8956 NP_001070868 Q73K not found in SNVbox database
733 NP_705833 S923N not found in SNVbox database
1299 NP_705833 D648Y not found in SNVbox database
3165 NP_705833 R163S not found in SNVbox database
4958 NP_001070868 P770L not found in SNVbox database
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr19:58862931 G>A maps to NM_130786.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:52595902 G>A maps to NM_138932.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:52595939 G>T maps to NM_138932.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:52570797 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:52595981 G>T maps to NM_138932.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:52566548 G>T maps to NM_138932.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:9254153 A>G maps to NM_000014.4 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:9265065 C>A maps to NM_000014.4 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:9243003 G>T maps to NM_000014.4 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:9247575 A>G maps to NM_000014.4 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:9225332 G>A maps to NM_000014.4 R1297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:9223110 G>A maps to NM_000014.4 F1389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:9227194 C>T maps to NM_000014.4 T1239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:9265015 G>T maps to NM_000014.4 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:9246089 C>T maps to NM_000014.4 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr12:9229526 A>G maps to NM_000014.4 P1119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr12:9232241 G>C maps to NM_000014.4 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:9020487 C>T maps to NM_144670.3 Y1256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:8990108 C>T maps to NM_144670.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:9002849 C>T maps to NM_144670.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:8976425 G>A maps to NM_144670.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:8988857 G>A maps to NM_144670.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:9008103 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:8998739 G>A maps to NM_144670.3 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:9000180 G>T maps to NM_144670.3 G574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:9020499 G>A maps to NM_144670.3 E1260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr12:8988221 T>C maps to NM_144670.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:43089669 G>A maps to NM_017436.4 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr3:137843366 G>A maps to NM_016161.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr12:53708532 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr12:125570873 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:125626750 C>T maps to NM_023928.3 D665D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr3:151545953 T>C maps to NM_001086.2 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:151532027 C>T maps to NM_001086.2 N26N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JS-01A-11D-A10B-09 chr3:151545848 G>A maps to NM_001086.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:151545575 G>T maps to NM_001086.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:151538231 A>G maps to NM_001086.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:151538225 C>T maps to NM_001086.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:151458472 G>T maps to NM_207365.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:151475238 C>T maps to NM_207365.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:12785476 G>A maps to NM_001103170.1 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:12785380 G>A maps to NM_001103170.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:67495182 G>A maps to NM_024666.3 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:67528764 G>A maps to NM_024666.3 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr15:67524164 T>A maps to NM_024666.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:67528842 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:69732722 C>T maps to NM_014911.3 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:69757230 C>T maps to NM_014911.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:70316687 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr16:70295026 G>A maps to ENST00000418685 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:70310907 G>A maps to ENST00000418685 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr16:70305778 G>A maps to ENST00000418685 Y200Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A056-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:44275059 G>A maps to NM_020745.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:44279876 G>A maps to NM_020745.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:41108274 G>A maps to NM_001136042.2 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:41102657 C>T maps to NM_001136042.2 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:57244432 G>A maps to NM_181806.2 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:57250507 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:57219672 A>T maps to NM_181806.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:57244366 C>T maps to NM_181806.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr4:57211379 A>G maps to NM_181806.2 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr4:57250441 A>G maps to NM_181806.2 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:57215479 G>A maps to NM_181806.2 R813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:57220219 A>G maps to NM_181806.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:57221513 G>A maps to NM_181806.2 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:105950306 G>A maps to NM_015423.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:105967582 C>T maps to NM_015423.2 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:105950306 G>A maps to NM_015423.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:105950306 G>A maps to NM_015423.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:105950306 G>A maps to NM_015423.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:105967613 C>T maps to NM_015423.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:121716599 C>T maps to NM_005763.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:121766507 A>G maps to NM_005763.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:121756942 G>A maps to NM_005763.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:121773657 C>T maps to NM_005763.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:121773639 G>T maps to NM_005763.3 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:8873371 C>T maps to NM_001127448.1 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:8873424 C>T maps to NM_001127448.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:107618266 C>A maps to ENST00000423487 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:107645371 C>T maps to NM_005502.3 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:107593328 C>T maps to NM_005502.3 W590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:107584856 G>A maps to NM_005502.3 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr9:107566904 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:107560836 G>T maps to NM_005502.3 I1662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:107548607 G>T maps to NM_005502.3 C2124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:107565590 C>T maps to NM_005502.3 K1522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr9:107602662 C>T maps to NM_005502.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:67190013 C>A maps to NM_080282.3 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:67186508 A>G maps to NM_080282.3 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:67145056 C>A maps to NM_080282.3 E1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:67160292 G>A maps to NM_080282.3 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:67212045 T>C maps to NM_080282.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:67217934 C>A maps to NM_080282.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:67197810 T>G did not map to a codon.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr17:67215690 T>C maps to NM_080282.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:67215827 C>A maps to NM_080282.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:215802257 C>T maps to NM_173076.2 L2506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:215854294 T>C maps to NM_173076.2 R1225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:215797378 T>C maps to NM_173076.2 Q2589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:215882814 C>A maps to NM_173076.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:215840738 C>T maps to NM_173076.2 E1717E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:215831577 G>A maps to NM_173076.2 R1960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:215855641 G>A maps to NM_173076.2 G1136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:215914499 T>G maps to NM_173076.2 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:215798867 C>T maps to NM_173076.2 L2538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:215882814 C>A maps to NM_173076.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:215884469 G>A maps to NM_173076.2 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr2:215848477 C>T maps to NM_173076.2 Q1425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:215884483 C>A maps to NM_173076.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:215910660 C>A maps to NM_173076.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr7:48450180 C>T maps to NM_152701.3 A4045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr7:48312403 C>T maps to NM_152701.3 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:48467391 C>T maps to NM_152701.3 N4163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:48237897 T>C maps to NM_152701.3 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:48619942 C>T maps to NM_152701.3 R4826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr7:48318113 G>A maps to NM_152701.3 L2441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:48528906 G>A maps to NM_152701.3 Q4419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:48314021 G>T maps to NM_152701.3 E1587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr7:48313303 T>C maps to NM_152701.3 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:48288847 A>G maps to NM_152701.3 E635E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:48411862 C>T maps to NM_152701.3 I3634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:48528846 G>A maps to NM_152701.3 Q4399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:48684217 G>A maps to NM_152701.3 Q4983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:48682990 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:48284223 G>A maps to NM_152701.3 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:48545930 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:48416036 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:48559827 G>A maps to NM_152701.3 S4663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:139916883 G>T maps to ENST00000355090 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:139917187 C>T maps to ENST00000355090 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:139909379 G>A maps to ENST00000355090 F1319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:139911976 G>A maps to ENST00000355090 Y823Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:139905963 G>A maps to ENST00000355090 F1928F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:139911722 G>A maps to ENST00000355090 Y856Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:139911707 G>A maps to ENST00000355090 Y861Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:139910598 T>C maps to ENST00000355090 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:2338039 G>T maps to NM_001089.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:2376013 G>A maps to NM_001089.2 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:2338189 G>T maps to NM_001089.2 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:2354116 G>A maps to NM_001089.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:2358562 G>A maps to NM_001089.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:2376200 G>A maps to NM_001089.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:2326767 G>A maps to NM_001089.2 G1674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:2358604 G>A maps to NM_001089.2 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr16:2354133 G>A maps to NM_001089.2 R435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:94488946 T>C maps to NM_000350.2 E1554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:94508377 G>T maps to NM_000350.2 T1089T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:94497501 G>A maps to NM_000350.2 C1320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:94505629 G>A maps to NM_000350.2 V1192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:94568672 G>T maps to NM_000350.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:94546151 G>A maps to NM_000350.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:94471007 C>A maps to NM_000350.2 E2046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:94548913 A>G maps to NM_000350.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:94502831 C>A maps to NM_000350.2 E1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:94508436 G>A maps to NM_000350.2 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:94526125 C>T maps to NM_000350.2 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:94497390 C>T maps to NM_000350.2 A1357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:67300807 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:67298915 C>T maps to ENST00000392677 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:67252411 C>T maps to ENST00000392677 T1249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:67310456 G>A maps to ENST00000392677 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:67298986 C>A maps to ENST00000392677 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:67257801 C>A maps to ENST00000392677 E1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:67251957 C>A maps to ENST00000392677 E1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:67293341 C>A maps to ENST00000392677 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:67111039 G>A maps to NM_080284.2 Q549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:67080433 C>T maps to NM_080284.2 T1441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:67101693 G>A maps to NM_080284.2 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:67109361 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:67101693 G>A maps to NM_080284.2 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:67119450 G>A maps to NM_080284.2 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:67077212 C>A maps to NM_080284.2 E1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:67083583 T>C maps to NM_080284.2 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:67082842 C>A maps to NM_080284.2 E1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:67094158 C>A maps to NM_080284.2 G1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:67079405 A>G maps to NM_080284.2 A1474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr17:67092822 G>A maps to NM_080284.2 F1080F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:1052031 C>T maps to NM_019112.3 C1018C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:1051162 G>T maps to NM_019112.3 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:1063823 G>A maps to NM_019112.3 V1971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:1044697 C>T maps to NM_019112.3 H390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:1058740 G>A maps to NM_019112.3 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:1056333 G>A maps to NM_019112.3 W1474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:1046291 C>T maps to NM_019112.3 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:1062224 C>T maps to NM_019112.3 S1875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:1041881 G>A maps to NM_019112.3 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:1043737 C>T maps to NM_019112.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:66937089 G>T maps to NM_007168.2 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr17:66881444 G>A maps to NM_007168.2 F1107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:66865862 T>C maps to NM_007168.2 Q1523Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:66872656 C>A maps to NM_007168.2 V1398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:66913551 C>T maps to NM_007168.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:66877281 G>A maps to NM_007168.2 D1299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:66920906 G>A maps to NM_007168.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:66878019 G>T maps to NM_007168.2 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:66902304 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr17:66924145 G>C maps to NM_007168.2 S395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:66898956 A>C maps to NM_007168.2 Y847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:66903978 G>T maps to NM_007168.2 S687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:66925271 G>T maps to NM_007168.2 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr17:66914188 C>T maps to NM_007168.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:66872632 G>T maps to NM_007168.2 T1406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:66865892 C>T maps to NM_007168.2 L1513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:67004273 G>A maps to NM_080283.3 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:67039670 C>T maps to NM_080283.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:66980227 G>A maps to NM_080283.3 R1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:67014721 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:67014665 G>A maps to NM_080283.3 Y885Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:87160738 G>T maps to NM_000927.3 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:87179870 C>T maps to NM_000927.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:87178785 G>A maps to NM_000927.3 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:87183157 G>T maps to NM_000927.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:87174270 G>T maps to NM_000927.3 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:87180118 A>G maps to NM_000927.3 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:87190588 C>A maps to NM_000927.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:87180058 G>T maps to NM_000927.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:87190588 C>A maps to NM_000927.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:87214996 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr7:87183162 G>A maps to NM_000927.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr7:87199539 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:87190588 C>A maps to NM_000927.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:87190703 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:87196105 A>G maps to NM_000927.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr7:87196161 G>A maps to NM_000927.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:87173567 G>T maps to NM_000927.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:229665985 T>G maps to NM_012089.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:229676433 G>A maps to NM_012089.2 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr2:169853171 G>A maps to NM_003742.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:169825857 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:169853230 A>G maps to NM_003742.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:169825989 A>G maps to NM_003742.2 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:169842772 G>A maps to NM_003742.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:169792838 C>T maps to NM_003742.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:169781177 C>A maps to NM_003742.2 E1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:87031456 G>T maps to NM_018849.2 I1272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:87079293 C>A maps to NM_018849.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:87053308 C>T maps to NM_018849.2 W708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:87080989 C>T maps to NM_018849.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:87083906 C>A maps to NM_018849.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:87032584 T>A maps to NM_018849.2 R1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:87043014 C>A maps to NM_018849.2 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:87035618 G>A maps to NM_018849.2 I1164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:87073032 C>A maps to NM_018849.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:87069126 T>C maps to NM_018849.2 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:87092220 G>A maps to NM_018849.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr7:87031486 C>A maps to NM_018849.2 T1262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:20685492 G>T maps to NM_001163941.1 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:20778695 G>A maps to NM_001163941.1 A986A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:20782534 C>A maps to NM_001163941.1 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:20795202 C>T maps to NM_001163941.1 R1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:20698247 G>A maps to NM_001163941.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:20762821 G>T maps to NM_001163941.1 E869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:20682909 C>T maps to NM_001163941.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:20698710 G>T maps to NM_001163942.1 *132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:20685504 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:20767946 G>A maps to NM_001163941.1 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:20792981 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr2:220077768 G>A maps to NM_005689.2 D608D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr2:220079779 G>A maps to NM_005689.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr2:220082511 C>T maps to NM_005689.2 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr2:220074722 C>T maps to NM_005689.2 W822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:74334620 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:74273294 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:74282220 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:74334631 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:74284922 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:74293701 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr23:74282206 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:74291396 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:74291497 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:74376053 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:74284991 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:74293779 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:74273407 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:74280153 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:74280062 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:74273248 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:74318804 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:74293594 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:74288926 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:74375953 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:74284961 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:74289196 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:150731000 C>T maps to ENST00000297504 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:150739067 G>A maps to ENST00000297504 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:150731003 G>T maps to ENST00000297504 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:150732673 C>T maps to ENST00000297504 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:123430706 G>T maps to NM_203444.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:123434458 A>G maps to NM_203444.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:123430616 G>A maps to NM_203444.2 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:16150073 G>A maps to ENST00000399408 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:16108482 G>T maps to ENST00000399408 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:16130427 G>A maps to ENST00000399408 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:16228313 C>T maps to ENST00000399408 I1368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr16:16101798 C>T maps to ENST00000399408 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr16:16165500 G>A maps to ENST00000399408 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:16162152 C>T maps to ENST00000399408 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr16:16232346 G>A maps to ENST00000399408 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr6:43410877 C>T maps to NM_033450.2 A771A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:43401088 G>A maps to NM_033450.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr6:43400812 C>T maps to NM_033450.2 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr16:48210868 G>A maps to NM_032583.3 H1168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:48258305 G>A maps to NM_032583.3 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:48247383 C>T maps to NM_032583.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:48258198 G>A maps to NM_032583.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:48230193 C>A maps to NM_032583.3 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:48249201 G>A maps to NM_032583.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr16:48221194 G>A maps to NM_032583.3 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:48248818 G>T maps to NM_032583.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:48247383 C>T maps to NM_032583.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:48145802 C>A maps to NM_033226.2 E670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:48180242 G>T maps to NM_033226.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:48121985 C>T maps to NM_033226.2 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:48180265 T>G maps to NM_033226.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:48139247 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:48149436 C>T maps to NM_033226.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:101578853 C>A maps to NM_000392.3 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:101579026 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:101590173 C>T maps to NM_000392.3 R911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:101590499 G>A maps to NM_000392.3 K925K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:101591776 C>T maps to NM_000392.3 F1049F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:101560265 C>T maps to NM_000392.3 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:101553751 C>A maps to NM_000392.3 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:101594171 C>A maps to NM_000392.3 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:101611294 C>T maps to NM_000392.3 C1515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:101594171 C>A maps to NM_000392.3 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:101560151 C>A maps to NM_000392.3 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr10:101591438 G>A maps to NM_000392.3 A985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:101559097 C>A maps to NM_000392.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:101569956 C>T maps to NM_000392.3 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:101603600 G>T maps to NM_000392.3 E1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:101610400 T>C maps to NM_000392.3 L1452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:48765055 C>T maps to NM_003786.3 I1480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:48733344 C>T maps to NM_003786.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:48736663 C>T maps to NM_003786.3 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:48753897 G>A maps to NM_003786.3 P1109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:48750846 G>A maps to NM_003786.3 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:48762137 C>T maps to NM_003786.3 D1394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:48738397 C>T maps to NM_003786.3 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:95686993 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:95829989 A>G maps to NM_005845.3 D566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr13:95847148 G>A maps to NM_005845.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:95723920 C>A maps to NM_005845.3 E1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:95847191 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:95673858 C>T maps to NM_005845.3 S1316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:95725483 G>A maps to NM_005845.3 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:95860132 C>A maps to NM_005845.3 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:95899261 A>C maps to NM_005845.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:183670984 A>G maps to NM_005688.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:183655743 G>A maps to NM_005688.2 R1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:183683247 G>A maps to NM_005688.2 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:183643384 C>T maps to NM_005688.2 T1390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:183700707 G>A maps to NM_005688.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:183669653 G>A maps to NM_005688.2 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:183706370 C>A maps to NM_005688.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:183689356 G>T maps to NM_005688.2 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:183667836 G>A maps to NM_005688.2 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:16308294 G>A maps to NM_001171.5 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:16278844 C>T maps to NM_001171.5 W638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr16:16308267 G>C maps to NM_001171.5 Y171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr16:16315595 G>C maps to NM_001171.5 Y43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:16302654 C>A maps to NM_001171.5 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:16281022 C>A maps to NM_001171.5 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:16302654 C>A maps to NM_001171.5 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:16315586 G>A maps to NM_001171.5 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:16253383 G>A maps to NM_001171.5 I1230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:16313416 G>A maps to NM_001171.5 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr16:16284062 G>C maps to NM_001171.5 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:17464342 G>A maps to ENST00000302539 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:17470188 C>T maps to ENST00000302539 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:17483201 G>A maps to ENST00000302539 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:17414606 G>A maps to ENST00000302539 F1560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:17418492 G>A maps to ENST00000302539 H1364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:17452500 G>A maps to ENST00000302539 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:17430061 G>T maps to ENST00000302539 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:17414606 G>A maps to ENST00000302539 F1560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:17417468 G>T maps to ENST00000302539 I1377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:17419335 G>A maps to ENST00000302539 I1255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:22035734 G>A maps to NM_005691.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:22059084 G>T maps to NM_005691.2 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:22028599 G>A maps to NM_005691.2 R694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:22001137 G>A maps to NM_005691.2 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:22078906 G>A maps to NM_005691.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr12:22015984 C>T maps to NM_005691.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:21962846 G>T maps to NM_005691.2 L1418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:22035765 G>A maps to NM_005691.2 H651H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr12:21997467 G>A maps to NM_005691.2 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153001833 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152991483 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152991505 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153006138 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153001659 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153002665 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:152991291 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:152991070 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:152991285 C>T did not map to a codon.
Sequencing variant TCGA-BG-A186-01A-11D-A12J-09 chr23:152990933 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:153005560 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152991458 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152991235 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152991540 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153005555 G>A did not map to a codon.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr23:152991141 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:153001624 C>T did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:152991297 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:40013123 T>C maps to NM_005164.3 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:39967519 A>G maps to NM_005164.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:39967591 G>A maps to NM_005164.3 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:40001402 C>A maps to NM_005164.3 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:40013024 G>A maps to NM_005164.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:39979984 G>A maps to NM_005164.3 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:39998579 G>A maps to NM_005164.3 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:40013227 C>A maps to NM_005164.3 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:94964527 C>T maps to ENST00000454898 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:94972192 C>T maps to ENST00000454898 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:94972161 C>T maps to ENST00000454898 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:94955468 A>G maps to ENST00000454898 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:74757033 G>T maps to NM_005050.3 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr14:74759862 G>A maps to NM_005050.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:74753135 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:74764640 G>A maps to NM_005050.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:146031298 T>G maps to NM_002940.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:146038504 C>T maps to NM_002940.2 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:146025660 C>T maps to NM_002940.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:30548196 C>T maps to NM_001025091.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:30553418 C>T maps to NM_001025091.1 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:150921084 A>G maps to NM_005692.3 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:150923468 C>A maps to NM_005692.3 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:150912715 G>A maps to NM_005692.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:183905931 A>G maps to NM_018358.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:183908822 C>T maps to NM_018358.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:183905736 C>T maps to NM_018358.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:43714662 C>T maps to NM_004915.3 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:43702514 C>T maps to NM_004915.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:43708137 C>A maps to NM_004915.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:89036121 T>C maps to NM_004827.2 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:89061129 G>A maps to NM_004827.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:89052331 C>A maps to NM_004827.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:89060952 C>T maps to NM_004827.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr4:89052284 C>T maps to NM_004827.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr4:89028403 G>C maps to NM_004827.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:44104811 G>A maps to NM_022437.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:44099403 G>A maps to NM_022437.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:44102301 G>A maps to NM_022437.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr2:44078855 C>T maps to NM_022437.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:44099148 G>A maps to NM_022437.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr2:44100947 C>T maps to NM_022437.2 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:44078819 G>A maps to NM_022437.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27351352 G>A maps to NM_032604.3 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:111705215 G>A maps to NM_018394.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:111710294 C>T maps to NM_018394.2 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:73152786 A>G maps to NM_148912.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr7:73150871 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr7:73151834 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:25290080 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:25282982 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:51352568 T>C maps to ENST00000337334 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:51345505 G>A maps to ENST00000337334 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:108882198 A>G maps to NM_032859.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52014986 C>T maps to NM_015407.4 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:52012370 C>T maps to ENST00000463937 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:52003621 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:89738470 C>T maps to NM_152924.4 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:89719184 C>T maps to NM_152924.4 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr15:89738581 C>T maps to NM_152924.4 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:89694985 G>A maps to NM_152924.4 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:19231712 C>A maps to NM_138340.4 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:23078708 C>T maps to NM_022060.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:23072379 C>T maps to NM_022060.2 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr14:23075424 C>T maps to NM_022060.2 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:43760008 C>T maps to NM_016006.4 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:58260448 C>T maps to NM_020676.5 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:58256756 G>A maps to NM_020676.5 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:58260421 G>A maps to NM_020676.5 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:58260448 C>T maps to NM_020676.5 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:17411870 G>A maps to NM_024527.4 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:27066125 A>G maps to NM_005470.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:27112186 G>T maps to NM_005470.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:27040683 T>C maps to NM_005470.3 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:27149699 G>A maps to NM_005470.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr10:27037651 T>C maps to NM_005470.3 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:204231626 G>T maps to ENST00000295851 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:204244966 G>T maps to ENST00000295851 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:204267368 G>A maps to ENST00000295851 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:204231626 G>T maps to ENST00000295851 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:47288151 C>T maps to NM_016428.2 N22N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:100617676 G>T maps to ENST00000471714 V137V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BG-A0M4-01A-11W-A10C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:100489770 C>T maps to ENST00000471714 K1510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:100621500 G>A maps to ENST00000471714 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:100470398 C>A maps to ENST00000471714 E1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr9:133759905 G>A maps to NM_007313.2 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:133730284 G>A maps to NM_007313.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:133755536 C>A maps to NM_007313.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:133730284 G>A maps to NM_007313.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:133730362 C>T maps to NM_007313.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:133750380 A>G maps to NM_007313.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:133738346 C>T maps to NM_007313.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:133748250 C>T maps to NM_007313.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr9:133760628 G>A maps to NM_007313.2 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:133747571 C>A maps to NM_007313.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:133748349 C>T maps to NM_007313.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:133750275 C>T maps to NM_007313.2 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:133760508 C>T maps to NM_007313.2 D963D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:179079564 G>A maps to NM_007314.3 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:179100500 G>A maps to NM_007314.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:179077239 C>T maps to NM_007314.3 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:179087846 G>A maps to NM_007314.3 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:179077835 C>A maps to NM_007314.3 G856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:116245084 G>A maps to ENST00000277895 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:116335206 G>A maps to ENST00000277895 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:116200818 G>A maps to ENST00000277895 F740F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:116233715 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:116335263 G>A maps to ENST00000277895 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:7986602 G>T maps to NM_001130083.1 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:7968818 C>T maps to NM_001130083.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:8062751 G>A maps to NM_001130083.1 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:8098872 C>T maps to NM_001130083.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:8037947 G>A maps to NM_001130083.1 I325I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A0JV-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr4:7968737 C>T maps to NM_001130083.1 K639K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:8010815 C>T maps to NM_001130083.1 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:8098905 G>A maps to NM_001130083.1 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:148577926 C>T maps to NM_014945.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:148586679 C>T maps to NM_014945.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:148577947 C>T maps to NM_014945.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:148577860 C>A maps to NM_014945.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:148627415 C>A maps to NM_014945.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:148630929 C>T maps to NM_014945.2 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:148619329 C>T maps to NM_014945.2 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:148610265 T>G maps to NM_014945.2 L271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:148563138 C>A maps to NM_014945.2 C46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:148577947 C>T maps to NM_014945.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:150554961 C>A maps to ENST00000416793 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr7:150554355 G>A maps to ENST00000416793 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:150553878 G>A maps to ENST00000416793 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:150555015 C>T maps to ENST00000416793 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:150555923 C>T maps to ENST00000416793 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:150554433 C>A maps to ENST00000416793 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:150558185 C>T maps to ENST00000416793 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:150557703 G>T maps to ENST00000416793 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr7:150555996 C>T maps to ENST00000416793 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:986861 G>A maps to NM_021962.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:915092 G>A maps to NM_021962.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr17:973326 G>A maps to NM_021962.2 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:915092 G>A maps to NM_021962.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:107781935 T>C maps to NM_139166.4 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:107782289 C>T maps to NM_139166.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:107782307 C>T maps to NM_139166.4 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:107782409 C>T maps to NM_139166.4 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr6:26598283 G>A maps to NM_013375.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:127399618 C>A maps to ENST00000361019 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:34184249 C>T maps to NM_145804.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:38167176 G>A maps to NM_001607.3 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:38164511 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:35578753 G>A maps to NM_198834.1 R1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:35518823 G>A maps to NM_198834.1 S1740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:35603864 G>T maps to NM_198834.1 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:35578753 G>A maps to NM_198834.1 R1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:35468471 G>A maps to NM_198834.1 R2187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:35656251 C>T maps to NM_198837.1 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:35600460 T>G maps to NM_198834.1 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:35564714 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:35538155 C>A maps to NM_198834.1 E1640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:35468546 C>A maps to NM_198834.1 E2162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:109678974 C>T maps to NM_001093.3 R1637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:109687840 C>T maps to NM_001093.3 L1908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:109703291 G>A maps to NM_001093.3 T2404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:109639481 C>T maps to NM_001093.3 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:109680381 G>A maps to NM_001093.3 P1721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:109644532 G>T maps to NM_001093.3 E978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:109696913 G>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:109617074 G>A maps to NM_001093.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:109704109 T>C maps to NM_001093.3 A2440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:109671822 G>A maps to NM_001093.3 P1440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:109702937 A>G maps to NM_001093.3 A2322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:109647013 G>A maps to NM_001093.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:109629525 C>T maps to NM_001093.3 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:109670596 C>T maps to NM_001093.3 F1375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:109692110 G>T maps to NM_001093.3 R2046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr12:109625925 G>A maps to NM_001093.3 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:109661651 C>T maps to NM_001093.3 D1275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:109703060 C>T maps to NM_001093.3 F2363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:109629662 G>A maps to NM_001093.3 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr12:109689901 C>T maps to NM_001093.3 R1948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:112174698 C>A maps to NM_001136538.1 Y566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:112167691 G>A maps to NM_001136538.1 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:112150334 G>T maps to NM_001136538.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:112191643 G>A maps to NM_001136538.1 Q993Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr3:132280028 G>A maps to NM_032169.4 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:132294650 G>A maps to NM_032169.4 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:132361546 C>A maps to NM_032169.4 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr3:132345593 G>A maps to NM_032169.4 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:134128474 C>A maps to NM_014384.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:134128971 C>A maps to NM_014384.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:134127028 C>T maps to NM_014384.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:134127028 C>T maps to NM_014384.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:128627080 C>T maps to NM_014049.4 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:128628221 C>A maps to NM_014049.4 C507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:128614259 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:128612492 G>T maps to NM_014049.4 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:128622957 G>T maps to NM_014049.4 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:128627036 G>T maps to NM_014049.4 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:211057553 T>C maps to NM_001608.3 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:211060040 C>A maps to NM_001608.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:211081231 A>C maps to NM_001608.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:211070472 C>A maps to NM_001608.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:211082809 C>A maps to NM_001608.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:211085455 G>T maps to NM_001608.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:211085513 G>A maps to NM_001608.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:76215150 C>T maps to ENST00000370834 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:76215150 C>T maps to ENST00000370834 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:76215150 C>T maps to ENST00000370834 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:121176213 C>T maps to NM_000017.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:124800182 G>T maps to NM_001609.3 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:124800005 G>T maps to NM_001609.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:124802674 C>T maps to NM_001609.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:124813265 C>T maps to NM_001609.3 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:124802674 C>T maps to NM_001609.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr10:124802659 C>A maps to NM_001609.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr17:7124095 G>T maps to ENST00000356839 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr17:7124100 G>A maps to ENST00000356839 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:7124897 C>T maps to ENST00000356839 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:89382101 C>T maps to NM_013227.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:89402265 C>T maps to NM_013227.3 S2150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:89402148 C>T maps to NM_013227.3 F2111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:89401938 C>T maps to NM_013227.3 F2041F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:89382239 C>T maps to NM_013227.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:89401707 C>T maps to NM_013227.3 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:89390594 C>T maps to NM_013227.3 Y517Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:89415279 C>T maps to NM_013227.3 I2384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr15:89398455 T>C maps to NM_013227.3 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:89385081 C>T maps to NM_013227.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:89402034 C>A maps to NM_013227.3 V2073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:7247263 C>T maps to NM_014716.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr17:7240104 C>T maps to NM_014716.3 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:7252363 C>T maps to NM_014716.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:195009959 C>T maps to NM_012287.5 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:195027950 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:1239516 G>T maps to NM_030649.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr1:1231486 C>G maps to NM_030649.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:1239504 C>T maps to NM_030649.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:108004961 G>T maps to NM_000019.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:226340194 G>A maps to NM_022735.3 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:226342429 T>C maps to NM_022735.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:43214118 T>C maps to NM_001135706.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:43214438 C>T maps to NM_001135706.1 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:27486316 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:27529611 G>T maps to NM_145698.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:27507112 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr10:27504517 G>A maps to ENST00000375888 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:180399324 C>A maps to NM_032360.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:15120969 C>A maps to NM_001039844.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:15120582 C>T maps to NM_001039844.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr10:15120549 C>G maps to NM_001039844.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:44097137 C>T maps to NM_032592.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:44100310 G>A maps to NM_032592.3 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:44069846 G>A maps to NM_001031854.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:44070017 C>T maps to NM_001031854.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr11:44073240 C>T maps to NM_001031854.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr17:61557755 C>T maps to NM_000789.3 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:61560409 C>T maps to NM_000789.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr17:61564378 C>A maps to NM_000789.3 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:61568596 G>T maps to NM_000789.3 E923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr17:61566371 G>A maps to NM_000789.3 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15593793 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15599496 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15609836 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:15605981 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:15607505 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:15607551 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:15618919 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:15584440 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:15610399 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:15589778 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:15609912 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:15610407 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:15599407 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:15618956 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:15596252 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:15580121 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15580080 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15589783 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15599471 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:15603679 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:15582153 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:15589852 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:15596383 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr9:19446223 G>A maps to ENST00000380376 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:19450630 G>A maps to NM_001010887.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:76637711 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:76709842 C>T maps to NM_018367.5 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:76696755 A>G maps to NM_018367.5 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:100490016 C>T maps to NM_000665.3 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:100490136 G>A maps to NM_000665.3 Y457Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:100490886 C>A maps to NM_000665.3 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:100491460 G>A maps to NM_000665.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr14:23549518 G>C maps to NM_014977.3 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:23549595 T>G maps to NM_014977.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:23528628 G>A maps to NM_014977.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:23548097 G>A maps to NM_014977.3 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:40024152 G>A maps to ENST00000401700 H1116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:40025729 C>T maps to ENST00000401700 S1060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:40028377 G>A maps to ENST00000401700 H944H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:40061038 C>T maps to ENST00000401700 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:40063715 G>A maps to ENST00000401700 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr17:40065316 G>A maps to ENST00000401700 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:40025821 G>A maps to ENST00000401700 R1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:40058047 G>A maps to ENST00000401700 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:135655981 C>A maps to NM_138326.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:135596288 G>T maps to NM_138326.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:32427335 C>T maps to NM_002197.2 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:32407314 G>T maps to NM_002197.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:32405566 C>T maps to NM_002197.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr9:32436331 C>T maps to NM_002197.2 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:32448913 C>T maps to NM_002197.2 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr9:32425906 T>C maps to NM_002197.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:32419039 C>T maps to NM_002197.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr9:32420963 C>T maps to NM_002197.2 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr9:32431733 C>T maps to NM_002197.2 Q582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:32436295 C>T maps to NM_002197.2 D716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr9:32449009 C>T maps to NM_002197.2 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:41903959 C>T maps to ENST00000396512 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:41919216 C>A maps to ENST00000396512 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:41920899 C>T maps to ENST00000396512 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:55050491 C>T maps to NM_015547.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:55069558 C>A maps to NM_015547.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:55066959 C>T maps to NM_015547.3 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:80655778 G>A maps to NM_130767.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:80655778 G>A maps to NM_130767.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:80681610 G>A maps to NM_130767.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:80655818 A>G maps to NM_130767.2 D133D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:80655778 G>A maps to NM_130767.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr5:80639994 G>A maps to NM_130767.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:80681625 A>C maps to NM_130767.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:24701830 C>T maps to NM_018473.3 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:24698280 C>T maps to NM_018473.3 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:74086503 T>C maps to NM_001037162.1 H195H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:6324685 G>A maps to NM_007274.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:6399559 C>T maps to NM_007274.3 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:6341326 C>T maps to NM_007274.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:44483899 G>A maps to NM_005469.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr20:44472334 G>A maps to NM_005469.3 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:23723960 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:23740814 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:23748996 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:23722830 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:23740087 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:23724805 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:23748961 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:73951751 A>G maps to NM_004035.6 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:73945863 C>T maps to NM_004035.6 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:58503000 G>A maps to NM_003500.3 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:58494664 G>A maps to NM_003500.3 Y646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:58519172 G>A maps to NM_003500.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr3:58510220 T>G maps to NM_003500.3 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:58519751 G>A maps to NM_003500.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:8417629 G>A maps to NM_003501.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:8375308 G>A maps to NM_003501.2 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:111551654 G>A maps to NM_001142807.1 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:111551708 G>A maps to NM_001142807.1 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr2:272205 C>T maps to NM_007099.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:277001 C>T maps to NM_004300.3 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:277494 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr2:277453 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:47266891 C>T maps to NM_001610.2 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:11687195 G>A maps to NM_001111036.1 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:11687970 G>A maps to NM_001111036.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:11686046 G>A maps to NM_001111036.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr19:11687261 G>A maps to NM_001111036.1 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:147119275 G>T maps to NM_016361.3 Y412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:147127349 G>A maps to NM_016361.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:147131809 C>T maps to NM_016361.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:141006294 G>T maps to NM_001037172.1 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:140979094 C>T maps to NM_001037172.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:141011815 C>A maps to NM_001037172.1 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr3:141011335 C>T maps to NM_001037172.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:141012038 G>T maps to NM_001037172.1 G479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr3:132061394 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:132068845 G>A maps to NM_001134194.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:51297163 C>A maps to NM_033068.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr22:51183295 G>A maps to NM_001097.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:51178319 G>A maps to NM_001097.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:6749282 G>T maps to NM_032489.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:6747494 G>A maps to NM_032489.2 R529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70823881 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70825569 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70832292 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:70814208 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70823820 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70830601 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70817886 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:70830620 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70830564 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:70817886 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:70823891 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:70823606 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr23:70823594 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:70823633 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70823683 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:70823865 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70823851 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:70823555 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:125542516 G>A maps to NM_001612.5 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:125542516 G>A maps to NM_001612.5 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:78486359 G>A maps to NM_015162.4 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:78474355 G>A maps to NM_015162.4 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:78487060 C>T maps to NM_015162.4 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:78486901 G>T maps to NM_015162.4 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:78500374 C>T maps to NM_015162.4 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:78486970 G>A maps to NM_015162.4 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr19:6166025 C>T maps to NM_030924.3 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:6185663 G>T maps to NM_030924.3 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:48549865 C>T maps to ENST00000427954 C492C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr17:48539804 C>T maps to ENST00000427954 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:89211712 C>T maps to NM_174917.2 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:185724530 C>T maps to NM_001995.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:185724637 G>A maps to NM_001995.2 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:185724637 G>A maps to NM_001995.2 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:185678787 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:223786112 T>C maps to NM_203372.1 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A052-01A-11W-A027-09 chr23:108911503 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:108906586 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:108924259 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:108887276 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:108921594 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:108924574 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:108926118 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:108911346 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:108912396 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:108921508 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:108912312 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:108921508 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:108926519 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:108926399 T>G did not map to a codon.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr23:108926598 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:108924604 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:108904759 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:108924303 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:108926377 T>C did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:108908698 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:108924309 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:108902741 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:108926473 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:114181349 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:114181415 G>A maps to NM_016234.3 W516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:131323839 T>C maps to NM_001009185.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:131309042 G>A maps to NM_001009185.1 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr5:131305833 G>A maps to NM_001009185.1 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:20693783 C>T maps to NM_052956.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr16:20648123 T>C maps to NM_052956.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:20696602 G>A maps to NM_052956.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:20648755 G>T maps to NM_052956.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:20696722 C>T maps to NM_052956.2 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr16:20634894 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:20635480 C>T maps to NM_052956.2 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:20480840 C>A maps to NM_001010845.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:20476852 C>T maps to NM_001010845.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:20476999 G>T maps to NM_001010845.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:20559729 C>T maps to NM_182617.3 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:20554316 C>A maps to NM_182617.3 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:20559406 C>A maps to NM_182617.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MU-01A-11D-A13L-09 chr16:20552095 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:20576006 C>T maps to NM_182617.3 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:20565100 A>G maps to NM_182617.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr16:20793080 C>T maps to NM_005622.3 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:20803440 T>C maps to NM_005622.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:20807742 G>T maps to NM_005622.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr16:20803421 A>G maps to NM_005622.3 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:7459136 G>A maps to NM_001080454.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr12:7469831 G>A maps to NM_001080454.1 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:20451736 G>A maps to NM_017888.2 E576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:20432619 C>T maps to NM_017888.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:20441036 G>T maps to NM_017888.2 G347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:20451725 C>T maps to NM_017888.2 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:25038444 G>A maps to NM_032501.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr20:24988466 G>A maps to NM_032501.2 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:81536890 G>A maps to NM_024560.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:229568513 C>T maps to NM_001100.3 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:229568140 G>A maps to NM_001100.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:229568847 G>A maps to NM_001100.3 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:229568856 G>A maps to NM_001100.3 C2C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:229568068 G>T maps to NM_001100.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:90695021 G>A maps to NM_001141945.1 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:90699345 G>A maps to NM_001141945.1 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr10:90707052 C>A maps to NM_001141945.1 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:56778213 G>A maps to NM_001017992.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:56778159 G>A maps to NM_001017992.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:56778459 G>A maps to NM_001017992.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:56777903 G>A maps to NM_001017992.2 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:35086973 G>A maps to NM_005159.4 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:35084452 C>A maps to NM_005159.4 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:74140687 C>A maps to NM_001615.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:179294016 T>G maps to NM_004301.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:100243895 G>A maps to NM_016188.4 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:111625339 C>T maps to NM_006687.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:111625021 C>T maps to NM_006687.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr9:111625558 G>A maps to NM_006687.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:111617181 G>A maps to NM_006686.3 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:18149619 G>A maps to NM_030812.2 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:18152998 G>A maps to NM_030812.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:18149829 G>A maps to NM_030812.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:8808403 G>A maps to NM_178525.3 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:8808364 G>A maps to NM_178525.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:8808271 G>A maps to NM_178525.3 Y260Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:69351508 G>A maps to NM_001130004.1 R493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:69392371 A>G maps to NM_001130004.1 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:69351508 G>A maps to NM_001130004.1 R493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:69343942 A>G maps to NM_001130004.1 F814F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:69360389 G>A maps to NM_001130004.1 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:69352155 G>A maps to NM_001130004.1 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:69360389 G>A maps to NM_001130004.1 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr14:69343804 C>T maps to NM_001130004.1 G860G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:69352206 G>A maps to NM_001130004.1 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:236889311 C>T maps to NM_001103.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:236907956 C>T maps to NM_001103.2 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:236920784 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:236902682 C>T maps to NM_001103.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:236900490 G>T maps to NM_001103.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:236906323 G>A maps to NM_001103.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:66318768 C>T maps to NM_001104.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:66322637 C>T maps to NM_001104.1 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:66323622 G>T maps to NM_001104.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:66325541 C>T maps to NM_001104.1 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:66325337 C>T maps to NM_001104.1 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr11:66323649 C>A maps to NM_001104.1 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr11:66319006 C>T maps to NM_001104.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:39214888 G>A maps to NM_004924.3 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:39205119 C>T maps to NM_004924.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:39214894 C>T maps to NM_004924.3 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:39200066 C>T maps to NM_004924.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:39200066 C>T maps to NM_004924.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr19:39200921 C>T maps to NM_004924.3 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:39200066 C>T maps to NM_004924.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr10:104241857 G>A maps to NM_005736.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:104247942 G>T maps to NM_005736.3 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:98275066 T>C maps to NM_005735.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:98274436 G>A maps to NM_005735.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:65473785 G>A maps to NM_001005386.2 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:114699798 G>T maps to NM_005721.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr7:152513582 G>A maps to NM_020445.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:152550658 G>A maps to NM_020445.4 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:149992432 C>A maps to ENST00000478393 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:37378855 G>A maps to NM_024855.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:37380857 C>T maps to NM_024855.3 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:37380812 A>G maps to NM_024855.3 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:100613874 C>T maps to NM_022496.3 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:100601503 G>T maps to NM_022496.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:53907117 G>A maps to NM_022899.4 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:53907173 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:53911279 C>T maps to NM_022899.4 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:53904044 T>C maps to NM_022899.4 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:127185530 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:127186017 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:127185630 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:127185733 A>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:127185927 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:127185113 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:127185452 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:127185348 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:127185675 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:127185621 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:127185067 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:127185240 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:127185681 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:127185803 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:127185477 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:127185446 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:2938642 C>T maps to NM_080431.4 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:2938675 G>A maps to NM_080431.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:2938954 G>A maps to NM_080431.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:2938642 C>T maps to NM_080431.4 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr2:158622505 G>T maps to NM_001111067.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:52369208 C>T maps to NM_020328.3 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:158412761 C>T maps to NM_145259.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:148676060 G>T maps to NM_001616.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:148684828 G>T maps to NM_001616.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:38518940 C>T maps to NM_001106.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:38524663 C>T maps to NM_001106.3 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:52309862 C>T maps to NM_001077401.1 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52308355 C>T maps to NM_001077401.1 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52312772 C>T maps to NM_001077401.1 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:52309937 C>T maps to NM_001077401.1 C389C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr12:52309847 C>T maps to NM_001077401.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:52307090 C>T maps to NM_001077401.1 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:52019950 C>T maps to ENST00000463937 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:52022997 G>A maps to ENST00000463937 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:52019950 C>T maps to ENST00000463937 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:67412588 C>T maps to NM_080658.1 L187L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BS-A0UV-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:54342822 G>A maps to ENST00000303536 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:54531899 C>A maps to NM_138448.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:43252947 C>T maps to NM_000022.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:43257797 G>A maps to NM_000022.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:43255233 G>A maps to NM_000022.2 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr20:43251281 C>T maps to NM_000022.2 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:43248477 G>T maps to NM_000022.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:123336625 T>C maps to NM_139243.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:123350879 C>T maps to NM_139243.3 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:123342497 G>T maps to NM_139243.3 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:84228702 C>T maps to NM_139174.3 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:84228741 C>T maps to NM_139174.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:43627325 A>G maps to ENST00000422466 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:43644043 G>A maps to ENST00000422466 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:43632483 G>T maps to ENST00000422466 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:43643137 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr15:43632500 C>T maps to ENST00000422466 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:58919935 G>A maps to NM_001110.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:42848998 G>A maps to NM_002390.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:127782690 G>A maps to NM_003474.4 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:127806765 G>A maps to NM_003474.4 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:127753528 G>A maps to NM_003474.4 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr10:127738176 G>A maps to NM_003474.4 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:127967503 G>T maps to NM_003474.4 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:127731687 G>A maps to NM_003474.4 C678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:127789753 G>A maps to NM_003474.4 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:155026792 C>A maps to NM_207197.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:155034728 G>A maps to NM_207197.1 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:155025153 T>C maps to NM_207197.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:155031239 C>T maps to NM_207197.1 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:155025093 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr1:155032819 G>A did not map to a codon.
Sequencing variant TCGA-BG-A186-01A-11D-A12J-09 chr1:155030436 C>T maps to NM_207197.1 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:155031200 C>T maps to NM_207197.1 R645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:9658086 G>T maps to NM_003183.4 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:9650167 G>A maps to NM_003183.4 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:9633092 G>A maps to NM_003183.4 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr2:9676878 G>A maps to NM_003183.4 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:9666373 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:39587421 C>A maps to NM_014237.2 S728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:156946857 G>A maps to ENST00000430702 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:156916127 C>T maps to ENST00000430702 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:156918707 G>A maps to ENST00000430702 C672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr5:156926670 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:156916127 C>T maps to ENST00000430702 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:156917388 G>A maps to ENST00000430702 C725C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:39607212 A>G maps to NM_001464.3 C616C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:39682416 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:39624517 G>A maps to NM_001464.3 C452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr14:70991180 C>T maps to NM_003814.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:70989380 G>A maps to NM_003814.4 C748C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:70990645 C>A maps to NM_003814.4 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:70925691 C>T maps to NM_003813.2 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:70924524 C>A maps to NM_003813.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:70925424 C>A maps to NM_003813.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr14:70926270 G>A maps to NM_003813.2 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:70925032 G>T maps to NM_003813.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr7:87759713 T>C maps to NM_021723.3 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:87797452 T>C maps to NM_021723.3 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr7:87759746 G>A maps to NM_021723.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr7:87810895 C>T maps to NM_021723.3 R829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:87808309 C>T maps to NM_021723.3 D787D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr2:207431959 C>T maps to NM_003812.2 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:207425918 G>T maps to NM_003812.2 G413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:207426961 G>A maps to NM_003812.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:207425918 G>T maps to NM_003812.2 G413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:207437916 C>T maps to NM_003812.2 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:207310143 G>T maps to NM_003812.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:24167699 G>A maps to NM_014265.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:24168891 G>T maps to NM_014265.4 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:24190189 C>T maps to NM_014265.4 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:175897576 G>T maps to NM_014269.4 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:175897113 A>G maps to NM_014269.4 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:175897857 C>A maps to NM_014269.4 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:175898313 C>A maps to NM_014269.4 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:175897842 A>G maps to NM_014269.4 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:175898247 G>A maps to NM_014269.4 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:175898601 C>T maps to NM_014269.4 C642C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:175897707 G>A maps to NM_014269.4 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:120437090 G>A maps to NM_021794.2 C623C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:120437438 G>A maps to NM_021794.2 C507C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:120437795 A>G maps to NM_021794.2 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:39114856 T>C maps to NM_145004.5 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:39007371 G>A maps to NM_145004.5 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr8:39044507 C>T maps to NM_145004.5 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:39022344 T>C maps to NM_145004.5 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:3654719 G>A maps to NM_025220.2 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:3655270 G>A maps to NM_025220.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:3657790 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:3655726 C>A maps to NM_025220.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:3653228 G>A maps to NM_025220.2 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:24349555 T>C maps to ENST00000380789 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:24349525 A>G maps to ENST00000380789 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:24359043 G>A maps to ENST00000380789 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:24324410 G>A maps to ENST00000380789 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:24339741 G>T maps to ENST00000380789 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:24348346 T>C maps to ENST00000380789 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:24365000 A>G maps to ENST00000380789 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:24300064 A>G maps to ENST00000380789 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:24349611 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:38940233 A>G maps to NM_003816.2 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr8:38874738 G>T maps to NM_003816.2 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr8:38934902 C>T maps to NM_003816.2 N618N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:24254846 G>T maps to NM_014479.3 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:24254939 C>T maps to NM_014479.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:28214690 C>T maps to NM_006988.3 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr21:28214980 G>A maps to NM_006988.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:8651355 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:8656852 G>A maps to NM_030957.2 C574C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:8661264 G>A maps to NM_030957.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:8661279 G>A maps to NM_030957.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr19:8662204 A>G maps to ENST00000393912 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:8651766 G>T maps to NM_030957.2 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:8670208 G>A maps to NM_030957.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:8650066 G>A maps to NM_030957.2 C997C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:33549440 G>A maps to NM_030955.2 C1391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:33576173 G>A maps to NM_030955.2 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:33649717 G>A maps to NM_030955.2 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:33624432 G>A maps to NM_030955.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:33662040 G>A maps to NM_030955.2 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:33576215 G>A maps to NM_030955.2 Y1305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:33624432 G>A maps to NM_030955.2 I682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:33751443 T>G maps to ENST00000515401 *233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:33662040 G>A maps to NM_030955.2 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:33577168 G>A maps to NM_030955.2 R988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:33751563 G>A maps to NM_030955.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:33683134 G>A maps to NM_030955.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:136305567 G>T maps to NM_139025.3 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:136289597 C>T maps to NM_139025.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:136310113 G>T maps to NM_139025.3 E851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:136298547 A>G maps to NM_139025.3 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:136279646 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:136324374 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:136324375 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:136324416 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:136324375 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:136305612 C>A maps to NM_139025.3 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:136324375 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:136303391 C>T maps to NM_139025.3 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:136323209 C>T maps to NM_139025.3 Y1357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:136295130 G>A maps to NM_139025.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr9:136308625 G>T maps to NM_139025.3 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:72520227 C>T maps to NM_139155.2 A1100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:72511869 C>T maps to NM_139155.2 Y875Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:72517719 C>A maps to NM_139155.2 C983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr10:72520506 C>T maps to NM_139155.2 G1193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:72509659 C>A maps to NM_139155.2 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:72518041 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:72520512 T>A maps to NM_139155.2 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:72494963 C>T maps to NM_139155.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:130332036 G>T maps to NM_139055.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:5191885 C>T maps to NM_139056.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:5235132 G>A maps to NM_139056.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr5:5239989 C>T maps to NM_139056.2 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:5262857 G>A maps to NM_139056.2 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr5:5319208 C>T maps to NM_139056.2 Y1211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:5306691 C>T maps to NM_139056.2 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:5306618 C>A maps to NM_139056.2 C1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr5:5146569 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:5239869 C>A maps to NM_139056.2 Y785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:5242272 G>A maps to NM_139056.2 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:5239953 C>T maps to NM_139056.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:5146498 C>T maps to NM_139056.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:5191796 G>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr15:100533336 G>A maps to NM_139057.2 C955C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:100533342 C>T maps to NM_139057.2 G953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:100594182 G>A maps to NM_139057.2 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:100801733 G>A maps to NM_139057.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:100802580 C>T maps to NM_139057.2 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:100801715 C>T maps to NM_139057.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:100533312 G>A maps to NM_139057.2 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:100636641 C>A maps to NM_139057.2 E686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:100801759 G>A maps to NM_139057.2 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:77326996 C>T maps to NM_199355.2 Q1055Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:77331220 C>T maps to NM_199355.2 E922E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:77353781 G>A maps to NM_199355.2 Y832Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:77398189 T>C maps to NM_199355.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:77401473 G>A maps to NM_199355.2 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:77359871 G>A maps to NM_199355.2 N641N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:129037264 G>T maps to NM_133638.3 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:129001190 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:129030516 C>T maps to NM_133638.3 R969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:128990095 A>G maps to NM_133638.3 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:128983477 T>C maps to NM_133638.3 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:129072811 G>C maps to NM_133638.3 V1175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:128862050 G>T maps to NM_133638.3 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:128864278 G>T maps to NM_133638.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:128983472 G>T maps to NM_133638.3 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:129070707 T>C maps to NM_133638.3 C1126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:178556935 A>C maps to NM_014244.4 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:178540981 G>A maps to NM_014244.4 V1174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:178559303 G>A maps to NM_014244.4 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:178580624 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:43777426 A>T maps to ENST00000389420 S1577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:43896194 C>T maps to ENST00000389420 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:43771263 A>C maps to ENST00000389420 V1633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:43833723 T>C maps to ENST00000389420 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr12:43944909 G>A maps to ENST00000389420 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:43884225 A>G maps to ENST00000389420 C363C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:43821125 G>A maps to ENST00000389420 Y1364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr12:43824175 A>G maps to ENST00000389420 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:43819314 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:43822566 G>C maps to ENST00000389420 R1175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:43833713 C>A maps to ENST00000389420 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:43884213 C>T maps to ENST00000389420 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:43887029 A>G maps to ENST00000389420 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:43896020 A>G maps to ENST00000389420 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:43944951 C>T maps to ENST00000389420 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:73184294 G>A maps to NM_014243.1 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr4:73414569 C>T maps to NM_014243.1 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:73185119 G>T maps to NM_014243.1 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:73169654 T>C maps to NM_014243.1 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:73433105 C>A maps to NM_014243.1 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:73280660 C>A maps to NM_014243.1 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:73175218 C>A maps to NM_014243.1 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:73185110 T>C maps to NM_014243.1 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:73186479 G>A maps to NM_014243.1 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:73149206 A>C maps to NM_014243.1 S1088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:161167853 G>A maps to NM_005099.4 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:161166069 G>A maps to NM_005099.4 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:161165327 A>G maps to NM_005099.4 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:28338344 C>T maps to NM_007038.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:28302266 G>A maps to NM_007038.3 C721C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:28296686 C>T maps to NM_007038.3 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:28302335 G>A maps to NM_007038.3 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:28296458 G>A maps to NM_007038.3 C902C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr21:28327085 G>A maps to NM_007038.3 H403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:64520823 A>G maps to NM_197941.2 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:64766673 A>G maps to NM_197941.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:64520822 G>A maps to NM_197941.2 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:64447674 G>A maps to NM_197941.2 C1114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:64595870 C>A maps to NM_197941.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:64769449 A>G maps to NM_197941.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:64755997 C>G maps to NM_197941.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:64510482 C>A maps to ENST00000464680 E905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:64766613 A>G maps to NM_197941.2 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr15:79060539 G>A maps to ENST00000258883 H860H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr15:79059934 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:130278492 G>A maps to NM_007037.4 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:130286151 G>A maps to NM_007037.4 H390H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:130286868 C>T maps to NM_007037.4 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:130286172 G>A maps to NM_007037.4 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:64587823 G>A maps to NM_182920.1 H1271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:64640045 G>A maps to NM_182920.1 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:64589726 G>A maps to NM_182920.1 Y1206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:64554055 G>A maps to NM_182920.1 G1504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr3:64592707 G>A maps to NM_182920.1 C1134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:64580080 T>C maps to NM_182920.1 R1403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:18817203 A>G maps to NM_001040272.4 G1301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:18721588 G>A maps to NM_001040272.4 E644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:18777226 G>A maps to NM_001040272.4 G1000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr9:18639250 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:18777580 G>A maps to NM_001040272.4 T1118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:18887910 G>A maps to NM_001040272.4 T1444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr9:18887910 G>A maps to NM_001040272.4 T1444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:18908467 C>T maps to NM_001040272.4 C1737C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:18675893 T>C maps to NM_001040272.4 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr9:18889710 G>A maps to NM_001040272.4 Q1536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:18680541 T>C maps to ENST00000380566 *440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:136405846 C>T maps to ENST00000393061 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:84553878 C>T maps to NM_207517.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:84539593 C>T maps to NM_207517.2 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:84651313 C>T maps to NM_207517.2 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:84683414 C>T maps to NM_207517.2 Y1365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:84611416 C>T maps to NM_207517.2 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:84651310 C>T maps to NM_207517.2 I977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr15:84373235 C>T maps to NM_207517.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr15:84592755 G>A maps to NM_207517.2 Q696Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:150531848 G>A maps to ENST00000369039 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:150529440 C>T maps to ENST00000369039 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:150530609 C>T maps to ENST00000369039 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:150531812 A>G maps to ENST00000369039 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:1506058 C>T maps to NM_213604.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:943792 A>G maps to NM_006869.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:943774 A>G maps to NM_006869.2 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:29258928 C>T maps to ENST00000394782 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:29283269 G>A maps to ENST00000394782 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:154562269 G>A maps to ENST00000292205 D920D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:154575054 C>T maps to ENST00000292205 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:154574187 C>T maps to ENST00000292205 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:154569288 G>A maps to ENST00000292205 H797H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr21:46596404 C>T maps to NM_015833.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:46624511 C>T maps to NM_015833.3 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:46596323 C>T maps to NM_015833.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:46595933 G>A maps to NM_015833.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr21:46640841 C>T maps to NM_015833.3 N653N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr21:46596383 G>T maps to NM_015833.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr21:46603319 C>T maps to NM_015833.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:1262946 G>A maps to NM_018702.2 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:1279696 G>A maps to NM_018702.2 Y484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr10:1262907 G>A maps to NM_018702.2 C555C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr10:1284303 G>A maps to NM_018702.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:1406014 G>A maps to NM_018702.2 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:1279777 G>A maps to NM_018702.2 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr16:75654583 C>T maps to NM_012091.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:143753712 G>A maps to NM_182503.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:143749815 G>A maps to NM_182503.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:33557703 C>A maps to ENST00000373441 C111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:33562393 C>T maps to ENST00000373441 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:33585675 G>T maps to ENST00000373441 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:33585650 G>A maps to ENST00000373441 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:33557721 A>G maps to ENST00000373441 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:78392231 C>A maps to NM_020421.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:41209497 G>A maps to NM_024876.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:41211271 G>A maps to NM_024876.3 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr8:145616096 G>A maps to NM_174922.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:145608338 G>A maps to NM_174922.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:45662326 C>T maps to NM_021116.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:45742985 G>A maps to NM_021116.2 E822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:45662326 C>T maps to NM_021116.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:45688396 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:45699688 C>T maps to NM_021116.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:45701797 C>T maps to NM_021116.2 C530C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:45725706 G>A maps to NM_021116.2 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:45717646 C>T maps to NM_021116.2 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:167825401 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:167871265 G>A maps to NM_018417.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:167849383 G>A maps to NM_018417.4 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:167874303 G>A maps to NM_018417.4 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:167830246 G>A maps to NM_018417.4 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:167802307 G>T maps to NM_018417.4 I1170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:167793961 G>A maps to NM_018417.4 I1294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:167805732 A>C maps to NM_018417.4 V1041V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:167847759 C>A maps to NM_018417.4 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:167849383 G>A maps to NM_018417.4 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:7743840 C>T maps to NM_020546.2 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:7520873 C>A maps to NM_020546.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:7757686 C>T maps to NM_020546.2 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:7802440 T>C maps to NM_020546.2 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:7717329 T>C maps to NM_020546.2 I561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:7773088 G>A maps to NM_020546.2 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:7695882 C>T maps to NM_020546.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:25042872 C>T maps to NM_004036.3 G1121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:25064177 G>A maps to NM_004036.3 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:25043703 G>A maps to NM_004036.3 G1047G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr2:25044481 G>A maps to NM_004036.3 Q1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:25046100 C>A maps to NM_004036.3 E954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:25048912 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:25050455 C>T maps to NM_004036.3 E818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:25045500 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:25061313 C>T maps to NM_004036.3 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24788643 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:24792141 G>A maps to NM_139247.3 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:24793332 C>A maps to NM_139247.3 G661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:123036913 C>T maps to NM_183357.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:123044183 C>T maps to NM_183357.2 K691K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:123046524 G>A maps to NM_183357.2 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:123010004 G>A maps to NM_183357.2 V1094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr3:123036922 C>T maps to NM_183357.2 A766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:123008729 G>A maps to NM_183357.2 S1133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:123010145 G>A maps to NM_183357.2 D1047D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:49168285 G>A maps to NM_015270.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:49171486 G>A maps to NM_015270.3 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:49167433 C>T maps to ENST00000395210 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:49168471 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:49170269 G>A maps to NM_015270.3 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr12:49162493 G>T maps to NM_015270.3 T1129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:49170269 G>A maps to NM_015270.3 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:49164672 G>A maps to NM_015270.3 N1044N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr16:50344746 C>T maps to NM_001114.3 C770C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:50347924 G>A maps to NM_001114.3 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:50340965 C>T maps to NM_001114.3 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr16:50339458 C>T maps to NM_001114.3 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:50324513 G>A maps to NM_001114.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:50342642 G>A maps to NM_001114.3 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:50345957 C>A maps to NM_001114.3 Y820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:131795962 G>T maps to NM_001115.2 S1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:131861934 G>A maps to NM_001115.2 C775C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:132052012 G>A maps to NM_001115.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:131916182 G>A maps to NM_001115.2 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr8:131792686 G>A maps to NM_001115.2 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:131922047 G>A maps to NM_001115.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:4015793 G>A maps to NM_001116.3 N1348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:4015870 G>A maps to NM_001116.3 R1323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:4165122 G>A maps to NM_001116.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:4164165 G>A maps to NM_001116.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:4016168 G>A maps to NM_001116.3 F1223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:4029276 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:4164452 C>A maps to NM_001116.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:4165112 G>A maps to NM_001116.3 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:4016168 G>A maps to NM_001116.3 F1223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:4016456 G>A maps to NM_001116.3 D1127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:31124987 G>A maps to ENST00000409489 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:31123754 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:31124972 G>A maps to ENST00000409489 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:2877671 G>T maps to NM_014189.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr4:2896373 C>T maps to NM_014189.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:2927769 G>T maps to NM_014189.2 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:70890609 G>A maps to NM_001185054.1 R710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:70904955 G>A maps to NM_001185054.1 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:70910752 A>G maps to NM_001185054.1 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:70903900 G>A maps to NM_001185055.1 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:70923523 G>A maps to NM_001185054.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:111878433 C>A maps to NM_016824.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:111876168 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:111860607 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:111881956 G>A maps to NM_016824.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:100205732 C>T maps to NM_000667.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr4:100205874 G>A maps to NM_000667.3 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:100205585 A>T maps to NM_000667.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:100232007 C>T maps to NM_000668.4 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:100261746 C>A maps to NM_000669.3 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:100266090 C>T maps to NM_000669.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:99997953 G>T maps to NM_000671.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:100128601 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:100128600 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:100334324 G>A maps to NM_000673.4 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:100349292 C>A maps to NM_000673.4 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:67355030 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:67361178 C>T maps to NM_144650.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:67372615 C>T maps to NM_144650.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:3504505 C>T maps to ENST00000415131 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:3517726 C>T maps to NM_018269.3 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:202915675 G>A maps to NM_015999.3 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:202915726 T>C maps to NM_015999.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:202914292 G>A maps to NM_015999.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:202911203 A>G maps to NM_015999.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:1863599 C>T maps to NM_024551.2 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:1890195 C>T maps to NM_024551.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:1887160 G>T maps to NM_024551.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:1863554 G>T maps to NM_024551.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:76349068 C>A maps to NM_006721.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:76153930 A>G maps to NM_006721.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:76153948 G>T maps to NM_006721.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:76153969 C>T maps to NM_006721.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr20:49509055 A>T maps to NM_181442.1 L732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:49508241 G>A maps to NM_181442.1 S1003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:49510334 G>A maps to NM_181442.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:49510577 G>A maps to NM_181442.1 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:49509855 G>A maps to NM_181442.1 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:49510334 G>A maps to NM_181442.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:49510577 G>A maps to NM_181442.1 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:49510398 T>C maps to NM_181442.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:49509855 G>A maps to NM_181442.1 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr18:77895890 C>T maps to NM_014913.3 G865G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:77893889 G>A maps to NM_014913.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr18:77894087 G>A maps to NM_014913.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:203134742 C>T maps to NM_001048230.1 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:24837105 C>A maps to NM_000675.4 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:24837243 G>A maps to NM_000675.4 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:112045904 G>T maps to NM_020683.6 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:112031458 C>T maps to NM_020683.6 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:112042688 G>T maps to NM_000677.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr1:112045871 G>A maps to NM_020683.6 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr15:73067392 C>T maps to NM_031284.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:73044514 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:73044593 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:73044752 G>A maps to NM_031284.4 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:119305409 A>T maps to NM_001125.2 K193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr13:114083297 C>T maps to NM_138430.3 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:114107710 G>A maps to NM_138430.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:114077253 G>A maps to NM_138430.3 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:36557404 C>T maps to NM_017825.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr1:36557392 C>T maps to NM_017825.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:36557320 G>A maps to NM_017825.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:36557677 C>T maps to NM_017825.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:26627683 C>T maps to NM_000680.2 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr8:26721684 T>A maps to ENST00000356368 K268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:26722357 A>G maps to ENST00000356368 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:26721721 C>T maps to ENST00000356368 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:26722237 G>A maps to ENST00000356368 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:26722279 C>T maps to ENST00000356368 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:26721630 G>A maps to ENST00000356368 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:26722108 G>A maps to ENST00000356368 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr8:26722357 A>G maps to ENST00000356368 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr5:159398961 C>A maps to NM_000679.3 C342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:4229160 G>A maps to NM_000678.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:4202229 G>A maps to NM_000678.3 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:4229310 G>A maps to NM_000678.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr20:4228602 G>A maps to NM_000678.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:112838029 G>A maps to NM_000681.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:112838083 C>A maps to NM_000681.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:96781456 C>T maps to NM_000682.5 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:96780784 G>A maps to NM_000682.5 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:96781108 C>T maps to NM_000682.5 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:96780853 G>A maps to NM_000682.5 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:96780814 C>T maps to NM_000682.5 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:96781537 C>T maps to NM_000682.5 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:96781354 G>A maps to NM_000682.5 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:96780780 G>A maps to NM_000682.5 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:96781138 C>T maps to NM_000682.5 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr2:96780733 G>A maps to NM_000682.5 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:3768656 G>A maps to NM_000683.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:115804637 C>T maps to NM_000684.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:115804448 G>A maps to NM_000684.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:148206507 C>T maps to NM_000024.5 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:148206963 C>A maps to NM_000024.5 C190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:148207506 G>A maps to NM_000024.5 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:67050270 C>T maps to NM_001619.3 D403D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr11:67051371 C>T maps to NM_001619.3 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:26091154 C>A maps to NM_005160.3 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:26063717 G>T maps to NM_005160.3 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:60883227 C>T maps to NM_175573.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:40762492 C>T maps to NM_000026.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:40742682 C>T maps to NM_000026.2 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:244579340 C>T maps to NM_001126.3 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:244583523 T>C maps to NM_001126.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:244574724 G>T maps to NM_001126.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:244572910 C>A maps to NM_001126.3 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:244586154 A>G maps to NM_001126.3 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:244574618 G>A maps to NM_001126.3 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:105207557 C>T maps to NM_199165.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:105211160 G>A maps to NM_199165.1 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr14:105212597 C>T maps to NM_199165.1 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44149707 C>T maps to NM_001129.3 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:44151763 G>A maps to NM_001129.3 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:19653049 C>T maps to NM_001114176.1 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:19653070 G>A maps to NM_001114176.1 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:89172476 C>T maps to NM_022767.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3057740 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:3053822 C>T maps to NM_198969.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:7774650 C>A maps to NM_001134647.1 E717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:7780516 G>A maps to NM_001134647.1 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:7802369 G>A maps to NM_001134647.1 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:148695421 C>T maps to NM_152406.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:148681985 C>T maps to NM_152406.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:148697446 C>T maps to NM_152406.2 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:148709335 C>T maps to NM_152406.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:148699263 C>T maps to NM_152406.2 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:148702272 C>T maps to NM_152406.2 H601H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:148695475 C>T maps to NM_152406.2 H371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr5:148687034 G>A maps to NM_152406.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:148709232 C>T maps to NM_152406.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:148699215 G>A maps to NM_152406.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:148712349 C>T maps to NM_152406.2 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:116073749 G>A maps to NM_001001936.1 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:116061184 G>A maps to NM_001001936.1 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:116061184 G>A maps to NM_001001936.1 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:116056817 T>C maps to NM_001001936.1 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:116061169 G>A maps to NM_001001936.1 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:116059088 T>C maps to NM_001001936.1 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:88047478 G>T maps to NM_001166693.1 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:88056765 C>A maps to NM_001166693.1 T1190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:88053512 C>T maps to NM_001166693.1 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:88055751 G>A maps to NM_001166693.1 Q1147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:87968115 G>A maps to NM_001166693.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:88053512 C>T maps to NM_001166693.1 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:87967977 G>A maps to NM_001166693.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:87968659 C>T maps to NM_001166693.1 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:88029434 G>T maps to NM_001166693.1 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:147743705 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:147967483 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:147733569 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:147743979 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:147733640 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:148044366 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:148068929 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:147582649 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:147743604 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:147919254 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:147985788 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:147743596 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:148037694 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:148044459 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:148055005 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:148059914 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:147743705 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:148035208 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:148037583 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:148037821 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:148072839 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:147582628 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:147743666 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:148044459 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:148059503 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr23:148044332 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:148037372 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:148072844 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:148039869 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:147743941 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:148035155 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:148037782 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:148048588 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:148037244 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:148037295 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:147743514 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:147743573 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:148062316 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:148068911 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:148044425 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:147743946 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:100623192 G>A maps to NM_001025108.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:100623772 G>A maps to NM_001025108.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:100623901 G>T maps to NM_001025108.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:132232070 C>A maps to NM_014423.3 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:132269970 T>C maps to NM_014423.3 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:132228041 C>T maps to NM_014423.3 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:132222063 G>A maps to NM_014423.3 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:132262890 C>T maps to NM_014423.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:132232206 G>C maps to NM_014423.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:12351389 G>A maps to NM_006796.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:12353103 G>A maps to NM_006796.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr18:12329638 T>C maps to NM_006796.2 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:74350010 A>G maps to NM_001133.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:74357674 C>T maps to NM_001133.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:74361073 A>G maps to NM_001133.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:74367575 C>T maps to NM_001133.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:74367596 C>T maps to NM_001133.2 C580C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:74364848 G>A maps to NM_001133.2 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76200751 C>A maps to NM_001145526.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr17:76201795 C>T maps to NM_001145526.1 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:76201776 C>T maps to NM_001145526.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:74309144 C>T maps to NM_001134.1 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:64794727 C>T maps to ENST00000422803 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:64778748 C>T maps to ENST00000422803 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:64780402 C>T maps to ENST00000422803 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:64819109 T>C maps to ENST00000422803 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:64780402 C>T maps to ENST00000422803 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:64779741 T>C maps to ENST00000422803 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr2:64794718 G>A maps to ENST00000422803 E653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:64819027 G>A maps to ENST00000422803 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:178360728 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:178355561 A>G maps to NM_000027.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:178361512 C>T maps to NM_000027.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:178363460 G>T maps to NM_000027.3 C23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:236659076 G>A maps to NM_001037131.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:236706449 G>T maps to NM_001037131.1 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:236957751 C>T maps to NM_001037131.1 C647C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr2:236708036 C>T maps to NM_001037131.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:236706463 G>A maps to NM_001037131.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:236649605 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr2:237028847 A>G maps to NM_001037131.1 E709E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:88769637 C>T maps to NM_133447.1 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:88769244 C>T maps to NM_133447.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:58128373 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:58122155 C>T maps to NM_001122772.1 K854K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:150815685 C>T maps to NM_031946.4 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:150784184 G>A maps to ENST00000469901 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:150839670 C>A maps to NM_031946.4 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:150815327 C>T maps to NM_031946.4 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:75435505 G>A maps to NM_001144000.1 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:75457420 G>T maps to NM_001144000.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:75457363 C>T maps to NM_001144000.1 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr10:51769798 C>T maps to NM_001077665.2 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:51769402 C>T maps to NM_001077665.2 H506H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:51465390 G>A maps to ENST00000416142 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:86838639 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:87066158 C>T maps to NM_152336.2 R846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:87531216 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:86807790 G>A maps to NM_152336.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:87217589 C>T maps to NM_152336.2 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr15:86807685 A>G maps to NM_152336.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr15:86822923 C>A maps to NM_152336.2 Y664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:86838484 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:86814937 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:87217524 G>T maps to NM_152336.2 E981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr11:47713755 T>G maps to ENST00000357610 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:47731940 C>A maps to ENST00000357610 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:49511377 C>A maps to NM_032785.3 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:49056627 G>A maps to NM_032785.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:49100153 C>A maps to ENST00000371838 *321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:27276789 C>A maps to NM_021831.5 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:27276359 T>G maps to NM_021831.5 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:27293064 C>A maps to NM_021831.5 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27277662 C>T maps to NM_021831.5 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27277662 C>T maps to NM_021831.5 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:27275942 G>A maps to NM_021831.5 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr2:27278548 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr6:32151708 C>T maps to ENST00000375070 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr7:100160513 C>A maps to NM_006076.4 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:100161565 G>A maps to NM_006076.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:76335459 G>A maps to NM_018046.4 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:76342416 A>G maps to NM_018046.4 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:76351385 G>T maps to NM_018046.4 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:76326660 C>T maps to NM_018046.4 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr5:76349791 G>A maps to NM_018046.4 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:76355439 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:76342239 C>T maps to NM_018046.4 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:141341161 C>T maps to NM_018238.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:141341708 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:141301080 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:141341095 G>T maps to NM_018238.3 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:100366417 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:100342056 G>T maps to ENST00000311030 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:100340250 C>T maps to ENST00000311030 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:100349966 G>T maps to ENST00000311030 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:100379224 T>C maps to ENST00000311030 D1365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr1:100356891 C>T maps to ENST00000311030 R978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:100336138 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr9:139571063 G>A maps to NM_006412.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:45391350 C>T maps to NM_001037553.1 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:45401009 C>T maps to NM_001037553.1 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:161560484 C>T maps to NM_020133.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:161560484 C>T maps to NM_020133.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr8:6588235 C>T maps to NM_018361.3 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:6612575 T>C maps to NM_018361.3 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:6590132 C>T maps to NM_018361.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:6612680 C>T maps to NM_018361.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:41469725 C>A maps to NM_178819.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr8:41476433 C>T maps to NM_178819.3 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:41469476 C>T maps to NM_178819.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:41476219 C>T maps to NM_178819.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:84509417 C>T maps to NM_032717.3 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:84518017 G>T maps to NM_032717.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:84518017 G>T maps to NM_032717.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:78805642 T>C maps to NM_001013619.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:78807407 G>T maps to NM_001013619.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr2:178386077 C>T maps to NM_003659.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:178310272 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:178310272 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:178346806 G>T maps to NM_003659.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:178301496 C>A maps to NM_003659.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:16840827 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:981386 C>T maps to NM_198576.2 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:982770 G>A maps to NM_198576.2 T1151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:982725 C>T maps to NM_198576.2 G1136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:978667 G>A maps to NM_198576.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:987132 C>T maps to NM_198576.2 D1863D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr16:67516694 G>A maps to NM_001138.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:230841815 G>A maps to NM_000029.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:230846431 T>C maps to NM_000029.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr1:230846278 G>A maps to NM_000029.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:230846278 G>A maps to NM_000029.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr1:230846278 G>A maps to NM_000029.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr1:230846200 G>T maps to NM_000029.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:88193855 G>T maps to ENST00000395847 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:88247608 C>T maps to ENST00000395847 E661E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:88190227 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:88272468 T>G maps to ENST00000395847 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:88203343 A>C maps to ENST00000395847 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:88204596 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:88233949 A>C maps to ENST00000395847 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr9:88248205 G>A maps to ENST00000395847 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:88296181 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:88247610 C>A maps to ENST00000395847 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:148459388 A>G maps to NM_032049.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:148459373 T>C maps to NM_032049.2 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:115304371 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:115304367 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:115304090 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:115303996 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:115304002 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:115303665 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:115304403 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:115304503 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:115304076 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:115304270 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:115303996 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:115304014 C>A did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:115304308 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:11806167 C>A maps to ENST00000476512 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr1:11808634 G>A maps to NM_001040196.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:241808765 C>T maps to NM_000030.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:241810792 C>T maps to NM_000030.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:241816982 C>T maps to NM_000030.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:35047908 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:35037139 G>A maps to NM_031900.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:34998916 C>T maps to NM_031900.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:35010121 C>A maps to NM_031900.3 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:35037139 G>A maps to NM_031900.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr5:35025867 T>C maps to NM_031900.3 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:109664977 A>G maps to NM_031279.3 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:109680995 G>A maps to NM_031279.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:109670609 G>A maps to NM_031279.3 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:109672162 A>G maps to NM_031279.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:109669186 A>G maps to NM_031279.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:247013925 T>C maps to ENST00000428671 R1832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:247004112 G>A maps to ENST00000428671 L2304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:247068847 T>C maps to ENST00000428671 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:247055198 C>T maps to ENST00000428671 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:247013094 T>C maps to ENST00000428671 E2109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:247024552 T>C maps to ENST00000428671 K1298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:247025373 G>A maps to ENST00000428671 R1246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr1:247021084 G>A maps to ENST00000428671 L1426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:247013966 C>A maps to ENST00000428671 E1819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:247013128 G>T maps to ENST00000428671 S2098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:247079623 C>T maps to ENST00000428671 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:247081594 G>A maps to ENST00000428671 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr1:247013190 C>T maps to ENST00000428671 S2077S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:110561082 C>T maps to NM_006621.4 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:110559065 G>T maps to NM_006621.4 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:110557409 C>T maps to NM_006621.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:110559348 T>C maps to NM_006621.4 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:110559065 G>T maps to NM_006621.4 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr7:129028948 G>A maps to NM_015328.3 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:27874531 G>A maps to NM_001029882.2 C1365C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:27876867 G>A maps to NM_001029882.2 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:27878212 C>T maps to NM_001029882.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:27874672 G>A maps to NM_001029882.2 S1318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:27874480 C>T maps to NM_001029882.2 P1382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:27875269 C>T maps to NM_001029882.2 W1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:135787132 G>A maps to NM_017651.4 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr6:135749883 T>A maps to NM_017651.4 K836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr6:135768163 C>T maps to NM_017651.4 W587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:135621672 G>A maps to NM_017651.4 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:62288805 G>A maps to NM_001620.1 I4361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:62298675 A>G maps to NM_001620.1 D1071D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:62300847 C>T maps to NM_001620.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62296545 G>A maps to NM_001620.1 V1781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62298396 G>A maps to NM_001620.1 I1164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:62290725 G>A maps to NM_001620.1 I3721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:62296323 G>A maps to NM_001620.1 I1855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:62298729 C>T maps to NM_001620.1 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:62300469 C>T maps to NM_001620.1 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:62288187 A>G maps to NM_001620.1 I4567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:62286993 G>A maps to NM_001620.1 I4965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:62292229 G>T maps to NM_001620.1 S3220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:62298627 G>T maps to NM_001620.1 I1087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:62296857 C>T maps to NM_001620.1 K1677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr11:62295516 T>C maps to NM_001620.1 L2124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:62286735 A>G maps to NM_001620.1 I5051I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:62286993 G>A maps to NM_001620.1 I4965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:62288733 G>T maps to NM_001620.1 I4385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:62294166 G>T maps to NM_001620.1 I2574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:62298191 C>A maps to NM_001620.1 G1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:62302486 A>G maps to NM_001620.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr11:62286962 T>A maps to NM_001620.1 K4976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr14:105408764 C>G maps to NM_138420.2 L4341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:105415166 G>A maps to NM_138420.2 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:105406087 C>A maps to NM_138420.2 E5234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:105408926 G>A maps to NM_138420.2 A4287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:105420052 G>A maps to NM_138420.2 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr14:105412391 G>A maps to NM_138420.2 A3132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr14:105409223 G>A maps to NM_138420.2 A4188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:105410996 G>A maps to NM_138420.2 V3597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr14:105407003 G>A maps to NM_138420.2 S4928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:105405817 C>A maps to NM_138420.2 E5324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:105408572 G>A maps to NM_138420.2 V4405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:105418214 G>T maps to NM_138420.2 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:105418763 G>A maps to NM_138420.2 F1008F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:105421097 C>T maps to NM_138420.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:105411530 G>A maps to NM_138420.2 D3419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:105416165 C>T maps to NM_138420.2 P1874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:105407899 C>A maps to NM_138420.2 G4630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:105419824 T>A maps to NM_138420.2 K655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105405236 T>C maps to NM_138420.2 G5517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105410996 G>A maps to NM_138420.2 V3597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105411353 G>A maps to NM_138420.2 F3478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105414254 C>T maps to NM_138420.2 P2511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105416894 C>T maps to NM_138420.2 P1631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105421097 C>T maps to NM_138420.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:105408860 C>A maps to NM_138420.2 G4309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:105412298 C>T maps to NM_138420.2 E3163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr14:105407054 C>T maps to NM_138420.2 L4911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:105407882 C>T maps to NM_138420.2 T4635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr14:105419204 C>T maps to NM_138420.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:105404879 T>C maps to NM_138420.2 K5636K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:105412733 C>T maps to NM_138420.2 Q3018Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:105407696 C>T maps to NM_138420.2 S4697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:105412136 G>A maps to NM_138420.2 L3217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr14:105407768 A>G maps to NM_138420.2 H4673H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr14:105414443 G>A maps to NM_138420.2 S2448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr14:105418658 G>T maps to NM_138420.2 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:17349712 C>T maps to NM_001621.4 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:17379758 G>A maps to NM_001621.4 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr5:434222 C>A maps to NM_020731.3 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:434768 C>T maps to NM_020731.3 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:428001 G>A maps to NM_020731.3 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:428028 C>T maps to NM_020731.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr5:376755 G>A maps to NM_020731.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr14:77935520 C>T maps to NM_012111.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:77928569 C>T maps to NM_012111.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:186338547 G>T maps to ENST00000273784 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:186338715 C>A maps to ENST00000273784 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:186331025 C>T maps to ENST00000273784 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:8757904 C>T maps to NM_020661.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:8757967 A>G maps to NM_020661.2 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:8756934 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:31584661 C>A maps to NM_001623.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:129289256 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:129283452 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129263958 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129270628 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129290562 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:129270075 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:129279544 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:129281789 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:129264057 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:129263604 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:129263581 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:129289203 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:129271119 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:129273773 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:129289227 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:21330771 C>T maps to NM_144704.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:21331352 C>T maps to NM_144704.2 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr22:21329050 C>T maps to NM_144704.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr6:143382167 G>T maps to NM_016108.2 G36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:143605275 C>T maps to NM_016108.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:106975248 C>T maps to NM_001624.2 L1086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:106968994 G>A maps to NM_001624.2 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:106973042 C>T maps to NM_001624.2 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:107009347 C>T maps to NM_001624.2 I1629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr6:106999813 C>T maps to NM_001624.2 G1392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr6:106968433 C>T maps to NM_001624.2 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:106987293 G>T maps to NM_001624.2 E1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:106968076 C>T maps to NM_001624.2 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:106991433 G>A maps to NM_001624.2 P1259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:107009237 C>T maps to NM_001624.2 R1593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:107009237 C>T maps to NM_001624.2 R1593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr6:107011703 G>A maps to NM_001624.2 L1660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:106969218 C>A maps to NM_001624.2 S971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:107008711 C>T maps to NM_001624.2 R1556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:106967944 C>T maps to NM_001624.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:106967861 G>T maps to NM_001624.2 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:26658087 C>T maps to NM_001039775.3 T1402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:26664036 G>A maps to NM_001039775.3 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:26664853 C>T maps to NM_001039775.3 K1153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr1:26650666 G>A maps to NM_001039775.3 Y1571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:26658051 G>A maps to NM_001039775.3 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:159043238 G>A maps to NM_004833.1 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:159035849 A>G maps to NM_004833.1 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:159033349 G>A maps to NM_004833.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:159036038 C>T maps to NM_004833.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:107252979 C>T maps to NM_001142416.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr4:107248611 G>A maps to NM_001142416.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:6057467 C>T maps to NM_006303.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:6337237 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:4832432 G>A maps to NM_018836.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:4772688 G>A maps to NM_018836.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:130630632 G>A maps to ENST00000223836 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr9:130635088 C>T maps to ENST00000223836 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:33478682 G>T maps to ENST00000398192 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:33487014 A>G maps to NM_001625.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:33480161 G>A maps to NM_001625.3 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:77987618 C>T maps to NM_174858.1 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:77763398 G>T maps to NM_174858.1 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:77987618 C>T maps to NM_174858.1 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:77984324 C>T maps to NM_174858.1 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:77806115 G>T maps to NM_174858.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:77987618 C>T maps to NM_174858.1 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:78024324 A>G maps to NM_174858.1 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:77987618 C>T maps to NM_174858.1 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:96912865 C>T maps to NM_152327.2 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:96917829 C>T maps to NM_152327.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:96924550 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:96922740 G>T maps to NM_152327.2 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:96922740 G>T maps to NM_152327.2 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr17:55183322 G>A maps to ENST00000427138 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:55187410 C>T maps to ENST00000427138 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:55183076 C>T maps to ENST00000427138 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:55182878 G>A maps to ENST00000427138 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:55183286 T>C maps to ENST00000427138 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:55163800 A>C maps to ENST00000427138 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:55187443 G>A maps to ENST00000427138 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:55183043 T>C maps to ENST00000427138 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:55184426 G>A maps to ENST00000427138 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr17:55182884 C>T maps to ENST00000427138 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:55183901 A>G maps to ENST00000427138 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:19861350 C>A maps to NM_007202.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:19835221 G>A maps to NM_007202.2 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:42882602 G>T maps to NM_016248.2 E1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:42877648 C>T maps to NM_016248.2 Y1589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:42875527 G>A maps to NM_016248.2 T882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:42876832 G>A maps to NM_016248.2 P1317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:42876970 A>C maps to NM_016248.2 I1363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr13:42877507 G>A maps to NM_016248.2 Q1542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr13:42874612 C>A maps to NM_016248.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:151673605 C>T maps to NM_005100.3 H1360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:151672474 G>A maps to NM_005100.3 G983G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:151672411 C>T maps to NM_005100.3 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:151673180 G>T maps to NM_005100.3 E1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:151673356 C>T maps to NM_005100.3 D1277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:151673456 G>T maps to NM_005100.3 E1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:151674175 C>T maps to NM_005100.3 V1550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:151671319 C>T maps to NM_005100.3 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:151674412 T>C maps to NM_005100.3 D1629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:151626919 C>T maps to NM_005100.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:151671527 G>T maps to NM_005100.3 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:151672060 C>T maps to NM_005100.3 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:151671830 A>C maps to NM_005100.3 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr6:151626886 A>G maps to NM_005100.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:151670762 G>T maps to NM_005100.3 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:151670333 G>T maps to NM_005100.3 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:86205639 T>C maps to NM_006738.4 G1589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:86270434 C>T maps to NM_006738.4 R2325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:86124559 G>A maps to NM_006738.4 V1087V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:86212990 T>C maps to NM_006738.4 C1681C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:86124749 G>T maps to NM_006738.4 E1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:86076891 G>T maps to NM_006738.4 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:86253826 T>C maps to NM_006738.4 L1854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:86251287 C>T maps to NM_006738.4 L1839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr15:86122492 C>T maps to NM_006738.4 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:86270684 G>T maps to NM_006738.4 E2364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr15:86122408 G>A maps to NM_006738.4 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:119054554 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:119037260 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:119054506 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:119048728 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:119037537 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:119048781 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:4737602 G>T maps to NM_006422.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:4737874 C>A maps to NM_006422.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr12:4737707 T>C maps to NM_006422.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:4735664 C>T maps to NM_006422.2 E801E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:4736927 C>T maps to NM_006422.2 K380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:4736006 G>T maps to NM_006422.2 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr12:4736231 G>A maps to NM_006422.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:49958223 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:49957088 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:49957537 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:49958667 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49958572 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49958689 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49958973 G>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:49958660 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:49957009 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:49957416 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49958459 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49958366 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49958505 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:49955614 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:49957287 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:49958393 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49957440 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49958252 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49963396 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:49957894 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:49957875 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:49958035 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:49958702 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:49962233 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:33243038 C>A maps to NM_004274.4 A1176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:33291249 C>T maps to NM_004274.4 Q1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:33068647 T>G maps to NM_004274.4 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:33015416 C>T maps to NM_004274.4 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:33204980 G>T maps to NM_004274.4 E1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:33292160 G>A maps to NM_004274.4 S1714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:33015295 T>G maps to NM_004274.4 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:33292238 C>A maps to NM_004274.4 V1740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:33015556 G>A maps to NM_004274.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:33015748 C>A maps to NM_004274.4 Y630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr14:33014830 G>T maps to NM_004274.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:33292208 C>T maps to NM_004274.4 S1730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:33290842 C>A maps to NM_004274.4 S1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:33292208 C>T maps to NM_004274.4 S1730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr14:33014800 A>G maps to NM_004274.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:33292238 C>A maps to NM_004274.4 V1740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:33293480 C>A maps to NM_004274.4 C2154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:131520623 G>T maps to ENST00000431975 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:131540860 G>T maps to ENST00000431975 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:15487823 G>T maps to NM_005858.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:15472540 T>C maps to NM_005858.2 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:15465845 G>A maps to NM_005858.2 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:15483053 G>A maps to NM_005858.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15471757 G>A maps to NM_005858.2 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15484042 G>A maps to NM_005858.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:15484700 G>A maps to NM_005858.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:15471714 G>A maps to NM_005858.2 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:91728999 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:91630472 C>T maps to NM_005751.4 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:91645450 C>T maps to NM_005751.4 C1207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:91651620 G>T maps to NM_005751.4 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:91603224 A>C maps to NM_005751.4 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:91631175 C>T maps to NM_005751.4 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:91687673 C>T maps to ENST00000265737 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:91674507 C>T maps to NM_005751.4 V1783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:91709427 G>T maps to NM_005751.4 E2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:91625057 G>T maps to NM_005751.4 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:91652198 G>T maps to NM_005751.4 E1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:91691742 G>T maps to NM_005751.4 E1974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:91694547 T>G maps to NM_005751.4 L1994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:91709327 A>G maps to NM_005751.4 E2627E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:91726194 C>T maps to NM_005751.4 R3308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:91735019 C>T maps to NM_005751.4 R3787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:91706313 T>G maps to NM_005751.4 L2253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:91631433 G>T maps to NM_005751.4 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:91724478 G>T maps to NM_005751.4 E3241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:91631004 G>T maps to NM_005751.4 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:91709327 A>G maps to NM_005751.4 E2627E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:91631046 G>T maps to NM_005751.4 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:91726037 G>A maps to NM_005751.4 R3255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:91632522 G>T maps to NM_005751.4 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:91630472 C>T maps to NM_005751.4 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:109827650 C>T maps to NM_001145128.2 Q1576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:109827993 G>A maps to NM_001145128.2 I1497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:109933287 C>A maps to NM_001145128.2 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:109863338 T>C maps to NM_001145128.2 V1087V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:109814754 G>A maps to NM_001145128.2 S1851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:109871345 C>A maps to NM_001145128.2 E971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:39469073 G>A maps to NM_024595.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:88391421 C>A maps to NM_018064.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:88385635 C>T maps to NM_018064.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:88387568 C>A maps to NM_018064.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:117129900 G>A maps to NM_030767.4 N550N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:117138676 C>A maps to ENST00000394574 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:117139234 C>T maps to NM_030767.4 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:117139759 G>A maps to NM_030767.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:117122195 A>G maps to NM_030767.4 V757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr9:117103985 C>T maps to NM_030767.4 T1298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:109394365 A>G maps to NM_152763.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:109358872 C>A maps to NM_152763.3 E811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:109358816 C>T maps to NM_152763.3 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:109377641 G>A maps to NM_152763.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:109394787 C>A maps to NM_152763.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:109369895 C>A maps to NM_152763.3 G623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:46035585 G>A maps to NM_153326.1 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:46035609 C>T maps to NM_153326.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:46034293 G>A maps to NM_153326.1 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:46034215 C>A maps to NM_153326.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:134221505 T>C maps to NM_020299.4 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:134215508 G>T maps to NM_020299.4 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:134262484 G>A maps to ENST00000418096 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:134260640 T>C maps to ENST00000418096 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr10:5011054 C>T maps to NM_001353.5 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:5014842 C>T maps to NM_001353.5 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:5037991 A>G maps to NM_001354.4 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:5144685 G>A maps to NM_003739.4 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:5247790 A>G maps to NM_001818.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:137798459 G>T maps to NM_005989.3 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:137773402 A>G maps to NM_005989.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:137792314 G>T maps to NM_005989.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:137782646 C>T maps to NM_005989.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:4872899 G>T maps to NM_001040177.1 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:19635076 G>T maps to NM_003689.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:19615047 G>A maps to NM_012067.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:19597298 A>G maps to NM_201252.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr14:105239692 C>T maps to NM_001014432.1 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:105239273 C>T maps to NM_001014432.1 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:105246524 G>A maps to NM_001014432.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:105237115 C>T maps to NM_001014432.1 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:50376378 C>T maps to ENST00000391835 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:40748485 C>T maps to NM_001626.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:40748464 C>T maps to NM_001626.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:243708870 C>A maps to NM_005465.3 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:243668574 G>T maps to NM_005465.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:243777038 G>T maps to NM_005465.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:243800977 G>A maps to NM_005465.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr1:243708874 T>C maps to NM_005465.3 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:243708870 C>A maps to NM_005465.3 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:53528906 A>C maps to ENST00000453503 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:52245449 C>T maps to ENST00000441729 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:52233335 T>C maps to ENST00000441729 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr3:52245356 C>T maps to ENST00000441729 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr3:52239986 G>A maps to ENST00000441729 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:55035646 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:55039944 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:55040032 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:55040038 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:55041309 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:55052394 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:55041441 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:55047635 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:55042167 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:55043988 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:55054237 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:55041375 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:55042157 C>T did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr4:74283929 T>C maps to NM_000477.5 D518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:74281974 C>T maps to NM_000477.5 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr4:74279231 C>T maps to NM_000477.5 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:74274451 C>T maps to NM_000477.5 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:74281974 C>T maps to NM_000477.5 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:105238966 C>T maps to NM_001627.2 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:105266045 T>C maps to NM_001627.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:105266354 C>T maps to NM_001627.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:49967184 C>A maps to NM_153329.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49971729 C>T maps to NM_153329.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:97376296 C>T maps to NM_002860.3 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:97397041 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr10:97402847 C>T maps to NM_002860.3 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:97371058 G>A maps to NM_002860.3 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:97380904 G>A maps to NM_002860.3 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:75520914 G>A maps to NM_000689.3 C464C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr9:75545818 G>A maps to NM_000689.3 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:75531909 G>A maps to NM_000689.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:58302897 G>A maps to NM_003888.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:58302862 C>A maps to NM_003888.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:58302913 G>A maps to NM_003888.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:58253042 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr15:58357767 C>T maps to NM_003888.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:101434199 C>T maps to NM_000693.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:101432768 C>T maps to NM_000693.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr15:101427778 C>T maps to NM_000693.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:38396761 C>A maps to NM_000692.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:125833456 G>A maps to ENST00000273450 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:125879822 G>T maps to ENST00000273450 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:125854466 G>A maps to ENST00000273450 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:125831636 G>A maps to ENST00000273450 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:125855660 G>A maps to ENST00000273450 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:125855660 G>A maps to ENST00000273450 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:105462658 A>G maps to NM_001034173.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:105456677 G>A maps to NM_001034173.3 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:105451901 G>A maps to NM_001034173.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:112227677 C>T maps to NM_000690.2 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:19642904 G>A maps to NM_000691.4 C344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:19646608 G>T maps to NM_000691.4 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:19642967 G>A maps to NM_000691.4 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:19643673 G>A maps to NM_000691.4 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:19575091 G>A maps to NM_001031806.1 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:19568331 G>A maps to NM_001031806.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:67434138 G>T maps to NM_001031615.1 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:67430748 A>G maps to NM_001031615.1 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:19199350 C>T maps to NM_003748.3 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:19199401 C>T maps to NM_003748.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr6:24503567 C>T maps to NM_170740.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:24515538 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:24503517 G>T maps to NM_170740.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:74538607 G>A maps to NM_005589.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:74538913 C>A maps to NM_005589.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr14:74533535 G>A maps to NM_005589.2 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:74533475 G>A maps to NM_005589.2 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:125885919 G>T maps to NM_001182.3 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:135254072 G>A maps to NM_022568.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:135239672 C>T maps to NM_022568.3 W448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr6:135254072 G>A maps to NM_022568.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:135260454 C>A maps to NM_022568.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:165636556 G>A maps to NM_000696.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:165649813 C>T maps to NM_000696.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:165632325 A>C maps to NM_000696.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr16:30080181 C>T maps to ENST00000395248 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr16:30081305 G>T maps to ENST00000395248 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr9:104189859 C>T maps to NM_000035.3 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:104187235 C>T maps to NM_000035.3 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:104189910 G>A maps to NM_000035.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr17:26900564 G>A maps to NM_005165.2 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr12:34177006 G>A maps to NM_032834.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:38714511 C>T maps to NM_001013620.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:52598174 C>T maps to NM_001004127.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:52598174 C>T maps to NM_001004127.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:50297714 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr22:50302891 C>T maps to NM_024105.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:110951599 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:111000879 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:110951613 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:110961416 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:111003158 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:110925440 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:110964895 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:110970113 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr23:110951322 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:110961460 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:110987995 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:110925470 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:110961468 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:110996042 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:110967047 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:110970086 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:111000887 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:111003135 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:110956460 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:110970086 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:110928194 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:110951352 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:110970187 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:110961438 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr23:110980097 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:110980080 T>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:111002970 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:110968235 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:110996022 A>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:95538364 G>A maps to NM_144988.3 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:129810193 G>A maps to NM_001136152.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:183963387 G>A maps to NM_005787.5 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:183960740 G>A maps to NM_005787.5 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:183963026 G>A maps to NM_005787.5 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:37524128 G>A maps to NM_013338.4 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:37569724 G>A maps to NM_013338.4 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:37524128 G>A maps to NM_013338.4 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:37569724 G>A maps to NM_013338.4 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:63876876 C>T maps to ENST00000263440 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:63872049 G>T maps to ENST00000263440 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr11:77812075 A>C maps to NM_024079.4 Y505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:77820568 A>G maps to NM_024079.4 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:77823696 G>A maps to NM_024079.4 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr11:77835215 C>T maps to NM_024079.4 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr11:77825035 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:77832182 C>A maps to NM_024079.4 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:77850595 C>T maps to NM_024079.4 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:111708317 A>G maps to ENST00000428306 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:111739390 G>A maps to ENST00000428306 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:111680412 C>A maps to ENST00000428306 E788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:111708221 G>A maps to ENST00000428306 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr2:29498333 C>A maps to NM_004304.3 G616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:29416200 G>A maps to NM_004304.3 Y1584Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:29420415 A>G maps to NM_004304.3 P1355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:29455239 G>A maps to NM_004304.3 D854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:29455188 G>A maps to NM_004304.3 N871N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:29432704 G>A maps to NM_004304.3 G1261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:29462581 G>T maps to NM_004304.3 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:29456523 G>A maps to NM_004304.3 N798N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr2:29551214 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:29551309 G>T maps to NM_004304.3 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:78142126 G>A maps to NM_006020.2 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:109527944 G>A maps to NM_001145375.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:109527908 C>T maps to NM_001145375.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr12:109527845 A>G maps to NM_001145375.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:43940667 G>A maps to NM_139178.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:43913678 C>T maps to NM_139178.3 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:43940667 G>A maps to NM_139178.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:102100134 A>G maps to NM_017621.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:36501473 C>A maps to NM_032878.3 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:36503927 G>A maps to ENST00000455847 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:107393165 A>T maps to ENST00000417449 I384I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A11U-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:3726078 G>T maps to ENST00000403787 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:3729222 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:3729224 T>C maps to ENST00000403787 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:73747143 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:73646280 G>T maps to NM_015120.4 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:73828397 T>A maps to NM_015120.4 P3982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:73675996 T>C maps to NM_015120.4 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:73718346 A>G maps to NM_015120.4 L3086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:73680163 T>C maps to NM_015120.4 S2169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:73800286 C>T maps to NM_015120.4 V3760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:73717275 T>C maps to NM_015120.4 S2729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:73681186 A>G maps to NM_015120.4 R2510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:73680157 C>A maps to NM_015120.4 I2167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:73717090 C>T maps to NM_015120.4 R2668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:73676389 G>A maps to NM_015120.4 E911E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:73800073 C>T maps to NM_015120.4 G3689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:73678633 A>G maps to NM_015120.4 V1659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr2:73679191 G>A maps to NM_015120.4 L1845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:73677301 G>A maps to NM_015120.4 Q1215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:73680136 A>G maps to NM_015120.4 L2160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:73828449 C>T maps to NM_015120.4 L4000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:73680641 A>C maps to NM_015120.4 R2329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:6913669 C>T maps to NM_000697.2 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:6902111 C>T maps to NM_000697.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr17:7976235 G>A maps to NM_001139.2 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:7976471 G>A maps to NM_001139.2 D640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:4539264 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:7950373 G>A maps to NM_001141.2 Q479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7948904 C>T maps to NM_001141.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:7948581 C>T maps to NM_001141.2 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:7948599 C>T maps to NM_001141.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:45878079 C>T maps to NM_000698.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:45935933 C>T maps to NM_000698.2 Y346Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:45941074 G>A maps to NM_000698.2 K655K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:45877989 C>T maps to NM_000698.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:45919566 C>A maps to NM_000698.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:45924145 C>T maps to NM_000698.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:31326239 G>A maps to NM_001629.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:8011798 G>A maps to ENST00000380149 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:8018934 C>A maps to ENST00000380149 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:8015444 C>T maps to ENST00000380149 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:8007503 C>A maps to ENST00000380149 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:8019006 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr17:8013592 A>G maps to ENST00000380149 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:8020256 C>T maps to ENST00000380149 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:233321170 C>T maps to NM_001631.3 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:233321362 G>A maps to NM_001631.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:233323080 C>A maps to NM_001631.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:113352322 C>A maps to NM_025144.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:113352007 G>A maps to NM_025144.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr4:113353462 C>T maps to NM_025144.3 C920C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr4:113353162 C>A maps to NM_025144.3 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr4:113350369 C>A maps to NM_025144.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:113359796 C>T maps to NM_025144.3 L1116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr18:56203686 G>T maps to NM_052947.3 S1244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:56202885 G>A maps to NM_052947.3 G1511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:56246302 C>A maps to NM_052947.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr18:56203527 A>G maps to NM_052947.3 A1297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:56247379 C>A maps to NM_052947.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:56204036 C>A maps to NM_052947.3 E1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr18:56203427 G>T maps to NM_052947.3 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:56171352 C>A maps to NM_052947.3 R2019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr18:56202714 A>T maps to NM_052947.3 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:56246924 G>A maps to NM_052947.3 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:56247607 C>A maps to NM_052947.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:85399978 G>A maps to NM_020778.4 Q872Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:85405881 G>A maps to NM_020778.4 E1584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:85383853 G>T maps to NM_020778.4 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:85406847 G>A maps to NM_020778.4 A1694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:85400512 G>A maps to NM_020778.4 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:85383413 C>T maps to NM_020778.4 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:85383931 G>A maps to NM_020778.4 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr15:85400326 T>C maps to NM_020778.4 H988H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr15:85370741 G>A maps to NM_020778.4 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:85402504 G>A maps to NM_020778.4 E1485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:85405948 C>T maps to NM_020778.4 R1607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:85384033 C>T maps to NM_020778.4 C710C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:85407714 C>T maps to NM_020778.4 I1716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:85405941 C>A maps to NM_020778.4 L1604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr15:85401199 C>T maps to NM_020778.4 D1279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:233246282 C>T maps to NM_001632.3 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:233244912 C>T maps to NM_001632.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:233244996 G>A maps to NM_001632.3 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:233245444 C>T maps to NM_001632.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:233272699 G>A maps to NM_031313.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:233272320 G>A maps to NM_031313.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr2:233272615 C>T maps to NM_031313.2 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:202609040 G>A maps to NM_020919.3 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:202617877 C>T maps to NM_020919.3 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:202598037 G>A maps to NM_020919.3 Y847Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:202587822 G>A maps to NM_020919.3 S1215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:202611450 G>A maps to NM_020919.3 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr2:202622443 C>T maps to NM_020919.3 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:46718472 C>T maps to NM_147129.3 W599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:46717114 C>A maps to NM_147129.3 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:46718394 G>A maps to NM_147129.3 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:46722782 C>T maps to NM_147129.3 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:46717763 C>T maps to NM_147129.3 Q719Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:46724714 G>A maps to NM_147129.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:202466515 G>A maps to NM_001168221.1 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:202358117 G>A maps to NM_001168221.1 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:202356832 G>A maps to NM_001168221.1 R1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:202466488 G>A maps to NM_001168221.1 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:202356832 G>A maps to NM_001168221.1 R1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:202356524 T>C maps to NM_001168221.1 Q1513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:202357559 T>C maps to NM_001168221.1 G1168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:202352462 G>A maps to NM_001168221.1 R1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:202358437 C>A maps to NM_001168221.1 E876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:202352429 G>A maps to NM_001168221.1 R1790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:202173901 G>A maps to NM_139163.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr2:202195492 C>T maps to NM_139163.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:202173901 G>A maps to NM_139163.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:202172322 G>A maps to NM_139163.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:202213015 G>A maps to NM_139163.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:202172322 G>A maps to NM_139163.2 F266F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:85674245 G>A maps to NM_006982.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:44289156 G>A maps to NM_021926.3 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:33989304 C>A maps to NM_001167595.1 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:33998883 A>G maps to NM_001167595.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:71472422 C>T maps to NM_016519.4 D440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:71465345 G>T maps to NM_016519.4 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:71459088 C>T maps to NM_016519.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:71472269 T>C maps to NM_016519.4 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr4:71471924 C>A maps to NM_016519.4 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:116831978 C>T maps to NM_001633.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr11:46568746 T>C maps to ENST00000458649 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:46455065 G>A maps to ENST00000458649 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr11:46564855 C>T maps to ENST00000458649 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr11:46563554 G>C maps to ENST00000458649 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr11:46563734 G>T maps to ENST00000458649 S611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:96350483 G>T maps to NM_152435.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:96354190 T>C maps to NM_152435.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:96346552 G>T maps to NM_152435.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:96354256 A>G maps to NM_152435.2 E223E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:11316787 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:11316675 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:11316221 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:11316691 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:56396222 C>A maps to ENST00000314566 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:56442016 C>T maps to NM_001144.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:56448256 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr12:53819660 C>T maps to NM_020547.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:53819305 C>T maps to NM_020547.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:53819537 C>A maps to NM_020547.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr12:53822696 C>G maps to NM_020547.2 Y290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:53819353 C>T maps to NM_020547.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr12:53819242 G>A maps to NM_020547.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:118076649 C>A maps to NM_001098526.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:110051210 C>T maps to NM_020703.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:110050859 G>A maps to NM_020703.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:47471705 C>T maps to NM_001143668.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:47471309 T>G maps to NM_001143668.1 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49756355 G>A maps to NM_198722.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:49756613 G>A maps to NM_198722.2 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:109441811 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:109444254 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:31850306 C>T maps to NM_001113402.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:31850306 C>T maps to NM_001113402.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:31882039 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:31825167 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:112022634 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:112035160 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:112022765 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:112022626 C>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:112024278 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:112054507 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:112022361 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:112022765 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:112053211 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:112048283 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:112065587 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:112066332 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:112058928 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:112065918 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:112066059 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:112034002 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:112033825 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:112065996 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:112025790 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:112034009 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:112065610 T>C did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:112065825 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:112054590 C>T did not map to a codon.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr23:112022698 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:94533474 G>A maps to NM_130847.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:94532845 G>T maps to NM_130847.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr3:134079138 G>A maps to ENST00000514516 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:134077520 G>T maps to ENST00000514516 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:134089921 C>T maps to ENST00000514516 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:115217474 C>T maps to NM_000036.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:115238108 G>T maps to NM_000036.2 S28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:115220136 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr1:115220123 C>T maps to NM_000036.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:110168330 G>A maps to ENST00000393689 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:10483243 C>T maps to NM_000480.2 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:10515029 G>C maps to NM_000480.2 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:10526103 T>C maps to NM_000480.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:38424451 G>T maps to NM_001635.3 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:38574605 G>A maps to NM_001635.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:38574563 G>A maps to NM_001635.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:38514955 C>A maps to NM_001635.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:38431465 C>T maps to NM_001635.3 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:38574563 G>A maps to NM_001635.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:38505846 G>A maps to NM_001635.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr3:49456431 A>G maps to NM_000481.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr4:71396937 C>T maps to NM_212557.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:104160190 T>C maps to NM_000699.2 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:104166535 G>T maps to ENST00000305865 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:104162264 C>G maps to ENST00000305865 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:104120213 C>T maps to NM_020978.3 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:104122070 T>C maps to NM_020978.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:104115857 C>T maps to ENST00000305865 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:104118161 C>T maps to NM_020978.3 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr1:104121953 A>G maps to NM_020978.3 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:66250634 C>A maps to NM_016627.4 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr2:112625609 A>G maps to NM_022662.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:112608478 C>T maps to NM_022662.2 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:112552435 G>A maps to NM_022662.2 I1444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:112601134 C>A maps to NM_022662.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:112605355 C>T maps to NM_022662.2 Q579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:112578835 G>A maps to NM_022662.2 F1062F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:112541502 T>G maps to NM_022662.2 I1678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:145916698 A>G maps to NM_014885.3 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:146017263 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:134201760 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:73983692 C>A maps to NM_173473.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:73990145 C>T maps to NM_173473.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:140082342 T>C maps to NM_013366.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:140076276 G>A maps to NM_013366.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr9:140079476 G>A maps to NM_013366.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr9:140070238 G>A maps to NM_013366.3 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr9:140076139 G>A maps to NM_013366.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:140080711 G>A maps to NM_013366.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:25408836 C>T maps to ENST00000510092 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:121756172 C>T maps to NM_016237.4 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:121779825 C>A maps to NM_016237.4 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:121746432 G>A maps to NM_016237.4 C706C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:121758185 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:110812080 C>T maps to NM_016238.2 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:21162121 T>C maps to NM_001097577.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:77269824 C>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr14:77272983 C>T maps to NM_015305.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr14:77275423 G>A maps to NM_015305.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:213180398 G>A maps to ENST00000310246 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:213178559 G>A maps to NM_144567.3 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:213168439 G>A maps to NM_144567.3 N526N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr8:6371356 A>G maps to NM_001147.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr8:6366552 G>T maps to NM_001147.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:6377417 C>T maps to NM_001147.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:853704 G>A maps to NM_015985.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:861900 G>A maps to NM_015985.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr20:896835 G>A maps to NM_015985.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:896646 C>A maps to NM_015985.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:178834781 C>A maps to NM_004673.3 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:178834479 C>T maps to NM_004673.3 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:178822892 C>A maps to NM_004673.3 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:129853994 G>A maps to NM_012098.2 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:129851352 G>A maps to NM_012098.2 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:129870605 C>T maps to NM_012098.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr9:129870656 G>A maps to NM_012098.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:129870901 C>A maps to NM_012098.2 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:63066773 G>T maps to NM_014495.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:63063482 T>C maps to NM_014495.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:63069784 G>A maps to NM_014495.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr1:63069701 C>T maps to NM_014495.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:63064413 C>T maps to NM_014495.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:101765652 C>T maps to NM_178127.4 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:101777953 C>A maps to NM_178127.4 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:101762054 A>C maps to NM_178127.4 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr11:101762090 C>T maps to NM_178127.4 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:41522529 G>A maps to NM_020478.4 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:41583425 G>A maps to ENST00000415018 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:41530062 G>A maps to ENST00000415018 I1635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:41566325 C>T maps to ENST00000415018 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:41526000 C>T maps to ENST00000415018 T1726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:41529948 A>C maps to ENST00000415018 V1673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:41543753 G>A maps to ENST00000415018 R1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:41550297 G>A maps to ENST00000415018 F1242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:41557060 C>A maps to ENST00000415018 E823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr8:41542068 C>T maps to ENST00000415018 Q1510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:41547777 G>A maps to ENST00000415018 C1357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:41556983 C>T maps to ENST00000415018 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:41530317 G>A maps to ENST00000415018 I1550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:41550297 G>A maps to ENST00000415018 F1242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:41575638 G>A maps to ENST00000415018 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr8:41572593 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:41521257 C>A maps to ENST00000415018 G1799G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:41550270 G>A maps to ENST00000415018 P1251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:41551614 C>T maps to ENST00000415018 Q1111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr8:41526060 G>A maps to ENST00000415018 D1706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr8:41573292 G>A maps to ENST00000415018 N493N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:41550297 G>A maps to ENST00000415018 F1242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:114264207 C>T maps to NM_001148.4 F1386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:114095618 G>A maps to NM_001148.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:114277819 A>G maps to NM_001148.4 L2682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:114278726 G>T maps to NM_001148.4 E2985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:114163335 C>T maps to NM_001148.4 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:114279995 C>T maps to NM_001148.4 R3408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:114277613 G>T maps to NM_001148.4 E2614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:114278086 C>A maps to NM_001148.4 I2771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:114199629 G>A maps to NM_001148.4 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:114276463 C>T maps to NM_001148.4 S2230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:114264207 C>T maps to NM_001148.4 F1386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:114277727 T>C maps to NM_001148.4 L2652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:114276103 G>A maps to NM_001148.4 V2110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:114277835 C>T maps to NM_001148.4 R2688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:114279328 C>T maps to NM_001148.4 D3185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr4:114260442 T>C maps to NM_001148.4 N1286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:114257038 C>T maps to NM_001148.4 I1139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:114262907 G>T maps to NM_001148.4 E1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:114275123 C>T maps to NM_001148.4 R1784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:114274468 C>T maps to NM_001148.4 I1565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:114208819 T>C maps to NM_001148.4 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:114277613 G>T maps to NM_001148.4 E2614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:61835107 G>T maps to NM_020987.2 S1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:61994478 G>A maps to NM_020987.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:61833168 G>A maps to NM_020987.2 P2490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:61833642 G>T maps to NM_020987.2 V2332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:61832247 G>A maps to NM_020987.2 N2797N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:61842461 G>A maps to NM_020987.2 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:61835607 T>C maps to NM_020987.2 S1677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:61994460 G>A maps to NM_020987.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr10:61835221 G>T maps to NM_020987.2 S1806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:61828829 G>A maps to NM_020987.2 Q3937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:61835919 G>T maps to NM_020987.2 S1573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:61819477 G>A maps to ENST00000503366 S1682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:61844448 G>A maps to NM_020987.2 R1329*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A11N-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:61815793 G>A maps to NM_020987.2 S4229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:61973179 G>C maps to NM_020987.2 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr10:61844448 G>A maps to NM_020987.2 R1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:61833753 T>C maps to NM_020987.2 E2295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:62038907 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr10:61958165 G>A maps to NM_020987.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:61828929 A>C maps to NM_020987.2 T3903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:61829127 T>C maps to NM_020987.2 G3837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:61831710 G>A maps to NM_020987.2 P2976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:61833636 G>A maps to NM_020987.2 I2334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:61828560 G>A maps to NM_020987.2 S4026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:61819570 G>A maps to ENST00000503366 V1651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:61833306 G>A maps to NM_020987.2 H2444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:61847918 G>A maps to NM_020987.2 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr10:61832730 C>T maps to NM_020987.2 L2636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:190559718 C>A maps to NM_144708.3 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:190584301 C>T maps to NM_144708.3 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:190584400 G>A maps to NM_144708.3 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:190557093 G>T maps to NM_144708.3 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:190611160 T>A maps to NM_144708.3 T1371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr2:190606137 C>A maps to NM_144708.3 I1257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:65239655 G>A maps to NM_182703.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:65242155 C>T maps to NM_182703.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:65226376 G>A maps to NM_182703.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:65223090 C>T maps to NM_182703.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:54517728 G>T maps to NM_153228.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr17:54403674 A>G maps to NM_153228.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr17:54428291 A>C maps to NM_153228.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:54534656 T>C maps to NM_153228.2 N452N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:54543715 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:4111230 G>T maps to NM_016376.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:4098276 C>T maps to NM_016376.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:4109625 T>G maps to NM_016376.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:4120393 C>T maps to NM_016376.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:4111296 C>T maps to NM_016376.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:4100729 C>T maps to NM_016376.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr17:4080533 G>A maps to NM_016376.3 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:4109763 A>G maps to NM_016376.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:14711332 G>A maps to NM_054027.4 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:14713075 G>A maps to NM_054027.4 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:14716836 G>T maps to NM_054027.4 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:14745984 G>A maps to NM_054027.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:14871448 G>A maps to ENST00000505140 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:14745984 G>A maps to NM_054027.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:139907828 T>A maps to ENST00000253810 P1766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:139864754 G>A maps to ENST00000253810 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr5:139916950 G>A maps to ENST00000253810 S2352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:139876837 C>T maps to ENST00000253810 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:139889652 C>T maps to ENST00000253810 L1331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:139908936 C>T maps to ENST00000253810 R2136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:139917080 G>T maps to ENST00000253810 G2396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr7:92015851 T>C maps to NM_019004.1 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:92000821 C>T maps to NM_019004.1 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr7:91972443 C>G maps to NM_019004.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:91924462 A>G maps to NM_019004.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:91980368 A>G maps to NM_019004.1 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:92015914 C>T maps to NM_019004.1 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr11:113267968 C>T maps to NM_178510.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:113264367 G>A maps to NM_178510.1 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:113265796 G>A maps to NM_178510.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:113265661 C>T maps to NM_178510.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:113265661 C>T maps to NM_178510.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr11:113270436 C>T maps to NM_178510.1 Y582Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:17394235 C>T maps to NM_152363.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:133331648 G>A maps to NM_015114.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr12:133324775 C>T maps to NM_015114.1 W330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:133306772 G>A maps to NM_015114.1 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:133324429 G>A maps to NM_015114.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:133313502 G>A maps to NM_015114.1 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:241419036 C>A maps to ENST00000401804 E1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:241463798 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:241494360 C>T maps to ENST00000401804 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:241446975 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:241468536 C>T maps to ENST00000401804 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:16655452 T>G maps to NM_020319.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:16640445 G>A maps to NM_020319.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr7:16649353 C>T maps to NM_020319.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:16649277 G>A maps to NM_020319.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:92675580 C>T maps to NM_014391.2 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:92675537 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:111536132 G>A maps to NM_017664.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A052-01A-11W-A027-09 chr16:89351186 G>T maps to NM_013275.4 S588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:89348320 G>A maps to NM_013275.4 G1543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:89355076 G>T maps to NM_013275.4 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:89345707 C>T maps to NM_013275.4 T2414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:89351701 C>T maps to NM_013275.4 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:89349409 C>T maps to NM_013275.4 E1180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:89349798 C>A maps to NM_013275.4 E1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:89351716 C>A maps to NM_013275.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:89371644 G>A maps to NM_013275.4 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:89371698 G>A maps to NM_013275.4 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr16:89352004 G>A maps to NM_013275.4 D315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr16:89347300 G>A maps to NM_013275.4 F1883F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr16:89350594 G>A maps to NM_013275.4 D785D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:89348419 C>T maps to NM_013275.4 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:89345737 C>T maps to NM_013275.4 T2404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr16:89355034 G>A maps to NM_013275.4 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr18:9254506 A>G maps to NM_015208.3 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:9254212 C>T maps to NM_015208.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:9254249 G>T maps to NM_015208.3 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr18:9208793 C>T maps to NM_015208.3 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:9257186 C>T maps to NM_015208.3 R1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:9211712 C>T maps to NM_015208.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:9257186 C>T maps to NM_015208.3 R1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr18:9275634 C>T maps to NM_015208.3 A1959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:110475265 C>T maps to NM_033121.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:110463602 C>T maps to NM_033121.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:110474085 G>A maps to NM_033121.1 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:27939426 G>A maps to NM_152345.4 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:70728417 G>A maps to NM_030816.4 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:70790584 C>T maps to NM_030816.4 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:70761922 C>A maps to NM_030816.4 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:67059648 G>A maps to NM_207354.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:5925028 G>A maps to NM_001009941.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:5926003 G>A maps to NM_001009941.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:5922266 G>A maps to NM_001009941.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:74005788 G>A maps to NM_032217.3 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:73968110 C>A maps to NM_032217.3 E1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr4:74013045 T>A maps to NM_032217.3 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:73984548 T>C maps to NM_032217.3 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:74005853 C>A maps to NM_032217.3 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr4:74124085 G>A maps to NM_032217.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr4:74005392 C>T maps to NM_032217.3 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:74019636 A>G maps to NM_032217.3 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:73957623 C>T maps to NM_032217.3 R1907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:99338292 G>A maps to NM_020349.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:99342383 C>T maps to NM_020349.2 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:99338109 C>T maps to NM_020349.2 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:69391160 T>C maps to NM_001098805.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:69421996 G>A maps to NM_001098805.1 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:69385695 G>T maps to NM_001098805.1 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr9:69423452 T>C maps to NM_001098805.1 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:69423671 G>A maps to NM_001098805.1 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr2:97507922 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:97505472 C>T maps to NM_144994.7 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:97506637 C>T maps to NM_144994.7 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:4210267 C>T maps to ENST00000262970 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:4216702 C>T maps to ENST00000262970 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:4216978 G>T maps to ENST00000262970 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:4212565 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:4222672 G>T maps to ENST00000262970 E1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:4216948 G>T maps to ENST00000262970 E688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:4208788 G>A maps to ENST00000262970 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:27324129 C>T maps to NM_014915.2 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:27324527 C>A maps to NM_014915.2 E951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:27294556 C>A maps to NM_014915.2 E1699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:27324293 C>A maps to NM_014915.2 E1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:27328954 C>A maps to NM_014915.2 E772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:27366265 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:27323939 G>A maps to NM_014915.2 R1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:33134099 C>T maps to NM_032139.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:33130327 G>A maps to NM_032139.2 Y350Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:33096836 C>T maps to NM_032139.2 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr19:33116815 C>T maps to NM_032139.2 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:33119683 G>T maps to NM_032139.2 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:33096836 C>T maps to NM_032139.2 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:33089122 C>T maps to NM_032139.2 A1027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:33090882 C>T maps to NM_032139.2 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:15736692 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:15836767 G>A maps to NM_015199.3 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:15755110 G>T maps to NM_015199.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:15751243 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:15727541 T>C maps to NM_015199.3 K682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:15727626 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:15836767 G>A maps to NM_015199.3 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:21192053 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:37438607 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:37436341 G>A maps to ENST00000374660 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:37442559 G>T maps to ENST00000374660 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:37478454 G>T maps to ENST00000374660 E891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:37508060 G>T maps to ENST00000374660 E1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:37506773 G>T maps to ENST00000374660 E1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:37422888 T>C maps to ENST00000374660 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:37430874 C>T maps to ENST00000374660 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:37436341 G>A maps to ENST00000374660 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:37431045 G>A maps to ENST00000374660 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr10:37421199 G>A maps to ENST00000374660 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:37478454 G>T maps to ENST00000374660 E891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:37442577 G>T maps to ENST00000374660 G540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:37422957 T>C maps to ENST00000374660 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:37419130 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr10:37430799 T>C maps to ENST00000374660 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:37438607 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:37438746 G>T maps to ENST00000374660 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr10:37486233 C>T maps to ENST00000374660 F943F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:14803792 G>T maps to NM_001145029.1 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:14797837 G>T maps to NM_001145029.1 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:14763814 T>C maps to NM_001145029.1 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:14777982 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:14852112 A>G maps to NM_001145029.1 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:14852377 G>T maps to NM_001145029.1 E1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr18:14797803 T>G maps to NM_001145029.1 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:14763742 C>T maps to NM_001145029.1 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:14791464 C>T maps to NM_001145029.1 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:14828289 T>C maps to NM_001145029.1 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:14752954 T>C maps to NM_001145029.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:14778015 G>A maps to NM_001145029.1 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:14763985 C>T maps to NM_001145029.1 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr18:14852377 G>T maps to NM_001145029.1 E1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:94030536 C>T maps to NM_032290.3 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:94022371 T>C maps to NM_032290.3 C690C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:94022374 A>G maps to NM_032290.3 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr12:52284407 G>A maps to NM_182608.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:52282511 C>A maps to NM_182608.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:52285056 C>T maps to NM_182608.3 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:145474506 G>A maps to NM_001039888.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:79854370 C>A maps to NM_001004441.2 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:145561262 G>A maps to NM_144698.3 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:97881190 G>A maps to NM_001164315.1 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:97875578 G>T maps to NM_001164315.1 E1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:97830153 T>C maps to NM_001164315.1 D493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:97810405 G>A maps to NM_001164315.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:97853094 G>A maps to NM_001164315.1 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:97877310 G>A maps to NM_001164315.1 K1132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:97911235 C>T maps to NM_001164315.1 R1638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:97853094 G>A maps to NM_001164315.1 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:97866100 T>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:97899537 C>T maps to NM_001164315.1 D1367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:97911147 G>A maps to NM_001164315.1 T1608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:97856887 G>T maps to NM_001164315.1 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:97810405 G>A maps to NM_001164315.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:97851206 T>C maps to NM_001164315.1 N667N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:98195399 C>A maps to NM_025190.3 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:98201511 C>T maps to NM_025190.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:98156526 C>A maps to NM_025190.3 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:97519314 G>A maps to NM_016466.5 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr17:48776889 G>A maps to NM_052855.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:82936080 C>T maps to ENST00000260047 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:197943492 C>T maps to NM_001195144.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:197948124 C>T maps to NM_001195144.1 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:197986076 G>A maps to NM_001195144.1 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:197872607 G>A maps to NM_001195144.1 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:197964556 G>A maps to NM_001195144.1 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:197866550 A>G maps to NM_001195144.1 C787C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:197953514 C>T maps to ENST00000424317 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:197878358 G>A maps to NM_001195144.1 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:197878304 C>T maps to NM_001195144.1 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:173616021 A>C maps to ENST00000367712 Y169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:173628340 C>A maps to ENST00000367712 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:94231574 C>T maps to NM_017704.2 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:10030315 C>T maps to NM_198798.1 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:10030572 G>A maps to NM_198798.1 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:10035112 C>T maps to NM_198798.1 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:10030293 C>T maps to NM_198798.1 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:10025098 C>T maps to NM_198798.1 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:10036278 C>T maps to NM_198798.1 R768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:10036232 C>T maps to NM_198798.1 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:125592222 G>A maps to NM_020337.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:125592469 T>C maps to NM_020337.2 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:125592222 G>A maps to NM_020337.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:125593602 C>A maps to NM_020337.2 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:125590831 C>T maps to NM_020337.2 T1200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:125593512 C>A maps to NM_020337.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr4:125591639 A>T maps to NM_020337.2 L931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:125590746 G>A maps to NM_020337.2 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr4:125590425 G>A maps to NM_020337.2 Q1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:56641948 G>A maps to NM_173595.3 D612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56641906 C>T maps to NM_173595.3 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56645969 G>A maps to NM_173595.3 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:56641520 G>A maps to NM_173595.3 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:56650864 A>G maps to NM_173595.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:56641861 G>A maps to NM_173595.3 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:56642655 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr12:56638435 C>A maps to NM_173595.3 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr12:56651121 C>T maps to NM_173595.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr12:56641843 C>T maps to NM_173595.3 K647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:71206810 C>T maps to NM_001115116.1 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:71206358 C>T maps to NM_001115116.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:55455721 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:55422897 G>A maps to NM_024669.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:55479341 C>A maps to NM_024669.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:55407119 G>A maps to NM_024669.2 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:55472101 C>T maps to NM_024669.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:90276736 T>C maps to ENST00000339746 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:90340651 T>C maps to ENST00000339746 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:117879984 G>A maps to ENST00000357099 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:117876202 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:117876921 T>C maps to ENST00000357099 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:34949576 C>T maps to NM_015245.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:34949576 C>T maps to NM_015245.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:34949576 C>T maps to NM_015245.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:34985817 C>T maps to NM_015245.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:35054096 C>T maps to ENST00000373990 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr6:35053568 G>A maps to NM_015245.2 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:100048961 T>C maps to NM_152788.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:99447015 G>A maps to NM_152788.3 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:99638149 C>A maps to NM_152788.3 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:99793421 T>C maps to NM_152788.3 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:100169374 T>C maps to NM_152788.3 Q304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:99139621 G>A maps to NM_181670.2 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:99225902 G>T maps to NM_152788.3 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:99174975 A>G maps to NM_152788.3 S1095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:99139599 G>A maps to NM_181670.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:4777132 C>T maps to NM_133450.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:4776997 G>A maps to NM_133450.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:4774771 G>A maps to NM_133450.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr16:4764172 G>A maps to NM_133450.2 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:21261573 C>T maps to NM_145865.2 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:101536358 G>A maps to ENST00000375018 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:101539718 C>A maps to ENST00000375018 G529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:101547143 G>A maps to ENST00000375018 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:101507924 G>A maps to ENST00000375018 D810D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:101530497 A>G maps to ENST00000375018 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:101546319 G>A maps to ENST00000375018 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:101536173 G>A maps to ENST00000375018 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr2:220099776 C>A maps to NM_001042410.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:220096686 C>T maps to NM_001042410.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr7:36435886 C>T maps to NM_018685.2 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:36464296 G>A maps to NM_018685.2 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:36466637 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:36447458 G>A maps to NM_018685.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:69949260 G>A maps to NM_018043.5 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:69951838 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:43591252 C>A maps to NM_018075.3 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:43602831 A>C maps to NM_018075.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr3:43474162 C>T maps to NM_018075.3 R618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:5841700 C>A maps to ENST00000356134 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:5722081 A>G maps to ENST00000356134 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:5908724 C>A maps to ENST00000356134 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:5685036 C>A maps to ENST00000356134 E863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:5708794 C>T maps to ENST00000356134 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:6031938 C>T maps to ENST00000356134 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:5722071 C>A maps to ENST00000356134 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr12:5853321 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:5672677 C>T maps to ENST00000356134 T929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:5687556 C>T maps to ENST00000356134 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:5939598 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:5963307 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:26660716 C>T maps to NM_031418.2 D690D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:26619975 C>T maps to NM_031418.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr11:26463463 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:26568995 T>C maps to NM_031418.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:26463573 G>A maps to NM_031418.2 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:26681907 G>T maps to NM_031418.2 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr11:26681883 C>T maps to NM_031418.2 R947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:26621224 C>T maps to NM_031418.2 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:26656601 G>C maps to NM_031418.2 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:101333127 G>T maps to ENST00000392977 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:101433759 C>T maps to ENST00000392977 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:101490407 C>T maps to ENST00000392977 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:101436110 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:101336314 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:101368631 C>A maps to ENST00000392977 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:101493478 C>T maps to ENST00000392977 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:101413865 C>T maps to ENST00000392977 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:101368631 C>A maps to ENST00000392977 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:101505474 G>T maps to ENST00000392977 E813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:101490413 C>T maps to ENST00000392977 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:22281249 C>T maps to NM_213599.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:22232853 A>G maps to NM_213599.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:22271795 G>T maps to NM_213599.2 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:22283789 C>T maps to NM_213599.2 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:22284575 G>T maps to NM_213599.2 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:22279290 G>T maps to NM_213599.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:22271809 C>T maps to NM_213599.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:45796858 C>T maps to NM_001142679.1 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:45795801 C>T maps to NM_001142679.1 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:45741977 C>T maps to NM_001142679.1 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:242147018 C>T maps to NM_001001891.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:242149768 C>T maps to NM_001001891.3 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:242139610 C>A maps to NM_001001891.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:17441045 G>A maps to NM_020959.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:17435670 A>G maps to NM_020959.2 A1062A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:17444520 G>A maps to NM_020959.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:428358 G>A maps to NM_001012302.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:69113063 T>C maps to NM_006305.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:100760860 C>A maps to NM_006401.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:100760860 C>A maps to NM_006401.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:100773571 C>T maps to NM_006401.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:165118506 G>A maps to NM_012403.1 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:165118695 T>C maps to NM_012403.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr4:165118818 C>T maps to NM_012403.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:165118482 G>A maps to NM_012403.1 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:48866507 G>T maps to NM_012404.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:150204165 A>G maps to NM_030920.3 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:150204194 T>A maps to NM_030920.3 K42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:150198947 C>A maps to NM_030920.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr15:90334185 G>A maps to NM_001150.2 N889N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:90340844 C>T maps to NM_001150.2 K706K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:90347125 C>T maps to NM_001150.2 W429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:90347776 G>A maps to NM_001150.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:90348694 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:90346988 G>A maps to NM_001150.2 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:90344340 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:90335726 G>T maps to NM_001150.2 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr15:90349631 C>T maps to NM_001150.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:90348389 C>T maps to NM_001150.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr15:90349769 C>A maps to NM_001150.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:69350207 G>T maps to NM_032208.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:80952820 A>C maps to NM_001145794.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:169102844 C>T maps to NM_007193.3 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:124696897 C>T maps to NM_001003954.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:60641360 G>T maps to NM_001002858.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:79522685 G>A maps to NM_005139.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:79525502 C>T maps to NM_005139.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:70015268 G>A maps to NM_001153.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:70015194 G>T maps to NM_001153.3 G7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr2:70008649 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:70015271 C>T maps to NM_001153.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:122590878 C>A maps to NM_001154.3 G261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:150515861 G>A maps to NM_001155.4 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:150512097 C>T maps to NM_001155.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:150512688 G>T maps to NM_001155.4 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:150497318 C>T maps to NM_001155.4 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:150514014 G>A maps to NM_001155.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:75156961 T>C maps to NM_004034.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr10:75139866 G>A maps to NM_004034.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr10:75158113 A>C maps to NM_004034.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr10:75156919 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr10:75139702 G>A maps to NM_004034.2 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr10:47756085 C>T maps to NM_001630.2 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:150960762 G>A maps to NM_003568.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:150960780 G>A maps to NM_003568.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:36570105 G>T maps to NM_001177506.1 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:36588261 G>A maps to NM_001177506.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:36677462 C>T maps to NM_001177506.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:36588255 G>A maps to NM_001177506.1 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:36713548 G>A maps to NM_001177506.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:40997350 C>T maps to NM_009590.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:41002253 C>A maps to NM_009590.2 Y720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:41004821 C>T maps to NM_003734.2 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:41004064 C>T maps to NM_003734.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr17:41004379 C>T maps to NM_003734.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:201470280 C>T maps to NM_001159.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:201507525 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:201499607 C>T maps to NM_001159.3 Y772Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:201507472 C>T maps to NM_001159.3 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:201515908 A>G maps to NM_001159.3 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:113186167 G>T maps to NM_018569.4 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:29752485 G>A maps to NM_001127.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:29735080 T>C maps to NM_001127.3 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:29754843 G>A maps to NM_001127.3 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:29759084 G>A maps to NM_001127.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:29754807 G>A maps to NM_001127.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr22:29735002 T>C maps to NM_001127.3 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:71803537 C>T maps to ENST00000423132 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:71790000 C>A maps to ENST00000423132 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:71779405 C>T maps to ENST00000423132 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:71823340 G>A maps to ENST00000423132 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:71773165 G>C maps to ENST00000423132 S716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr16:71768541 T>C maps to ENST00000423132 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:71782172 G>A maps to ENST00000423132 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:71790015 G>A maps to ENST00000423132 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr14:24033003 C>A maps to NM_003917.2 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:24035051 G>A maps to NM_003917.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:16314295 C>T maps to NM_001130524.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr19:16318898 C>T maps to NM_001130524.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:16344305 C>T maps to NM_001130524.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:10694698 A>G maps to ENST00000453102 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr19:10692243 G>A maps to ENST00000453102 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:10690389 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:10689639 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15870607 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:15870611 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15870607 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:50308788 C>T maps to NM_014203.2 C830C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:50298987 G>A maps to NM_014203.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:50303355 C>T maps to NM_014203.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:50295284 G>A maps to NM_014203.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr19:50302905 G>A maps to NM_014203.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:50285819 G>A maps to NM_014203.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:1010601 G>T maps to ENST00000332231 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:33925288 G>A maps to NM_001030006.1 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:33925250 G>T maps to NM_001030006.1 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:183901337 C>T maps to ENST00000411763 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:183899974 C>T maps to ENST00000411763 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:47341790 C>A maps to NM_004069.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:47341793 G>A maps to NM_004069.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:47342727 G>A maps to NM_004069.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:77436966 C>T maps to NM_003664.3 Q550Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:77334941 G>A maps to NM_003664.3 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:77316566 C>A maps to NM_003664.3 E981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:77423876 G>A maps to NM_003664.3 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:77396842 C>A maps to NM_003664.3 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:77311298 G>T maps to NM_003664.3 I1022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:77335049 G>A maps to NM_003664.3 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:77334941 G>A maps to NM_003664.3 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr15:83332567 G>T maps to NM_004644.3 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:83346109 G>A maps to NM_004644.3 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:83333168 G>A maps to NM_004644.3 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:83350215 G>T maps to NM_004644.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:83333168 G>A maps to NM_004644.3 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:83332687 C>T maps to NM_004644.3 K748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:83345365 G>T maps to NM_004644.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:83333195 G>A maps to NM_004644.3 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:83345365 G>A maps to NM_004644.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:83328709 G>T maps to NM_004644.3 I995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr19:2109917 G>A maps to ENST00000355272 L1102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:2120979 G>A maps to ENST00000355272 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:2121045 C>T maps to ENST00000355272 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:2121229 G>A maps to ENST00000355272 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:2109870 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:2115262 G>A maps to ENST00000355272 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:2123375 G>A maps to ENST00000355272 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:75884225 T>C maps to NM_207012.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:75898124 G>A maps to NM_207012.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:42022667 C>A maps to NM_006803.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:42025186 C>T maps to NM_006803.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:114443858 G>A maps to NM_006594.2 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:114443858 G>A maps to NM_006594.2 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr1:114438526 C>T maps to NM_006594.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr15:51276217 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:51250834 G>A maps to NM_007347.3 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:51226827 G>T maps to NM_007347.3 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:51223082 G>T maps to NM_007347.3 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:51250834 G>A maps to NM_007347.3 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:51250804 T>C maps to NM_007347.3 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:51242072 C>A maps to NM_007347.3 S456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:51233687 G>A maps to NM_007347.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr15:51285770 G>A maps to NM_007347.3 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:99699378 G>A maps to ENST00000429084 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:99074072 G>T maps to NM_181861.1 G647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:99080652 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:99093184 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:99126245 G>T maps to NM_181861.1 G1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:99102434 G>T maps to NM_181861.1 E932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:99042271 T>C maps to NM_181861.1 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:72082852 G>A maps to NM_001163.3 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:72130932 G>A maps to NM_001163.3 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:72082780 G>A maps to NM_001163.3 N480N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr9:72130950 G>A maps to NM_001163.3 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:72071288 G>A maps to NM_001163.3 I554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JS-01A-11D-A10B-09 chr15:29346179 C>T maps to NM_005503.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:29393974 C>T maps to NM_005503.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:29393974 C>T maps to NM_005503.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:3759746 C>T maps to NM_004886.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr11:6422802 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6416810 G>A maps to ENST00000389906 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:6423907 C>T maps to ENST00000389906 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:6424728 C>A maps to ENST00000389906 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:26825127 A>G maps to NM_019043.3 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:26800806 T>G maps to NM_019043.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr10:26856407 C>T maps to NM_019043.3 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:40823917 G>A maps to NM_004307.1 N694N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:40825733 G>T maps to NM_004307.1 S620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:40892409 G>A maps to NM_004307.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:40892409 G>A maps to NM_004307.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:40818227 G>A maps to NM_004307.1 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:139941576 G>A maps to ENST00000231029 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:112128190 C>T maps to NM_001127510.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:112177095 G>A maps to NM_001127510.2 Q1935Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:112177900 C>T maps to NM_001127510.2 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:112178364 C>A maps to NM_001127510.2 S2358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:112177900 C>T maps to NM_001127510.2 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr5:112174008 T>C maps to NM_001127510.2 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:112103078 G>A maps to NM_001127510.2 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:112175277 C>T maps to NM_001127510.2 H1329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:112103070 G>T maps to NM_001127510.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:112173571 G>T maps to NM_001127510.2 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:112175920 G>T maps to NM_001127510.2 E1544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:112162824 G>T maps to NM_001127510.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:112179273 T>C maps to NM_001127510.2 I2661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:112177048 C>T maps to NM_001127510.2 R1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr5:112154722 C>T maps to NM_001127510.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:112177900 C>T maps to NM_001127510.2 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:112177999 C>T maps to NM_001127510.2 R2237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:112179273 T>C maps to NM_001127510.2 I2661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:112175586 A>G maps to NM_001127510.2 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr5:112163651 C>T maps to NM_001127510.2 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr5:112175272 C>T maps to NM_001127510.2 Q1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:112177900 C>T maps to NM_001127510.2 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:112177476 A>G maps to NM_001127510.2 K2062K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:112173916 C>T maps to NM_001127510.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:112175638 C>T maps to NM_001127510.2 R1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:10485769 C>T maps to ENST00000423585 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr20:57036547 G>A maps to NM_153360.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr20:57035929 C>T maps to NM_153360.1 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:159558032 C>T maps to NM_001639.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49714447 G>A maps to ENST00000438011 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:20924079 G>A maps to NM_080649.1 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:20924969 C>T maps to NM_080649.1 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:20925228 T>C maps to NM_080649.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:55033703 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:55028731 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:55028812 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr23:55029467 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:55028708 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:55027999 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:55028777 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:55028688 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:55033332 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:55033510 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:55032974 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:55028007 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:55033052 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:55033779 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:55028006 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:55033664 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:55033349 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:55033425 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:55027008 A>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:63571482 T>G maps to NM_031301.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr11:43357458 T>A maps to NM_001142930.1 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:43364194 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:43343640 C>T maps to NM_001142930.1 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:43364266 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:43342373 C>T maps to NM_001142930.1 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:43340246 C>T maps to NM_001142930.1 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr11:43348098 C>T maps to NM_001142930.1 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:43345003 G>T maps to NM_001142930.1 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:10500409 G>A maps to NM_198544.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:10511633 C>A maps to NM_198544.3 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:68753218 G>T maps to NM_173545.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:57004319 C>T maps to NM_005161.4 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:57003770 G>A maps to NM_005161.4 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:57003355 C>A maps to NM_005161.4 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:36362858 C>T maps to NM_001024807.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:36365458 G>A maps to NM_001024807.1 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:36369534 G>A maps to NM_001024807.1 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:129993531 G>A maps to NM_001642.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:130010378 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr11:130010308 G>A maps to NM_001642.2 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:129992358 C>T maps to NM_001642.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:130013853 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:116707816 G>A maps to NM_000039.1 R34*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BS-A0TA-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:116691981 C>T maps to NM_000482.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:116661545 C>T maps to NM_052968.4 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr11:116662399 G>T maps to NM_052968.4 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:21251265 G>A maps to NM_000384.2 Q588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:21230967 A>G maps to NM_000384.2 S2924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr2:21239324 G>T maps to NM_000384.2 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:21229334 G>A maps to NM_000384.2 L3469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:21234033 C>T maps to NM_000384.2 P1902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:21234576 G>A maps to NM_000384.2 V1721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:21232175 G>A maps to NM_000384.2 R2522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:21225458 C>A maps to NM_000384.2 E4279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:21228795 G>A maps to NM_000384.2 V3648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:21234849 G>T maps to NM_000384.2 I1630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:21239396 T>C maps to NM_000384.2 E1082E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:21225915 G>A maps to NM_000384.2 I4126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:21229371 G>A maps to NM_000384.2 S3456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:21258577 G>A maps to NM_000384.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:21238248 C>T maps to NM_000384.2 W1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:21256186 G>A maps to NM_000384.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr2:21230829 T>C maps to NM_000384.2 V2970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:21237330 G>T maps to NM_000384.2 L1277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:21249713 G>A maps to NM_000384.2 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:21233604 G>A maps to NM_000384.2 A2045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr2:21224817 G>A maps to NM_000384.2 H4492H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:7805367 G>T maps to NM_001644.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:41029195 G>A maps to NM_006789.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:39357417 C>T maps to NM_001193289.1 Y67Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:39357417 C>T maps to NM_001193289.1 Y67Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:39382369 C>T maps to ENST00000402182 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:39382327 T>C maps to ENST00000402182 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr22:39414353 C>T maps to ENST00000396762 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:39418970 C>A maps to NM_152426.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:39427761 C>T maps to NM_152426.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:39428282 C>T maps to NM_152426.3 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr22:39421619 G>A maps to NM_152426.3 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:39421595 T>C maps to NM_152426.3 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:39474960 A>G maps to NM_021822.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:183617355 A>G maps to NM_203454.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:45448438 C>T maps to NM_001646.1 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:195300752 G>A maps to ENST00000421243 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:56755607 G>A maps to NM_001638.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:64212956 C>A maps to NM_000042.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:64224245 C>A maps to NM_000042.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:64224234 C>T maps to NM_000042.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:64224206 G>A maps to NM_000042.2 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:64210702 C>A maps to NM_000042.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:36624250 G>A maps to ENST00000451256 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:36587875 C>A maps to ENST00000332987 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:36122397 C>T maps to NM_030642.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:36055570 A>G maps to NM_030641.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:31624283 C>T maps to NM_019101.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:23899018 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:23925875 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:84310864 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:84310875 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:84342676 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:84310907 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:84329025 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:84329384 G>T did not map to a codon.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr23:84309353 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:27425569 C>T maps to NM_000484.3 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:27327982 C>T maps to NM_000484.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:27327991 G>A maps to NM_000484.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr21:27269928 C>A maps to NM_000484.3 E674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:27369711 C>T maps to NM_000484.3 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr21:27372429 C>T maps to NM_000484.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:58577835 C>A maps to NM_006380.2 G51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:58524950 C>T maps to NM_006380.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:58543773 C>A maps to NM_006380.2 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:58543806 G>A maps to NM_006380.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:58529255 G>A maps to NM_006380.2 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:57276170 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:57291324 T>C maps to NM_012096.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:105589094 C>T maps to NM_018171.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:105568109 G>A maps to NM_018171.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:105569832 C>A maps to NM_018171.3 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr12:105589096 G>A maps to NM_018171.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr12:105569824 A>G maps to NM_018171.3 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:105569832 C>A maps to NM_018171.3 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:88876198 G>A maps to NM_000485.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr16:88876489 G>A maps to NM_000485.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:154295789 C>T maps to NM_080429.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:154295497 C>T maps to NM_080429.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:241631643 G>T maps to ENST00000429564 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:241619820 C>T maps to NM_001102467.1 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:241621969 G>A maps to NM_001102467.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr2:241622182 G>T maps to NM_001102467.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:50344654 C>T maps to NM_000486.5 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:33442345 G>A maps to NM_004925.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:24442316 G>A maps to NM_001650.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:24436258 A>C maps to NM_001650.4 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:24440777 G>T maps to NM_001650.4 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:50369414 C>A maps to NM_001652.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:33387084 G>A maps to NM_001170.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:33385865 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:25235780 C>A maps to NM_001169.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:25228649 C>T maps to NM_001169.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:25232798 G>A maps to NM_001169.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:58467201 G>A maps to NM_020980.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:58467153 C>T maps to NM_020980.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:58467216 G>A maps to NM_020980.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:115298703 C>T maps to NM_173800.4 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:115346436 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:115350224 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:115320351 C>T maps to NM_173800.4 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:115346440 C>T maps to NM_173800.4 N699N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:115335463 G>A maps to NM_173800.4 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:35212574 A>G maps to NM_014691.2 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:35174840 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:35155184 G>A maps to NM_014691.2 F1304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:35155082 G>A maps to NM_014691.2 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:35167017 G>A maps to NM_014691.2 G1095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:35178824 C>A maps to NM_014691.2 E907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:35252990 C>A maps to NM_014691.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr15:35210540 C>T maps to NM_014691.2 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr23:66905912 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:66905928 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:66943613 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:66765653 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr23:66941742 G>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:66942692 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:66765745 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:66931476 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:66942712 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:66931245 C>T did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:66905967 G>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:66863241 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:66765965 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:66765541 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:66765038 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr23:47428206 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:47426707 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47422680 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:47426820 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:47430281 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:47430354 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47428243 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47428956 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:47428425 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47422454 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:47426521 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47428973 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47424531 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47426443 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47430283 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47429357 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:72410565 G>A maps to NM_001040118.2 D778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:72422183 G>A maps to NM_001040118.2 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:72437798 C>T maps to NM_001040118.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:36150116 G>T maps to NM_015230.2 I970I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:36230357 C>A maps to NM_015230.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:36069783 G>A maps to NM_015230.2 D1620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:36168669 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:36214941 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:36230795 C>A maps to NM_015230.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:36214941 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:36134857 A>G maps to NM_015230.2 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:36230519 C>A maps to NM_015230.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:36166722 C>T maps to NM_015230.2 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:36212316 A>G maps to NM_015230.2 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:36230519 C>A maps to NM_015230.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:36069767 G>A maps to NM_015230.2 R1626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr4:36168642 G>A maps to NM_015230.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:36152574 G>T maps to NM_015230.2 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:36189075 C>A maps to NM_015230.2 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:36214941 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:36230519 C>A maps to NM_015230.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:36081836 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:36150116 G>T maps to NM_015230.2 I970I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:36122869 C>T maps to NM_015230.2 T1275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:36134992 C>T maps to NM_015230.2 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:141052476 C>T maps to NM_022481.5 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:141038025 A>G maps to NM_022481.5 A1144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:141059792 C>T maps to NM_022481.5 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:143694540 C>T maps to NM_015193.3 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:143694919 C>T maps to NM_015193.3 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:118468454 C>T maps to ENST00000359415 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:118463512 C>T maps to ENST00000359415 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:118468454 C>T maps to ENST00000359415 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:228285049 C>T maps to NM_001024228.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:49333819 C>T maps to NM_001659.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:49334752 G>A maps to NM_001659.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:127230164 G>T maps to NM_001662.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:61917492 C>A maps to ENST00000370275 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:61909471 C>A maps to NM_175609.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:61917525 G>A maps to ENST00000370275 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr20:61907459 C>T maps to NM_175609.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:43203103 G>A maps to NM_014570.4 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:43231424 G>A maps to NM_014570.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:43195059 G>A maps to NM_014570.4 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:68111233 G>A maps to NM_006421.3 R1829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:68137247 G>A maps to NM_006421.3 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:68138301 G>A maps to NM_006421.3 R1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:68140362 A>G maps to NM_006421.3 D1142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:68178265 C>A maps to NM_006421.3 E700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:68179664 C>A maps to NM_006421.3 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:68165757 C>A maps to NM_006421.3 E876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr8:68170429 G>A maps to NM_006421.3 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:68138301 G>A maps to NM_006421.3 R1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr8:68211494 G>A maps to NM_006421.3 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:68200213 C>A maps to NM_006421.3 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr8:68163586 G>A maps to NM_006421.3 Q933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:68170429 G>A maps to NM_006421.3 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr20:47611055 G>C maps to NM_006420.2 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:47569405 C>T maps to NM_006420.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr20:47607654 C>T maps to NM_006420.2 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:47628533 C>T maps to NM_006420.2 F1277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:47606199 C>T maps to NM_006420.2 I931I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:47589779 C>T maps to NM_006420.2 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:47612369 G>T maps to NM_006420.2 E1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:47626855 C>T maps to NM_006420.2 N1224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr20:47591367 G>A maps to NM_006420.2 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr20:47591334 C>T maps to NM_006420.2 C566C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:47645143 C>T maps to NM_006420.2 R1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:153750842 G>T maps to NM_001025595.1 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:62337719 A>G maps to NM_003224.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr6:131904241 T>C maps to ENST00000356962 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr6:131902518 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr14:68112428 C>A maps to NM_001172.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:121289571 A>G maps to NM_001012659.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:121305071 G>A maps to NM_001012659.1 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:121303896 G>A maps to NM_001012659.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:46700968 C>T maps to NM_004308.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:46702649 G>A maps to NM_004308.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr11:46700688 C>T maps to NM_004308.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:148886205 G>A maps to NM_024605.3 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:148985620 G>A maps to NM_024605.3 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:148768337 G>T maps to NM_024605.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:148830881 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:148984316 G>A maps to NM_024605.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:148787910 G>T maps to NM_024605.3 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:148653563 G>T maps to NM_024605.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:32921920 T>C maps to NM_014783.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:32925186 C>T maps to NM_014783.3 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:32926191 C>T maps to NM_014783.3 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:32917392 C>T maps to NM_014783.3 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:32928564 G>T maps to NM_014783.3 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr15:30927691 C>T maps to NM_001039841.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:30927321 A>C maps to NM_001039841.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:30925788 G>A maps to NM_001039841.1 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:32099582 C>A maps to NM_018287.5 E682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:32097673 C>A maps to NM_018287.5 E757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:32103219 C>A maps to NM_018287.5 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:32143118 C>A maps to NM_018287.5 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:32197564 C>T maps to NM_018287.5 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr10:32197450 A>G maps to NM_018287.5 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:143986207 G>T maps to NM_018460.3 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:144244966 C>T maps to NM_018460.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:24931555 C>T maps to NM_001006634.1 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:24990312 C>A maps to NM_001006634.1 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:24931537 A>G maps to NM_001006634.1 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:24953417 C>T maps to NM_001006634.1 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:24966022 C>T maps to NM_001006634.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:129955210 C>A maps to NM_033515.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:129921906 C>T maps to NM_033515.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:129962958 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:99019329 C>T maps to NM_032900.4 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr10:98994991 G>T maps to NM_032900.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:98988841 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:98989534 C>A maps to NM_032900.4 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:99024581 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:110451545 G>A maps to NM_020809.2 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:110461422 G>A maps to NM_020809.2 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:110485314 G>T maps to NM_020809.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:110485284 G>A maps to NM_020809.2 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:110501433 G>A maps to NM_020809.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:110461422 G>A maps to NM_020809.2 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:110451613 G>A maps to NM_020809.2 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:110457039 G>A maps to NM_020809.2 R439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:110451830 G>A maps to NM_020809.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:110450672 G>A maps to NM_020809.2 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:110457031 A>G maps to NM_020809.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr11:110477467 C>A maps to NM_020809.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr10:24922401 T>C maps to NM_020824.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:24896782 G>T maps to NM_020824.3 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:24873607 G>A maps to NM_020824.3 I1870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:24910064 T>C maps to NM_020824.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr10:24908435 C>T maps to NM_020824.3 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:24880905 G>T maps to NM_020824.3 P1304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:24908804 G>A maps to NM_020824.3 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:24873775 G>A maps to NM_020824.3 S1814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr10:24873526 G>T maps to NM_020824.3 G1897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:24886904 G>A maps to NM_020824.3 R1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:24910127 G>A maps to NM_020824.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:24889678 G>A maps to NM_020824.3 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:24909163 G>A maps to NM_020824.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:24880895 G>A maps to NM_020824.3 R1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:49667845 C>A maps to ENST00000417912 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:49667830 C>T maps to ENST00000417912 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:49663092 G>A maps to ENST00000417912 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr10:49667827 G>A maps to ENST00000417912 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:49662201 G>A maps to ENST00000417912 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:86915790 C>A maps to NM_001025616.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr4:86916301 C>T maps to NM_001025616.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:86921731 C>T maps to NM_001025616.2 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:69015005 C>A maps to NM_001007231.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:69034576 C>T maps to NM_001007231.2 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:68962345 G>A maps to NM_001007231.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:69034493 G>T maps to NM_001007231.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:69034594 G>A maps to NM_001007231.2 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:69049842 C>A maps to NM_001007231.2 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:142393655 G>A maps to NM_015071.4 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:142500551 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:142437265 G>T maps to NM_015071.4 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:43481983 G>A maps to ENST00000428638 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:43481687 G>A maps to ENST00000428638 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:43473940 G>A maps to ENST00000428638 F695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:6850869 G>T maps to ENST00000383472 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:6873406 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:94639997 G>A maps to NM_004815.3 G1071G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:94652060 C>A maps to NM_004815.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:94650463 A>G maps to NM_004815.3 C691C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:94650987 A>G maps to NM_004815.3 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:94639451 G>A maps to NM_004815.3 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161019396 C>T maps to NM_001025598.1 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:161017741 C>T maps to NM_001025598.1 E1023E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:161017596 C>A maps to NM_001025598.1 E1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:161018565 C>A maps to NM_001025598.1 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:161017881 C>A maps to NM_001025598.1 E977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:161021227 C>T maps to NM_001025598.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:161021227 C>T maps to NM_001025598.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:119109720 C>T maps to NM_020754.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:119121119 G>A maps to NM_020754.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:119134756 G>A maps to NM_020754.2 E1327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:119102035 C>A maps to NM_020754.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:119135032 G>A maps to NM_020754.2 E1419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:119101984 C>T maps to NM_020754.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:119135074 A>C maps to NM_020754.2 V1433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:119120753 C>T maps to NM_020754.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:119101137 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:119121095 C>T maps to NM_020754.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:119134300 C>T maps to NM_020754.2 R1175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr3:119133187 G>A maps to NM_020754.2 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:119102006 G>T maps to NM_020754.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:119128400 G>A maps to NM_020754.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:119132788 G>A maps to NM_020754.2 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr3:119109677 G>A maps to NM_020754.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:119132839 G>A maps to NM_020754.2 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:128993397 C>T maps to NM_001142685.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:128840853 C>T maps to NM_001142685.1 A1404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:128844628 G>A maps to NM_001142685.1 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:128844223 G>A maps to NM_001142685.1 C942C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr11:128848791 C>T maps to NM_001142685.1 K651K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:128844388 G>A maps to NM_001142685.1 V887V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:129062072 A>G maps to NM_001142685.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:128856517 C>T maps to NM_001142685.1 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36268515 C>A maps to ENST00000221905 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:36272094 C>T maps to ENST00000007510 H342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:36273545 C>T maps to ENST00000007510 H426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:36277903 C>T maps to ENST00000007510 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:36271945 C>T maps to ENST00000007510 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:36279174 G>A maps to ENST00000007510 R1236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:130220540 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:130220540 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:130217157 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:130220338 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:130215713 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:130217156 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:130219950 A>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:130217833 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:130218320 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:130218607 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:130219570 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr23:130220355 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:130219663 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:130222640 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:130217716 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:130220305 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr23:130217928 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:130218321 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:130218896 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:145756181 G>A maps to NM_025251.1 I1018I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:153178234 T>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:153184499 T>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:153175477 C>T did not map to a codon.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr23:153187213 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153178165 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153175681 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153185123 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153185023 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:153174591 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153174576 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153184623 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:153174958 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:153176392 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153176610 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153184316 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153186164 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:32559967 A>G maps to NM_001030055.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:32560486 C>T maps to NM_001030055.1 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:32560510 T>G maps to NM_001030055.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:32561113 C>T maps to NM_001030055.1 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:32563238 C>T maps to NM_001030055.1 R1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:32624001 G>T maps to NM_001030055.1 E1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:32623886 G>A maps to NM_001030055.1 W1414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:32624024 T>C maps to NM_001030055.1 I1460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:11206861 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:11682552 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:11174697 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:11682470 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:11196300 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:11308556 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:11162266 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:11166830 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:11204424 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:11206962 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:11215097 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:11196219 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:11204428 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:11206926 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:11215105 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:11682615 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:11174724 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:11682722 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:11682615 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:11682729 C>G did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:11157567 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:11215099 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:11682705 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:11196324 T>C did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:11162283 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:11160389 T>C did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:11197521 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:11160422 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:11187647 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:57871262 C>T maps to ENST00000393797 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:57867452 C>A maps to ENST00000393797 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:57869325 C>A maps to ENST00000393797 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:79826889 C>G maps to NM_004309.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:15103493 C>T maps to NM_001175.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:42396803 G>A maps to NM_199002.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:42392164 C>T maps to NM_199002.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:42396731 G>A maps to NM_199002.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:42409407 G>A maps to NM_199002.1 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:1844557 C>T maps to ENST00000398564 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:1876700 C>T maps to ENST00000398564 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:1871716 G>A maps to ENST00000398564 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:1871951 G>A maps to ENST00000398564 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:1872032 C>T maps to ENST00000398564 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr8:1857535 C>T maps to ENST00000398564 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr8:1812584 C>T maps to ENST00000398564 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:1882047 G>A maps to ENST00000398564 T1079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:1851514 C>T maps to ENST00000398564 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:1851514 C>T maps to ENST00000398564 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:17914018 G>A maps to NM_018125.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:18014075 C>T maps to NM_018125.3 F1006F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr1:17928657 C>T maps to NM_018125.3 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:156949030 C>T maps to NM_198236.1 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156946840 G>A maps to NM_198236.1 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:156912496 G>T maps to NM_198236.1 S1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:156948166 G>A maps to NM_198236.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:156908252 T>C maps to NM_198236.1 S1383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:156909690 G>A maps to NM_198236.1 R1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:156908225 G>A maps to NM_198236.1 G1392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:156941578 G>A maps to NM_198236.1 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:120347454 T>G maps to NM_015313.2 T1121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:120331409 C>T maps to NM_015313.2 R853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:120351113 G>A maps to NM_015313.2 E1404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:120331409 C>T maps to NM_015313.2 R853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:120312519 G>A maps to NM_015313.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:120300509 G>A maps to NM_015313.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:120322336 G>T maps to NM_015313.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:120348881 G>T maps to NM_015313.2 E1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:120308037 G>T maps to NM_015313.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:120312811 G>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:120348878 T>C maps to NM_015313.2 L1183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:8218235 G>A maps to NM_173728.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:8222124 T>C maps to NM_173728.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr17:8218493 C>T maps to NM_173728.3 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:8215489 G>T maps to NM_173728.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr17:8222647 G>A maps to NM_173728.3 W735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:8216417 C>T maps to NM_173728.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr17:8224301 C>A maps to NM_173728.3 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:3379971 C>T maps to NM_014448.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:3389647 C>T maps to NM_014448.3 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr11:73022286 G>A maps to NM_014786.3 E868E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:73076912 C>T maps to NM_014786.3 H1972H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:73022127 C>T maps to NM_014786.3 D815D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:73022638 G>T maps to NM_014786.3 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr11:73021005 C>T maps to NM_014786.3 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7511966 C>T maps to NM_001130955.1 Y362Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7523423 A>G maps to NM_001130955.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7529498 C>T maps to NM_001130955.1 R755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:7523495 G>A maps to NM_001130955.1 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:7506652 T>C did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:7509210 C>T maps to NM_001130955.1 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:16525125 G>A maps to NM_153213.3 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:16525156 G>A maps to NM_153213.3 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:155936258 C>T maps to NM_001162383.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:155932765 C>A maps to NM_001162383.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:56779405 G>A maps to NM_001128615.1 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:56771256 G>A maps to NM_001128615.1 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:56992907 C>T maps to NM_001128615.1 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:143884022 C>A maps to NM_001003702.2 *485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:148997781 G>A maps to NM_001001669.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:106473934 G>T maps to ENST00000420470 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:106510417 A>G maps to ENST00000420470 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:131797620 C>T maps to NM_015320.2 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:131797874 C>T maps to NM_015320.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:131799474 C>T maps to NM_015320.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:131704101 T>C maps to NM_015320.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:144060517 C>T maps to NM_005435.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:144075858 C>T maps to NM_005435.3 S1512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:144075924 C>T maps to NM_005435.3 A1534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:144070292 C>A maps to NM_005435.3 I1352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr7:144061060 C>T maps to NM_005435.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:144059983 G>A maps to NM_005435.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr7:144075924 C>T maps to NM_005435.3 A1534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr7:144069807 G>A maps to NM_005435.3 S1336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:144070323 C>T maps to NM_005435.3 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:144060592 A>G maps to NM_005435.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:144060940 G>A maps to NM_005435.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr7:144075892 C>T maps to NM_005435.3 R1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:144077104 C>T maps to NM_005435.3 R1584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr23:135757255 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:135764991 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:135790897 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135767903 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135767873 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135827432 C>A did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:135790897 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135750258 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135767889 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135772867 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:135772878 G>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135751651 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135790902 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135795434 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:135762942 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135762982 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135790889 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135861631 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135795498 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135814322 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135750225 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135754266 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135772824 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135750205 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135751651 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135761710 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135770137 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135829751 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135789113 A>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:135863010 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:135861591 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:111955336 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:111885598 G>T maps to NM_001113511.1 G261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:111896630 G>T maps to NM_001113511.1 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:111953839 C>T maps to ENST00000218789 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr13:111940782 C>G maps to NM_001113511.1 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:111935592 G>A maps to NM_001113511.1 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr13:111870105 C>A maps to NM_001113511.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:62885776 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:62944433 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:62898268 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:62974185 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr23:62885816 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:62875607 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:62898284 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:62875575 A>G did not map to a codon.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr23:62917004 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:62898398 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:62944503 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:62875389 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:62944489 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:27056216 C>T maps to NM_006015.4 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:27106179 G>T maps to NM_006015.4 E1931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:27100206 C>T maps to NM_006015.4 R1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr1:27100182 C>T maps to NM_006015.4 Q1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:27105869 C>T maps to NM_006015.4 C1827C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:27107096 C>T maps to NM_006015.4 R2236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:27058067 T>A maps to NM_006015.4 Y592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:27087960 C>T maps to NM_006015.4 R750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:27088641 G>T did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:27057726 C>T maps to NM_006015.4 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr1:27105585 G>T maps to NM_006015.4 E1733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:27057641 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr1:27105549 C>T maps to NM_006015.4 R1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:27087439 G>T maps to NM_006015.4 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr1:27087502 C>T maps to NM_006015.4 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:27100206 C>T maps to NM_006015.4 R1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JS-01A-11D-A10B-09 chr1:27105552 C>T maps to NM_006015.4 R1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:27087502 C>T maps to NM_006015.4 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:27092751 G>T maps to NM_006015.4 G925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:27105678 G>T maps to NM_006015.4 E1764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K0-01A-11W-A062-09 chr1:27106532 G>A maps to NM_006015.4 W2048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr1:27101053 C>T maps to NM_006015.4 R1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:27105552 C>T maps to NM_006015.4 R1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:27106287 C>T maps to NM_006015.4 L1967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:27059259 C>T maps to NM_006015.4 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr1:27087960 C>T maps to NM_006015.4 R750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr1:27057972 C>T maps to NM_006015.4 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr1:27099324 C>T maps to NM_006015.4 Q1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr1:27100206 C>T maps to NM_006015.4 R1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:27097809 C>A maps to NM_006015.4 P1133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr1:27097801 C>T maps to NM_006015.4 Q1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr1:27100175 C>A maps to NM_006015.4 Y1324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr1:27101134 C>T maps to NM_006015.4 Q1473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr1:27100942 C>T maps to NM_006015.4 Q1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr1:27099946 C>T maps to NM_006015.4 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:27057960 C>T maps to NM_006015.4 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr1:27100206 C>T maps to NM_006015.4 R1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr1:27087502 C>T maps to NM_006015.4 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:27100119 C>T maps to NM_006015.4 Q1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:27107150 C>G maps to NM_006015.4 Y2254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:27105563 T>C maps to NM_006015.4 I1725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:27097629 G>A maps to NM_006015.4 W1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:27093042 G>T maps to NM_006015.4 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr1:27106860 C>T maps to NM_006015.4 R2158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:27101299 C>T maps to NM_006015.4 R1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr1:27106527 G>T maps to NM_006015.4 E2047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr1:27099946 C>T maps to NM_006015.4 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr1:27100194 C>T maps to NM_006015.4 Q1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:27087502 C>T maps to NM_006015.4 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:27057918 C>T maps to NM_006015.4 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:27106860 C>T maps to NM_006015.4 R2158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr1:27099097 C>T maps to NM_006015.4 Q1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr1:27107194 C>A maps to NM_006015.4 S2269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:157099434 G>A maps to ENST00000367148 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:157527905 C>T maps to ENST00000367148 I1917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:157527626 C>T maps to ENST00000367148 F1824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:157528310 G>A maps to ENST00000367148 W2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:157528934 C>T maps to ENST00000367148 G2260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:157527962 C>T maps to ENST00000367148 P1936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:157527506 C>T maps to ENST00000367148 D1784D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:157510788 C>A maps to ENST00000367148 S1228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:157528949 C>A maps to ENST00000367148 I2265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:157527626 C>T maps to ENST00000367148 F1824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr6:157528377 C>T maps to ENST00000367148 L2075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr6:157520005 G>T maps to ENST00000367148 G1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:157527494 C>T maps to ENST00000367148 D1780D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr6:157517354 C>T maps to ENST00000367148 Q1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:46246048 T>G maps to NM_152641.2 T1381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:46242675 T>G maps to NM_152641.2 Y546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:46125023 G>T maps to NM_152641.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:46233124 T>C maps to NM_152641.2 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:46245257 C>T maps to NM_152641.2 Q1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:960102 C>T maps to NM_005224.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr19:971938 C>A maps to NM_005224.2 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:968402 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr19:960102 C>A maps to NM_005224.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr15:74885485 A>G maps to ENST00000395077 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr14:58814484 T>C maps to NM_002892.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:58795015 C>A maps to NM_002892.3 S215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:58796296 G>A maps to NM_002892.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:58827757 C>A maps to NM_002892.3 S693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr14:58831833 T>A maps to NM_002892.3 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:58831390 C>T maps to NM_002892.3 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr14:58832862 G>A maps to NM_002892.3 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr14:58796244 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:58825934 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:58832907 G>A maps to NM_002892.3 P1161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:235345626 T>C maps to NM_016374.5 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:235345058 G>T maps to NM_016374.5 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:235345463 G>A maps to NM_016374.5 R924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:235345025 C>A maps to NM_016374.5 E1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:235377220 G>T maps to NM_016374.5 C568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:235383711 C>A maps to NM_016374.5 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:235403669 G>A maps to NM_016374.5 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:235345286 C>A maps to NM_016374.5 E983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:235345767 A>G maps to NM_016374.5 R822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:235357357 C>A maps to NM_016374.5 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:97218025 C>T maps to NM_212481.1 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr10:63850869 G>T maps to NM_032199.2 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:63845620 G>T maps to NM_032199.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:63816910 G>A maps to NM_032199.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:63852311 A>G maps to NM_032199.2 A1030A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:63851570 C>T maps to NM_032199.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:63759943 T>C maps to NM_032199.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr10:63851072 C>T maps to NM_032199.2 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr10:63850618 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:63852146 A>G maps to NM_032199.2 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:63829494 G>T maps to NM_032199.2 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:63845620 G>T maps to NM_032199.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:63760042 G>A maps to NM_032199.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:63759856 C>T maps to NM_032199.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr10:63850785 C>T maps to NM_032199.2 Q522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:72810460 G>A maps to NM_005744.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:72859454 G>A maps to NM_005744.3 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:49011155 C>T maps to NM_006321.2 H265H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:48965218 C>T maps to NM_006321.2 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:49017026 G>A maps to NM_006321.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:49011194 G>T maps to NM_006321.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:101789448 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:175798732 C>T maps to NM_173664.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:175793459 C>T maps to NM_173664.4 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr5:175798759 G>A maps to NM_173664.4 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:175793399 C>T maps to NM_173664.4 D67D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:175793411 G>A maps to NM_173664.4 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100243395 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100228732 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100240747 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100241885 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100243395 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100242406 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100243423 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100228733 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100245652 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100241808 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100243192 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100243408 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100245653 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:160395403 C>T maps to NM_025047.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:53409127 C>T maps to NM_019087.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr11:64786117 C>T maps to NM_001667.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:57284395 G>T maps to NM_012106.3 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:57282554 C>T maps to NM_012106.3 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:12728193 C>T maps to NM_005738.4 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:18962932 C>T maps to NM_178815.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:97499518 C>T maps to NM_177976.1 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:97499057 C>A maps to NM_177976.1 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:123467036 G>A maps to NM_018694.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:123465893 G>A maps to ENST00000392433 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:123466013 T>C maps to ENST00000392433 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:69151115 C>T maps to NM_006407.3 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:69153774 A>G maps to NM_006407.3 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:153577100 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:153616394 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:153616510 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr2:153616486 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:202103612 C>T maps to NM_138795.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:102738997 T>C maps to NM_031905.3 *344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:109274288 C>T maps to NM_032131.4 N550N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:109274313 G>T maps to NM_032131.4 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr6:109220942 C>T maps to NM_032131.4 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:109294630 G>T maps to NM_032131.4 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:109274396 A>G maps to NM_032131.4 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:23319618 G>T maps to NM_173081.3 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr10:23287151 C>T maps to NM_173081.3 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:23287211 T>C maps to NM_173081.3 N437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:23321904 G>T maps to NM_173081.3 G788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:23319618 G>T maps to NM_173081.3 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:23257234 G>T maps to NM_173081.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:23297786 G>T maps to NM_173081.3 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:28273985 A>G maps to NM_018076.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:28283879 C>T maps to NM_018076.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:28283879 C>T maps to NM_018076.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:28151479 G>A maps to NM_018076.2 N894N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr10:28274002 G>A maps to NM_018076.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:28149592 G>A maps to NM_018076.2 A994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:28229608 C>T maps to NM_018076.2 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:28274123 T>G maps to NM_018076.2 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr10:28272819 A>G maps to NM_018076.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr16:31477778 C>T maps to ENST00000408912 R888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:31477234 G>A maps to ENST00000408912 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr16:31473905 G>A maps to ENST00000408912 Q441Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:137993337 C>T maps to ENST00000469044 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:137964075 A>G maps to ENST00000470821 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:137986044 C>T maps to ENST00000469044 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:232081415 C>A maps to ENST00000359743 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:232141378 C>T maps to ENST00000359743 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:232087533 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:232156154 C>T maps to ENST00000359743 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:232104681 C>A maps to ENST00000359743 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100808480 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:100809055 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100808675 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100809148 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:100808557 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:100808642 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100808589 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:100809046 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100808913 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100807972 C>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:100808979 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:100809031 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100808973 T>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:100911899 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:100912396 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100911495 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100912261 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100911058 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100912322 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:100911752 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100911658 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:100911744 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:100912473 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:100912397 G>A did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:100911500 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100910806 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100911097 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100912561 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100911684 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100910919 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:100911495 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:100911097 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100880540 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100880686 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100880045 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100880876 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100880884 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:100880983 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100880988 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100880987 T>G did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:100880132 C>T did not map to a codon.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr23:100880349 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101858296 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:101857763 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:101857884 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:101857175 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101858401 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:101858704 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:101857238 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:101857323 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:101857866 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:101857363 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:100871173 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100871578 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100871303 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100871211 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:150786564 C>A maps to NM_001668.3 G701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:150802421 G>A maps to NM_001668.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:150807020 G>A maps to NM_001668.3 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:150786551 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:80806723 C>T maps to NM_014862.3 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:80845054 C>T maps to NM_014862.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:80867350 C>T maps to NM_014862.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:80750278 C>T maps to NM_014862.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:13395689 G>A maps to ENST00000403290 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr11:13387106 G>T maps to ENST00000403290 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:13378563 G>T maps to ENST00000403482 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:27533237 G>T maps to NM_020183.3 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:27573350 C>T maps to NM_020183.3 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:27533180 G>T maps to NM_020183.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:27555569 A>G maps to NM_020183.3 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:27533180 G>T maps to NM_020183.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:98955968 G>A maps to NM_006409.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr7:98951745 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:98988863 C>T maps to NM_005720.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:52849356 A>G maps to NM_006628.4 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:35723366 C>T maps to ENST00000458225 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr3:35725304 C>T maps to ENST00000458225 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:35729247 G>A maps to ENST00000458225 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:69496308 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:69497576 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69489987 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69495978 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69489204 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69497580 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69496000 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr23:69500108 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:69500418 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:69489722 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:74988471 G>A maps to NM_004041.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:74979999 G>A maps to NM_004041.3 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:4623510 C>T maps to ENST00000412477 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr9:140508785 C>T maps to NM_152285.2 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:140508800 G>A maps to NM_152285.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:18119562 C>T maps to NM_015683.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:18119352 C>T maps to NM_015683.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:18119890 C>A maps to NM_015683.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:18119523 C>T maps to NM_015683.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:90672559 G>A maps to NM_020801.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:90670774 G>A maps to NM_020801.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:90669529 G>T maps to NM_020801.2 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:90670774 G>A maps to NM_020801.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:98511278 C>A maps to NM_183376.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:98511278 C>T maps to NM_183376.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:4902816 G>A maps to NM_001080523.1 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:4891231 G>A maps to NM_001080523.1 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr22:51065260 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:51064489 G>A maps to ENST00000395624 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:78181426 G>A maps to NM_000046.3 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:2835949 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:2838737 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:2825590 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:2833627 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:2828813 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:2843681 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:2828814 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:2836182 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:2843797 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:2825572 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:2864056 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:2867584 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:2867734 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:2873506 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:2873544 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:2876329 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:2876442 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:2856147 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:2853103 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:2876410 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:2876406 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:2867351 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:2853011 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:2876420 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:2998958 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:3030573 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:3021809 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:2999044 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:3002626 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:3028180 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:3002466 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:3030449 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:3007606 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:3028229 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:3030315 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:66352834 C>T maps to NM_014960.3 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:66381274 C>T maps to NM_014960.3 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:66303840 G>A maps to NM_014960.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:66347800 G>A maps to NM_014960.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:66381268 G>A maps to NM_014960.3 W349*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BG-A0M8-01A-12D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr17:66416354 C>T maps to NM_014960.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr17:66416387 G>A maps to NM_014960.3 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:2951221 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:2947342 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:2933328 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr23:2924727 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:2933042 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:2942142 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:2936643 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:2951076 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr23:2933043 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:2928152 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:2947302 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:2951168 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:2933376 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:2947307 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:149681717 C>T maps to NM_001012301.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:149677373 G>A maps to NM_001012301.2 Y371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr5:149677384 G>A maps to NM_001012301.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:114823684 G>A maps to NM_024590.3 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:114899960 C>T maps to NM_024590.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr4:114824026 A>G maps to NM_024590.3 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:114899594 T>C maps to NM_024590.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:94939058 C>T maps to NM_198150.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:94918805 C>A maps to NM_198150.2 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr5:94927196 C>T maps to NM_198150.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:94927196 C>T maps to NM_198150.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:3681249 C>T maps to NM_004314.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:14993624 G>A maps to NM_021071.2 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:14994060 G>A maps to NM_021071.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:3661225 G>A maps to NM_001079536.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:44401667 C>A maps to ENST00000438616 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:19967491 C>T maps to NM_001670.2 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr22:19960709 G>A maps to NM_001670.2 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:25022874 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:25022795 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:104636764 G>T maps to NM_020682.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:104660432 C>T maps to NM_020682.3 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:17927342 G>A maps to NM_004315.4 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:17942295 G>A maps to NM_004315.4 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:52002997 G>A maps to NM_019893.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr10:51994201 C>T maps to NM_019893.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:131104231 G>A maps to NM_018482.2 G853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:131191523 G>A maps to NM_018482.2 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:131072851 G>A maps to NM_018482.2 P1055P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:131140287 G>T maps to NM_018482.2 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:131138204 G>T maps to NM_018482.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:131067039 G>A maps to NM_018482.2 I1109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:131226909 A>G maps to NM_018482.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:9496335 G>T maps to NM_003887.2 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:9463364 C>T maps to NM_003887.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:9496328 T>C maps to NM_003887.2 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:9514946 C>T maps to NM_003887.2 H540H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:9508555 C>T maps to NM_003887.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:23759633 C>T maps to NM_017707.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr7:150878313 G>A maps to ENST00000422024 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:15306083 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:15311419 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15306045 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:15306079 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:15333552 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:15307632 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:15315762 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:15333675 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:15315695 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:15311416 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:15333570 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:15306079 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:15332525 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15307641 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15320903 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15333607 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:15333673 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:63445031 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:63445392 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:63444938 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:63445377 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:63444875 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:63444797 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:63445192 G>T did not map to a codon.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr23:63445395 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:63444994 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:63445392 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:63445467 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:63445297 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:63444982 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:63444859 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:63445356 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:63445504 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:5683745 G>A maps to NM_024701.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:5683814 G>A maps to NM_024701.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr10:5682557 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:57317239 C>A maps to ENST00000295941 E2617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:123276903 C>T maps to NM_080928.3 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:123276903 C>T maps to NM_080928.3 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:123276903 C>T maps to NM_080928.3 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:123256273 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:123276903 C>T maps to NM_080928.3 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:42248387 C>T maps to NM_080863.4 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:42254990 C>T maps to NM_080863.4 C359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:76387785 G>A maps to NM_080868.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:94423269 G>T maps to NM_016150.3 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:94401049 C>T maps to ENST00000434324 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:94405570 G>A maps to ENST00000434324 C500C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:94405675 C>T maps to ENST00000434324 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:53941718 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:53992688 G>A maps to NM_001164165.1 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:95166953 G>A maps to NM_016116.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:177142386 C>A maps to NM_080874.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:177138037 C>A maps to NM_080874.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:177146492 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:177190067 T>C maps to NM_080874.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:132400296 G>A maps to NM_017873.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:132400903 G>A maps to NM_017873.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr9:132401493 G>A maps to NM_017873.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:132400260 G>A maps to NM_017873.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:132401755 G>A maps to NM_017873.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:101188568 C>T maps to NM_198243.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr15:101152627 C>T maps to NM_198243.2 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:101188568 C>T maps to NM_198243.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:48543595 G>A maps to NM_024095.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:48543405 C>A maps to NM_024095.3 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:15266967 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:15270502 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:15287988 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:15262644 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:30189431 G>A maps to NM_032204.3 Y612Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:30209526 A>C maps to NM_032204.3 L242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:30197097 C>A maps to NM_032204.3 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:100957932 G>A maps to NM_006828.2 D2112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:100957932 G>A maps to NM_006828.2 D2112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:100957859 G>A maps to NM_006828.2 R2137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:101109737 G>A maps to NM_006828.2 R883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:101053535 G>A maps to NM_006828.2 F1695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:101091989 C>A maps to NM_006828.2 G1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:101037617 A>C maps to NM_006828.2 T1814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:101054907 G>A maps to NM_006828.2 F1614F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:100957859 G>A maps to NM_006828.2 R2137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:101053535 G>A maps to NM_006828.2 F1695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:101296562 C>A maps to NM_006828.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:101110384 G>A maps to NM_006828.2 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:101248281 G>A maps to NM_006828.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr12:103352372 G>A maps to NM_004316.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:103352360 G>A maps to NM_004316.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:8959453 C>T maps to NM_020646.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:108169123 C>T maps to NM_203436.2 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:108169003 G>A maps to NM_203436.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:119228760 C>T maps to NM_014034.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11M-01A-11D-A122-09 chr19:14232343 C>T maps to NM_018154.2 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:14237046 G>A maps to NM_018154.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7011805 C>T maps to NM_080912.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:155309119 G>A maps to ENST00000368346 R2839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:155448163 C>T maps to ENST00000368346 Q1499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:155450122 A>T maps to ENST00000368346 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:155491081 C>A maps to ENST00000368346 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:155313252 G>A maps to ENST00000368346 H2720H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:155330094 T>C maps to ENST00000368346 K2269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr1:155491094 C>T maps to ENST00000368346 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:155451183 C>A maps to ENST00000368346 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:155452189 G>A maps to ENST00000368346 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:155317518 G>A maps to ENST00000368346 D2582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:155365307 C>T maps to ENST00000368346 K2015K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:155307458 G>A maps to ENST00000368346 R2968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:155340767 G>T maps to ENST00000368346 I2118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:155490893 T>C maps to ENST00000368346 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:155450467 T>C maps to ENST00000368346 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:155307542 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:155491081 C>A maps to ENST00000368346 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:155491081 C>A maps to ENST00000368346 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:37964579 G>A maps to NM_004674.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:37972508 T>G maps to NM_004674.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:65548107 G>A maps to NM_000048.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:1752166 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:1755374 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr23:1742064 G>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:1746603 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:1743170 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:1761816 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:1536958 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:1540687 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:1536925 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:1544547 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:1537901 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:1540709 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:1540580 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:1546992 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:1540670 G>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:1537889 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:1557995 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:1537963 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:12856258 C>T maps to NM_004317.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:12848477 C>T maps to NM_004317.2 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:97483910 G>A maps to NM_183356.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:97493673 A>G maps to NM_183356.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:97493579 C>A maps to NM_183356.3 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:97484018 G>A maps to ENST00000454046 N395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:190532635 T>C maps to NM_019048.2 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:190531089 G>T maps to NM_019048.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:3402369 C>A maps to NM_000049.2 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:3397695 T>C maps to NM_000049.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:51015426 G>A maps to NM_001114598.1 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr19:51017735 T>G maps to NM_001024656.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:104559027 C>T maps to NM_001080464.1 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:62577985 C>A maps to NM_020164.4 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:29912543 C>T maps to NM_181718.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr16:29912846 G>A maps to NM_181718.3 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:29912387 G>A maps to NM_181718.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr22:26830225 G>A maps to NM_020437.4 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:197065197 C>A maps to NM_018136.4 E2973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:197059057 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:197060074 G>A maps to NM_018136.4 R3181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:197072569 T>C maps to NM_018136.4 G1937G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:197073913 A>C maps to NM_018136.4 S1489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:197093432 A>C maps to NM_018136.4 L1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:197061161 G>A maps to NM_018136.4 R3107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:197073648 G>A maps to NM_018136.4 R1578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:197073076 C>T maps to NM_018136.4 R1768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:197113223 C>A maps to NM_018136.4 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:197059509 C>T maps to NM_018136.4 W3215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:197062189 G>A maps to NM_018136.4 R3096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:197062286 T>A maps to NM_018136.4 I3063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:197086987 C>T maps to NM_018136.4 Q1332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:197072812 T>C maps to NM_018136.4 R1856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr1:197112406 A>G maps to NM_018136.4 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:197060161 G>A maps to NM_018136.4 R3152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:197094247 G>A maps to NM_018136.4 Q1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:197072148 G>A maps to NM_018136.4 R2078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr1:197115333 C>T maps to NM_018136.4 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:197065197 C>A maps to NM_018136.4 E2973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:197112015 C>A maps to NM_018136.4 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:197073349 G>A maps to NM_018136.4 S1677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:197057451 G>A maps to NM_018136.4 G3365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr1:197056093 T>A maps to NM_018136.4 R3390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:95232982 C>A maps to NM_017680.4 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:79954310 C>T maps to ENST00000306729 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:62159728 C>T maps to NM_025080.3 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:62124493 G>A maps to NM_025080.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62156694 C>T maps to NM_025080.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62159030 C>T maps to NM_025080.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:62159009 C>T maps to NM_025080.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:133333846 G>A maps to NM_000050.4 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:133376395 C>A maps to NM_000050.4 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:133329717 C>T maps to NM_000050.4 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:133355783 C>T maps to NM_000050.4 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:130743507 G>A maps to ENST00000514044 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:130743721 C>A maps to ENST00000514044 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:130737347 A>G maps to ENST00000446270 *398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:130743297 G>A maps to ENST00000514044 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:130742899 A>G maps to ENST00000514044 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:130743387 G>A maps to ENST00000514044 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:96789645 T>A maps to NM_001002036.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:96799276 C>T maps to NM_001002036.3 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:96799758 C>T maps to NM_001002036.3 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:176852107 G>A maps to ENST00000281881 D1091D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:176833449 G>A maps to ENST00000281881 Y1293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:176852056 C>T maps to ENST00000281881 P1108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:176915078 C>T maps to ENST00000281881 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:176838137 G>A maps to ENST00000281881 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:176857270 G>A maps to ENST00000281881 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:119380660 G>A maps to ENST00000313400 S1099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:119495711 G>T maps to ENST00000313400 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:119495744 C>T maps to ENST00000313400 P818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:119802230 G>A maps to ENST00000313400 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:119202919 G>A maps to ENST00000313400 F1250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:119380747 C>T maps to ENST00000313400 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:119737521 G>A maps to ENST00000313400 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr9:119495723 G>A maps to ENST00000313400 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:119202919 G>A maps to ENST00000313400 F1250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:119625983 C>A maps to ENST00000313400 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:119625954 G>A maps to ENST00000313400 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:119802181 G>A maps to ENST00000313400 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:119568047 G>A maps to ENST00000313400 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr9:119583044 T>C maps to ENST00000313400 K686K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:119202919 G>A maps to ENST00000313400 F1250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:31016180 C>T maps to ENST00000375687 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr20:30956919 G>A maps to ENST00000375687 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:31024196 G>T maps to ENST00000375687 E1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:31024985 C>T maps to ENST00000375687 Q1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:31023106 C>T maps to ENST00000375687 D864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr20:31019208 C>T maps to ENST00000375687 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr20:31022446 G>T maps to ENST00000375687 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:25966175 T>C maps to NM_018263.4 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:25965638 C>T maps to NM_018263.4 E1189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:25982439 G>A maps to NM_018263.4 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:26068392 C>A maps to NM_018263.4 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:25982439 G>A maps to NM_018263.4 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:26068356 C>A maps to NM_018263.4 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:25965155 T>C maps to NM_018263.4 V1350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:25982439 G>A maps to NM_018263.4 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:25978921 G>T maps to NM_018263.4 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:31323012 G>A maps to NM_030632.1 Q1067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr18:31323171 C>T maps to NM_030632.1 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:31263406 G>T maps to NM_030632.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr18:31324281 C>A maps to NM_030632.1 S1490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr18:31187632 G>T maps to NM_030632.1 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:31250666 G>T maps to NM_030632.1 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:31318762 C>T maps to NM_030632.1 C465C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr18:31325493 C>G maps to NM_030632.1 V1894V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:31324929 G>A maps to NM_030632.1 Q1706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr18:31326387 C>T maps to NM_030632.1 N2192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:117003775 T>C maps to NM_130768.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:117003621 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:117008761 C>T maps to NM_130768.2 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:117008575 A>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:117021075 C>A maps to NM_130768.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:117067565 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr7:117003733 A>G maps to NM_130768.2 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:89514550 C>A maps to NM_032810.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:89544352 G>A maps to NM_032810.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:89516600 G>A maps to NM_032810.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:124357228 C>T maps to NM_014109.3 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:124371872 G>A maps to NM_014109.3 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:124346502 C>A maps to NM_014109.3 E1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:124357184 G>T maps to NM_014109.3 S886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:124383522 G>A maps to NM_014109.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:124340601 G>A maps to NM_014109.3 A1232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr8:124361664 G>A maps to NM_014109.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:124382175 A>G maps to NM_014109.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:124358424 T>C maps to NM_014109.3 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:124359506 G>A maps to NM_014109.3 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:124360509 G>A maps to NM_014109.3 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:124359506 G>A maps to NM_014109.3 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr2:24033195 G>C maps to NM_017552.1 S815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:24056817 C>A maps to NM_017552.1 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:23974916 C>A maps to NM_017552.1 *1459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:24107637 C>A maps to NM_017552.1 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:23980783 A>G maps to NM_017552.1 N1194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:1454312 G>T maps to NM_018188.3 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:1469361 C>T maps to NM_018188.3 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:1421958 C>T maps to NM_031921.4 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:1417922 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:1396237 G>A maps to NM_001039211.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:1391199 C>T maps to NM_001039211.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:29221687 C>T maps to NM_024857.3 R1802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:29162436 C>A maps to NM_024857.3 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr17:29162451 T>G maps to NM_024857.3 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:29187578 G>T maps to NM_024857.3 E1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:29214208 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:29203537 G>T maps to NM_024857.3 E1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:29214371 C>T maps to NM_024857.3 R1414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr17:29162841 T>C maps to NM_024857.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:29221044 C>A maps to NM_024857.3 S1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:29161339 G>T maps to NM_024857.3 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:3907777 G>A maps to NM_033064.4 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3905606 C>T maps to NM_033064.4 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:3885800 C>T maps to NM_033064.4 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:3907732 C>T maps to NM_033064.4 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:123600643 G>A maps to NM_001001976.1 Y370Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:51213528 T>G maps to NM_005171.4 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:51189732 C>T maps to NM_005171.4 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:51203237 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:175962218 G>A maps to NM_001880.2 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:175983055 C>A maps to NM_001880.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr19:50436267 C>T maps to NM_001193646.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161790889 C>T maps to NM_007348.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161830047 G>T maps to NM_007348.2 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:161833096 C>T maps to NM_007348.2 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:161789541 A>C maps to NM_007348.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:161771971 A>G maps to NM_007348.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:161789497 G>T maps to NM_007348.2 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:161833096 C>T maps to NM_007348.2 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:161928389 C>T maps to NM_007348.2 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:161833096 C>T maps to NM_007348.2 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:161751784 T>C maps to NM_007348.2 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:32084592 C>T did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr6:32087732 C>T maps to NM_004381.4 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr6:32089054 G>A maps to NM_004381.4 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:53918425 G>A maps to NM_001130059.1 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53918345 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:14578384 G>A maps to NM_018179.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr12:14610168 G>T maps to NM_018179.3 E700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:14576841 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:14576891 C>T maps to NM_018179.3 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:14578316 G>T maps to NM_018179.3 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:14591173 G>A maps to NM_018179.3 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:14628903 T>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr12:14576891 C>T maps to NM_018179.3 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:14649175 C>T maps to NM_018179.3 R1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:14587304 T>C maps to NM_018179.3 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:14613979 C>T maps to NM_018179.3 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:14649175 C>T maps to NM_018179.3 R1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:14578391 G>T maps to NM_018179.3 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:10575767 C>T maps to NM_024997.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:10531983 C>A maps to NM_024997.2 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:234201050 C>T maps to ENST00000392018 C550C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:234183423 C>T maps to ENST00000392018 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:234191390 C>T maps to ENST00000392018 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:234198558 G>A maps to ENST00000392018 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:234191390 C>T maps to ENST00000392018 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr11:64675054 G>A maps to ENST00000421419 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:64681309 G>A maps to ENST00000421419 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:64681915 G>A maps to ENST00000421419 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:64678181 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:64673063 G>T maps to ENST00000421419 I1145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:64669628 C>T maps to ENST00000421419 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:64679716 G>A maps to ENST00000421419 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:96752178 C>T maps to NM_018036.5 T2050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:96777591 G>A maps to NM_018036.5 S1341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:96757943 G>A maps to NM_018036.5 R1858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr14:96784188 G>T maps to NM_018036.5 I961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr14:96779400 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:96752103 G>A maps to NM_018036.5 H2075H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:96769483 G>A maps to NM_018036.5 R1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:112253159 G>T maps to NM_022488.3 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:112256680 G>A maps to NM_022488.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107381399 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107381198 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:107377296 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107393386 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107396214 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:107381217 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:242606084 C>A maps to ENST00000337606 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:242590685 C>T maps to ENST00000337606 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:242606117 C>T maps to ENST00000337606 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:242606096 C>T maps to ENST00000337606 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:63282316 G>T maps to NM_032852.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:63282316 G>T maps to NM_032852.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:63284764 G>T maps to NM_032852.2 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr1:63282471 T>C maps to NM_032852.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr1:63269477 T>C maps to NM_032852.2 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:63269478 G>T maps to NM_032852.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:63284685 G>A maps to NM_032852.2 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr19:10659703 C>T maps to NM_032885.4 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:10662718 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:11406153 C>T maps to NM_006395.2 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr3:11340198 C>G maps to NM_006395.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr3:11421448 C>A maps to NM_006395.2 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:220088369 G>A maps to NM_024085.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:220087551 A>G maps to NM_024085.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:220089806 G>A maps to NM_024085.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:150710497 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:150715068 A>C maps to NM_173681.5 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:150721408 A>T maps to NM_173681.5 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr7:150721500 G>A maps to NM_173681.5 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr7:150715497 C>T maps to NM_173681.5 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:293485 C>T maps to ENST00000409479 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:293229 G>A maps to ENST00000409479 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:292900 C>T maps to ENST00000409479 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:290055 C>T maps to ENST00000409479 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:292568 T>C maps to ENST00000409479 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:216190746 C>T maps to NM_004044.6 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr2:216203587 C>T maps to NM_004044.6 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:216200801 G>A maps to NM_004044.6 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:216211585 G>A maps to NM_004044.6 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:51095134 G>A maps to ENST00000358385 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:51094835 C>T maps to ENST00000358385 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:38526415 A>G maps to NM_001135673.1 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:38525332 C>A maps to NM_001135673.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:38570526 C>T maps to NM_001135673.1 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:63410892 G>A maps to NM_015459.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:63419975 G>T maps to NM_015459.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:63410930 G>A maps to NM_015459.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr11:108186547 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:108173606 G>T maps to NM_000051.3 E1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:108126972 C>A maps to NM_000051.3 S719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:108172482 C>A maps to NM_000051.3 A1762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:108153591 T>C maps to NM_000051.3 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:108121755 G>T maps to NM_000051.3 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:108180946 T>C maps to NM_000051.3 V1941V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:108203491 C>T maps to NM_000051.3 R2598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:108216595 C>T maps to NM_000051.3 R2849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:108235934 C>T maps to NM_000051.3 R2993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:108119761 G>T maps to NM_000051.3 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:108170567 C>T maps to NM_000051.3 T1711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:108186741 C>T maps to NM_000051.3 R2034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr11:108158325 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:108115661 G>A maps to NM_000051.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:108236202 C>T maps to NM_000051.3 R3047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr11:108175400 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:108106456 C>A maps to NM_000051.3 S131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:108216507 C>A maps to NM_000051.3 V2819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:108121784 C>T maps to NM_000051.3 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:108206667 T>C maps to NM_000051.3 L2750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:108216507 C>T maps to NM_000051.3 V2819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:108205738 C>A maps to NM_000051.3 S2685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:81078016 C>T maps to NM_015251.2 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:81078223 C>T maps to NM_015251.2 D707D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:7044822 G>A maps to NM_001940.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:7050098 C>A maps to NM_001940.3 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr4:94750130 C>T maps to NM_005172.1 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:151125894 G>A maps to NM_004045.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:151125929 G>A maps to NM_004045.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr15:25963466 G>A maps to NM_024490.3 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:25924552 G>A maps to NM_024490.3 R1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:26026237 G>A maps to NM_024490.3 H194H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:25972388 G>A maps to NM_024490.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:25972388 G>A maps to NM_024490.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:25959217 G>A maps to NM_024490.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:25972355 G>A maps to NM_024490.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:25981249 G>A maps to NM_024490.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr15:25924529 G>A maps to NM_024490.3 D1486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:25981249 G>A maps to NM_024490.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:25953352 G>A maps to NM_024490.3 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:25924907 C>T maps to NM_024490.3 P1360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr5:160114969 G>A maps to NM_025153.2 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:160047852 G>T maps to NM_025153.2 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:160059357 G>A maps to NM_025153.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:160067516 G>T maps to NM_025153.2 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:160113174 G>A maps to NM_025153.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:160016700 G>T maps to NM_025153.2 A1216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:160039780 G>A maps to NM_025153.2 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:160042857 T>C maps to NM_025153.2 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:160049460 G>A maps to NM_025153.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:160059309 G>A maps to NM_025153.2 C482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:160076230 A>G maps to NM_025153.2 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr5:160071241 A>G maps to NM_025153.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:160025833 G>T maps to NM_025153.2 I1169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:160025857 G>T maps to NM_025153.2 V1161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:160061418 G>A maps to NM_025153.2 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr5:160042866 C>A maps to NM_025153.2 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:160114940 G>A maps to NM_025153.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:160039852 G>T maps to NM_025153.2 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:47563078 A>G maps to NM_020453.3 K885K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:47527648 C>T maps to NM_020453.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:47537562 G>T maps to NM_020453.3 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:47514772 G>T maps to NM_020453.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:113479818 C>T maps to NM_032189.3 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:113488932 C>T maps to NM_032189.3 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:113488968 C>T maps to NM_032189.3 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:113496632 C>T maps to NM_032189.3 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:113487178 C>T maps to NM_032189.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr13:113487172 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:182554198 C>T maps to NM_014616.1 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:182563300 G>T maps to NM_014616.1 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:182547476 T>C maps to NM_014616.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:182553888 C>T maps to NM_014616.1 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:182563300 G>T maps to NM_014616.1 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:182597359 G>T maps to NM_014616.1 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:182605447 T>G maps to NM_014616.1 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:182554144 C>T maps to NM_014616.1 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr3:182614510 C>T maps to NM_014616.1 G1002G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:182554144 C>T maps to NM_014616.1 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:182584108 G>A maps to NM_014616.1 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:182563300 G>T maps to NM_014616.1 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:182577013 C>A maps to NM_014616.1 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:182591615 C>T maps to NM_014616.1 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:138882258 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:138857000 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:138844259 T>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:138870438 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:138878620 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:138879463 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:138857054 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:138864866 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:138878557 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:138864758 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:138813829 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:138856892 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:138869344 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:138878610 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:138879361 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:138901559 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:138823227 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:138820183 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:138882263 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:138850444 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:138856924 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:138864876 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:138878610 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:138856924 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:138850482 A>T did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:138878542 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:138857080 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:138867458 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:138871547 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:138823215 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:138864853 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:138867414 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:138882269 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:138886709 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:138901559 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:138844170 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:138825741 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:138844170 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:138864758 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:138880850 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:138869377 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:138882266 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:138901536 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:138864758 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:138820075 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:138813830 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:138828013 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:138864758 G>A did not map to a codon.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr23:138820119 C>G did not map to a codon.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr23:138884419 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:25262660 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:25280519 C>A maps to NM_001185085.1 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:25274960 G>A maps to NM_001185085.1 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:25264531 G>T maps to NM_001185085.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:19757090 G>A maps to NM_020410.2 T1057T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:17313327 C>T maps to NM_022089.2 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:17332012 G>A maps to NM_022089.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:194180198 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:194169269 G>A maps to NM_024524.3 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:193272545 C>A maps to NM_032279.2 G15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:193185117 C>A maps to NM_032279.2 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:193130066 A>G maps to NM_032279.2 F1036F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:193120533 C>T maps to NM_032279.2 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:193232515 C>A maps to NM_032279.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:193185120 G>A maps to NM_032279.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr3:193175185 G>T maps to NM_032279.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr3:193019038 G>A maps to NM_198505.2 Y912Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:193036798 C>A maps to NM_198505.2 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:193023394 A>G maps to NM_198505.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr3:193039578 C>T maps to NM_198505.2 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr3:193019017 A>G maps to NM_198505.2 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:116944181 G>A maps to NM_000701.7 K952K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:116933513 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:116941304 C>T maps to NM_000701.7 D729D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:116944184 C>A maps to NM_000701.7 I953I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:116935579 G>A maps to NM_000701.7 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:160104994 C>T maps to NM_000702.3 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:160098786 C>T maps to NM_000702.3 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr1:160100374 C>T maps to NM_000702.3 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:160090700 C>T maps to NM_000702.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:160100269 G>A maps to NM_000702.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr1:160105085 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr1:160093163 C>T maps to NM_000702.3 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:160099120 A>G maps to NM_000702.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:160090742 C>T maps to NM_000702.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:160105024 C>T maps to NM_000702.3 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:160100290 G>A maps to NM_000702.3 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr19:42482314 G>A maps to ENST00000441343 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:42490096 C>T maps to ENST00000441343 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:42473691 C>A maps to ENST00000441343 V861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr19:42474632 C>T maps to ENST00000441343 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:42473004 A>G maps to ENST00000441343 V917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:42471848 G>A maps to ENST00000441343 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:42489180 G>A maps to ENST00000441343 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:160144415 G>A maps to NM_144699.3 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:160125932 G>A maps to NM_144699.3 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:160144368 G>T maps to NM_144699.3 G715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:160141393 G>A maps to NM_144699.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:160144033 G>T maps to NM_144699.3 E709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:169094254 C>T maps to NM_001677.3 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:169080696 G>T maps to NM_001677.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:169096472 G>T maps to NM_001677.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:141595721 G>T maps to NM_001679.2 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:141644432 A>T maps to NM_001679.2 K244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:119504646 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:119512554 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119504677 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:119509328 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:119509347 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:119509333 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:119509381 T>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:119496049 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:119500467 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr16:28898594 G>A maps to NM_173201.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:28914723 C>T maps to NM_173201.3 D981D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:28890057 G>T maps to NM_173201.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:28898837 C>A maps to NM_173201.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:28909720 G>A maps to NM_173201.3 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:28913585 G>C maps to NM_173201.3 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:28912071 C>T maps to NM_173201.3 N645N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr16:28905900 C>T maps to NM_173201.3 C420C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:110778477 C>T maps to NM_170665.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:110778799 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr12:110783911 G>T maps to NM_170665.3 E950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:3833680 G>A maps to NM_174953.1 I886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:3832630 C>T maps to NM_174953.1 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:3846704 G>A maps to NM_174953.1 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:3840714 G>A maps to NM_174953.1 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:3840876 G>A maps to NM_174953.1 I718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:3850885 G>A maps to NM_174953.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:3833629 C>T maps to NM_174953.1 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:3844885 G>A maps to NM_174953.1 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:90004245 G>A maps to ENST00000428670 R763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:89985068 G>A maps to ENST00000428670 R1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:89997645 G>A maps to ENST00000428670 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:90013984 G>A maps to ENST00000428670 H540H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:89984922 G>A maps to ENST00000428670 A1196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:89996870 G>T maps to ENST00000428670 I1003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:90010803 G>A maps to ENST00000428670 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:89985068 G>A maps to ENST00000428670 R1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:90004245 G>A maps to ENST00000428670 R763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:10401789 G>A maps to NM_001001331.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:10430012 G>T maps to NM_001001331.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:10443805 G>A maps to NM_001001331.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:10387187 G>A maps to NM_001001331.2 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:10420035 G>A maps to NM_001001331.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:10401728 G>A maps to NM_001001331.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr3:10379871 C>T maps to NM_001001331.2 R1136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:10420041 G>A maps to NM_001001331.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:152813315 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152815520 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr23:152845457 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152807164 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152815153 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152818553 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152823574 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152835089 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:152835147 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:152806989 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:152823590 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:152821671 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:152845729 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:152830437 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr23:152845746 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr23:152806994 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152815060 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152830557 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:152813326 G>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:152815081 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:152807349 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:152818574 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:152826284 C>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:152821593 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:203677129 C>A maps to NM_001001396.1 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:203693058 C>T maps to NM_001001396.1 S1025S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:203702352 C>T maps to NM_001001396.1 I1104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:203667385 G>T maps to NM_001001396.1 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:203668843 C>T maps to NM_001001396.1 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:203680139 C>T maps to NM_001001396.1 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:203681231 G>T maps to NM_001001396.1 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:203667373 G>T maps to NM_001001396.1 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:203670028 C>T maps to NM_001001396.1 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:130720166 G>A maps to NM_001001486.1 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:130686223 G>A maps to NM_001001486.1 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:130717181 C>T maps to NM_001001486.1 F812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:130699475 G>T maps to NM_001001486.1 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr3:130717234 T>C did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr3:130673918 G>T maps to NM_001001486.1 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:84492938 C>T maps to ENST00000416219 N760N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:84449125 G>T maps to ENST00000416219 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36042362 C>T maps to NM_000704.2 Q957Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:36051478 G>A maps to NM_000704.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:36049580 C>T maps to NM_000704.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:36047937 G>A maps to NM_000704.2 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:114306015 G>T maps to NM_000705.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr13:114306018 G>A maps to NM_000705.3 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:114309165 C>T maps to NM_000705.3 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr18:43666115 G>A maps to NM_001001937.1 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:43669848 T>G maps to NM_001001937.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:57032910 C>A maps to NM_001686.3 G490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:57036483 G>T maps to NM_001686.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:57038656 T>C maps to NM_001686.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr12:57038731 G>A maps to NM_001686.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:7839116 C>T maps to NM_001001973.1 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:7844302 C>T maps to NM_001001973.1 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:57605476 G>A maps to NM_006886.2 R14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:111996904 C>T maps to NM_001688.4 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:46970884 G>T maps to ENST00000513347 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:54059199 C>T maps to NM_005176.5 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:99057757 G>T maps to NM_001198879.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:43036025 C>T maps to NM_001165877.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:35279736 G>A maps to ENST00000429238 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:50798936 C>A maps to ENST00000358473 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr14:50792375 G>T maps to NM_001003803.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:50790813 C>A maps to NM_001003803.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153663811 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153664153 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153664097 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153662666 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:153657559 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153660173 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153664079 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:153663829 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:153662051 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:153660231 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:81608495 C>A maps to NM_001017971.1 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:81608618 C>T maps to NM_001017971.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:81608537 C>T maps to NM_001017971.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:40460120 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:40450606 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:40458917 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:40448368 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:40450600 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:40464865 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:40456835 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:40456896 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:40639276 C>T maps to NM_001130020.1 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:40613028 C>T maps to NM_001130020.1 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:40647724 C>T maps to NM_001130020.1 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:40630565 C>T maps to NM_001130020.1 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:124212354 G>T maps to NM_012463.3 G183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:124228354 C>A maps to NM_012463.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:124233272 G>T maps to NM_012463.3 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:138440457 A>G maps to NM_130840.2 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr7:138444494 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:138430004 G>A maps to NM_130840.2 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:138455905 G>A maps to NM_130840.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr7:138417771 C>T maps to NM_130840.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:44442812 C>A maps to NM_004047.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:44442839 C>A maps to NM_004047.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:87153736 G>A maps to NM_152565.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:87151850 C>T maps to NM_152565.1 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr8:87162504 G>A maps to NM_152565.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:149575805 C>T maps to ENST00000479613 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:113503589 G>A maps to NM_001690.3 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:113517214 C>T maps to NM_001690.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr3:113507613 A>T maps to NM_001690.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:71190747 A>G maps to NM_001692.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:71187159 C>T maps to NM_001692.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:71170844 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:71191987 C>A maps to NM_001692.3 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr2:71189966 G>A maps to NM_001692.3 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:20077844 G>T maps to NM_001693.3 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:20069654 G>T maps to NM_001693.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:20072361 C>A maps to NM_001693.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:20070410 C>T maps to NM_001693.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:104065050 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr8:104054636 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:10863007 C>T maps to NM_001039362.1 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:10917778 G>A maps to NM_001039362.1 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:10911982 G>A maps to NM_001039362.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:10912015 C>T maps to NM_001039362.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:67817376 C>A maps to NM_015994.3 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:18080957 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:46739760 G>A maps to NM_080653.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:46739261 C>A maps to NM_080653.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:46739832 G>A maps to NM_080653.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:128505429 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr9:117359932 G>A maps to NM_004888.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:117354908 G>T maps to NM_004888.3 E54*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:31514326 G>A maps to NM_130463.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:198509756 G>A maps to ENST00000489986 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:198492613 G>A maps to ENST00000489986 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:54684727 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:54656138 G>A maps to NM_015941.2 N463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:54727286 C>A maps to NM_015941.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:77264625 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:77284778 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr23:77276502 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:77254124 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:77243855 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:77245423 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:77294362 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:77301011 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:77264619 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:77289286 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77243987 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77244765 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77245141 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77268456 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77286913 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77289292 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77298096 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:77254023 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:77284933 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:77298875 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:77268477 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:77296086 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:77301868 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:77243739 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:77243984 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:77268585 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:77245007 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:77254092 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:77298247 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:77245217 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:77267069 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:77270197 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:77284773 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:77275826 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:77244037 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:77286985 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:52523857 C>T maps to NM_000053.2 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:52534421 G>A maps to NM_000053.2 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr13:52515283 G>A maps to NM_000053.2 S1163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr13:52542741 A>G maps to NM_000053.2 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:52544885 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:42571221 G>A maps to NM_006095.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:42627684 G>A maps to NM_006095.2 Y70Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:42415025 C>T maps to NM_006095.2 G1134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:42416728 G>A maps to NM_006095.2 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:42487676 C>T maps to NM_006095.2 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:42592880 C>T maps to NM_006095.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:42557993 T>C maps to NM_006095.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:26148971 C>A maps to NM_016529.4 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:26163783 C>T maps to NM_016529.4 R720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:26343276 C>T maps to NM_016529.4 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:26402263 C>T maps to NM_016529.4 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:26108339 G>T maps to ENST00000381648 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:26125474 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr13:26117486 C>T maps to NM_016529.4 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr13:26343297 C>T maps to NM_016529.4 H833H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:26104728 A>G maps to NM_016529.4 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:26413706 C>T maps to NM_016529.4 N967N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:26343360 C>T maps to NM_016529.4 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:55398982 G>A maps to NM_005603.4 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:55335658 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:55361837 G>A maps to NM_005603.4 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:55336653 C>A maps to NM_005603.4 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:55368293 C>T maps to NM_005603.4 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:55336594 G>A maps to NM_005603.4 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr18:55359124 G>A maps to NM_005603.4 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:55336653 C>A maps to NM_005603.4 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:154318927 C>A maps to NM_020452.3 S1033S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:154307036 C>T maps to NM_020452.3 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:154316886 C>T maps to NM_020452.3 I717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:154319199 C>A maps to NM_020452.3 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:154317882 C>T maps to NM_020452.3 F885F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:154318753 G>A maps to NM_020452.3 P975P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr1:154318945 C>T maps to NM_020452.3 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:1805408 C>A maps to NM_138813.2 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:1802600 G>A maps to NM_138813.2 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:1800384 C>A maps to NM_138813.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:50189644 T>C maps to NM_024837.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:50212511 C>T maps to NM_024837.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:50223501 C>A maps to NM_024837.2 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:50288949 C>T maps to NM_024837.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:50212511 C>T maps to NM_024837.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:50223393 C>A maps to NM_024837.2 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:50288949 C>T maps to NM_024837.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr15:50212483 G>A maps to NM_024837.2 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:50158639 G>T maps to NM_024837.2 V1023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:50223382 T>C maps to NM_024837.2 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:50217857 G>A maps to NM_006045.1 F1012F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:50273518 G>A maps to NM_006045.1 Y488Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:50234076 G>A maps to NM_006045.1 D789D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:50329564 G>A maps to NM_006045.1 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr20:50241781 C>T maps to NM_006045.1 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr20:50217872 G>A maps to NM_006045.1 I1007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:50230251 G>A maps to NM_006045.1 F845F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:50312683 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:77108157 C>T maps to NM_198531.3 F955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:76914502 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:76856499 G>A maps to NM_198531.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:77067104 C>T maps to NM_198531.3 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:77097281 C>T maps to NM_198531.3 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr18:77133985 C>T maps to NM_198531.3 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:77107909 C>A maps to NM_198531.3 I941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:77108157 C>T maps to NM_198531.3 F955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:47101578 C>A maps to NM_022745.3 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:47110889 A>G maps to NM_022745.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:17925167 G>A maps to NM_145691.3 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:35814293 T>G maps to NM_001141972.1 *166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:35747014 C>A maps to NM_080650.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:35834650 G>A maps to NM_080650.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:28564464 C>T maps to NM_016311.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:28564486 T>G maps to NM_016311.3 *107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:142185357 G>A maps to NM_001184.3 S2235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:142281202 G>T maps to NM_001184.3 C347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr3:142224145 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:142186841 G>T maps to NM_001184.3 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:142241617 C>T maps to NM_001184.3 A1406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:142257363 C>A maps to NM_001184.3 E1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:142232476 G>A maps to NM_001184.3 R1503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:142257448 A>C maps to NM_001184.3 V1200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:142168413 G>A maps to NM_001184.3 R2598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:142269003 G>A maps to NM_001184.3 F982F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:142215936 G>A maps to NM_001184.3 R1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr3:142285035 C>T maps to NM_001184.3 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:48500824 C>T maps to NM_130384.1 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:48491530 C>T maps to NM_130384.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr3:48501271 G>T maps to NM_130384.1 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:3581672 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:3577039 C>T maps to NM_139321.2 R1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:3553579 G>T maps to NM_139321.2 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:3619483 C>T maps to NM_139321.2 R1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:3564617 C>T maps to NM_139321.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:3515956 G>A maps to NM_139321.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:3619483 C>T maps to NM_139321.2 R1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr20:3543019 C>T maps to NM_139321.2 Y515Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr20:3565435 C>A maps to NM_139321.2 A1031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:116887485 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:117001449 T>C maps to NM_207303.2 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:116879955 G>T maps to NM_207303.2 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr10:116930835 T>C maps to NM_207303.2 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:117045862 G>T maps to NM_207303.2 E791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:117226685 G>A maps to NM_207303.2 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:117045868 G>T maps to NM_207303.2 E793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:117045790 G>T maps to NM_207303.2 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:76812924 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:76872182 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:76938630 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:76907773 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:76814284 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:76829805 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:76918943 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:76939401 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:76939495 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:76849198 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:76891464 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:76907824 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:76909624 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:76920257 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:76937083 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:76938051 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:76939108 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:76907771 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:76912115 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:76938211 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:76972614 T>G did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:76764012 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:76889165 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:76907710 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:76909626 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:76920184 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:76937677 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:76938148 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:76938340 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:76938006 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:76778763 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:76874294 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:76891465 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:76937610 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:76938188 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr23:76939715 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:76849265 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:76872160 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:76778767 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:76889095 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:76938926 T>G did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:76937070 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr23:76937520 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:76874314 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:76888804 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:76920171 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:76938306 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:76939377 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:76814237 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:76845383 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:76938686 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:76814238 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:76874346 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:76909645 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:76937873 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:76938994 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:76939652 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:76953079 C>T did not map to a codon.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr23:76907621 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:76938906 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:76937747 T>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:76829735 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:76776375 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:76875918 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:76937235 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:76939163 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:76940498 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:76972658 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr6:16306868 G>A maps to NM_000332.3 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:16328250 G>A maps to NM_000332.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:16327539 G>A maps to NM_000332.3 Y334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:16307034 G>T maps to NM_000332.3 S658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:16326648 G>A maps to NM_000332.3 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:16327257 G>T maps to NM_000332.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:16327530 C>T maps to NM_000332.3 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr6:16326632 G>A maps to NM_000332.3 R637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:46096204 G>A maps to NM_013236.3 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:46098593 A>T maps to NM_013236.3 K172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:111893868 C>T maps to NM_002973.3 A1236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr12:111954024 C>T maps to NM_002973.3 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:111907942 G>A maps to NM_002973.3 Y1095Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:111990712 C>T maps to NM_002973.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:111907918 C>T maps to NM_002973.3 A1103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:111951256 C>A maps to NM_002973.3 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:111956086 C>T maps to NM_002973.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:111962998 G>A maps to NM_002973.3 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:28845716 C>T maps to NM_148414.1 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:28846967 G>A maps to NM_148414.1 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:28847782 C>T maps to NM_148414.1 P1092P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr16:28838192 C>T maps to NM_148414.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:92560141 C>A maps to ENST00000359819 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr14:92537315 C>T maps to ENST00000359819 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:92548703 C>A maps to ENST00000359819 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:13337194 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:13337984 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:13337100 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13337038 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13337216 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13338019 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:13337649 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:13337039 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:13337837 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:13338017 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr3:63981735 C>T maps to NM_001177387.1 Y746Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:63975860 C>T maps to NM_001177387.1 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr3:63976487 C>T maps to NM_001177387.1 C545C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:105260698 G>A maps to NM_020725.1 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:105254971 G>A maps to NM_020725.1 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr7:105278903 G>A maps to NM_020725.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:105254974 G>A maps to NM_020725.1 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:105260693 G>A maps to NM_020725.1 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:105305535 C>T maps to NM_020725.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:110032746 G>A maps to NM_153340.4 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:110030325 C>A maps to NM_153340.4 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:110033933 G>T maps to NM_153340.4 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:42273431 G>A maps to NM_020218.1 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:42272137 C>T maps to NM_020218.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr9:93983104 C>T maps to NM_001698.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:93978385 G>A maps to NM_001698.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:74754242 G>A maps to ENST00000412627 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:74753946 G>A maps to ENST00000258081 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:54958152 C>A maps to NM_198437.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr20:54961463 G>A maps to NM_198437.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:1309523 G>A maps to NM_001127230.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:8110513 G>A maps to NM_004217.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:8110893 G>T maps to NM_004217.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr17:8108251 G>A maps to NM_004217.2 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr17:8108284 C>T maps to NM_004217.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr19:57746704 C>T maps to NM_001015878.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:69599556 C>T maps to NM_015570.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:70255894 G>A maps to NM_015570.2 P1231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:70250998 C>T maps to NM_015570.2 F761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:70255978 A>C maps to NM_015570.2 R1259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr7:70252291 G>A maps to NM_015570.2 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:34158855 G>T maps to NM_020371.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:58191779 T>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:58201263 G>A maps to NM_006576.3 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr12:58201378 G>A maps to NM_006576.3 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:32612989 G>A maps to NM_015060.1 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:63541221 G>A maps to NM_000706.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:63543728 G>A maps to NM_000706.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:63544217 G>A maps to NM_000706.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:206225009 C>T maps to NM_000707.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:206224655 C>T maps to NM_000707.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153171296 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:153171374 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153171405 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153171601 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:153171577 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153171046 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr23:153171161 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153171601 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69457031 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69459688 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69454573 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69460100 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69459729 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:69459658 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:69459692 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:69460115 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:69261668 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69261771 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69263837 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69264267 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr23:69263461 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69261810 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69263345 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:69263812 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69263092 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69262152 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69263462 C>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:69263052 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:69269732 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:69263812 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:396833 C>T maps to NM_003502.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:364544 G>A maps to NM_003502.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:63533045 C>T maps to NM_004655.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:63533560 G>A maps to NM_004655.3 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:63545705 G>A maps to NM_004655.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:63554432 C>T maps to NM_004655.3 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:63533620 C>T maps to NM_004655.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:41744489 G>A maps to NM_021913.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:41762392 C>T maps to NM_021913.3 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr19:41736911 C>T maps to NM_021913.3 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr19:41745067 G>C did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:41765472 G>A maps to NM_021913.3 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:41762479 T>C maps to NM_021913.3 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:79168753 C>A maps to ENST00000269392 E682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr17:79172772 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:79177379 G>A maps to ENST00000269392 C181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr17:79173250 C>T maps to ENST00000269392 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:28365574 A>G maps to NM_022461.3 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:28380025 A>C maps to NM_022461.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr3:28373867 G>A maps to NM_022461.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:103851074 G>A maps to NM_148174.2 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:103842138 T>C maps to NM_148174.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:829697 C>T maps to NM_001700.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:45008528 C>T maps to NM_004048.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:235658046 G>A maps to ENST00000366599 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:168726103 C>T maps to NM_020981.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:168725563 C>A maps to NM_020981.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:193150199 C>A maps to NM_003783.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr1:193149789 G>A maps to NM_003783.3 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:41032797 G>A maps to NM_033172.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:41033355 G>A maps to NM_033172.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:41032582 G>T maps to NM_033172.1 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:41032582 G>T maps to NM_033172.1 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:41032926 T>G maps to NM_033172.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:41032582 G>T maps to NM_033172.1 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:31843411 G>T maps to NM_194318.3 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:31897936 C>T maps to NM_194318.3 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:31789215 G>A maps to NM_194318.3 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:134252699 C>T maps to NM_054025.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr11:134251881 G>A maps to NM_054025.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:134253579 G>A maps to NM_054025.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:71603870 G>A maps to NM_080742.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:71571446 G>A maps to NM_080742.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:62449642 C>T maps to NM_006577.5 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:62449790 C>T maps to NM_006577.5 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:122690866 A>T maps to NM_030765.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:122691607 C>T maps to NM_030765.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:182988323 G>A maps to NM_032047.4 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:182988299 C>A maps to NM_032047.4 Y238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:232263032 C>T maps to NM_145236.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:232263242 C>T maps to NM_145236.2 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:232263404 C>T maps to NM_145236.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:232263146 C>T maps to NM_145236.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:232262879 C>T maps to NM_145236.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:232263161 C>T maps to NM_145236.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:232263221 C>T maps to NM_145236.2 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:67183440 G>A maps to NM_033309.2 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:67183689 G>A maps to NM_033309.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr16:67183836 G>A maps to NM_033309.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:81006368 G>A maps to NM_001009905.1 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr17:80992967 G>A maps to NM_001009905.1 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:80904841 G>A maps to NM_001009905.1 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:80914641 T>G maps to NM_001009905.1 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:58020744 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:47230248 G>A maps to NM_153446.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:47243580 C>T maps to NM_153446.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr17:47246167 G>A maps to NM_153446.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:47218677 C>T maps to NM_153446.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr12:670529 C>T maps to NM_173593.3 D970D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:661659 T>C maps to NM_173593.3 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:667190 C>T maps to NM_173593.3 Y848Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:657443 C>T maps to NM_173593.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:666858 C>T maps to NM_173593.3 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:668560 C>T maps to NM_173593.3 G954G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:379965 C>T maps to NM_178537.4 F863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:379965 C>T maps to NM_178537.4 F863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:373206 T>C maps to NM_178537.4 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:375741 G>A maps to NM_178537.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr1:44456098 G>A maps to ENST00000309519 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:44450724 C>T maps to ENST00000309519 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161144905 G>A maps to NM_003779.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:161141752 G>A maps to NM_003779.3 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:161141605 T>C maps to NM_003779.3 *394W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:161143647 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:161143495 G>A maps to NM_003779.3 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:118943070 G>A maps to NM_212543.1 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr3:118931502 G>A maps to NM_212543.1 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr18:29210977 G>A maps to NM_004775.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:29207070 C>A maps to NM_004775.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:104240249 G>T maps to ENST00000297574 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:104240297 C>T maps to ENST00000297574 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:104225228 G>A maps to ENST00000297574 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:104133521 G>A maps to NM_001701.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr9:104124838 C>T maps to NM_001701.3 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:104133418 T>G maps to NM_001701.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:104125257 C>A maps to NM_001701.3 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:104130512 G>A maps to NM_001701.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:117161705 G>A maps to NM_012104.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr11:117161766 T>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:42615304 C>A maps to NM_012105.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:42647523 C>A maps to NM_012105.3 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr21:42613750 A>C maps to NM_012105.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:42609655 G>A maps to NM_012105.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:42629206 C>T maps to NM_012105.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr21:30715069 T>C maps to NM_206866.1 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:90642207 G>A maps to NM_001170794.1 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:90660378 G>A maps to NM_001170794.1 H482H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:90642534 G>A maps to NM_001170794.1 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:90661284 G>A maps to NM_001170794.1 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:90660987 C>T maps to NM_001170794.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr6:90660033 C>T maps to NM_001170794.1 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:64039219 C>T maps to NM_032989.2 E81E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AX-A05Z-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:104026937 G>A maps to NM_001015049.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr14:104026328 G>C maps to NM_001015049.2 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:104026333 G>A maps to NM_001015049.2 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:104027072 G>T maps to NM_001015049.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:79414845 G>A maps to ENST00000436173 Q1316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:79427565 C>A maps to ENST00000436173 P2012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:79405435 C>A maps to ENST00000436173 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:79411841 C>T maps to ENST00000436173 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:79428757 C>T maps to ENST00000436173 L2357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:79409856 C>T maps to ENST00000436173 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:79428954 C>T maps to ENST00000436173 F2422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:79414806 G>A maps to ENST00000436173 G1303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:79414441 C>T maps to ENST00000436173 R1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:40750788 C>T maps to NM_014952.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:40757604 C>A maps to NM_014952.3 C708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr15:40752063 C>A maps to NM_014952.3 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:40752063 C>T maps to NM_014952.3 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:40754306 C>T maps to NM_014952.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:143562690 T>G maps to NM_001702.2 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:143562621 C>A maps to NM_001702.2 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:143603471 C>T maps to NM_001702.2 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:143614790 C>T maps to NM_001702.2 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:143566105 C>A maps to NM_001702.2 Y763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:143569734 C>A maps to NM_001702.2 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:143599542 C>T maps to NM_001702.2 G954G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr8:143604035 A>G maps to NM_001702.2 G1070G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:143614790 C>T maps to NM_001702.2 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:32210255 C>T maps to NM_001703.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr1:32196472 G>A maps to NM_001703.2 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:32222008 G>A maps to NM_001703.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:69653725 C>T maps to NM_001704.2 H345H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:69646409 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:69684662 G>T maps to NM_001704.2 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:70070804 G>T maps to NM_001704.2 G1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr6:70049293 C>T maps to NM_001704.2 A1119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:69349236 G>T maps to NM_001704.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:69759193 C>T maps to NM_001704.2 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr6:69758209 T>C maps to NM_001704.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:69653763 C>A maps to NM_001704.2 S358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:70071235 C>T maps to NM_001704.2 D1357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:69349110 G>T maps to NM_001704.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:69666667 G>T maps to NM_001704.2 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr6:70048879 G>A maps to NM_001704.2 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:69665970 G>A maps to NM_001704.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr6:70082333 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:79031767 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:79059299 C>T maps to ENST00000435091 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:79080547 G>A maps to NM_017451.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:79073732 C>T maps to NM_017451.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:97949384 G>A maps to NM_018842.4 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:97935800 C>T maps to NM_018842.4 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:97946560 G>A maps to NM_018842.4 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:97939784 C>T maps to NM_018842.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:97939784 C>T maps to NM_018842.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:38494162 G>A maps to NM_025045.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:1384733 C>T maps to NM_003933.4 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:1394142 C>T maps to NM_003933.4 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:1394063 C>T maps to NM_003933.4 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:1394474 C>T maps to NM_003933.4 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:1397934 G>A maps to NM_003933.4 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:1394284 G>A maps to NM_003933.4 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:1398282 G>A maps to NM_003933.4 L1147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr16:1396450 C>T maps to NM_003933.4 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:1391137 G>A maps to NM_003933.4 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:33541921 T>C maps to ENST00000360661 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:28971209 G>A maps to NM_012342.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr4:102946404 C>T maps to NM_017935.4 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:88068926 G>A did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr16:88071598 C>T maps to NM_001173543.1 H420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52436833 C>T maps to NM_004656.2 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52442615 T>C maps to NM_004656.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:52437234 G>A maps to NM_004656.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:215646107 G>A maps to NM_000465.2 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:215646172 G>T maps to NM_000465.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:215634033 G>A maps to NM_000465.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:215593651 G>A maps to NM_000465.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr2:215610464 A>G maps to NM_000465.2 Y597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:135458441 G>A maps to NM_020064.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:135458486 C>A maps to NM_020064.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:135458450 G>A maps to NM_020064.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:91182707 C>T maps to NM_020063.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:91182269 G>A maps to NM_020063.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:91182392 C>T maps to NM_020063.1 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:91182683 G>C maps to NM_020063.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:91182449 C>T maps to NM_020063.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:91182158 C>T maps to NM_020063.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:96715278 T>C maps to NM_021570.3 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr9:96714571 G>A maps to NM_021570.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:129321248 G>A maps to NM_003658.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:129312795 G>A maps to NM_003658.4 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:17275537 C>T maps to NM_006317.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:64756888 C>T maps to NM_138456.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:212870361 G>T maps to NM_018664.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr19:49464138 C>T maps to NM_138761.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:35295279 C>A maps to NM_013448.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:35245607 G>A maps to NM_013448.2 R784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:35243688 A>T maps to NM_013448.2 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:35245551 G>T maps to NM_013448.2 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:35280180 C>A maps to NM_013448.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr14:35233935 G>A maps to NM_013448.2 D1251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:35222875 C>T maps to NM_013448.2 S1503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:35262019 C>A maps to NM_013448.2 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:72892157 C>A maps to NM_032408.3 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:72873949 C>T maps to NM_032408.3 K1116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:72903721 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:72863915 G>A maps to NM_032408.3 C1228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr7:72892037 A>G maps to NM_032408.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:56996499 A>G maps to NM_013449.3 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr12:56999092 G>A maps to NM_013449.3 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:56992455 G>A maps to NM_013449.3 R1888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr12:56998973 C>T maps to NM_013449.3 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:56992655 C>A maps to NM_013449.3 G1850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr12:56994976 C>T maps to NM_013449.3 Q1429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:160194178 G>A maps to NM_013450.2 G1853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:160193465 G>T maps to NM_013450.2 S1928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:160303360 G>A maps to NM_013450.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr2:160206388 G>A maps to NM_013450.2 R1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:160255347 G>A maps to NM_013450.2 R986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:160245926 G>A maps to NM_013450.2 R1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:160181374 A>C maps to NM_013450.2 V2100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr19:47725104 A>G maps to NM_001127240.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:27141377 A>G maps to NM_003986.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:66290968 G>A maps to NM_024649.4 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:76740009 A>C maps to NM_024685.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:76739616 A>G maps to NM_024685.3 N716N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:73007663 G>T maps to NM_033028.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:73029293 G>A maps to NM_033028.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:170356009 T>C maps to ENST00000419050 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:122774221 G>A maps to NM_176824.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:122774170 G>A maps to NM_176824.1 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:122770017 G>A maps to NM_176824.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:33427630 G>T maps to NM_198428.2 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:33217123 T>C maps to NM_198428.2 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:33384197 G>A maps to NM_198428.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:33427641 T>C maps to NM_198428.2 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:107435525 C>T maps to NM_001142568.1 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:107491738 G>T maps to NM_001142568.1 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:107520086 C>T maps to NM_001142568.1 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr3:107493570 C>T maps to NM_001142568.1 R641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:107429364 C>T maps to NM_001142568.1 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:107520023 C>T maps to NM_001142568.1 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr3:107491582 G>T maps to NM_001142568.1 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr3:107520038 G>A maps to NM_001142568.1 T883T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:45322316 G>A maps to NM_005581.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:45322388 C>A maps to NM_005581.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:45317469 C>T maps to NM_005581.3 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156628037 G>A maps to NM_021948.3 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:156618579 G>A maps to NM_021948.3 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:156622107 G>T maps to NM_021948.3 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:156618361 G>T maps to NM_021948.3 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:156616617 C>T maps to NM_021948.3 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:156628428 C>T maps to NM_021948.3 C844C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152989045 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152988653 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr23:152966425 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152966184 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:152969515 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:75267741 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:75271173 G>A maps to NM_001170714.1 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:94140444 C>T maps to NM_003567.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr20:52645023 G>A maps to NM_003657.2 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:52644977 C>A maps to NM_003657.2 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:115113346 G>A maps to NM_005872.2 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:115112626 T>C maps to NM_005872.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:59445703 C>T maps to ENST00000407086 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:59152366 G>T maps to ENST00000407086 E736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:59067517 G>T maps to ENST00000407086 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:49493048 G>A maps to NM_198799.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:24989524 C>A maps to NM_001178093.1 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:49299747 A>G maps to NM_001190.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:49300262 C>T maps to NM_001190.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:49303011 G>A maps to NM_001190.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:49299963 C>G maps to NM_001190.3 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:127522500 G>T maps to NM_016567.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:165547332 T>A maps to NM_000055.2 K497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:165547467 G>A maps to NM_000055.2 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:165547489 G>T maps to NM_000055.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:165491208 G>A maps to NM_000055.2 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:165548829 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:41928177 C>T maps to NM_000709.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:41928954 G>T maps to NM_000709.3 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:41916645 C>T maps to NM_000709.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:41928926 C>T maps to NM_000709.3 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:41916711 G>A maps to NM_000709.3 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:80910651 G>A maps to NM_183050.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:80982904 C>T maps to NM_183050.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:80877485 G>A maps to NM_183050.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:31122465 T>C maps to NM_005881.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr16:31122050 A>T maps to NM_005881.2 K229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:85733522 C>T maps to NM_003921.4 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr2:60687937 G>T maps to NM_022893.3 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:60689325 G>A maps to NM_022893.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:60689530 A>G maps to NM_022893.3 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:60689437 G>A maps to NM_022893.3 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr2:60688810 G>A maps to NM_022893.3 H412H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:99641777 C>T maps to NM_138576.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:99642458 C>T maps to NM_138576.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr14:99641792 G>A maps to NM_138576.2 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:99642347 C>T maps to NM_138576.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:52402140 G>T maps to NM_020396.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:52404509 G>A maps to NM_020396.2 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:111907696 C>T maps to NM_138621.3 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:111921748 C>T maps to NM_138621.3 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:111886261 C>T maps to NM_207002.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr2:111881510 G>A maps to NM_138621.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:50170335 C>T maps to NM_138639.1 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:50173528 C>T maps to NM_138639.1 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:50173591 C>T maps to NM_138639.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:18138482 G>A maps to NM_015367.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:18210086 C>T maps to NM_015367.2 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:45259555 C>T maps to NM_005178.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:45260629 C>T maps to NM_005178.4 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:187449516 G>A maps to NM_001706.4 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:187443417 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:187446845 G>A maps to NM_001706.4 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr3:187442757 G>A maps to NM_001706.4 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:187449603 T>G maps to NM_001706.4 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:187447565 G>T maps to NM_001706.4 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:187446172 C>T maps to NM_001706.4 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr17:6930406 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:6929794 C>T maps to NM_181844.3 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:6930372 C>T maps to NM_181844.3 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:6930051 C>T maps to NM_181844.3 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:6930333 C>T maps to NM_181844.3 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:6927917 C>T maps to NM_181844.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:6927917 C>T maps to NM_181844.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:72951687 C>T maps to NM_001707.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:30904014 C>A maps to NM_004765.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:30904039 C>T maps to NM_004765.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr16:30899187 A>G maps to NM_004765.2 *218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:147091958 G>A maps to NM_004326.2 Q666Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:147095727 C>A maps to NM_004326.2 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:147091586 T>C maps to NM_004326.2 H542H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr11:118769750 G>A maps to NM_182557.2 D1291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:118770842 G>A maps to NM_182557.2 G1063G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:118774021 G>A maps to NM_182557.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:136600940 G>A maps to NM_014739.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:136596814 C>T maps to NM_014739.2 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:136589370 C>A maps to NM_014739.2 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:136599391 G>A maps to NM_014739.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr16:81324076 C>A maps to NM_017429.2 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:81298345 G>A maps to NM_017429.2 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:81324058 C>T maps to NM_017429.2 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:81324160 C>T maps to NM_017429.2 C541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:112085726 G>T maps to ENST00000430950 *352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:112065434 G>T maps to NM_031938.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:112050079 G>A maps to NM_031938.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:112064223 G>A maps to NM_031938.4 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:112086951 G>T maps to NM_031938.4 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:39922132 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:39913587 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:39933842 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:39934079 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:39916462 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:39932557 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:39934007 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:39934251 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:39921467 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:39930371 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:39933944 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr23:39932474 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:39922070 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:39937152 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:39922960 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:39933047 G>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:39921479 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:39911597 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:39932569 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:39937151 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr23:39932116 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:39913222 T>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:39913152 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:39921420 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:39932068 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:39933021 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:39932908 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:39921605 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:39922157 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:39933751 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:39935768 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:39932679 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:39931657 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:39922895 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:39930237 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:39933286 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:39937176 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:39921452 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:39916550 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:39930237 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:39931667 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:39932638 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:39921436 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:39922185 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:39932844 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:39933377 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:39934213 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:39934312 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:39934334 G>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:39922121 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:39923699 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:39934046 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:39932428 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:39922895 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr23:39921443 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:129148541 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr23:129147410 C>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:129171431 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:129147216 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:129150145 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:129148887 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129148181 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129150141 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129154986 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129159111 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129162818 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129173211 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129147516 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129149143 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129162795 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:129147629 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr23:129150015 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:129149113 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:129190002 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:129139267 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:129185901 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:129146998 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:129148826 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:129156884 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr23:129147886 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:129173244 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:129148371 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:129156884 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:129150033 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:129148814 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:129148790 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:129149155 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:129156915 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:129162689 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:129184760 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:129147376 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:129189947 G>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:129147461 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr23:129139239 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:129148975 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:129156884 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:23603585 G>A maps to NM_004327.3 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:23656783 C>T maps to NM_004327.3 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr22:23656201 C>T maps to NM_004327.3 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:219525886 C>T maps to NM_004328.4 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:219526920 C>T maps to NM_004328.4 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:197238824 G>A maps to NM_203315.2 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:197249619 G>A maps to NM_203315.2 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:96730957 C>A maps to NM_000710.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:96707033 G>A maps to NM_000623.3 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:96707783 C>A maps to NM_000623.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:27679879 G>T maps to NM_001143810.1 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:70759923 G>A maps to NM_018429.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:70818602 A>G maps to NM_018429.2 T1738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:70785436 G>T maps to NM_018429.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:70858141 C>A maps to NM_018429.2 S2513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:70757753 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:70820039 G>T maps to NM_018429.2 E1888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:70763226 G>T maps to NM_018429.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:70808181 G>T maps to NM_018429.2 E1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:70785300 G>A maps to NM_018429.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr5:70785354 A>G maps to NM_018429.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr5:70805342 G>A maps to NM_018429.2 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:40970644 T>C maps to NM_003766.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:40967951 G>A maps to NM_003766.3 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr14:101004527 G>A maps to NM_020836.3 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:101005565 G>A maps to NM_020836.3 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:18221870 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr23:18189322 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:18213497 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18195759 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:18221837 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:18213473 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:18221623 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:18189289 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:18192280 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:18192349 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:18183236 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:18192194 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:18198648 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:18195787 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:18234645 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:18219963 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr23:18189183 C>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:18194131 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:18198720 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:107391626 G>A maps to NM_001080450.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr6:107390738 G>A maps to NM_001080450.2 D552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:107390102 G>A maps to NM_001080450.2 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:107390786 G>A maps to NM_001080450.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:42122191 A>G maps to NM_207406.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:42122211 G>A maps to NM_207406.3 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:42145871 G>A maps to NM_207406.3 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:42119570 G>T maps to NM_207406.3 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:42145525 G>A maps to NM_207406.3 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:49224863 G>A maps to NM_024603.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:49202043 C>T maps to NM_024603.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:49227038 C>G maps to NM_024603.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:49193580 C>A maps to NM_024603.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:56880152 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:13481450 C>T maps to ENST00000396900 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:13534808 T>C maps to ENST00000396900 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:13541787 C>T maps to ENST00000396900 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:61727034 C>T maps to NM_001139443.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:61725823 C>T maps to ENST00000435278 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr11:61725715 C>T maps to NM_001139443.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:12864106 C>T maps to NM_017682.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:12865483 C>A maps to NM_017682.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:12864160 C>T maps to NM_017682.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr19:12865501 C>A maps to NM_017682.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:70078334 A>G maps to ENST00000393365 *73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:70070998 G>A maps to NM_032735.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr12:70070770 G>A maps to NM_032735.2 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:70066682 G>A maps to NM_032735.2 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr12:70087466 G>A maps to NM_032735.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr7:93625531 G>A maps to ENST00000425626 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102318105 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102317996 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:102317885 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:102317847 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:102318054 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:102564540 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:102564785 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:102564816 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:102564853 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:102471151 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:102471205 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102471241 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101409071 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:101409008 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:14743704 C>T maps to NM_016561.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:17479685 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:17475612 C>T maps to NM_001195.3 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:17475473 C>A maps to NM_001195.3 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:17492713 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:133119094 C>T maps to NM_003571.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:133169166 A>G maps to NM_003571.2 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:133169265 T>C maps to NM_003571.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:133169274 C>T maps to NM_003571.2 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:133118939 C>T maps to NM_003571.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:133119094 C>A maps to NM_003571.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:133191328 C>T maps to NM_003571.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:133185785 G>T maps to NM_003571.2 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr3:133191301 G>A maps to NM_003571.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:156212600 G>A maps to ENST00000368276 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:152772343 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152770130 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:152772035 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152771477 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152772328 A>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152773750 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr23:152770302 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:152771380 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:102004497 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:102004291 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:102005424 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:102005451 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102004410 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr23:102005023 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102004249 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:102004530 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:102005287 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:102004348 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:102004497 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:102005156 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:102005451 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:5025214 C>T maps to NM_003670.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:78415121 C>T maps to NM_001713.2 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr5:78417159 C>T maps to NM_001713.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:60556152 G>A maps to NM_001080512.1 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:60573645 C>T maps to NM_001080512.1 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:60558966 G>A maps to NM_001080512.1 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr10:60549560 C>T maps to NM_001080512.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:32487523 G>A maps to NM_001714.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:32369266 G>A maps to NM_001714.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:32481303 C>T maps to NM_001714.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr12:32490520 C>T maps to NM_001714.2 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:32481147 G>T maps to NM_001714.2 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:32369266 G>A maps to NM_001714.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr12:32480564 C>T maps to NM_001714.2 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:95483010 C>T maps to NM_001003800.1 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr9:95482728 G>A maps to NM_001003800.1 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:95491389 C>T maps to NM_001003800.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:18232940 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:43524621 C>T maps to NM_001197.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:127821522 C>T maps to NM_139343.1 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:127816724 G>A maps to NM_139343.1 N288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:127825780 C>T maps to NM_139343.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:127809842 C>T maps to NM_139343.1 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:51685944 G>T maps to NM_016293.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr12:51685721 G>A maps to NM_016293.2 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:22478955 G>A maps to NM_018688.4 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:102248381 G>T maps to NM_001166.3 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr11:102221166 G>A maps to NM_001166.3 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:102220611 T>G maps to NM_001166.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:102248841 T>C maps to NM_001166.3 C595C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:102206865 G>A maps to NM_182962.1 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:102201973 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:76219692 C>T maps to NM_001012270.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:32703728 G>A maps to NM_016252.3 T2365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:32750028 G>T maps to NM_016252.3 E3900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:32640614 C>T maps to NM_016252.3 C752C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:32724694 C>T maps to NM_016252.3 V2850V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:32735647 G>A maps to NM_016252.3 T3431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:32740506 T>C maps to NM_016252.3 C3673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:32724748 C>T maps to NM_016252.3 H2868H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:32667223 G>T maps to NM_016252.3 E1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:32667406 T>C maps to NM_016252.3 N1374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:32824934 C>T maps to NM_016252.3 R4654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr2:32690158 T>C maps to NM_016252.3 L1761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:32639967 G>T maps to NM_016252.3 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:32707633 C>T maps to NM_016252.3 S2560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:32836582 T>C maps to NM_016252.3 D4776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:32740825 C>T maps to NM_016252.3 L3780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:32725072 G>A maps to NM_016252.3 S2976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:32690173 T>C maps to NM_016252.3 A1766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:32832644 C>T maps to NM_016252.3 R4732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:32724665 G>T maps to NM_016252.3 E2841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:32726951 A>G maps to NM_016252.3 R3068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:32770834 G>T maps to NM_016252.3 E4240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr2:32640932 G>A maps to NM_016252.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:32658771 T>C maps to NM_016252.3 H1103H. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A11Y-01A-21D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:61869288 T>C maps to NM_139317.1 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr20:61870902 G>T maps to NM_139317.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:53793278 C>A maps to NM_033341.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:103474150 G>T maps to NM_017693.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:103492014 G>T maps to NM_017693.3 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr13:103492160 T>C maps to NM_017693.3 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:121986483 C>T maps to NM_001001786.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:11403592 C>T maps to ENST00000427279 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:11405574 C>T maps to ENST00000427279 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:11412315 C>T maps to ENST00000427279 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:11406541 C>T maps to ENST00000427279 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:11418935 C>T maps to ENST00000427279 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:11412357 C>A maps to ENST00000427279 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:91337523 A>G maps to NM_000057.2 G1049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:91295089 T>C maps to NM_000057.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:91326079 C>T maps to NM_000057.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:91293196 C>T maps to NM_000057.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:91346817 C>T maps to NM_000057.2 A1142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:91358382 C>A maps to NM_000057.2 I1376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:91358441 T>A maps to NM_000057.2 L1396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:28601215 C>A did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:28598321 G>C maps to NM_000386.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:97983644 C>T maps to NM_013314.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr10:97964349 G>A maps to NM_013314.3 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56113368 G>A maps to NM_001487.3 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr7:43846818 C>T maps to NM_000712.3 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:43840109 C>T maps to NM_000712.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:40953834 G>A maps to NM_000713.2 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr19:40964285 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:169346189 T>G maps to NM_003666.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:169346070 G>T maps to NM_003666.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr1:169345877 G>A maps to NM_003666.2 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr1:169347744 C>T maps to NM_003666.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:40398071 A>G maps to NM_001003940.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A052-01A-11W-A027-09 chr15:40398214 G>A maps to NM_001003940.1 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr15:40398145 G>A maps to NM_001003940.1 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:22615488 C>A maps to NM_005180.6 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:22618326 G>A maps to NM_005180.6 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr8:22037926 T>C maps to NM_006129.4 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:22054865 C>T maps to NM_006129.4 N680N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr8:22056729 C>A maps to ENST00000313857 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:22054346 C>T maps to NM_006129.4 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:22066961 C>T maps to NM_006129.4 C860C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:50659057 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:50659398 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:50659105 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:50653979 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:50659067 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr23:50653985 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr23:50653945 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr23:50659597 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:6759007 G>T maps to NM_001200.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:6750844 C>T maps to NM_001200.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr20:6750797 C>T maps to NM_001200.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr20:6750886 G>A maps to NM_001200.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr4:79763641 G>A maps to NM_198892.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:79782541 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr4:79747296 A>G maps to NM_198892.1 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:79800023 G>T maps to NM_198892.1 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr4:79792102 G>A maps to NM_198892.1 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:79782541 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:55638952 C>T maps to NM_021073.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:55739584 C>A maps to NM_021073.2 G27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr6:55623844 G>A maps to NM_021073.2 N391N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:55739341 C>A maps to NM_021073.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr6:7880554 A>G maps to NM_001718.4 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:7879305 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr20:55748339 G>A maps to NM_001719.2 Y354Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr20:55777546 C>T maps to NM_001719.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:40228844 C>T maps to NM_001720.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:40230343 C>T maps to NM_001720.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:33976920 G>A maps to NM_133468.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr7:34182937 C>T maps to NM_133468.3 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr7:34118742 G>A maps to NM_133468.3 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:88679140 C>T maps to NM_004329.2 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:88671995 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr4:96051102 G>T maps to ENST00000440890 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:203242262 C>T maps to NM_001204.6 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:203383609 A>G maps to NM_001204.6 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:203420176 C>T maps to NM_001204.6 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:43292930 G>A maps to NM_014753.3 Q683Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:43316000 C>T maps to NM_014753.3 R939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:43289380 C>T maps to NM_014753.3 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:43292422 C>T maps to NM_014753.3 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr10:43316000 C>T maps to NM_014753.3 R939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:43315743 C>T maps to NM_014753.3 R881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:15568078 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15527514 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15548112 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:15540508 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr23:15560256 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:15560269 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:15527468 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:15549481 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:15540558 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:15543426 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:15543482 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:15555383 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:15555404 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:15527514 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:15560134 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15540683 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15543479 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:15564971 C>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:15540477 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:15564932 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:83936885 G>A maps to NM_001717.3 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:83926484 G>A maps to NM_001717.3 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:83933378 G>A maps to NM_001717.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:83935605 G>A maps to NM_001717.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:83926718 G>T maps to NM_001717.3 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:16419598 G>A maps to NM_017637.5 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:16436042 C>A maps to NM_017637.5 E717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:16419316 G>A maps to NM_017637.5 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr9:16419574 C>T maps to NM_017637.5 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:16727881 G>A maps to NM_017637.5 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:16435689 G>T maps to NM_017637.5 I834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:16436741 G>A maps to NM_017637.5 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr9:16552541 C>A maps to NM_017637.5 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:59970199 G>A maps to NM_004330.2 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:59972497 T>C maps to NM_004330.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:133784269 C>T maps to NM_004052.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr1:151010105 G>A maps to NM_138278.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:113002256 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:112968672 G>A maps to ENST00000273395 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:112991419 G>A maps to ENST00000273395 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:113002318 G>A maps to ENST00000273395 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr3:113004236 G>A maps to ENST00000273395 P995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr3:113003293 C>T maps to ENST00000273395 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr4:13615172 C>T maps to NM_148894.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:13603509 C>A maps to NM_148894.2 E1672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:13603609 G>A maps to NM_148894.2 I1638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:13602661 T>C maps to NM_148894.2 V1954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:13578511 G>A maps to NM_148894.2 D2996D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:13602067 G>A maps to NM_148894.2 F2152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:13604638 C>T maps to NM_148894.2 S1295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:13584297 G>T maps to NM_148894.2 T2832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:13602499 G>A maps to NM_148894.2 Y2008Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:13612568 G>A maps to NM_148894.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr4:13602067 G>A maps to NM_148894.2 F2152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:13597535 A>G maps to NM_148894.2 G2684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:13578610 G>T maps to NM_148894.2 S2963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:13605993 T>G maps to NM_148894.2 R844R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:13602067 G>A maps to NM_148894.2 F2152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:13602067 G>A maps to NM_148894.2 F2152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:149871662 T>G maps to NM_016074.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:149871842 C>T maps to NM_016074.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:134346661 G>T maps to NM_001724.4 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:134346627 G>A maps to NM_001724.4 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:134346693 C>T maps to NM_001724.4 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:3119667 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:3152778 C>T maps to NM_004332.2 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:36938937 T>C maps to NM_001725.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:36953196 C>T maps to NM_001725.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:36953196 C>A maps to NM_001725.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:65850179 C>T maps to ENST00000321892 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:65882298 C>T maps to ENST00000321892 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:65972026 T>C maps to ENST00000321892 V3019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:65850453 A>T maps to ENST00000321892 K338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:65905779 T>G maps to ENST00000321892 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:65907644 C>T maps to ENST00000321892 I1341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:65941525 T>C maps to ENST00000321892 G2360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr17:65850650 T>C maps to ENST00000321892 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:140508717 G>T maps to NM_004333.4 C194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:140482851 G>T maps to NM_004333.4 S428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:140454023 G>A maps to NM_004333.4 H568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:112117113 C>T maps to NM_006768.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr12:112110569 C>T maps to NM_006768.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:112096634 G>A maps to NM_006768.3 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr12:112103456 G>A maps to NM_006768.3 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:41245530 C>A maps to ENST00000471181 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:41223139 G>A maps to ENST00000471181 T1619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:41234450 G>A maps to ENST00000471181 R1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:41246506 C>T maps to ENST00000471181 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:41201211 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:41226450 A>T maps to ENST00000471181 S1546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:41244934 C>T maps to ENST00000471181 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:41245719 T>G maps to ENST00000471181 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:32907424 A>T maps to NM_000059.3 K604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:32918717 T>C maps to NM_000059.3 L2289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:32893220 A>G maps to NM_000059.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:32907142 G>T maps to NM_000059.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:32911180 G>T maps to NM_000059.3 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:32929415 G>T maps to NM_000059.3 E2476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:32914848 C>T maps to NM_000059.3 N2119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:32929303 T>C maps to NM_000059.3 D2438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr13:32929039 C>T maps to NM_000059.3 T2350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:32911682 C>A maps to NM_000059.3 S1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:32912812 G>T maps to NM_000059.3 E1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr13:32914476 C>T maps to NM_000059.3 N1995N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:154327608 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:154348305 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr23:154305453 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:154301688 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:154345002 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr23:154317626 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154319105 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154348283 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:154307012 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:154348404 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:50191477 C>T maps to ENST00000342989 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50181064 C>A maps to ENST00000342989 E944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:32940704 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:32943249 T>C maps to ENST00000395289 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:136913282 C>T maps to NM_007371.3 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:136913405 G>A maps to NM_007371.3 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr9:136901325 G>A maps to NM_007371.3 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:136901246 C>A maps to NM_007371.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:136901430 G>A maps to NM_007371.3 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:136913390 C>T maps to NM_007371.3 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr9:136901204 G>A maps to NM_007371.3 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:136907016 C>T maps to NM_007371.3 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:136913309 G>A maps to NM_007371.3 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:15366192 G>A maps to NM_058243.2 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:15383823 T>C maps to NM_058243.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:15350021 C>T maps to NM_058243.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:15366918 A>T maps to NM_058243.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:50353863 G>A maps to NM_001173984.2 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:50368631 C>A maps to NM_001173984.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:50353168 C>A maps to NM_001173984.2 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:137502261 C>T maps to NM_139199.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:137502261 C>T maps to NM_139199.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:137506841 G>A maps to NM_139199.1 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:137497812 C>A maps to NM_139199.1 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr5:137496602 G>A maps to NM_139199.1 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:137486475 T>C maps to NM_139199.1 S1026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:137499033 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:137501617 C>A maps to NM_139199.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:864600 C>T maps to NM_001009877.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:878567 C>T maps to NM_001009877.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:876275 G>A maps to NM_001009877.2 D388D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A103-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr5:879939 C>T maps to NM_001009877.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:92467669 G>A maps to ENST00000347608 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:92428329 C>T maps to ENST00000347608 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:92442824 G>T maps to ENST00000347608 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:92446228 T>G maps to ENST00000347608 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:92459750 G>T maps to ENST00000347608 E755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:92433817 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:92446847 G>T maps to ENST00000347608 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:92470742 G>T maps to ENST00000347608 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:92442824 G>T maps to ENST00000347608 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:92459797 T>C maps to ENST00000347608 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:92446295 G>T maps to ENST00000347608 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:92446295 G>T maps to ENST00000347608 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:92445133 C>T maps to ENST00000347608 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:28268665 G>A maps to NM_004899.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:28210899 C>T maps to NM_004899.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:105693075 G>T maps to NM_001519.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:105722866 G>A maps to NM_001519.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105677501 G>A maps to NM_001519.2 D651D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:105739058 C>T maps to NM_001519.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:105685509 G>A maps to NM_001519.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:37702417 G>A maps to NM_018310.3 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:37702559 C>T maps to NM_018310.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:37702169 C>A maps to NM_018310.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr8:37706117 T>C maps to NM_018310.3 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:59761064 C>T maps to NM_032043.2 Q1114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr17:59885947 C>T maps to NM_032043.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:59871020 T>C maps to NM_032043.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:59924494 T>C maps to NM_032043.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:59761117 C>A maps to NM_032043.2 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:59853824 T>C maps to NM_032043.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:59878763 C>T maps to NM_032043.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:34924950 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:34925419 G>A maps to NM_018321.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr5:34925518 T>A maps to NM_018321.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:66108473 G>A maps to NM_001024957.1 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr14:36331797 C>T maps to NM_032352.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:36300614 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:36334962 G>A maps to NM_032352.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:166779475 C>A maps to ENST00000360961 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:9781321 C>T maps to NM_001003694.1 C413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:9788072 G>A maps to NM_001003694.1 E1138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:9775908 C>T maps to NM_001003694.1 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:9780874 C>T maps to NM_001003694.1 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:9787262 G>T maps to NM_001003694.1 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:9787379 C>T maps to NM_001003694.1 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:9781273 C>T maps to NM_001003694.1 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:9775986 C>T maps to NM_001003694.1 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:9784767 C>T maps to NM_001003694.1 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:9783720 C>T maps to NM_001003694.1 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:36198325 G>A maps to NM_015695.2 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:36168896 T>C maps to NM_015695.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:36175166 G>A maps to NM_015695.2 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr6:36181951 C>T maps to NM_015695.2 R926R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:135570440 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:135572635 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:135574250 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135572319 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135574406 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:135574247 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135570561 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135574119 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:135572531 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135572509 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:135574150 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135572433 G>A did not map to a codon.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr23:135570304 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135570693 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135574301 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:135570621 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135574329 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:135574295 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:55812938 C>T maps to NM_032430.1 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:55805752 C>T maps to NM_032430.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:55817693 C>T maps to NM_032430.1 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr11:1466583 G>A maps to NM_003957.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:1475825 C>T maps to NM_003957.2 H552H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr21:40608667 G>A maps to NM_018963.3 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:40559166 C>A maps to NM_018963.3 E2250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:40604372 C>A maps to NM_018963.3 E940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:40568601 C>T maps to NM_018963.3 S2131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:40590105 G>A maps to NM_018963.3 R1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:40608670 C>T maps to NM_018963.3 A872A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:40559236 T>C maps to NM_018963.3 V2226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:40578100 G>A maps to NM_018963.3 R1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:40568742 A>G maps to NM_018963.3 N2084N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:40568601 C>T maps to NM_018963.3 S2131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:40604197 G>A maps to NM_018963.3 R969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:40590151 C>T maps to NM_018963.3 P1195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:79945464 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:79948520 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:79975092 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:79936859 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:79942390 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:79952253 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:79955510 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:79990691 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:79938119 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:79945583 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:79947443 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:80047447 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:79932557 T>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:79973126 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:80001134 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:79932301 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:79937996 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:79942390 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:79932611 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:79979254 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:79947593 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:79965029 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:79990650 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:80001077 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:79942390 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:79945289 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:79984299 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:79984338 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:79980544 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:79960224 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:79947635 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:79973249 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:79979261 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:79985480 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:79999588 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:79932847 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:79932715 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:79975092 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:79984260 T>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:79932479 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:79938046 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:79948475 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:79978264 G>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:79988954 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:79945474 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:79936866 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:79991558 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:79999580 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:79952302 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:80064786 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:32841953 C>T maps to NM_001143888.1 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:580778 C>T maps to NM_001728.2 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:580727 C>T maps to NM_001728.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr3:49699435 G>A maps to NM_003458.3 A3386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:49689742 C>T maps to NM_003458.3 T918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49691614 G>A maps to NM_003458.3 T1542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49694789 C>T maps to NM_003458.3 R2601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:49701952 C>T maps to NM_003458.3 G3902G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:49695088 C>T maps to NM_003458.3 I2700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:49699165 C>T maps to NM_003458.3 Y3296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:49694068 A>G maps to NM_003458.3 S2360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:49690732 G>A maps to NM_003458.3 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr3:49690324 G>A maps to NM_003458.3 A1112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:49701928 C>T maps to NM_003458.3 S3894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:49694977 C>T maps to NM_003458.3 S2663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:49699984 C>T maps to NM_003458.3 S3569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:49680203 C>T maps to NM_003458.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr3:49691963 A>C maps to NM_003458.3 R1659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:55472942 C>T maps to NM_057176.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:55470702 C>T maps to NM_057176.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:55472946 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:55472813 G>A maps to NM_057176.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr9:116132394 C>G maps to NM_017688.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:15707182 G>A maps to ENST00000382346 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr4:15704839 C>T maps to ENST00000382346 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:15713433 C>T maps to ENST00000382346 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:17514944 G>A maps to NM_004335.2 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr11:122852119 G>T maps to NM_001098169.1 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:93717040 C>A maps to NM_003972.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:93722342 G>T maps to NM_003972.2 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:93778595 A>G maps to NM_003972.2 Q1589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:93778692 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:93713613 G>T maps to NM_003972.2 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:93767939 C>T maps to NM_003972.2 R1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:93744019 A>G maps to NM_003972.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr15:83698936 G>A maps to NM_025238.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:108029082 C>T maps to NM_001018072.1 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:107914390 C>A maps to NM_001018072.1 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:108008923 T>C maps to NM_001018072.1 H662H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:108013883 G>A maps to NM_001018072.1 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:108011213 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:124057285 C>T maps to ENST00000368994 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:124066802 C>T maps to ENST00000368994 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:124091964 C>T maps to ENST00000368994 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:124094412 G>A maps to ENST00000368994 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:124094412 G>A maps to ENST00000368994 S395S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BG-A18B-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:1986552 C>T maps to NM_017797.3 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:1987251 C>T maps to NM_017797.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:1990817 G>A maps to NM_017797.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:1990752 G>A maps to NM_017797.3 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:11903588 G>T maps to NM_014962.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr20:11903545 G>A maps to NM_014962.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr20:11903890 C>A maps to NM_014962.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:11899024 T>C maps to NM_014962.2 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:11903663 G>T maps to NM_014962.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:11903728 T>C maps to NM_014962.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:105716945 G>A maps to NM_033271.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:93709113 C>T maps to NM_001002860.2 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:93761137 A>C maps to NM_001002860.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:93712230 A>G maps to NM_001002860.2 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:93709302 T>C maps to NM_001002860.2 G905G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:93717989 T>C maps to NM_001002860.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:93760917 C>A maps to NM_001002860.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:92606758 C>T maps to NM_183242.3 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:38142949 G>A maps to NM_052893.1 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:38312861 G>A maps to NM_052893.1 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:38548204 C>A maps to NM_052893.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:75681097 G>A maps to NM_001729.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:75681118 G>A maps to NM_001729.2 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:75695352 A>G maps to NM_001729.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:75695343 C>A maps to NM_001729.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:15686739 C>A maps to NM_000060.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr3:15686712 T>C maps to NM_000060.2 H450H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:15686643 T>G maps to NM_000060.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:15685950 A>G maps to NM_000060.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:15686415 A>G maps to NM_000060.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:52525557 C>T maps to NM_152265.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr21:18970964 C>T maps to NM_001130914.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:111365928 C>T maps to NM_017589.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100611137 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100630136 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100614294 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:100630207 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100617569 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:100617555 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:100612523 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:100630194 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:100615740 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100615677 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100609633 C>T did not map to a codon.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr23:100624985 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:100614308 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:26509239 C>T maps to NM_001732.2 C473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:26509188 C>A maps to NM_001732.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:26508936 C>T maps to NM_001732.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr6:26468467 G>A maps to NM_007049.3 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:26459991 C>A maps to NM_007049.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:26459751 G>T maps to NM_007049.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:26468545 C>T maps to NM_007049.3 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:26463514 C>T maps to NM_007049.3 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:26468780 C>A maps to ENST00000265424 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:26388358 T>C maps to NM_001197237.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:26388484 G>A maps to NM_001197237.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:26390423 G>T maps to NM_001197237.1 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:26390356 C>A maps to NM_001197237.1 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:26392963 C>T maps to NM_001197237.1 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:26392963 C>T maps to NM_001197237.1 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:26406326 G>A maps to NM_007048.5 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:26373140 C>T maps to NM_001197246.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:26452182 T>C maps to NM_006994.4 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:26444392 G>A maps to NM_006994.4 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:26446178 C>T maps to NM_006994.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:26444443 C>T maps to NM_006994.4 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:26444374 G>A maps to NM_006994.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:26446037 C>T maps to NM_006994.4 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:32362539 G>A maps to ENST00000468270 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr6:32362626 G>A maps to ENST00000468270 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:32364112 C>A maps to ENST00000468270 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:180432367 G>A maps to NM_197975.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:180431745 C>T maps to NM_197975.2 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:180431432 C>T maps to NM_197975.2 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:180338411 G>A maps to NM_001040462.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:180374689 G>A maps to NM_024850.2 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:180335640 C>T maps to NM_001040462.2 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:180374630 C>T maps to NM_024850.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:180338454 G>T maps to NM_001040462.2 G172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr5:180477301 C>T maps to NM_152547.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:103296369 C>T maps to NM_033637.2 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:111415132 C>A maps to NM_004336.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:111415132 C>A maps to NM_004336.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:40502377 G>A maps to ENST00000412359 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:116640870 C>A maps to NM_032725.3 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:99015050 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:105564574 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:105564688 A>G maps to NM_007073.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:105577342 G>A maps to NM_007073.4 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:105564608 G>A maps to NM_007073.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:56389718 G>A maps to NM_004758.2 H821H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:56403725 G>A maps to NM_004758.2 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:56386645 G>A maps to NM_004758.2 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr17:56405068 G>A maps to NM_004758.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:56386509 G>A maps to NM_004758.2 R1375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:56393432 G>A maps to NM_004758.2 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:56388997 G>A maps to NM_004758.2 I1005I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:56388243 C>A maps to NM_004758.2 E1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:201683614 G>A maps to ENST00000452790 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr10:77807058 C>T maps to NM_032024.3 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:15138391 G>A maps to NM_153244.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:21414798 C>A maps to NM_001010896.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:115885668 C>T maps to NM_018017.2 T863T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:115895995 C>A maps to NM_018017.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:115891900 A>G maps to NM_018017.2 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:115887397 G>A maps to NM_018017.2 R739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:115904347 C>A maps to NM_018017.2 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:98742652 C>A maps to NM_015652.2 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:98744014 T>C maps to NM_015652.2 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:124457437 T>C maps to NM_001010912.1 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:135168878 G>A maps to NM_001098483.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:96970502 C>T maps to NM_207321.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:96970508 T>G maps to NM_207321.2 Y238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:96979658 T>C maps to NM_207321.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:96985102 C>T maps to NM_207321.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:127436517 G>A maps to ENST00000356792 Q1020Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:127442316 G>T maps to ENST00000356792 E1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:127429068 T>A maps to ENST00000356792 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr10:127429206 T>G maps to ENST00000356792 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:127436430 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:21804798 C>T maps to NM_207371.3 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:21805749 C>T maps to NM_207371.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:102749104 G>T maps to NM_021830.4 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:102750213 A>G maps to NM_021830.4 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:102750628 C>T maps to NM_021830.4 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:72539472 G>A maps to NM_152710.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:72541715 C>A maps to NM_152710.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:72539472 G>A maps to NM_152710.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:72541721 G>A maps to NM_152710.2 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:72532312 C>T maps to NM_152710.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:72532303 C>T maps to NM_152710.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:72541686 G>A maps to NM_152710.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:72531152 C>T maps to NM_152710.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr10:99968653 C>T maps to ENST00000314594 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:99968053 C>A maps to ENST00000314594 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:99991444 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:99968338 A>G maps to ENST00000314594 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:71391595 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:11894093 G>A maps to NM_153256.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:75671523 C>T maps to NM_001001791.2 K125K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A177-01A-21D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:99349899 C>T maps to NM_001009997.2 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:33103362 C>T maps to ENST00000375025 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:32863454 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:33135307 T>G maps to ENST00000375025 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:50532818 G>A maps to NM_001135196.1 Q743Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:50531438 C>T maps to NM_001135196.1 H283H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:50530649 C>T maps to NM_001135196.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:50533580 C>T maps to NM_001135196.1 A997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:50531153 C>T maps to NM_001135196.1 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:50532374 G>A maps to NM_001135196.1 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr10:50533700 C>A maps to NM_001135196.1 S1037S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr10:50531009 C>A maps to NM_001135196.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:103753314 G>A maps to NM_024541.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:115526206 C>T maps to NM_182601.1 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:115527102 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr10:115540500 G>A maps to NM_001193435.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:115533996 C>T maps to NM_182601.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:115540377 C>T maps to NM_001193435.1 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:124712451 G>A maps to NM_024942.3 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:128193240 C>T maps to NM_001004298.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:128153394 G>T maps to NM_001004298.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:128193575 C>A maps to NM_001004298.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr10:128192817 T>C maps to NM_001004298.2 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:128153289 A>T maps to NM_001004298.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:134261360 G>T maps to NM_173541.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:134261318 G>A maps to NM_173541.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:118084836 T>C maps to NM_198515.2 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:118117391 C>T maps to NM_198515.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:118117438 A>G maps to NM_198515.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:111753294 C>T maps to NM_022761.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:61557966 G>A maps to NM_014206.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr11:8948673 G>A maps to NM_020643.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:68029139 G>A maps to NM_022338.3 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:68029928 C>T maps to NM_022338.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr11:68030294 G>A maps to NM_022338.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:76162953 C>A maps to ENST00000393457 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:76257148 G>A maps to ENST00000393457 V1195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:76239457 G>A maps to ENST00000393457 Q715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:76170983 T>C maps to ENST00000393457 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:33566439 C>T maps to ENST00000389726 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:33565499 C>T maps to ENST00000389726 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:33682430 C>T maps to ENST00000389726 F1719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:33596360 C>T maps to ENST00000389726 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:33566751 C>T maps to ENST00000389726 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:33689438 C>T maps to ENST00000389726 I1769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr11:33667422 A>G maps to ENST00000389726 A1576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:33565286 A>G maps to ENST00000389726 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:33572758 C>A maps to ENST00000389726 A934A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:33628319 C>A maps to ENST00000389726 P1380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:33573675 G>A maps to ENST00000389726 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:33565124 G>A maps to ENST00000389726 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:33667381 C>T maps to ENST00000389726 L1563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:6231333 C>A maps to NM_173525.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:6232256 C>T maps to NM_173525.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:6232256 C>T maps to NM_173525.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:128772608 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:62435058 G>A maps to ENST00000431002 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr11:47183179 G>A maps to NM_001003677.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:47183134 A>G maps to NM_001003677.1 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:71822258 G>A maps to NM_014042.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr11:111154825 C>T maps to NM_198498.1 Y11Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:93494692 C>T maps to ENST00000354421 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:93494832 G>A maps to ENST00000354421 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:122795636 G>A maps to NM_024806.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:122756574 A>G maps to NM_024806.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:122774794 G>A maps to NM_024806.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:122774677 G>A maps to NM_024806.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:122830152 G>T maps to NM_024806.2 *779Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:108263971 C>A maps to NM_152587.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:108302474 C>A maps to NM_152587.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:108263932 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:77580782 C>T maps to NM_024684.2 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:101951949 C>T maps to NM_032930.2 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:101951949 C>T maps to NM_032930.2 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:86056715 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:86017480 T>C maps to NM_016401.3 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:82643837 C>A maps to NM_145018.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:82641315 G>A maps to NM_145018.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:63585754 C>T maps to NM_138471.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:64717284 G>T maps to NM_001037225.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:64707152 C>T maps to NM_001037225.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:109294541 G>A maps to NM_207645.3 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:109294442 C>T maps to NM_207645.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:111385526 C>T maps to NM_207430.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:111385530 G>T maps to NM_207430.2 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:61533109 C>T maps to NM_001127392.1 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr11:61539127 C>T maps to NM_001127392.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:61543556 C>T maps to NM_001127392.1 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr11:61533504 C>T maps to NM_001127392.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:111167005 G>A maps to ENST00000355430 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:45928444 C>T maps to NM_001080446.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:91347328 G>T maps to NM_152638.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr12:91347790 G>T maps to NM_152638.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr12:107365081 T>C maps to NM_152261.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:82796815 C>T maps to NM_032230.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:88436684 G>T maps to NM_001009894.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:88433989 A>G maps to NM_001009894.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:88436684 G>T maps to NM_001009894.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:110205844 C>T maps to NM_032829.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:110206321 G>A maps to NM_032829.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:32138388 C>T maps to NM_018169.3 S1500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:32138841 A>G maps to NM_018169.3 E1651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:32136501 C>T maps to NM_018169.3 N871N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:32138430 C>T maps to NM_018169.3 S1514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:32136111 A>G maps to NM_018169.3 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:32135910 A>G maps to NM_018169.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:32137705 G>T maps to NM_018169.3 E1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:32138187 G>A maps to NM_018169.3 T1433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:21679817 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:4609417 G>A maps to NM_020374.2 N442N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:4627416 G>A maps to NM_020374.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:4643427 G>T maps to NM_020374.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:4626355 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:4634483 C>A maps to NM_020374.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:4645320 C>A maps to NM_020374.2 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:40114782 A>G maps to NM_001031748.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:40076805 G>A maps to NM_001031748.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:40034796 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:40078719 A>T maps to NM_001031748.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:103872167 C>A maps to NM_001099336.1 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:103696194 G>A maps to NM_001099336.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:103872167 C>A maps to NM_001099336.1 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr12:103700091 C>T maps to NM_001099336.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:117155698 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:88376878 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:88390423 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:88379773 G>A maps to NM_152589.1 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:112702993 G>C maps to NM_001109662.2 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:112668574 A>G maps to NM_001109662.2 A1912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:112607325 G>A maps to NM_001109662.2 G3891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr12:112617163 C>T maps to NM_001109662.2 T3503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:112657287 G>A maps to NM_001109662.2 R2154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:112616817 C>T maps to NM_001109662.2 E3588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:112674830 G>A maps to NM_001109662.2 R1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:112690233 G>A maps to NM_001109662.2 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr12:112654999 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:112622299 G>A maps to NM_001109662.2 S3318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:112691861 C>T maps to NM_001109662.2 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:112677782 G>T maps to NM_001109662.2 A1497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:112620881 G>A maps to NM_001109662.2 F3484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:112623013 C>T maps to NM_001109662.2 T3080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:112694252 T>C maps to NM_001109662.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:112688836 T>C maps to NM_001109662.2 G1046G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:113629183 C>T maps to NM_032848.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:113624751 C>T maps to NM_032848.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:6806530 G>A maps to NM_153685.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:6806468 G>A maps to NM_153685.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:48884615 C>T maps to NM_152319.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:64664446 T>G maps to NM_001170633.1 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:64746821 C>T maps to NM_001170633.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:64746761 T>G maps to NM_001170633.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:64746745 C>A maps to NM_001170633.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:64746806 C>T maps to NM_001170633.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:64661028 T>C maps to NM_001170633.1 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr12:64679738 C>T maps to NM_001170633.1 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:14976264 C>A maps to NM_175874.3 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:97085075 G>A maps to ENST00000342887 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:97087498 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:97084962 G>T maps to ENST00000342887 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:97051677 G>T maps to ENST00000342887 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:97147572 G>A maps to ENST00000342887 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:97052057 G>A maps to ENST00000342887 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:97137180 G>A maps to ENST00000342887 E832E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:97073531 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:97073483 C>T maps to ENST00000342887 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:97147572 G>A maps to ENST00000342887 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr12:97114340 C>G maps to ENST00000342887 Y746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:64588302 C>T maps to ENST00000311915 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:64587846 G>A maps to ENST00000311915 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:14959565 C>A maps to NM_001013698.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:14959515 G>A maps to NM_001013698.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:27235080 G>A maps to ENST00000398815 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:25148921 G>A maps to NM_001101339.1 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:25148958 C>T maps to NM_001101339.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:31491641 C>A maps to NM_032849.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:31495937 C>T maps to NM_032849.3 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:31491569 T>G maps to NM_032849.3 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:113333489 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr14:57114170 C>T maps to NM_017799.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:57088287 C>T maps to NM_017799.3 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:57088257 C>T maps to NM_017799.3 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:57084005 C>T maps to NM_017799.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:90769175 C>T maps to NM_017970.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:90769175 C>T maps to NM_017970.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr14:90783147 G>A maps to NM_017970.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:90769175 C>T maps to NM_017970.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:90755278 C>A maps to NM_017970.2 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:90769175 C>T maps to NM_017970.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:90778778 C>T maps to NM_017970.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr14:90767597 C>T maps to NM_017970.2 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:57947361 G>A maps to NM_018168.2 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:76668170 G>T maps to NM_017926.2 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:76644342 G>A maps to NM_017926.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:76621241 C>A maps to NM_017926.2 S179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr14:76638220 G>T maps to NM_017926.2 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:31917607 G>T maps to NM_080664.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:60591099 T>C maps to ENST00000404681 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr14:60582711 A>G maps to ENST00000404681 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:93670071 G>A maps to NM_032490.4 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr14:93670071 G>A maps to NM_032490.4 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:91662797 T>C maps to NM_001102368.1 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:91655455 C>T maps to NM_001102368.1 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:91636379 C>T maps to NM_001102368.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:91636379 C>T maps to NM_001102368.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:52460479 C>T maps to NM_016039.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:52460479 C>T maps to NM_016039.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:52458134 C>T maps to NM_016039.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:77292852 C>T maps to NM_194287.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:77294700 G>A maps to NM_194287.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:77327103 C>T maps to NM_194287.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:50459557 G>A maps to NM_001012706.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr14:50550481 G>A maps to NM_001014830.1 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:24771467 G>A maps to NM_174913.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:45369695 C>T maps to NM_001017923.1 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:45369823 C>T maps to NM_001017923.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:45369898 G>A maps to NM_001017923.1 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:58606091 G>A maps to ENST00000438670 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr14:58563613 A>G maps to ENST00000438670 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:58471515 C>A maps to ENST00000438670 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:58563624 C>A maps to ENST00000438670 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:58604927 C>T maps to ENST00000438670 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:58605623 C>T maps to ENST00000438670 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr14:58605635 A>G maps to ENST00000438670 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:60936270 C>A maps to NM_174978.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:60933683 C>T maps to NM_174978.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:60935175 C>A maps to NM_174978.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:60951622 C>A maps to NM_174978.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:74203772 A>G maps to NM_001043318.1 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:74205421 G>A maps to NM_001043318.1 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr14:74206063 G>T maps to NM_001043318.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:74186045 C>T maps to NM_001043318.1 Q1032Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr14:74187999 C>T maps to NM_001043318.1 S979S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:74186036 C>T maps to NM_001043318.1 E1035E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:74523862 C>T maps to NM_025057.2 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:74523940 G>T maps to NM_025057.2 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:95912350 G>T maps to NM_152592.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:95905952 G>A maps to NM_152592.3 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:95932291 G>A maps to NM_152592.3 Y201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:95932342 G>A maps to NM_152592.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:95905456 C>T maps to NM_152592.3 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr14:95916408 G>A maps to NM_152592.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:105964952 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:105964988 C>T maps to ENST00000392523 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:23456735 G>A maps to NM_021944.2 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:24921751 C>T maps to NM_018958.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:24922123 G>A maps to NM_018958.2 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:24923485 C>T maps to NM_018958.2 D824D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr15:24922474 C>T maps to NM_018958.2 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr15:24921559 C>T maps to NM_018958.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:24924139 G>A maps to NM_018958.2 Q1042Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:24922693 C>T maps to NM_018958.2 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr15:24923809 A>G maps to NM_018958.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr15:24921898 G>A maps to NM_018958.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:24923587 G>A maps to NM_018958.2 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:24922937 G>T maps to NM_018958.2 E642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:24922927 C>A maps to NM_018958.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:34388109 C>T maps to NM_020154.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:81428906 G>T maps to ENST00000458088 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:81427690 C>A maps to ENST00000458088 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr15:81436088 C>T maps to ENST00000458088 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:76496124 C>T maps to NM_152335.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:76452493 C>T maps to NM_152335.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:76452493 C>T maps to NM_152335.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:34438977 C>A maps to NM_024713.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:93015692 T>C maps to NM_153040.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr15:93015449 G>A maps to NM_153040.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:49663591 G>A maps to NM_152647.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:49833921 C>A maps to NM_152647.2 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:49860461 G>A maps to NM_152647.2 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:49867306 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr15:49907355 G>A maps to NM_152647.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:49620866 G>A maps to NM_152647.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:49623994 C>T maps to NM_152647.2 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:90451587 G>A maps to ENST00000398333 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:90451590 G>A maps to ENST00000398333 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:90454038 G>A maps to ENST00000398333 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:90447198 C>A maps to ENST00000398333 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:75500554 T>C maps to NM_015492.4 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:83680236 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:83680251 G>A maps to NM_144597.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:36950032 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:36872138 G>A maps to NM_001130010.1 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:90142600 C>T maps to NM_152259.3 Y649Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:90167072 C>T maps to NM_152259.3 R1178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:90137784 C>T maps to NM_152259.3 R561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:90143869 C>T maps to NM_152259.3 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:90159717 C>A maps to NM_152259.3 I984I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:90168260 C>T maps to NM_152259.3 R1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr15:90167983 C>T maps to NM_152259.3 N1481N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:90162961 C>T maps to NM_152259.3 R1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:90167497 C>T maps to NM_152259.3 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:90152047 C>T maps to NM_152259.3 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr15:90127734 C>T maps to NM_152259.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr15:90162952 C>T maps to NM_152259.3 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:90143869 C>T maps to NM_152259.3 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:45270717 C>T maps to NM_152448.1 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr15:65899780 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr15:65899517 C>T maps to ENST00000420799 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:40630782 G>A maps to NM_207380.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr15:40627574 C>T maps to NM_207380.2 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:39544830 C>A maps to NM_207445.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:39544641 C>A maps to NM_207445.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:34640465 C>T maps to ENST00000438749 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:34643006 G>A maps to ENST00000438749 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:34646776 C>T maps to ENST00000438749 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr15:34640629 G>A maps to ENST00000438749 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:34649251 G>T maps to ENST00000438749 E1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:34647756 C>T maps to ENST00000438749 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:90784178 G>A maps to NM_001013657.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:90784985 C>T maps to NM_001013657.2 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr15:74032682 G>A maps to NM_001039614.1 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:74043395 G>A maps to NM_001039614.1 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:613377 G>A maps to ENST00000293874 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:1399448 G>A maps to NM_001001410.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:15675164 C>T maps to NM_033201.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:81095297 G>T maps to NM_152337.2 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:81095484 G>A maps to NM_152337.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:4562820 G>A maps to ENST00000359075 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr16:4563796 C>T maps to ENST00000359075 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:29828322 G>A maps to NM_024516.3 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:29828311 G>T maps to NM_024516.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:29756125 G>A maps to NM_175900.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:58036535 C>T maps to NM_024598.3 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:58052892 C>G maps to NM_024598.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:31504903 G>A maps to ENST00000430477 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:31505065 G>T maps to NM_022744.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:31502227 G>A maps to NM_022744.2 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:31510620 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:31503569 T>C maps to NM_022744.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:31504487 G>A maps to ENST00000436843 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:2510898 C>T maps to NM_025108.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:19580864 C>A maps to NM_020314.5 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:19627503 G>A maps to NM_020314.5 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:19640035 C>T maps to NM_020314.5 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:19693579 C>T maps to NM_020314.5 R888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr16:89785531 A>T maps to ENST00000261625 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:89774352 G>A maps to NM_004913.2 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:67159902 C>T maps to NM_025187.3 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:67168321 C>T maps to NM_025187.3 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:67178213 G>A maps to NM_025187.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:67165199 A>G maps to NM_025187.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:4790426 G>T maps to NM_139170.2 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:4790620 C>T maps to NM_139170.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:4787836 C>T maps to NM_139170.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr16:9210687 T>C maps to NM_014117.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:9210636 C>T maps to NM_014117.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr16:1884268 T>C maps to NM_001163560.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:1894964 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:1912117 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:85743854 G>A maps to NM_206967.2 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:49407854 C>A maps to NM_144602.2 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:49412502 T>C maps to NM_144602.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:2259671 G>A maps to NM_182563.3 H158H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:2260804 G>A maps to NM_182563.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:2260263 G>A maps to NM_182563.3 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr16:2259443 C>T maps to NM_182563.3 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr16:2259562 G>A maps to NM_182563.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:58150046 A>G maps to NM_013242.2 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:58149953 G>A maps to NM_013242.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:58149953 G>A maps to NM_013242.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr16:67702349 A>G maps to NM_001012984.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:46843569 T>C maps to NM_001001436.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:19725738 C>A maps to NM_001012991.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr16:19718306 G>A maps to NM_001012991.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:19726275 G>A maps to NM_001012991.2 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:19721872 G>A maps to NM_001012991.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr16:5094396 T>A maps to ENST00000422873 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:5110302 G>A maps to ENST00000350219 Q203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:5097882 A>G maps to ENST00000350219 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:5105259 G>T maps to ENST00000350219 C323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:5108550 G>T maps to ENST00000350219 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:5112432 G>A maps to ENST00000350219 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:5105322 G>A maps to ENST00000350219 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:1476196 T>C maps to NM_001010878.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:80373403 G>T maps to NM_175902.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:80363249 G>A maps to NM_175902.4 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr17:80369394 G>A maps to NM_175902.4 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:80352204 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:42744122 G>T maps to NM_001145080.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:42743999 C>T maps to NM_001145080.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:42744067 T>G maps to NM_001145080.2 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr17:26207380 A>G maps to ENST00000503642 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:26207173 C>T maps to ENST00000508862 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72948148 C>T maps to NM_030630.2 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:72958420 G>A maps to NM_030630.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:17957466 C>T maps to NM_024052.4 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:56620383 T>C maps to NM_001038704.1 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:56621042 G>A maps to NM_001038704.1 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10614367 T>G maps to NM_020233.4 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:42232677 C>T maps to NM_024032.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:42225981 C>T maps to NM_024032.3 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:42225699 G>T maps to NM_024032.3 G177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:42226247 C>A maps to NM_024032.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr17:79202838 C>A maps to NM_144679.2 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr17:45487055 C>T maps to NM_152347.4 N759N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:45412708 G>T maps to NM_152347.4 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:45490178 T>C maps to NM_152347.4 N773N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:45422454 G>T maps to NM_152347.4 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:45490160 C>A maps to NM_152347.4 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:45425280 G>T maps to NM_152347.4 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:27086643 G>A maps to NM_018182.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:27086835 C>T maps to NM_018182.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:58506895 A>G maps to NM_181707.2 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:58503527 G>T maps to NM_181707.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:34191894 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:34185484 T>C maps to NM_152781.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:34191159 G>A maps to ENST00000417195 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:34192270 G>A maps to NM_152781.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:54872502 A>C maps to NM_001085430.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr17:79516257 C>T maps to NM_025161.5 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:79518009 G>A maps to NM_025161.5 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7330357 C>T maps to NM_175734.4 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:7330704 G>A maps to NM_175734.4 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:72588475 C>A maps to NM_152460.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:72588424 C>T maps to NM_152460.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:35734887 G>T maps to NM_173625.3 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:35746296 G>A maps to NM_173625.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:71232107 C>T maps to NM_017941.4 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:3721768 A>G maps to NM_001114118.1 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:3746385 G>T maps to NM_001114118.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:3716499 C>T maps to NM_001114118.1 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr17:3721642 C>T maps to NM_001114118.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:79632452 C>T maps to NM_001039842.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr17:36997510 G>A maps to NM_001080465.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:36993442 G>T maps to NM_001080465.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:36997561 G>A maps to NM_001080465.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr18:13645226 C>T maps to NM_181481.3 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:13621164 G>A maps to NM_181481.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:33558800 A>G maps to NM_031446.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:43796214 G>A maps to NM_145055.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr18:52265327 C>T maps to NM_173629.1 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:30791940 G>A maps to NM_001105528.1 D719D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:30846938 C>T maps to NM_001105528.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr18:30913352 C>A maps to NM_001105528.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:51886947 G>A maps to ENST00000382911 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:51904606 G>A maps to ENST00000382911 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr18:51888208 T>C maps to ENST00000382911 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:51900603 T>G maps to ENST00000382911 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:51898867 T>C maps to ENST00000382911 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr18:51888166 C>T maps to ENST00000382911 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr18:51888292 C>G maps to ENST00000382911 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:73139487 G>A maps to NM_001037331.2 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr18:73139425 G>A maps to NM_001037331.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:73130744 G>A maps to NM_001037331.2 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr18:21109677 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr18:21104432 C>T maps to NM_013326.3 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:21104435 C>T maps to NM_013326.3 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:21096387 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:4668620 C>A maps to NM_019107.3 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr19:30193873 G>A maps to NM_001031726.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:757668 C>T maps to NM_173481.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:757197 G>A maps to NM_173481.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:1234249 G>A maps to ENST00000382477 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:1235857 G>A maps to ENST00000382477 F49F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A5-A0GH-01A-21W-A062-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-A5-A0VP-01A-21D-A10B-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3620797 G>T maps to NM_021231.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:33464383 G>A maps to NM_152266.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:16612031 G>A maps to NM_032207.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:16614048 G>A maps to NM_032207.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:16611601 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:16620725 C>T maps to NM_032207.2 H522H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:7573219 C>T maps to NM_198534.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:40829983 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:51301651 C>A maps to NM_199249.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:13888894 C>T maps to NM_014047.2 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:41248637 G>A maps to NM_198476.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36257684 C>T maps to NM_001039887.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:36252949 C>A maps to NM_001039887.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:36258919 G>A maps to NM_001039887.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:14000018 G>A maps to ENST00000454313 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:14000018 G>A maps to ENST00000454313 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:7742553 C>A maps to NM_174918.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:1011890 G>A maps to NM_001033026.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:1014349 C>T maps to NM_001033026.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr19:1014259 G>A maps to NM_001033026.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:50978583 G>A maps to ENST00000391816 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:10197687 C>T maps to NM_018381.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:10197960 C>T maps to NM_018381.2 N60N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:51768868 C>T maps to NM_173635.1 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119760465 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119760637 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:119760439 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:119760269 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:119760843 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:119760606 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:119760819 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:22986014 C>T maps to NM_000491.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:22987677 C>T maps to NM_000491.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr1:22987359 G>A maps to NM_000491.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:22987338 C>T maps to NM_000491.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:22986020 C>A maps to NM_000491.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:5336702 G>T maps to NM_001212.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:5341483 A>G maps to NM_001212.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:22974152 C>T maps to NM_172369.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:22974152 C>T maps to NM_172369.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:22974050 C>T maps to NM_172369.3 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:22970665 C>T maps to NM_172369.3 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:43037693 G>A maps to NM_006688.3 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr17:43037705 C>T maps to NM_006688.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:43044894 G>T maps to NM_006688.3 Y174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr10:16562569 G>A maps to NM_001010908.1 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:77042738 G>A maps to ENST00000392445 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:77044047 G>T maps to ENST00000392445 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:77040154 G>A maps to ENST00000392445 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:77043770 G>A maps to ENST00000392445 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:77042643 G>T maps to ENST00000392445 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:77043642 C>T maps to ENST00000392445 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:159776465 G>A maps to NM_031908.4 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:159776714 G>A maps to NM_031908.4 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:34020767 G>A maps to NM_181435.4 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr5:34043167 C>T maps to NM_181435.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:34028946 C>T maps to NM_181435.4 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:119210088 G>A maps to NM_015645.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:37578505 G>A maps to NM_182486.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:37578410 G>T maps to NM_182486.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:37581462 G>T maps to NM_182486.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:37578263 G>T maps to NM_182486.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr4:15444374 C>T maps to NM_001135170.1 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:15437387 T>C maps to NM_001135170.1 V14V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:24890236 G>A maps to NM_178540.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:24895132 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:24468299 C>T maps to NM_001007537.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:24470992 G>A maps to NM_001007537.1 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:7241268 C>T maps to ENST00000290575 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:7188501 G>A maps to ENST00000290575 H498H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:7187964 C>T maps to ENST00000290575 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:7188603 C>T maps to ENST00000290575 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:7241270 G>A maps to ENST00000290575 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:7188420 C>T maps to ENST00000290575 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:7188558 G>A maps to ENST00000290575 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:7189576 G>A maps to ENST00000290575 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:7254515 G>A maps to NM_016546.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:7249139 G>A maps to NM_016546.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:7249385 G>A maps to NM_016546.2 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:7249439 G>A maps to NM_016546.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:7260891 G>A maps to NM_016546.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:7175769 C>T maps to NM_001734.3 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:7177213 C>T maps to NM_001734.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:7174371 G>A maps to NM_001734.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:7174371 G>A maps to NM_001734.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:7174371 G>A maps to NM_001734.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr12:7177396 C>G maps to NM_001734.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:244541859 C>T maps to NM_001012970.1 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:244552290 C>T maps to NM_001012970.1 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:244541859 C>T maps to NM_001012970.1 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:244552322 T>C maps to NM_001012970.1 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:244735827 A>G maps to NM_001130957.1 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:244735713 G>A maps to NM_001130957.1 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:244735956 C>T maps to NM_001130957.1 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:244747199 C>T maps to NM_001130957.1 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:244640841 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:172437649 G>A maps to NM_139240.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:172417598 G>A maps to NM_139240.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:200880685 G>A maps to NM_018265.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:200878059 C>T maps to NM_018265.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:200860790 G>A maps to NM_018265.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:200870063 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:38152063 G>T maps to NM_017850.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:162825016 G>A maps to NM_178550.4 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:169812865 T>C maps to NM_018186.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:169818642 C>T maps to NM_018186.2 D687D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:169771775 C>T maps to NM_018186.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:169388304 G>T maps to ENST00000367806 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:169388366 C>A maps to ENST00000367806 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:169390860 C>A maps to ENST00000367806 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:169390740 G>A maps to ENST00000367806 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:207198313 G>A maps to NM_023938.5 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:207196103 C>T maps to NM_023938.5 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:207196679 G>A maps to NM_023938.5 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:231488758 T>G maps to NM_032018.4 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:11008739 C>A maps to NM_001170754.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:11024202 A>G maps to NM_001170754.1 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:170961421 G>A maps to NM_001163629.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:170964609 G>A maps to NM_001163629.1 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:170928648 G>T maps to NM_001163629.1 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:170928656 C>A maps to NM_001163629.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:170961349 G>A maps to NM_001163629.1 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:170965692 G>A maps to NM_001163629.1 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:231374788 C>T maps to ENST00000421623 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:231364894 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:231362495 C>A maps to ENST00000421623 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:26162311 C>T maps to NM_024037.1 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:67561051 T>G maps to NM_001013674.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr1:57209922 A>C maps to NM_001004303.4 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:57207871 T>C maps to NM_001004303.4 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:75072552 C>T maps to NM_001002912.4 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:75038567 G>A maps to NM_001002912.4 V942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:75086448 A>G maps to NM_001002912.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:75112383 G>T maps to NM_001002912.4 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:75078488 G>T maps to NM_001002912.4 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:75039053 C>T maps to NM_001002912.4 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:75102073 G>A maps to NM_001002912.4 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:3807282 G>A maps to NM_207356.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:3807204 G>A maps to NM_207356.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:206239519 A>G maps to NM_001007544.1 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:206239530 C>A maps to NM_001007544.1 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:11766674 C>T maps to NM_198545.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:11772430 C>T maps to NM_198545.3 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:154173033 C>T maps to NM_001010979.1 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:230979198 G>A maps to NM_032800.2 H276H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:230979495 G>A maps to NM_032800.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:24696261 T>G maps to ENST00000374409 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:43748671 C>T maps to NM_001164829.1 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:43748761 C>T maps to NM_001164829.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:162353029 C>T maps to NM_001135240.1 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:162353172 C>T maps to NM_001135240.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:186352233 C>A maps to NM_017847.5 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:186375246 C>T maps to NM_017847.5 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:234519527 A>G maps to ENST00000424237 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:228288867 C>T maps to NM_024319.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr1:28208884 G>A maps to NM_001105556.1 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:28209250 C>T maps to NM_001105556.1 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:28209376 G>A maps to NM_001105556.1 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr1:28211826 C>T maps to NM_001105556.1 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:154192368 G>A maps to NM_001098616.1 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:154180113 G>A maps to NM_001098616.1 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:178485748 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:43233228 C>T maps to NM_024097.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:85718385 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr1:197871862 G>A maps to NM_001024594.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150252086 C>T maps to NM_024579.3 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:150252067 C>T maps to NM_024579.3 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:226180123 C>T maps to NM_152608.3 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:226180156 G>A maps to NM_152608.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:226173191 C>T maps to NM_152608.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:226182982 A>G maps to NM_152608.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:151020502 A>C maps to NM_017860.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156384454 G>A maps to ENST00000357975 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:223568232 C>T maps to NM_152610.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:223568644 C>T maps to NM_152610.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:223568687 G>A maps to NM_152610.2 *624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:223567257 G>A maps to NM_152610.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr1:209956961 G>A maps to NM_152485.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:209956502 G>A maps to NM_152485.2 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:156262963 G>A maps to NM_144580.1 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:156263367 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:2129534 C>A maps to ENST00000378545 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:60505659 C>A maps to NM_152377.2 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:111890343 G>T maps to NM_181643.4 G70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:172579294 C>T maps to ENST00000367723 Q1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:172501884 C>G maps to ENST00000367723 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:172560207 G>A maps to ENST00000367723 E1122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:172526829 G>T maps to ENST00000367723 G369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:172501864 G>T maps to ENST00000367723 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:172555058 T>C maps to ENST00000367723 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:172502430 G>A maps to ENST00000367723 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:172501618 G>T maps to ENST00000367723 G3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:172579350 G>A maps to ENST00000367723 E1391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr1:34677872 G>A maps to NM_001134734.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:34666478 C>T maps to NM_001134734.1 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:34662855 G>A maps to NM_001134734.1 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:34667832 G>A maps to NM_001134734.1 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:34663000 C>T maps to NM_001134734.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr1:34684295 G>A maps to NM_001134734.1 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr1:34662915 C>T maps to NM_001134734.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:34666495 C>A maps to NM_001134734.1 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:229462598 C>T maps to NM_145257.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:31911916 G>T maps to ENST00000437789 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:31902181 G>T maps to ENST00000418949 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:31902132 C>A maps to ENST00000418949 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:61574980 G>A maps to NM_017896.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr20:42826066 G>A maps to NM_016470.6 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:31035491 G>A maps to NM_080616.3 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr20:31062427 G>A maps to NM_080616.3 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr20:35517719 C>T maps to NM_080628.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:35748235 G>A maps to ENST00000343811 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr20:35748242 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr20:2796054 T>G maps to NM_080739.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:34568466 C>A maps to ENST00000373973 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:34560589 C>T maps to ENST00000373973 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:34575336 C>A maps to ENST00000373973 S246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:61167680 G>T maps to NM_178463.3 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:61167680 G>T maps to NM_178463.3 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:3233328 G>T maps to NM_001009984.1 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:3236732 C>T maps to NM_001009984.1 Q1060Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:3268336 G>T maps to NM_001009984.1 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:3297422 C>A maps to NM_001009984.1 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:62187762 G>A maps to NM_024059.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr20:62187306 C>T maps to NM_024059.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:5843955 C>T maps to NM_152504.2 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr20:5753579 G>A maps to NM_152504.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:58645816 C>T maps to NM_173644.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:61430979 G>A maps to NM_018270.4 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:35236155 C>A maps to NM_018840.4 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:35240736 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr20:35236137 C>T maps to NM_018840.4 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:35240689 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:20209005 G>A maps to ENST00000389655 E685E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:20037374 T>C maps to ENST00000389655 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:20269503 A>G maps to ENST00000389655 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:20150029 C>T maps to ENST00000389655 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:20172057 G>T maps to ENST00000389655 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:20269266 C>T maps to ENST00000389655 F940F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:3734841 C>A maps to ENST00000405186 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:3736208 G>A maps to NM_001039140.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:3739200 G>A maps to NM_001039140.1 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:24950232 C>T maps to NM_020531.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:24954344 G>A maps to NM_020531.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:5090090 G>A maps to NM_001009923.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr20:34843651 C>T maps to NM_015511.3 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:55052039 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:55048439 T>C maps to ENST00000357348 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:17968817 C>A maps to NM_052865.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:17968817 C>A maps to NM_052865.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:17956472 C>T maps to NM_052865.2 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:17956381 C>T maps to NM_052865.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:56730521 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:10541415 G>A maps to NM_001009608.1 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:10603748 C>T maps to NM_001009608.1 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:258994 C>A maps to NM_153269.1 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:257869 C>T maps to NM_153269.1 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr20:270290 C>T maps to NM_153269.1 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:264665 C>A maps to NM_153269.1 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr20:264602 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:45751811 G>A maps to ENST00000397956 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr21:45751862 A>G maps to ENST00000397956 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:47588516 T>C maps to NM_001142854.1 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr21:47588450 G>A maps to NM_001142854.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr21:47722413 C>T maps to NM_058180.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr21:33976521 C>A maps to NM_021254.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:33980026 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr21:33979956 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:33887346 G>A maps to NM_058187.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr21:19165818 G>A maps to NM_001100420.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:19169401 G>T maps to NM_001100420.1 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr21:19165737 G>A maps to NM_001100420.1 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr22:38343315 G>A maps to NM_032561.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:38343372 G>A maps to NM_032561.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:38340510 G>A maps to NM_032561.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:32330337 A>T maps to NM_015372.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:32808068 G>T maps to NM_014306.4 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:32789917 C>T maps to NM_014306.4 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:19839076 G>A maps to NM_024627.5 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:19839604 C>T maps to NM_024627.5 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:19839193 G>T maps to NM_024627.5 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:19839609 G>A maps to NM_024627.5 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr22:29456528 C>T maps to NM_015370.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:29454996 C>T maps to NM_015370.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:29456528 C>T maps to NM_015370.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:29456528 C>T maps to NM_015370.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr22:46643084 G>T maps to NM_207327.4 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:32547506 G>A maps to NM_001010859.1 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:23955487 C>A maps to NM_016449.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:43319186 C>T maps to NM_015500.1 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:118986848 C>T maps to NM_014807.3 N669N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr11:118982001 C>A maps to NM_014807.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:118984983 G>A maps to NM_014807.3 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:73796729 A>G maps to ENST00000334126 C1281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:73881798 A>G maps to ENST00000334126 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:73872601 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:73789271 A>C maps to ENST00000334126 A1497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:73809190 G>A maps to ENST00000334126 R948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr11:73748712 C>T maps to ENST00000334126 Q1897Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr2:99767294 T>C maps to NM_144706.2 *126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:27800639 G>T maps to NM_032266.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:27803795 C>T maps to NM_032266.3 R1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27800200 G>A maps to NM_032266.3 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27800429 G>T maps to NM_032266.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27802247 G>T maps to NM_032266.3 E937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:27802912 C>T maps to NM_032266.3 G1158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:27803795 C>T maps to NM_032266.3 R1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:27800303 G>T maps to NM_032266.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:27803795 C>T maps to NM_032266.3 R1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:27001214 C>T maps to NM_017877.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:27001108 C>T maps to NM_017877.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:106688348 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:106690391 G>T maps to NM_032411.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:106690391 G>T maps to NM_032411.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:106690498 G>A maps to NM_032411.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:70408295 G>A maps to NM_017880.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:70377562 C>T maps to NM_017880.1 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:20939833 C>A maps to ENST00000381090 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:20939874 G>A maps to ENST00000381090 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:24262036 C>A maps to NM_025203.2 G110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:24253985 C>T maps to NM_025203.2 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:24260579 A>G maps to NM_025203.2 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:200824580 C>T maps to NM_024520.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:88825972 G>A maps to NM_152670.2 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:99412604 G>T maps to NM_207362.2 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:99448879 G>A maps to NM_207362.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:99454585 G>A maps to NM_207362.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr2:99439463 C>T maps to NM_207362.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:99438761 G>A maps to NM_207362.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:37475276 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:37474630 A>G maps to NM_144736.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:232458411 C>T maps to NM_152614.2 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:219222368 A>G maps to NM_198559.1 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:219222457 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:219232216 C>A maps to NM_198559.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr2:219222776 C>T maps to NM_198559.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:55449430 G>T maps to NM_152385.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:55436829 C>A maps to NM_152385.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:55439917 G>T maps to NM_152385.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:55403065 C>A maps to NM_152385.2 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:74803652 C>A maps to NM_138804.3 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:74802594 T>C maps to NM_138804.3 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:74808866 C>A maps to NM_138804.3 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr2:85836599 G>A maps to NM_001013649.3 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr2:200790179 G>A maps to NM_153689.5 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr2:200790023 A>G maps to NM_153689.5 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:26785554 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:29295462 G>A maps to NM_001029883.1 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:29296125 G>T maps to NM_001029883.1 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:29287818 G>A maps to NM_001029883.1 H1261H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr2:29295351 C>T maps to NM_001029883.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:29295798 G>T maps to NM_001029883.1 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZP-01A-21D-A10M-09 chr2:29296590 A>C maps to NM_001029883.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:29295282 G>A maps to NM_001029883.1 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:29294888 G>A maps to NM_001029883.1 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:120097547 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:120097478 G>A maps to NM_001017927.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:170502560 C>T maps to NM_001085447.1 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:170518875 G>A maps to NM_001085447.1 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:170506892 T>C maps to NM_001085447.1 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:170531149 C>A maps to NM_001085447.1 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr2:209049698 C>T maps to NM_001099334.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:228476340 C>T maps to NM_020161.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:228497738 G>A maps to NM_020161.3 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr2:228476205 A>G maps to NM_020161.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:24384417 G>A maps to NM_001145710.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:24362272 G>T maps to NM_001145710.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:85066423 C>T maps to ENST00000409520 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:85097861 T>C maps to ENST00000409520 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:6686257 G>A maps to NM_000064.2 N1229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:6692942 C>A maps to NM_000064.2 E1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:6702213 C>T maps to NM_000064.2 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:6711018 C>T maps to NM_000064.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:6712411 G>A maps to NM_000064.2 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:6714439 C>T maps to NM_000064.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:6678191 G>T maps to NM_000064.2 L1607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:6697716 C>T maps to NM_000064.2 E843E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:6719389 G>T maps to NM_000064.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:6693006 C>T maps to NM_000064.2 W1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:6694484 G>A maps to NM_000064.2 F1037F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:6697782 G>A maps to NM_000064.2 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:6692942 C>A maps to NM_000064.2 E1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr19:6710652 G>A maps to NM_000064.2 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:8212517 C>T maps to NM_004054.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:8211782 G>A maps to NM_004054.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:8212016 A>C maps to NM_004054.2 Y255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr12:8212517 C>T maps to NM_004054.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:8212791 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:119458110 G>T maps to NM_033364.3 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:119458110 G>T maps to NM_033364.3 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:119466039 G>T maps to NM_033364.3 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:112724778 A>C maps to NM_015412.3 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:112736429 T>C maps to NM_015412.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:14708363 G>T maps to NM_016474.4 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:14700408 G>T maps to NM_016474.4 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:14695971 G>T maps to NM_016474.4 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:14711468 G>A maps to NM_016474.4 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:14695971 G>T maps to NM_016474.4 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:14712401 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:14712424 G>A maps to NM_016474.4 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:14744742 G>A maps to NM_032137.4 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:14724408 G>A maps to NM_032137.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:14801421 C>T maps to NM_032137.4 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:14724531 T>C maps to NM_032137.4 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:14799018 C>T maps to NM_032137.4 D694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr3:14731510 C>T maps to NM_032137.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:44441951 G>T maps to NM_173826.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:44441955 T>G maps to NM_173826.3 L332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:10146026 C>T maps to NM_001164839.1 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr3:128292334 T>A maps to NM_007354.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:118865431 T>G maps to NM_152539.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:118865521 T>C maps to NM_152539.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:8675471 C>T maps to NM_015931.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:8661619 G>A maps to NM_015931.1 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:155493537 C>A maps to ENST00000340171 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:155520325 G>A maps to ENST00000340171 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:37476485 C>A maps to NM_178339.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:129023553 G>A maps to NM_001006109.1 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:88205224 G>T maps to NM_173824.3 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:88205419 G>T maps to NM_173824.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:43121930 G>A maps to NM_032806.4 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:43122761 C>T maps to NM_032806.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:43122629 G>T maps to NM_032806.4 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr3:196234757 T>A maps to NM_001077657.1 *215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr3:196234997 G>A maps to NM_001077657.1 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:50324117 C>T maps to NM_153215.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:157318169 A>C maps to NM_001130001.1 *134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:143704657 T>C maps to NM_173552.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:143708673 C>T maps to NM_173552.3 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:143704468 G>T maps to NM_173552.3 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:49313873 T>C maps to NM_198562.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:49308714 G>A maps to NM_198562.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:69058987 A>G maps to ENST00000383701 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:69026858 T>C maps to ENST00000383701 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:69054289 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:69056968 C>T maps to ENST00000383701 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:58923424 G>T maps to ENST00000394474 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:58792128 A>C maps to ENST00000482387 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:58923403 T>C maps to ENST00000394474 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr3:58852331 C>T maps to ENST00000482387 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:184801061 G>T maps to NM_001025266.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:184800965 C>T maps to NM_001025266.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:47552636 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:207317902 C>A maps to NM_000715.3 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:207288840 G>T maps to NM_000715.3 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:207314501 C>A maps to NM_000715.3 S442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:207314518 G>T maps to NM_000715.3 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:207305077 A>G maps to NM_000715.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:207287556 C>T maps to NM_000715.3 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:207314568 G>A maps to NM_000715.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:207314518 G>T maps to NM_000715.3 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:207314568 G>A maps to NM_000715.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:207314475 C>A maps to NM_000715.3 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:207262893 G>A maps to NM_001017367.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:207262706 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:207262915 C>T maps to NM_001017367.1 R14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:100463217 C>T maps to NM_032149.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:100434273 C>T maps to NM_032149.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:100434255 G>A maps to NM_032149.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:37592018 C>T maps to NM_018302.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr4:113462391 G>A maps to NM_018392.4 Y1877Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:113482132 A>G maps to NM_018392.4 V1572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:113524703 C>T maps to NM_018392.4 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:113468454 G>A maps to NM_018392.4 R1862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:113469532 G>A maps to NM_018392.4 R1784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:81256978 C>A maps to ENST00000508675 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:81791202 C>T maps to ENST00000508675 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:81791202 C>T maps to ENST00000508675 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:170663163 C>A maps to NM_017867.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr4:128938541 C>T maps to ENST00000454347 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:128949985 T>C maps to ENST00000454347 C352C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr4:130023849 G>T maps to NM_001099783.1 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:98761993 C>A maps to NM_174952.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:99055574 C>A maps to NM_174952.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:159836342 C>T maps to NM_152543.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:140201261 C>T maps to ENST00000260011 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:140187925 G>A maps to ENST00000260011 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:140187818 G>T maps to ENST00000260011 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:5977675 C>A maps to ENST00000324058 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:146650364 A>G maps to NM_001080531.1 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:146651090 C>T maps to NM_001080531.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:123723778 G>A maps to NM_001735.2 A1523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:123800200 G>A maps to NM_001735.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr9:123805330 T>C maps to NM_001735.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:123789500 T>C maps to NM_001735.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:123737134 G>A maps to NM_001735.2 I1313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:133295577 C>T maps to NM_020199.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr5:133304206 G>A maps to NM_020199.2 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:134782259 G>T maps to NM_130848.2 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:31538781 G>T maps to NM_018356.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:31538507 A>G maps to NM_018356.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:175722167 G>T maps to ENST00000443967 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:175763723 G>T maps to ENST00000443967 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr5:175717342 G>A maps to ENST00000443967 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:175763860 G>A maps to ENST00000443967 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr5:175722148 C>A maps to ENST00000443967 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr5:175716730 A>G maps to ENST00000443967 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:175764132 T>C maps to ENST00000443967 Y780Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr5:43446551 T>C maps to NM_022483.4 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:43487108 C>A maps to NM_198566.2 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr5:43502518 A>G maps to NM_198566.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:2752464 C>T maps to NM_178569.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:2752555 C>T maps to NM_178569.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:2752846 G>A maps to NM_178569.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr5:154203062 G>T maps to NM_032385.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr5:37227085 A>G maps to NM_023073.3 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:37157770 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:37183563 G>A maps to NM_023073.3 D1573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:37157442 A>G maps to ENST00000509849 P1701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:37164387 G>A maps to NM_023073.3 F2525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:37221294 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:37244686 C>T maps to NM_023073.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:37121876 G>T maps to NM_023073.3 L2955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:37167255 C>T maps to NM_023073.3 Q2431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:37125425 C>A maps to NM_023073.3 E2906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:37186481 G>A maps to NM_023073.3 F1365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:37183287 C>T maps to NM_023073.3 S1665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:37231002 C>A maps to NM_023073.3 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr5:37168961 T>C maps to NM_023073.3 Q2388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:37148343 G>A maps to NM_023073.3 F2746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:37164387 G>A maps to NM_023073.3 F2525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:37196094 G>A maps to NM_023073.3 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:37245881 C>T maps to NM_023073.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:37183341 A>G maps to NM_023073.3 L1647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:37184917 C>A maps to NM_023073.3 E1485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:37107880 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:60455811 C>A maps to NM_001048249.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:60455811 C>A maps to NM_001048249.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:64956624 C>T maps to NM_001093755.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:64920768 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:179271181 T>C maps to NM_016175.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr5:125968273 G>A maps to NM_207408.1 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:7835499 C>A maps to NM_001089584.1 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:41911208 G>A maps to NM_175921.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr5:41917323 G>T maps to NM_175921.4 G270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:41912262 C>T maps to NM_175921.4 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:159821051 G>A maps to NM_022090.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:159821207 A>G maps to NM_022090.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:159821869 A>G maps to NM_022090.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:159822196 A>G maps to NM_022090.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:159822374 G>A maps to NM_022090.3 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:442831 C>A maps to NM_138464.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:442835 G>A maps to NM_138464.2 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:41149517 A>G maps to NM_001115131.1 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:41201733 G>A maps to NM_001115131.1 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:41160373 G>A maps to NM_001115131.1 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:41181572 G>T maps to NM_001115131.1 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:41142994 C>A maps to NM_001115131.1 E913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:41159277 C>A maps to NM_001115131.1 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr6:34214371 G>C maps to NM_178508.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:34574487 G>A maps to NM_024294.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:34614408 C>T maps to NM_024294.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:165703463 C>A maps to NM_144980.3 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:165715645 G>A maps to NM_144980.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:165715723 G>A maps to NM_144980.3 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:165715270 G>T maps to NM_144980.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:41036689 A>G maps to NM_145063.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:88123614 C>T maps to NM_001031743.2 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:121624896 C>A maps to ENST00000275159 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:121563366 G>A maps to ENST00000275159 R713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:121427284 C>A maps to ENST00000275159 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:121638730 T>C maps to ENST00000275159 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:121434285 C>A maps to ENST00000275159 E1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr6:2623873 G>A maps to NM_152554.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr6:4099433 T>G did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr6:4099330 G>A maps to NM_001085401.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:4130388 C>T maps to NM_001085401.1 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:107361338 T>C maps to NM_001142470.1 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:151789809 T>C maps to NM_024573.1 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:151789674 C>T maps to NM_024573.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:151789602 T>C maps to NM_024573.1 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:74072872 C>T maps to NM_001017361.2 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:36294422 G>A maps to NM_001010903.4 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:36298146 G>A maps to NM_001010903.4 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:36291091 C>T maps to NM_001010903.4 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:31691695 C>T maps to NM_138272.1 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:31691596 C>T maps to NM_138272.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:31805191 C>A maps to NM_001040438.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:170156510 G>A maps to NM_018341.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:170175416 G>T maps to NM_018341.1 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:151894523 C>T maps to ENST00000367290 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:151917591 C>T maps to ENST00000367290 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:151859217 C>A maps to ENST00000367290 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:151857536 G>T maps to ENST00000367290 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:40950022 G>T maps to NM_000587.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:40962229 G>T maps to NM_000587.2 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:40937773 C>T maps to NM_000587.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:40945298 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:40962262 G>T maps to NM_000587.2 G580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:40950022 G>T maps to NM_000587.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:40959672 G>T maps to NM_000587.2 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:40947898 G>T maps to NM_000587.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:40959677 G>A maps to NM_000587.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:40972527 C>T maps to NM_000587.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:40723678 C>T maps to NM_001193311.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:40789049 C>T maps to NM_001193311.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:86826041 C>T maps to NM_024315.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr7:42949864 G>T maps to NM_001099858.1 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:42949760 T>G maps to NM_001099858.1 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:42950226 G>T maps to NM_001099858.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:6634070 G>A maps to NM_024067.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:6634124 T>C maps to NM_024067.2 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:6639488 G>T maps to NM_024067.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:6639937 G>A maps to NM_024067.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr7:25176292 T>C maps to NM_138811.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:25194753 G>A maps to NM_138811.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:25175617 G>A maps to NM_138811.3 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:142637497 C>T maps to NM_178829.4 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:142636704 G>A maps to NM_178829.4 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:30197085 G>A maps to NM_152793.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:99752783 C>T maps to NM_018275.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:99755321 G>A maps to NM_018275.3 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:43679204 G>A maps to NM_018224.2 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:129855956 C>T maps to NM_145268.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:23737907 G>A maps to NM_199136.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr7:134853704 G>A did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr7:134851581 C>T maps to NM_024033.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:112124969 C>T maps to NM_182597.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:48092407 G>A maps to ENST00000430738 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:48089548 G>T maps to ENST00000430738 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:120629921 A>T maps to NM_024913.4 K83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:120782098 C>T maps to NM_024913.4 H653H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr7:120655805 C>T maps to NM_024913.4 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:120767274 G>A maps to NM_024913.4 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr7:120655843 G>A maps to NM_024913.4 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:112462250 G>A maps to NM_152556.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:112461938 G>A maps to NM_152556.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:112461938 G>A maps to NM_152556.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:112461938 G>A maps to NM_152556.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr7:112462250 G>A maps to NM_152556.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:112555362 A>G maps to NM_152556.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:89909143 G>T maps to NM_001039706.2 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:89915626 G>T maps to NM_001039706.2 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:89903408 T>G maps to NM_001039706.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:89887434 T>C maps to NM_001039706.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr7:47698582 C>T maps to NM_001123065.1 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:47857721 A>G maps to NM_025031.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:57333290 A>G maps to NM_000562.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:57320597 C>A maps to NM_000562.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:57399005 A>G did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:57411608 G>A maps to NM_000066.2 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:139841139 C>T maps to NM_000606.2 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:144124501 A>G maps to NM_173687.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr8:146278810 C>T maps to ENST00000444534 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:146278728 G>A maps to ENST00000444534 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr8:146278036 C>T maps to ENST00000444534 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:96047720 C>T maps to NM_152416.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:96064457 G>A maps to NM_152416.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr8:96059355 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:442494 G>A maps to NM_175075.3 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:442597 G>T maps to NM_175075.3 S120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:442446 T>C maps to NM_175075.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:67592035 C>A maps to NM_019607.1 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:67591961 G>T maps to NM_019607.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:67786818 C>T maps to NM_173518.4 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:67808544 A>T maps to NM_173518.4 K474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:67786681 C>A maps to NM_173518.4 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:99105522 G>T maps to NM_173549.2 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:99101454 G>A maps to NM_173549.2 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:99101899 G>T maps to NM_173549.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:144650347 G>A maps to NM_001100878.1 D576D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:144650398 G>A maps to NM_001100878.1 H559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:27927153 G>T maps to ENST00000341513 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:27903133 G>A maps to ENST00000341513 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:27913552 G>A maps to ENST00000341513 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:27880889 C>A maps to ENST00000341513 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:27931915 C>T maps to ENST00000341513 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:27915772 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:27925084 C>T maps to ENST00000341513 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:27931973 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:27884560 G>A maps to ENST00000341513 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:38370054 G>T maps to NM_207412.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:39315906 G>A maps to NM_001737.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:39306778 C>T maps to NM_001737.3 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:39311416 G>A maps to NM_001737.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:39285309 A>G maps to NM_001737.3 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr5:39341263 G>A maps to NM_001737.3 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:39315888 A>C maps to NM_001737.3 Y286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:35662263 G>A maps to NM_032818.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:35663301 G>A maps to ENST00000378382 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:98643527 G>T maps to NM_001010895.2 G153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:98728962 C>T maps to NM_001010895.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:98728882 C>T maps to NM_001010895.2 R674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr9:27294314 G>A maps to NM_020641.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr9:131588378 G>A maps to NM_016390.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:130471895 C>T maps to NM_001012502.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:130472931 G>A maps to NM_001012502.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:7799575 A>G maps to NM_033428.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:104238825 C>T maps to NM_032342.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:104238266 A>G maps to NM_032342.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:104238360 G>A maps to NM_032342.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:104239110 G>A maps to NM_032342.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35825876 C>T maps to NM_001012446.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:96097678 G>A maps to NM_001098808.1 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:96097789 C>T maps to NM_001098808.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:96097783 C>T maps to NM_001098808.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr9:35045623 C>T maps to NM_203299.2 Q1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:35045391 A>C maps to NM_203299.2 S922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:35042955 C>T maps to NM_203299.2 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr9:35042263 C>T maps to NM_203299.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:72472894 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:72520868 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr9:139927564 C>G maps to NM_207511.1 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:112963590 C>T maps to NM_001012993.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:88842857 C>A maps to NM_001010907.1 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:89771649 A>C maps to NM_001001709.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:140146279 C>A maps to ENST00000388931 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:34379097 G>T maps to ENST00000412555 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:97730038 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:97555101 A>C maps to NM_001193329.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:77613612 G>A maps to NM_152420.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:77614686 C>T maps to NM_152420.1 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:116190499 A>G maps to ENST00000451722 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:5361150 C>T maps to NM_018465.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:91606755 C>T maps to ENST00000375850 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:91606044 G>A maps to NM_001001938.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr9:91606831 C>T maps to NM_001001938.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr9:132377822 G>A maps to NM_199350.3 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:132377859 G>T maps to NM_199350.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr9:132381881 C>T maps to NM_199350.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr9:132381902 C>T maps to NM_199350.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:86570523 C>T maps to NM_032307.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:86570358 C>T maps to NM_032307.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:214922 G>A maps to NM_152569.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:4617926 C>A maps to ENST00000454239 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:27556773 C>T maps to NM_018325.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:27548559 G>A maps to NM_018325.2 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:132597418 G>T maps to NM_016520.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:90498905 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:90500559 C>T maps to NM_178828.4 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:90502590 T>C maps to NM_178828.4 D1063D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:90502266 C>T maps to NM_178828.4 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:90503514 G>A maps to NM_178828.4 E1371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr9:90502146 C>T maps to NM_178828.4 T915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:90501327 C>T maps to NM_178828.4 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:90499926 G>A maps to NM_178828.4 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:90502500 G>A maps to NM_178828.4 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:115451845 C>T maps to NM_021218.1 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr9:115456310 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:26887477 C>A maps to NM_024828.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:26842372 G>A maps to NM_024828.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:26887348 C>A maps to NM_024828.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:114490224 C>A maps to NM_173521.3 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:114486075 C>T maps to NM_173521.3 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr9:114449073 C>T maps to NM_173521.3 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr9:114543277 C>T maps to ENST00000374283 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:114490224 C>A maps to NM_173521.3 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:114453995 C>A maps to NM_173521.3 E1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:74526730 C>T maps to NM_182505.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr9:139733724 C>T maps to NM_001173988.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:117405517 G>A maps to ENST00000374049 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:15729610 A>C maps to NM_173550.2 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:15874546 G>A maps to NM_173550.2 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:15727868 G>A maps to NM_173550.2 E565E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:15777757 C>A maps to NM_173550.2 A944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:15729648 G>A maps to NM_173550.2 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:15784505 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr9:15657180 G>A maps to NM_173550.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:15594149 G>T maps to NM_173550.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:15777643 G>A maps to NM_173550.2 K906K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:15920348 C>T maps to NM_173550.2 R1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:15591503 G>T maps to NM_173550.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:15729753 G>A maps to NM_173550.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:15744279 G>T maps to NM_173550.2 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr9:15874669 C>G maps to ENST00000432954 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:77676185 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:77684836 G>A maps to NM_017881.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:136249638 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:136270544 G>T maps to NM_153710.3 *681Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:136265580 G>A maps to NM_153710.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:136268043 G>A maps to NM_153710.3 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:86250586 G>T maps to NM_001738.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr8:86250486 G>A maps to NM_001738.3 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:86250540 C>A maps to NM_001738.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:50149676 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr17:50008394 G>A maps to NM_001082534.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:49731061 C>T maps to NM_001082534.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:49710966 G>T maps to NM_001082534.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:50008394 G>A maps to NM_001082534.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr15:63632937 A>C maps to NM_001218.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:63619358 G>A maps to NM_001218.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr15:63619394 G>A maps to NM_001218.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:63618507 C>T maps to NM_001218.3 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:63638888 G>A maps to NM_001218.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:63632964 C>T maps to NM_001218.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:86163042 G>T maps to NM_198584.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:86178893 G>T maps to NM_198584.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:150235798 C>A maps to NM_012113.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr8:86352100 C>A maps to NM_005181.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:86358459 G>A maps to NM_005181.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:86360300 C>T maps to NM_005181.3 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:87960426 C>T maps to NM_001739.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:15768188 C>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15794932 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:15782842 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:15800677 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:15782765 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:15782790 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:15800722 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:15768176 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:9009385 G>A maps to ENST00000413627 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:66881123 C>T maps to NM_005182.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr8:61135236 G>A maps to NM_004056.4 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:35679201 G>T maps to NM_001216.2 G310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:231683286 C>T maps to NM_001130850.1 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:49885130 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:49933932 G>T maps to NM_001079670.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:24458435 C>T maps to NM_012295.3 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr22:24479194 G>A maps to NM_012295.3 Q921Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr22:24455782 G>A maps to NM_012295.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:24459458 C>T maps to NM_012295.3 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:24562612 G>T maps to NM_012295.3 E1672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:24437717 A>G maps to NM_012295.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:20837267 C>T maps to NM_001100619.2 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr18:20837358 A>C did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr20:60968646 C>T maps to NM_031215.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:121088469 A>G maps to NM_031205.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:121099016 T>C maps to NM_001033677.1 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:121098561 C>T maps to NM_001033677.1 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:67287375 G>A maps to NM_016366.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr11:67223185 C>T maps to NM_145200.3 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr19:48543969 G>A maps to NM_019855.3 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr18:21739589 T>C maps to NM_138644.1 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:21736377 G>T maps to NM_012189.2 G305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:65157237 A>G maps to ENST00000371073 E1273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:65124554 A>G maps to ENST00000371073 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:65157243 A>G maps to ENST00000371073 *1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:13419321 G>A maps to NM_023035.2 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:13470566 G>A maps to NM_023035.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:13419321 G>A maps to NM_023035.2 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:13446663 G>A maps to NM_023035.2 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:13411431 A>G maps to NM_023035.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:13445201 G>T maps to NM_023035.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:13365962 G>A maps to NM_023035.2 F1571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr19:13370417 G>A maps to NM_023035.2 L1454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:13340963 G>T maps to NM_023035.2 S1824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:13370439 G>A maps to NM_023035.2 Y1446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:13482540 G>A maps to NM_023035.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr9:141015950 C>T maps to ENST00000277549 L2175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:140901289 C>T maps to ENST00000277549 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:140953553 C>T maps to ENST00000277549 Y1500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr9:141014729 G>A maps to ENST00000277549 S2049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:140953037 C>T maps to ENST00000277549 F1443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:140852045 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:141006874 C>T maps to ENST00000277549 D1819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:140865907 G>A maps to ENST00000277549 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:141006877 G>A maps to ENST00000277549 A1820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr9:140846826 G>A maps to ENST00000277549 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:140952623 C>A maps to ENST00000277549 I1411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:140878699 G>A maps to ENST00000277549 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:140952614 C>T maps to ENST00000277549 F1408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:141016213 G>A maps to ENST00000277549 G2262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:140881242 C>T maps to ENST00000277549 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:141015155 C>A maps to ENST00000277549 R2105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:140991060 G>A maps to ENST00000277549 A1741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr9:141016069 C>T maps to ENST00000277549 F2214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:140772630 C>T maps to ENST00000277549 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:140907681 C>T maps to ENST00000277549 I755I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:2714264 C>T maps to NM_199460.2 V1013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:2676846 C>T maps to NM_199460.2 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:2717778 C>T maps to NM_199460.2 I1173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:2715776 G>T maps to NM_199460.2 G1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:2774032 C>T maps to NM_199460.2 C1473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr12:2705141 G>T maps to NM_199460.2 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:2800289 G>A maps to NM_199460.2 A2197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:2595354 C>A maps to NM_199460.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:2774769 C>A maps to NM_199460.2 V1522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:2706647 G>T maps to NM_199460.2 E967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:2602491 C>T maps to NM_199460.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:53757497 C>T maps to NM_001128840.1 C568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:53837584 G>A maps to NM_001128840.1 S1857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:53756493 G>A maps to NM_001128840.1 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:53787672 C>T maps to NM_001128840.1 V1250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:53760985 C>T maps to NM_001128840.1 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:53820925 G>T maps to NM_001128840.1 E1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:53736668 G>T maps to NM_001128840.1 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:53783457 G>T maps to NM_001128840.1 E1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:53820925 G>T maps to NM_001128840.1 E1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:53757881 G>A maps to NM_001128840.1 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:53835224 G>A maps to NM_001128840.1 P1727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:53700438 G>A maps to NM_001128840.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:53694193 G>T maps to NM_001128840.1 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:53779688 C>T maps to NM_001128840.1 I1015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:53781412 C>T maps to NM_001128840.1 F1084F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:53783312 C>T maps to NM_001128840.1 I1111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr3:53804452 C>T maps to NM_001128840.1 N1306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr3:53757968 G>A maps to NM_001128840.1 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr3:53844072 G>A maps to NM_001128840.1 S1980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:181724386 C>T maps to ENST00000357570 C1281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:181745317 T>C maps to ENST00000357570 L1741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr1:181731718 C>T maps to ENST00000357570 R1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:181686227 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:181762880 G>A maps to ENST00000357570 A1993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:181767669 G>A maps to ENST00000357570 P2214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:181741294 C>T maps to ENST00000357570 N1689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:181684472 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:181702644 C>T maps to ENST00000357570 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:181701756 C>T maps to ENST00000357570 F845F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:181701630 G>A maps to ENST00000357570 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:181731769 G>T maps to ENST00000357570 E1556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:181726216 G>A maps to ENST00000357570 E1428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:181724386 C>T maps to ENST00000357570 C1281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:181480508 G>A maps to ENST00000357570 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:181690997 C>A maps to ENST00000357570 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:181726159 C>T maps to ENST00000357570 V1409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr1:181702602 C>T maps to ENST00000357570 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:181767561 C>T maps to ENST00000357570 H2178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:181750659 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:181708365 C>T maps to ENST00000357570 G1232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr1:181689470 C>T maps to ENST00000357570 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:181689945 G>A maps to ENST00000357570 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:49084507 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:49086967 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:49061648 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:49071846 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:49074455 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:49083562 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49063525 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49066120 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49068729 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49086967 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49068759 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49072884 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49079032 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49086729 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49061720 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49063046 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49066118 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49066121 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49066861 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49067485 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49069215 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49083397 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49083554 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:49071614 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:49079041 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr23:49074245 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49065677 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49067542 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49088170 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49071568 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49074954 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49081222 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49088170 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr23:49087400 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:49061735 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:49081241 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:49071876 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:49061796 C>G did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:49066445 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:49071558 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:49062094 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:49062204 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:49069145 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49070353 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49071983 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:49087766 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr23:49082399 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr23:49070329 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:49069161 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:49079224 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:49088146 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr23:49075802 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:49062162 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:49067820 G>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:49075396 G>C did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:48696107 C>T maps to NM_018896.3 F1840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:48684337 C>T maps to NM_018896.3 G1500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr17:48696014 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:48699061 G>A maps to NM_018896.3 E1989E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:48681530 G>A maps to NM_018896.3 A1395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:48653163 C>T maps to NM_018896.3 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:48681623 C>T maps to NM_018896.3 F1426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:48684316 C>T maps to NM_018896.3 Y1493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:48694807 G>A maps to NM_018896.3 Q1677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:48677099 A>G maps to NM_018896.3 R1190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:48681623 C>T maps to NM_018896.3 F1426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:1269006 C>A maps to NM_021098.2 S1975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:1250369 C>T maps to NM_021098.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:1250543 C>T maps to NM_021098.2 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:1248711 T>C maps to NM_021098.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:1250546 C>T maps to NM_021098.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:1255241 C>T maps to NM_021098.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:1255241 C>T maps to NM_021098.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:1265027 C>T maps to NM_021098.2 F1662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:1261242 C>T maps to NM_021098.2 I1433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:1256106 C>A maps to NM_021098.2 V869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:1268292 C>T maps to NM_021098.2 F1843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:39966948 G>A maps to NM_021096.3 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:40066072 C>T maps to NM_021096.3 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:40066841 T>C maps to NM_021096.3 C1474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr22:40075173 G>A maps to NM_021096.3 S1706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr22:40080412 C>A maps to NM_021096.3 G1979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:201029872 G>T maps to NM_000069.2 Y1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:201052332 G>T maps to NM_000069.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:201046149 G>A maps to NM_000069.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr1:201027534 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:201012449 G>T maps to NM_000069.2 A1669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:201030394 C>T maps to NM_000069.2 Q1085Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:201054600 C>T maps to NM_000069.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:201038597 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:201044635 G>A maps to NM_000069.2 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:201028412 C>T maps to NM_000069.2 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:201052359 G>A maps to NM_000069.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:81596484 G>A maps to NM_000722.2 D834D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:81589141 G>T maps to NM_000722.2 I990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:81594915 A>G maps to NM_000722.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:81746369 G>T maps to NM_000722.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:81591262 G>A maps to NM_000722.2 F971F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:81588593 G>T maps to NM_000722.2 V1052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:81662205 G>A maps to NM_000722.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:81601172 C>T maps to NM_000722.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:81746396 G>A maps to NM_000722.2 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:81624251 G>A maps to NM_000722.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:50471833 G>A maps to ENST00000435965 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:50403760 G>T maps to ENST00000435965 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:50417158 G>T maps to ENST00000435965 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:50417203 G>A maps to ENST00000435965 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:50418453 G>A maps to ENST00000435965 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:50417155 C>T maps to ENST00000435965 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:50417173 G>A maps to ENST00000435965 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr3:50404451 C>T maps to ENST00000435965 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:54925477 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:55003825 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:54933870 G>T maps to NM_018398.2 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:54354485 G>A maps to NM_018398.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:55018672 T>C maps to NM_018398.2 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:54905606 C>T maps to NM_018398.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:54914834 G>A maps to NM_018398.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:54354504 G>T maps to NM_018398.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:54871256 C>T maps to NM_018398.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:54676213 G>A maps to NM_018398.2 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:54930880 G>A maps to NM_018398.2 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:54661878 T>C maps to NM_018398.2 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:55018660 T>C maps to NM_018398.2 N861N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:1910208 G>A maps to NM_172364.4 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:2017176 G>A maps to NM_172364.4 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:2016687 G>T maps to NM_172364.4 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:1992155 C>T maps to NM_172364.4 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:1969368 G>A maps to NM_172364.4 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:1965271 G>T maps to NM_172364.4 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:2022200 G>T maps to NM_172364.4 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:37340097 G>A maps to NM_000723.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:37341039 G>A maps to NM_000723.3 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:37347837 C>T maps to NM_000723.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:37333569 G>A maps to NM_199247.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:37331661 T>G maps to NM_000723.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:37343134 A>G maps to NM_000723.3 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:18828487 G>T maps to NM_201596.2 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:18789793 C>T maps to NM_201596.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:18823140 G>A maps to NM_201596.2 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:18828571 C>A maps to NM_201596.2 Y634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:18789739 G>T did not map to a codon.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr10:18807317 A>G maps to NM_201596.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:18787375 C>T maps to NM_201596.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:49220845 G>A maps to NM_000725.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:152727043 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:152695632 T>G maps to NM_000726.3 *521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:152739811 G>A maps to NM_000726.3 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:152698527 C>T maps to NM_000726.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:152695727 C>A maps to NM_000726.3 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:152711847 T>A maps to NM_000726.3 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:37098567 G>A maps to NM_006078.3 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:36962409 G>A maps to NM_006078.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:36983539 G>A maps to NM_006078.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:36960868 G>A maps to NM_006078.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:36960823 G>A maps to NM_006078.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr22:36962538 C>T maps to NM_006078.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:24373000 C>T maps to NM_006539.3 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:24372799 C>T maps to NM_006539.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:24372778 C>T maps to NM_006539.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:24366238 C>T maps to NM_006539.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr16:24372968 C>T maps to NM_006539.3 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:24366208 C>T maps to NM_006539.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:24366220 C>T maps to NM_006539.3 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:65021037 C>T maps to NM_014405.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:54445390 C>T maps to NM_031896.4 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:27458471 C>T maps to NM_004341.3 L1346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:27448715 G>A maps to NM_004341.3 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:27455314 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27459322 C>T maps to NM_004341.3 R1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:27447334 G>T maps to NM_004341.3 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:27457441 C>T maps to NM_004341.3 F1225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:27465747 C>T maps to NM_004341.3 F2129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:27446602 T>C maps to NM_004341.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:27455513 C>T maps to NM_004341.3 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:27460617 G>A maps to NM_004341.3 A1532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27459282 C>T maps to NM_004341.3 G1402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:27464927 G>A maps to NM_004341.3 V2011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:27464040 G>A maps to NM_004341.3 L1918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:27447677 G>C maps to NM_004341.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:115047298 A>G maps to NM_014333.3 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:115099934 G>A maps to NM_014333.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr11:115102157 A>G maps to NM_014333.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:86114880 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:86010736 C>T maps to NM_153184.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:86115893 C>T maps to NM_153184.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:86010618 G>A maps to NM_153184.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:86115930 T>G maps to NM_153184.3 *438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GE-01A-11W-A062-09 chr1:159169658 G>A maps to NM_021189.3 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:159162450 G>T maps to NM_021189.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:159162506 C>T maps to NM_021189.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:159159662 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:159159606 C>T maps to NM_021189.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr1:159163348 C>T maps to NM_021189.3 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr1:159162506 C>T maps to NM_021189.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:159161786 C>T maps to NM_021189.3 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:44127537 C>A maps to NM_145296.1 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:44130336 C>T maps to NM_145296.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:44131330 C>T maps to NM_145296.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:44129245 G>A maps to NM_145296.1 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:62452082 T>C maps to ENST00000383709 Q1166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:62499369 C>A maps to NM_183394.2 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:62556581 T>A maps to ENST00000383709 K537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:62570978 C>T maps to ENST00000383709 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:62631467 G>A maps to ENST00000383709 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr3:62631413 G>A maps to ENST00000383709 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:62477081 A>G maps to ENST00000383709 D986D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:62518672 G>T maps to ENST00000383709 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:62570924 G>A maps to ENST00000383709 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:62459934 G>A maps to ENST00000383709 V1130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:62451071 C>T maps to ENST00000383709 G1207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:62522215 G>T maps to ENST00000383709 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:62739271 G>A maps to ENST00000383709 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr3:62385241 G>A maps to ENST00000383709 R1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr7:122261572 G>A maps to NM_001167940.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:122255307 G>A maps to NM_001167940.1 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:122526061 C>T maps to NM_001167940.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:122028791 G>A maps to NM_001167940.1 T1007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:122303553 C>A maps to NM_001167940.1 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:122194637 G>A maps to NM_001167940.1 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:121960332 A>C maps to NM_001167940.1 T1263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:121985671 G>A maps to NM_001167940.1 R1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:122033592 G>T maps to NM_001167940.1 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr7:122261660 C>T maps to NM_001167940.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr7:122028745 G>A maps to NM_001167940.1 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:121960373 G>A maps to NM_001167940.1 R1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:122078449 G>A maps to NM_001167940.1 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:122526172 C>T maps to NM_001167940.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:122033565 C>A maps to NM_001167940.1 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:7373700 C>A maps to NM_001170692.1 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:7356337 C>A maps to NM_001170692.1 E740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:7374202 G>A maps to NM_001170692.1 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr6:7373472 T>G maps to NM_001170692.1 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:7373964 C>A maps to NM_001170692.1 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:7374028 C>T maps to NM_001170692.1 Q341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:91078155 G>A maps to NM_004929.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:71416659 C>T maps to NM_001740.4 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:71419499 C>T maps to NM_001740.4 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:71406122 C>A maps to NM_001740.4 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:71408671 G>T maps to NM_001740.4 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:14990395 G>A maps to NM_001741.2 D125D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BS-A0UF-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:54105643 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:54105604 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:54107929 G>A maps to NM_020898.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:46939645 G>T maps to ENST00000448105 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:93055880 G>T maps to NM_001164737.1 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:93108737 G>A maps to NM_001164737.1 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:93108740 C>A maps to NM_001164737.1 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr7:93108744 G>A maps to NM_001164737.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:188211015 A>G maps to NM_005795.4 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr2:188223834 G>T maps to NM_005795.4 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:188243719 G>A maps to NM_005795.4 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:134613552 A>G maps to NM_033138.3 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:134625841 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:134642828 C>T maps to NM_033138.3 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:134644830 C>A maps to NM_033138.3 S723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:134625988 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:105218160 G>A maps to NM_001001412.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:105206947 C>T maps to NM_015916.4 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr10:105206878 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:105207004 G>A maps to NM_015916.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:47112209 C>T maps to NM_005184.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr19:47111526 G>A maps to NM_005184.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:5541281 C>T maps to NM_017422.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:1848296 C>T maps to NM_138705.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr19:13051443 A>G maps to NM_004343.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:16593512 C>T maps to NM_145046.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:16590028 G>A maps to NM_145046.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:16594785 C>T maps to NM_145046.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:128399844 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:9803387 G>A maps to NM_003656.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:9801417 C>T maps to NM_003656.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:9801417 C>T maps to NM_003656.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:12811796 C>T maps to NM_153498.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:12833166 C>T maps to NM_153498.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:12870786 C>A maps to NM_153498.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:209779759 C>A maps to NM_020439.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:149633036 C>A maps to NM_015981.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr7:44281816 G>A maps to NM_001220.4 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:44260221 G>A maps to NM_001220.4 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:44260221 G>A maps to NM_001220.4 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:114381390 G>T maps to ENST00000515496 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:114680520 C>A maps to ENST00000515496 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr10:75606988 C>T maps to ENST00000423381 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr10:75585105 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:110814129 C>T maps to NM_001744.4 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr5:110819921 C>T maps to NM_001744.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:3786428 T>A maps to ENST00000381771 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:121681926 C>A maps to NM_172214.2 *534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:49898419 T>C maps to NM_024046.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:49898209 G>T maps to NM_024046.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr3:49898376 G>A maps to NM_024046.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:49898889 G>A maps to NM_024046.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:134077129 G>T maps to NM_001745.2 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:138709866 C>T maps to ENST00000409386 T1420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:138714913 G>A maps to ENST00000409386 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:138714940 C>T maps to ENST00000409386 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:138773529 C>T maps to ENST00000409386 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:138774924 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr9:138713134 C>T maps to ENST00000409386 T1135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:138774829 G>A maps to ENST00000409386 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr9:138774889 G>A maps to ENST00000409386 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr9:138710416 C>T maps to ENST00000409386 A1346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:138703328 C>T maps to ENST00000409386 K1556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:7730996 C>T maps to NM_015215.2 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr1:7724478 C>A maps to NM_015215.2 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:7723932 C>T maps to NM_015215.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:7796453 C>T maps to NM_015215.2 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:7723926 C>T maps to NM_015215.2 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:6880284 T>C maps to NM_015215.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:7725108 C>T maps to NM_015215.2 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:4885026 G>A maps to NM_015099.3 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:4877706 G>T maps to NM_015099.3 C663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:4872577 G>A maps to NM_015099.3 R1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr17:4876926 A>C maps to NM_015099.3 A718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:4877004 G>T maps to NM_015099.3 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr17:4883017 G>A maps to NM_015099.3 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:67703957 G>A maps to NM_018448.3 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:67675716 G>A maps to NM_018448.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:67699925 G>A maps to NM_018448.3 K826K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:67691358 T>C maps to NM_018448.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:67691340 G>T maps to NM_018448.3 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:67675791 G>A maps to NM_018448.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:67696163 G>A maps to NM_018448.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:67696163 G>A maps to NM_018448.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:67699463 T>C maps to NM_018448.3 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:67699745 A>G maps to NM_018448.3 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:12854862 G>T maps to NM_001162499.1 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:12859013 G>A maps to NM_001162499.1 E861E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:12854768 C>T maps to NM_001162499.1 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:76991253 G>A maps to NM_138793.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:76993332 G>T maps to NM_138793.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:76993521 G>A maps to NM_138793.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76993560 C>T maps to NM_138793.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:76989736 G>A maps to NM_138793.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:76993488 G>A maps to NM_138793.3 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:179142898 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr5:179151704 G>A maps to ENST00000415618 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:179155617 A>G maps to ENST00000415618 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:40535836 C>T maps to NM_001105530.1 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:40535913 G>A maps to NM_001105530.1 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:40533226 G>T maps to NM_001105530.1 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:17421881 C>T maps to NM_006366.2 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:17507509 C>T maps to NM_006366.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:17556592 G>T maps to NM_006366.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:64974100 C>T maps to NM_005186.3 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:64953461 C>T maps to NM_005186.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr11:64977562 G>A maps to NM_005186.3 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:241531518 C>T maps to NM_023083.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:241533434 G>A maps to NM_023083.3 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr2:241530422 C>T maps to NM_023083.3 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:44140063 C>T maps to NM_007058.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:44141018 G>T maps to NM_007058.3 G243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr6:44145042 C>T maps to NM_007058.3 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:44148498 G>A maps to NM_007058.3 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:44147732 G>A maps to NM_007058.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr6:44140157 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:44140675 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr6:44145027 T>C maps to NM_007058.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:39224961 G>A maps to NM_144691.3 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:39225503 C>A maps to NM_144691.3 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:30964803 T>C maps to ENST00000295055 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:223940572 C>T maps to NM_001748.4 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:223934867 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:223938638 C>A maps to NM_001748.4 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:42691701 G>A maps to NM_000070.2 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:42652185 C>T maps to NM_000070.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:42703157 C>T maps to NM_000070.2 D780D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr11:76823687 C>T maps to ENST00000360841 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:76834861 G>A maps to ENST00000360841 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:76831934 T>C maps to ENST00000360841 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:110489869 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:110491854 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:110494142 A>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:110507158 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:110489921 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:110490640 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:110497576 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:110494890 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:110491965 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:110494200 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:110494310 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:110495672 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:110507062 A>G did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:110491214 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:110489921 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:110491189 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:110496272 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:110495645 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:110495636 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:110507059 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr3:15253636 T>C maps to NM_014296.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:15292435 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:15274171 C>T maps to NM_014296.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:15262461 C>T maps to NM_014296.2 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:15259990 T>C maps to NM_014296.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:15265039 G>T maps to NM_014296.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:15283702 C>T maps to NM_014296.2 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:230930951 G>A maps to NM_006615.2 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:230898526 C>T maps to NM_006615.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:230927674 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:230928236 G>A maps to NM_006615.2 W596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:230891100 G>T maps to NM_006615.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:230903322 C>T maps to NM_006615.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:230903322 C>T maps to NM_006615.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:34120907 G>T maps to NM_005898.4 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:34119323 G>A maps to NM_203364.2 W694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:34118180 T>C maps to NM_005898.4 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:30869573 C>A maps to NM_001002259.1 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:30869586 C>T maps to NM_001002259.1 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:30862859 T>C maps to NM_001002259.1 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:30862865 C>T maps to NM_001002259.1 T1118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:30877364 G>A maps to NM_001002259.1 D642D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:30881757 C>A maps to NM_001002259.1 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:5914949 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr19:5915236 A>T maps to ENST00000394521 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr12:75683398 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:75683543 C>A maps to NM_032606.3 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:75672827 C>A maps to ENST00000442339 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:75683520 A>G maps to NM_032606.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:75710175 C>T maps to NM_032606.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:35910637 T>G maps to NM_144647.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:113201660 C>T maps to NM_006135.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr7:116557837 C>A maps to NM_006136.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:116544242 G>T maps to NM_006136.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:18891438 C>T maps to NM_033328.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr1:19705071 C>T maps to ENST00000375145 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr22:37893106 C>T maps to NM_014550.3 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:37903886 G>A maps to NM_014550.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:37912212 G>A maps to NM_014550.3 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:37893138 C>A maps to NM_014550.3 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:37891894 G>A maps to NM_014550.3 C725C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:2962373 G>A maps to NM_032415.4 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:2976855 G>A maps to NM_032415.4 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:2979559 G>A maps to NM_032415.4 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:2951847 G>A maps to NM_032415.4 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:2959199 C>T maps to NM_032415.4 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:2987362 C>T maps to NM_032415.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:2962845 G>A maps to NM_032415.4 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr7:2984009 G>A maps to NM_032415.4 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:2951847 G>A maps to NM_032415.4 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:2955003 G>A maps to NM_032415.4 F902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:2959067 G>A maps to NM_032415.4 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:2998265 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr7:2946423 G>A maps to NM_032415.4 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:78165264 G>A maps to NM_024110.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:78172275 G>A maps to NM_024110.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:78163589 G>A maps to NM_024110.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:104915167 G>T maps to NM_001017534.1 Y75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:104914258 T>G maps to NM_052889.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:104971459 G>A maps to NM_001007232.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:40843440 A>G maps to NM_032587.3 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:40852694 C>T maps to NM_032587.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:40853620 G>A maps to NM_032587.3 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:40853548 T>C maps to NM_032587.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:40852399 A>G maps to NM_032587.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:40852687 C>A maps to NM_032587.3 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:40843252 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:40843491 C>T maps to NM_032587.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:40853917 C>A maps to NM_032587.3 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:48735209 G>A maps to ENST00000377461 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:111274593 A>G maps to NM_018210.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:111287813 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:11031117 C>T maps to NM_199141.1 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K0-01A-11W-A062-09 chr19:11032430 T>C maps to NM_199141.1 *609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:11015738 C>T maps to NM_199141.1 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr11:67186368 G>A maps to NM_001166222.1 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr11:67191963 C>T maps to NM_001166222.1 A915A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A16X-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr11:67191927 C>T maps to NM_001166222.1 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:3028124 C>T maps to NM_001014437.2 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:3039850 T>C maps to NM_001014437.2 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:3022406 G>A maps to NM_001014437.2 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:3039931 G>A maps to NM_001014437.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:3061139 G>T maps to NM_001014437.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:3069196 G>A maps to NM_001014437.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr11:3039979 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:3039964 G>A maps to NM_001014437.2 N470N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:3061100 G>T maps to NM_001014437.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:3039694 G>T maps to NM_001014437.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:3023226 G>A maps to NM_001014437.2 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:25297531 G>A maps to NM_018272.3 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:25308310 A>C maps to NM_018272.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:25299968 G>A maps to NM_018272.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:25308315 C>A maps to NM_018272.3 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:25263126 A>G maps to NM_018272.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:25297502 A>G maps to NM_018272.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr12:25311419 G>T maps to NM_018272.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr12:25307270 C>T maps to NM_018272.3 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:25297468 C>A maps to NM_018272.3 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:38324582 C>T maps to NM_007359.4 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:38318011 G>T maps to NM_007359.4 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:44624276 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:44695086 C>T maps to NM_138423.3 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr15:44671900 T>G maps to NM_138423.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:44705544 C>T maps to NM_138423.3 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:40914765 C>T maps to NM_170589.3 H794H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:40916719 C>A maps to NM_170589.3 R1446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:40920329 C>T maps to NM_170589.3 N1839N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:40914334 C>T maps to NM_170589.3 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:40944293 G>T maps to NM_170589.3 E2162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:40917514 G>T maps to NM_170589.3 E1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr15:40915287 T>C maps to NM_170589.3 T968T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:40901080 C>T maps to NM_170589.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:40917802 G>T maps to NM_170589.3 E1807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:40914528 A>G maps to NM_170589.3 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:40914901 G>T maps to NM_170589.3 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:40937891 A>G maps to NM_170589.3 S2002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:40914901 G>T maps to NM_170589.3 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:41394218 A>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:41414857 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:41469178 T>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:41485869 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:41419029 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:41379833 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:41437688 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:41485941 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:41379783 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41394208 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41495910 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:41390379 G>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:41419047 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:41519787 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:41646533 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:41437685 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:41712417 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:41419025 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41437630 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:41420831 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:41390294 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:41446201 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:41712456 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:41519762 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:41448819 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:41712456 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:41420819 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:2235359 C>T maps to NM_020764.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:2233700 G>A maps to NM_020764.3 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:73502915 C>T maps to NM_020753.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:104901167 T>C maps to NM_033292.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:104901929 C>A maps to NM_033292.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:104900470 G>T maps to NM_033292.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:202073853 G>A maps to NM_032977.3 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:202050824 C>T maps to NM_032977.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:202050694 C>A maps to NM_032977.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:202073862 A>G maps to NM_032977.3 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:202050824 C>T maps to NM_032977.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:202073853 G>A maps to NM_032977.3 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:202050563 G>T maps to NM_032977.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:15164692 C>T maps to NM_012114.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:142997110 C>T maps to NM_032982.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:143001854 C>T maps to NM_032982.2 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:143001009 C>T maps to NM_032982.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:142988671 A>G maps to NM_032982.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:142997044 A>G maps to NM_032982.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:142997325 C>T maps to NM_032982.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:185550640 G>A maps to NM_032991.2 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:185553080 A>G maps to NM_032991.2 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:185553521 G>A maps to NM_032991.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:104819263 C>T maps to NM_001225.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:104871207 C>T maps to NM_001136112.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:104866558 G>T maps to NM_001136112.1 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:104877933 A>C maps to NM_001136112.1 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:104893890 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:104893890 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:104879651 G>T maps to NM_001136112.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:104866558 G>T maps to NM_001136112.1 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:110612144 G>A maps to NM_001226.3 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:115489169 C>A maps to NM_033338.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:115457281 G>A maps to NM_033338.4 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:202137665 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:202134317 C>T maps to NM_001228.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:202149671 C>A maps to NM_001080125.1 C371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:202150038 C>T maps to NM_001080125.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:202136316 C>T maps to NM_001080125.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:202149879 G>T maps to NM_001080125.1 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:202136316 C>A maps to NM_001080125.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:202131314 G>T maps to NM_001080125.1 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr2:202137499 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:202137359 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:202137458 C>T maps to NM_001080125.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:202149905 G>A maps to NM_001080125.1 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:202149962 T>C maps to NM_001080125.1 C468C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:15831169 A>G maps to NM_001229.3 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:15819479 G>A maps to NM_001229.3 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:15833558 C>A maps to NM_001229.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:160163621 G>T maps to NM_001231.4 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:160165778 C>T maps to NM_001231.4 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:160162629 C>T maps to NM_001231.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:160162629 C>T maps to NM_001231.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:160162629 C>T maps to NM_001231.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:160165799 C>T maps to NM_001231.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:160171102 G>A maps to NM_001231.4 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:160165305 C>T maps to NM_001231.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:116275560 G>A maps to NM_001232.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:116311117 G>T maps to NM_001232.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:122002978 G>A maps to NM_001178065.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121981093 C>T maps to NM_001178065.1 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121981222 C>T maps to NM_001178065.1 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:122002711 C>T maps to NM_001178065.1 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:121980484 C>T maps to NM_001178065.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:121980560 C>T maps to NM_001178065.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:122003014 C>A maps to NM_001178065.1 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr3:121980529 C>T maps to NM_001178065.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:121980796 C>T maps to NM_001178065.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:55027242 T>C maps to NM_020356.3 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:55027224 T>A maps to NM_020356.3 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:55027368 T>C maps to NM_020356.3 H379H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:55027302 G>A maps to NM_020356.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:55027494 C>A maps to NM_020356.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:96077013 C>T maps to ENST00000508830 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:96100977 A>G maps to ENST00000508830 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:96065398 G>A maps to ENST00000508830 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:96073606 G>T maps to ENST00000508830 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:10714088 G>A maps to NM_001079843.1 C675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr1:10710784 C>T maps to NM_001079843.1 P948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:10699877 C>T maps to NM_001079843.1 K1467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:10708003 G>A maps to NM_001079843.1 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:10699931 C>T maps to NM_001079843.1 Q1449Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:10710793 G>A maps to NM_001079843.1 H945H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:34470860 T>C maps to NM_001752.3 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr11:34477667 C>T maps to NM_001752.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:65792902 G>A maps to NM_053054.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65793010 G>A maps to NM_053054.3 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:65792929 G>A maps to NM_053054.3 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:65793186 G>A maps to NM_053054.3 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:65792875 G>T maps to NM_053054.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:65788060 G>T maps to NM_053054.3 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:65792950 A>G maps to NM_053054.3 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:65792902 G>A maps to NM_053054.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:65788348 G>T maps to NM_053054.3 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:65789293 G>A maps to NM_053054.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:43940190 G>A maps to NM_172095.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:43939281 G>T maps to NM_172095.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr5:134343744 C>T maps to NM_178019.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:26520291 G>A maps to NM_198137.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:26524847 G>A maps to NM_198137.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:26526473 C>T maps to NM_198137.1 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:26524886 G>A maps to NM_198137.1 W263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:92102803 G>A maps to NM_024764.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:92159550 C>T maps to NM_024764.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:92195793 A>C maps to NM_024764.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:38853432 G>A maps to NM_021185.4 K812K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:38848931 G>T maps to NM_021185.4 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:38851130 C>A maps to NM_021185.4 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:38851265 C>T maps to NM_021185.4 Y582Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:38861407 C>T maps to NM_021185.4 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:38858146 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:38857914 C>T maps to NM_021185.4 N911N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:8787396 C>A maps to NM_001234.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:32194885 G>A maps to NM_005093.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:32210985 C>T maps to NM_005093.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:32232289 C>T maps to NM_005093.3 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:88967924 G>A maps to NM_005187.5 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:88952427 G>A maps to NM_005187.5 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:88964557 G>A maps to NM_005187.5 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr16:67070624 A>T maps to NM_022845.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:119169185 C>T maps to NM_005188.2 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr11:119149249 C>T maps to NM_005188.2 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:119149278 C>T maps to NM_005188.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr11:119103240 G>A maps to NM_005188.2 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:105438962 C>T maps to NM_170662.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:105470462 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr3:105400580 G>A maps to NM_170662.3 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:105377966 G>A maps to NM_170662.3 V932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:105452900 A>G maps to NM_170662.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:45303673 G>T maps to NM_012116.3 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr19:45303698 G>T maps to NM_012116.3 *475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:107398713 C>T maps to NM_024814.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:107399642 A>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr18:70209101 C>T maps to NM_182511.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:70209170 G>A maps to NM_182511.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:54579089 C>T maps to NM_080617.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:54579143 C>T maps to NM_080617.4 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr20:54579188 G>A maps to NM_080617.4 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:37444774 C>T maps to NM_001757.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:169923336 T>C maps to NM_032783.4 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:169911456 C>T maps to NM_032783.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:44486374 G>A maps to ENST00000398168 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:44474093 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr21:44488637 G>A maps to ENST00000398168 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr21:44488682 G>A maps to ENST00000398168 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:154704 G>A maps to ENST00000377447 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:162469 C>A did not map to a codon.
Sequencing variant TCGA-AP-A05D-01A-11W-A027-09 chr9:154617 T>G maps to ENST00000377447 *251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:154704 G>A maps to ENST00000377447 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:114251403 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:114253266 G>T maps to NM_172003.3 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:69238294 G>T maps to NM_001085457.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:69205471 G>A maps to NM_001085457.1 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:77755581 C>T maps to NM_005189.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:77757577 C>A maps to NM_005189.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr17:77757652 C>T maps to NM_005189.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:26246055 C>T maps to NM_016587.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:26251821 T>A maps to NM_016587.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr7:26245998 A>G maps to NM_016587.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:77808648 G>A maps to NM_003655.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:77808933 G>A maps to NM_003655.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:54645971 G>A maps to NM_012117.2 C59C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:39262765 G>A maps to NM_014292.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:77768907 G>A maps to NM_020649.2 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:14037872 C>T maps to NM_017721.4 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:14037636 G>T maps to NM_017721.4 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:52821312 A>T maps to NM_032449.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr1:52823511 G>T maps to NM_032449.2 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:15511839 C>T maps to NM_001080522.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:15542571 C>T maps to NM_001080522.2 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:15581688 A>G maps to NM_001080522.2 V1290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:15556735 C>A maps to NM_001080522.2 S843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:15575940 C>T maps to NM_001080522.2 R1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:15480406 C>T maps to NM_001080522.2 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:15517515 G>A maps to NM_001080522.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr4:15529272 T>A maps to NM_001080522.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:97769593 A>T maps to NM_001159747.1 K12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:97776058 G>A maps to NM_001159747.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:97787005 C>T maps to NM_001159747.1 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:70507138 G>A maps to NM_018237.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:70520793 C>T maps to NM_018237.2 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11M-01A-11D-A122-09 chr10:70520793 C>T maps to NM_018237.2 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr10:70547773 G>T maps to NM_018237.2 E991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr10:70507313 C>T maps to NM_018237.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:57103372 C>A maps to NM_133459.3 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:57106929 C>T maps to NM_133459.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:57134046 G>A maps to NM_133459.3 C159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:42907037 T>C maps to NM_001296.4 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:42906581 C>T maps to NM_001296.4 H196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:57550207 G>A maps to NM_033212.3 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:66564453 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:66504495 G>T maps to NM_024781.2 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr18:66504140 T>C maps to NM_024781.2 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr18:66542022 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:55761007 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:55771188 G>A maps to ENST00000339012 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:55771105 G>T maps to ENST00000339012 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:55750886 G>T maps to ENST00000339012 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:15132168 C>T maps to NM_173482.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:56160420 C>T maps to NM_013301.2 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:219896005 G>T maps to NM_194302.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:219886631 G>T maps to NM_194302.2 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:219869089 C>T maps to NM_194302.2 E1713E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:219887048 C>T maps to NM_194302.2 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:219868975 T>C maps to NM_194302.2 P1751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:219868911 C>A maps to NM_194302.2 E1773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:219888009 G>A maps to NM_194302.2 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:219888958 A>G maps to NM_194302.2 G791G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:110605759 A>G maps to NM_017918.4 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:110581349 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:47769288 T>C maps to NM_145020.3 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:47778122 A>G maps to NM_145020.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:47753753 C>T maps to NM_145020.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:186379439 A>G maps to NM_152775.3 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:186382294 C>A maps to NM_152775.3 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:186379558 C>A maps to NM_152775.3 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:186379837 C>A maps to NM_152775.3 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr4:186392096 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:186379705 C>A maps to NM_152775.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:185593504 G>A maps to NM_152683.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:185603479 C>T maps to NM_152683.2 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:114611038 T>C maps to NM_001040440.2 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:114620506 G>C maps to NM_001040440.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:58287999 G>A maps to NM_014157.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:58296369 G>T maps to NM_014157.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:58292312 G>A maps to NM_014157.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:48800673 C>T maps to NM_144577.3 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:48801451 C>T maps to NM_144577.3 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:48815310 G>A maps to NM_144577.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:48806905 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:48800331 C>T maps to NM_144577.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:48801291 C>T maps to NM_144577.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr19:48814868 G>A maps to NM_144577.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:48801291 C>T maps to NM_144577.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:21989344 C>T maps to NM_152612.2 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:21990875 C>T maps to NM_152612.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:21990875 C>T maps to NM_152612.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:21989159 C>T maps to NM_152612.2 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr22:21989098 C>T maps to NM_152612.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:46963753 C>A maps to NM_144716.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48920066 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48920040 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48919623 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48921976 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48924827 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27851362 A>G maps to ENST00000435516 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:27850467 C>A maps to ENST00000435516 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:27850683 C>A maps to ENST00000435516 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:44432990 C>A maps to NM_144974.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:68616151 C>T maps to NM_176816.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:68602701 C>A maps to NM_176816.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:68595925 G>A maps to NM_176816.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr7:23651023 G>A maps to NM_138771.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr7:23651032 T>A maps to NM_138771.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:216865 T>C maps to NM_145265.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:31617798 T>C maps to NM_194300.2 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:31690787 G>A maps to NM_194300.2 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:31682891 A>C maps to NM_194300.2 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:31682571 A>C maps to NM_194300.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:31692200 G>T maps to NM_194300.2 E965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:31683146 G>A maps to NM_194300.2 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr7:31617534 G>A maps to NM_194300.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:42775101 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:42751219 G>T maps to NM_144719.3 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:42799773 G>A maps to NM_144719.3 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:42781242 G>A maps to NM_144719.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:13873500 C>T maps to NM_030818.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:13868258 C>T maps to NM_030818.2 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:13868234 C>T maps to NM_030818.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:13869786 C>T maps to NM_030818.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:92940567 C>T maps to NM_017667.2 N613N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:92985358 G>A maps to NM_017667.2 E914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:92963445 C>T maps to NM_017667.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:92883210 G>A maps to NM_017667.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:92985326 G>T maps to NM_017667.2 E904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:92881983 C>T maps to NM_017667.2 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:92970743 T>G maps to NM_017667.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:92883210 G>A maps to NM_017667.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:92881983 C>T maps to NM_017667.2 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:92935204 T>G maps to NM_017667.2 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:42209292 G>A maps to NM_024821.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:42209813 C>T maps to NM_024821.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:42209813 C>T maps to NM_024821.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:57757010 C>A maps to NM_032269.5 Y502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:57760191 C>T maps to NM_032269.5 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:128441310 G>T maps to NM_022742.3 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:128457825 C>A maps to NM_022742.3 P1126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:128441513 C>T maps to NM_022742.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:128447454 G>T maps to NM_022742.3 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:128450374 C>T maps to NM_022742.3 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:128441289 G>T maps to NM_022742.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:128434763 A>G maps to NM_022742.3 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr7:128457825 C>A maps to NM_022742.3 P1126P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D1-A17Q-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:128434402 G>A maps to ENST00000249367 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:79638852 C>T maps to NM_199287.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:79639634 G>T maps to NM_199287.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:109432452 G>A maps to NM_144978.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:109429100 T>C maps to NM_144978.1 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:109421437 G>T maps to NM_144978.1 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:123649992 T>C maps to NM_022757.4 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:123633886 G>T maps to NM_022757.4 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:223168953 C>T maps to NM_153038.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:223168953 C>T maps to NM_153038.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179720079 T>G maps to NM_173648.3 I1018I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:179733852 G>T maps to NM_173648.3 V795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179732750 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179742842 C>A maps to NM_173648.3 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:179701835 C>A maps to NM_173648.3 S1370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:179702404 G>A maps to NM_173648.3 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr2:74708941 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:16608557 C>A maps to NM_014695.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:16593800 C>T maps to NM_014695.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:16612847 G>T maps to NM_014695.1 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:16664885 C>T maps to NM_014695.1 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:16608691 G>T maps to NM_014695.1 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:16630874 T>C maps to NM_014695.1 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:16665750 C>A maps to NM_014695.1 S1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:16593854 G>A maps to NM_014695.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:16638656 A>G maps to NM_014695.1 E1024E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:16608616 G>T maps to NM_014695.1 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:16638714 C>T maps to NM_014695.1 Q1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:16667309 C>T maps to NM_014695.1 Q1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:16593809 G>A maps to NM_014695.1 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:76908092 G>T maps to NM_020879.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:76922472 C>T maps to NM_020879.2 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:76908092 G>T maps to NM_020879.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:76908403 C>T maps to NM_020879.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:76903055 C>T maps to NM_020879.2 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:76908353 G>T maps to NM_020879.2 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:76885679 G>T maps to NM_020879.2 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:76797068 G>A maps to NM_020879.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:76891534 C>T maps to NM_020879.2 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:106118173 G>T maps to NM_001008723.1 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:106124613 A>G maps to NM_001008723.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:106124518 G>T maps to NM_001008723.1 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:106130775 G>T maps to NM_001008723.1 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:106118140 G>T maps to NM_001008723.1 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:106209948 G>T maps to NM_001008723.1 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:106207547 G>A maps to NM_001008723.1 T783T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:106130712 G>T maps to NM_001008723.1 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:106118173 G>T maps to NM_001008723.1 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:106209870 G>T maps to NM_001008723.1 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:106209948 G>T maps to NM_001008723.1 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:106125685 G>T maps to NM_001008723.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:159033085 C>A maps to NM_138803.3 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:159166097 A>G maps to NM_138803.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:24854702 G>A maps to NM_001130726.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:124875085 G>T maps to NM_025004.2 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:124908452 A>G maps to NM_025004.2 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr2:197530398 C>T maps to NM_001080539.1 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:197521494 C>T maps to NM_001080539.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:197559843 T>G maps to NM_001080539.1 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:197586392 C>T maps to NM_001080539.1 R803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:197597217 C>T maps to NM_001080539.1 R1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:197537073 G>A maps to NM_001080539.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr2:197597261 T>G maps to NM_001080539.1 Y1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr2:197590729 A>G maps to NM_001080539.1 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:11531868 G>A maps to NM_145045.4 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:119066178 C>A maps to NM_001145018.1 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:49900947 C>T maps to NM_144688.4 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:30769668 C>T maps to NM_001017437.2 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:77288599 C>T maps to NM_001042784.1 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:77305284 C>A maps to NM_001042784.1 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:77278634 C>A maps to NM_001042784.1 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:77283468 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:77288467 C>T maps to NM_001042784.1 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:77255227 T>G maps to NM_001042784.1 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:77276509 C>T maps to NM_001042784.1 Q751Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:133379674 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:133378948 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:133379393 T>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:133378856 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:133379033 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:133379248 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:133379480 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:133379758 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:133378921 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:133379391 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:133379093 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:133379652 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:133379093 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:133379031 T>A did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:93667455 C>T maps to NM_206886.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:93649648 C>T maps to NM_206886.2 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:93649648 C>T maps to NM_206886.2 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr1:93724432 T>C maps to NM_206886.2 Y1343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:93651946 C>T maps to NM_206886.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:93720072 C>T maps to NM_206886.2 R1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:93677753 C>T maps to NM_206886.2 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:93682251 T>C maps to NM_206886.2 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:159856362 C>T maps to NM_012337.2 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:159858194 C>A maps to NM_012337.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:159854303 C>T maps to NM_012337.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:159842947 C>A maps to NM_012337.2 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:159854246 C>T maps to NM_012337.2 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:159863008 C>T maps to NM_012337.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:159856359 C>T maps to NM_012337.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:159858191 C>A maps to NM_012337.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:49099755 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49099432 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49099631 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49103351 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49106159 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49099750 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49106138 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:49104878 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:44458224 C>T maps to NM_152499.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:44459606 C>T maps to NM_152499.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:44461478 C>T maps to NM_152499.1 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:27614246 G>A maps to NM_018246.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:3673372 T>C maps to NM_152492.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:3680307 G>T maps to NM_152492.2 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:3670735 C>T maps to NM_152492.2 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:3670800 C>T maps to NM_152492.2 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:139097217 C>A maps to NM_015439.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:12940505 C>T maps to NM_031455.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:12940570 G>A maps to NM_031455.3 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:12940625 C>T maps to NM_031455.3 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:43032077 C>T maps to NM_001080850.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:43032077 C>T maps to NM_001080850.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:43042695 G>A maps to NM_001080850.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:43022057 A>G maps to NM_001080850.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:43119672 G>T maps to NM_001080850.2 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:43042836 A>G maps to NM_001080850.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:43032077 C>T maps to NM_001080850.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:74572366 C>T maps to ENST00000321288 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:74536465 C>T maps to ENST00000321288 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:74626274 C>T maps to ENST00000321288 H901H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:74627404 G>A maps to ENST00000321288 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:27362371 G>A maps to NM_030771.1 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:27371946 C>A maps to NM_030771.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:27371810 G>T maps to NM_080654.2 S225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:27362270 G>A maps to NM_030771.1 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:27384545 G>A maps to NM_030771.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:49281842 T>A maps to NM_178173.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:49282171 T>C maps to ENST00000366429 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:49293751 G>A maps to NM_178173.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:49282086 G>A maps to NM_178173.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:49293754 A>G maps to NM_178173.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:49293878 G>T maps to NM_178173.3 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:126138548 G>A maps to ENST00000505024 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:126154467 G>A maps to ENST00000505024 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:126153212 G>A maps to ENST00000505024 E540E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:96310956 G>T maps to NM_182496.2 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:96312707 G>T maps to NM_182496.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:96273518 G>A maps to NM_182496.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:180361934 T>C maps to NM_181426.1 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:180359913 C>A maps to NM_181426.1 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:180337680 G>T maps to NM_181426.1 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr3:180379668 C>A maps to NM_181426.1 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:78022463 C>T maps to NM_017950.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:78055497 C>T maps to NM_017950.2 C572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:78013915 C>T maps to NM_017950.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:78071124 G>T maps to NM_017950.2 E1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:78021184 C>T maps to NM_017950.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:78014005 C>T maps to NM_017950.2 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr17:78023993 C>T maps to NM_017950.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:94772671 C>T maps to NM_001042399.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:94761836 C>A maps to NM_001042399.1 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:94763805 C>A maps to NM_001042399.1 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:94797038 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:94703806 G>A maps to NM_001042399.1 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:8644937 C>A maps to NM_144681.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:42757951 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:61829343 G>A maps to NM_020198.2 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:61833605 A>G maps to NM_020198.2 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:128753054 C>T maps to NM_024768.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:191098621 C>T maps to NM_178335.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:191047492 G>A maps to NM_178335.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr3:191074904 C>T maps to NM_178335.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr3:48475151 A>G maps to NM_024661.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr3:48474423 C>T maps to NM_024661.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:107097153 C>A maps to NM_032600.2 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:107096926 G>T maps to NM_032600.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:107097381 C>T maps to NM_032600.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:80141711 C>T maps to ENST00000445854 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:80153186 A>T maps to ENST00000445854 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:80086461 A>G maps to ENST00000445854 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr12:82746931 A>G maps to NM_014167.4 *242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:82746940 C>A maps to NM_014167.4 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:82750940 G>A maps to NM_014167.4 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:61612435 C>A maps to ENST00000395341 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:61572396 T>C maps to ENST00000395341 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:61612435 C>A maps to ENST00000395341 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:119978477 C>T maps to NM_178499.3 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:119773055 G>A maps to NM_178499.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr12:119968852 C>T maps to NM_178499.3 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:46519481 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:46506287 G>A maps to NM_001080402.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:123262118 C>T maps to NM_201435.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:123285824 G>T maps to NM_201435.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:123265729 T>G maps to NM_201435.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:123281893 G>A maps to NM_201435.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:111296458 G>A maps to NM_152591.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:111319069 G>T maps to NM_152591.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:111296554 G>A maps to NM_152591.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:111336735 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:120499524 T>C maps to NM_207311.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:120499608 G>T maps to NM_207311.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:120436357 C>T maps to NM_207311.2 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:120499536 C>T maps to NM_207311.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr12:120518738 C>T maps to NM_207311.2 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:49315111 C>T maps to NM_033124.4 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:49312056 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:49298127 G>A maps to NM_033124.4 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:49298131 G>T maps to NM_033124.4 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:56651312 G>T maps to NM_001141947.1 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:56649298 T>C maps to NM_001141947.1 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:56651187 C>A maps to NM_001141947.1 S631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:56653484 C>A maps to NM_001141947.1 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:56653470 C>T maps to NM_001141947.1 R851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:56653887 C>T maps to NM_001141947.1 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:93122237 G>T maps to NM_181645.3 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:93127692 C>A maps to NM_181645.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:93170812 T>A maps to NM_181645.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:93090125 C>T maps to NM_181645.3 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:93148235 G>T maps to NM_181645.3 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:93127650 A>G maps to NM_181645.3 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:93097387 T>A maps to NM_181645.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr18:52604147 G>A maps to NM_025214.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:150565606 G>T maps to NM_015621.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:32740747 G>T maps to NM_001026383.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:32740747 G>T maps to NM_001026383.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:32833193 G>T maps to NM_001026383.1 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:52439799 G>T maps to NM_031290.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:52440035 G>A maps to NM_031290.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:49200594 T>C maps to NM_022903.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49200893 G>A maps to NM_022903.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:49200657 C>T maps to NM_022903.3 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:32637618 G>A maps to NM_001008391.2 N414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:32636284 C>A maps to NM_001008391.2 G527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:32636194 C>A maps to NM_001008391.2 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:32657318 C>A maps to NM_001008391.2 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:32657369 C>A maps to NM_001008391.2 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:32675583 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:32697465 C>T maps to NM_001008391.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:32624458 A>G maps to NM_001008391.2 N1046N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:32635271 C>T maps to NM_001008391.2 E864E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:32697533 C>A maps to NM_001008391.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:32720834 C>A maps to NM_001008391.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:32657318 C>A maps to NM_001008391.2 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:32676427 C>A maps to NM_001008391.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:32635561 C>A maps to NM_001008391.2 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:32636275 C>A maps to NM_001008391.2 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:32720834 C>A maps to NM_001008391.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:32635450 C>A maps to NM_001008391.2 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:32781674 C>A maps to NM_001008391.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:132287064 C>T maps to ENST00000434330 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:132285770 G>A maps to NM_138770.1 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:130897480 C>T maps to NM_207310.1 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:130897489 G>T maps to NM_207310.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:130897663 C>T maps to NM_207310.1 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr2:37319060 A>T maps to ENST00000379187 K111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:37319177 C>T maps to ENST00000379187 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:37315545 G>T maps to ENST00000379187 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:100605242 T>C maps to NM_019083.2 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:100606481 A>G maps to NM_019083.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:775023 G>A maps to ENST00000439619 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr3:112335606 G>T maps to ENST00000447230 G768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:112349023 G>T maps to ENST00000447230 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:86097147 G>A maps to NM_001156474.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:86120374 A>C maps to NM_001156474.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:96117176 T>C maps to NM_024725.3 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:96117406 C>A maps to NM_024725.3 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:96117769 C>A maps to NM_024725.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:96092309 A>G maps to NM_024725.3 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:96117596 G>A maps to NM_024725.3 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:96117178 C>A maps to NM_024725.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:118882957 C>T maps to NM_198489.1 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr2:56602994 A>G maps to NM_001080433.1 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:56611478 G>T maps to NM_001080433.1 G551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:56611399 G>T did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr2:56420000 G>A maps to NM_001080433.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr2:56603036 C>T maps to NM_001080433.1 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:66359430 G>A maps to NM_018219.2 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:66358212 G>A maps to NM_018219.2 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:55561945 C>A maps to ENST00000436346 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:55561786 G>A maps to ENST00000436346 Q724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:55544423 C>A maps to ENST00000436346 E1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:55573405 G>A maps to ENST00000436346 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:55549774 T>C maps to ENST00000436346 V1017V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:55559735 G>A maps to ENST00000436346 R941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:55582839 G>T maps to ENST00000436346 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:55555482 G>A maps to ENST00000436346 R982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:55559781 G>A maps to ENST00000436346 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:55562164 C>A maps to ENST00000436346 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr2:55559799 T>C maps to ENST00000436346 Q919Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:55562110 C>A maps to ENST00000436346 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:64120585 G>A maps to NM_032251.5 G1187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr11:64111488 G>A maps to NM_032251.5 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:64121207 C>T maps to NM_032251.5 R1285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:91770292 G>A maps to NM_001080414.2 S1129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:91804868 G>A maps to NM_001080414.2 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:91766311 G>A maps to NM_001080414.2 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:91804432 C>T maps to NM_001080414.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:91739598 C>T maps to NM_001080414.2 E1819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:91780389 C>T maps to NM_001080414.2 K590K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:85396651 C>T maps to NM_152723.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr11:85396684 G>A maps to NM_152723.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr19:47761874 C>T maps to NM_015603.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:82984873 G>A maps to NM_021825.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:28605448 C>T maps to NM_018318.3 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:124422353 C>A maps to NM_025140.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:118732461 C>T maps to NM_019044.4 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:118766197 A>G maps to NM_019044.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:118758438 C>T maps to NM_019044.4 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:4262015 C>T maps to NM_018074.4 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:4258330 C>T maps to NM_018074.4 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:4247163 A>G maps to NM_018074.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:7043264 G>A maps to NM_153376.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:7043294 G>A maps to NM_153376.2 N457N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr4:7043111 G>A maps to NM_153376.2 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr19:41825632 G>A maps to NM_052848.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:41828580 A>G maps to NM_052848.1 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:169026164 T>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:169028401 G>A maps to NM_017785.4 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:169018167 G>A maps to NM_017785.4 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:169025478 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:169031138 T>G maps to NM_017785.4 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:169020365 A>G maps to NM_017785.4 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:169015447 C>T maps to NM_017785.4 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:169021583 C>T maps to NM_017785.4 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:36170078 G>T maps to NM_005893.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:36169537 C>T maps to NM_005893.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:36170536 G>A maps to NM_005893.2 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:42299711 G>A maps to NM_000729.4 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:26483748 G>A maps to NM_000730.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:26484820 G>A maps to NM_000730.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr4:26484776 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:26490891 G>A maps to NM_000730.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:26490891 G>A maps to NM_000730.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr11:6291528 C>T maps to NM_176875.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:6292298 C>T maps to NM_176875.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6281274 C>T maps to NM_176875.2 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:6292314 C>T maps to NM_176875.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:6292307 C>T maps to NM_176875.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:6292298 C>T maps to NM_176875.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:32612835 C>A maps to NM_002986.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:34310857 G>A maps to NM_032962.4 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:34325398 G>T maps to NM_032965.4 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:228681052 C>T maps to NM_004591.2 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:57394394 C>T maps to NM_002990.4 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:32598793 C>T maps to ENST00000378569 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:32598133 A>G maps to ENST00000394627 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:32647286 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:45115610 C>T maps to NM_001029835.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:45104115 C>T maps to NM_001029835.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:37012891 C>T maps to NM_003914.3 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:37014166 C>T maps to NM_003914.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:37016338 C>A maps to NM_003914.3 S415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:37011836 T>C maps to NM_003914.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:68471357 T>C maps to NM_031966.2 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:20779834 T>C maps to NM_182849.1 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:20779872 G>A maps to NM_182849.1 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:59409032 G>T maps to NM_004701.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:59415774 G>A maps to NM_004701.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:50054373 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:50052735 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:50056936 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:50085295 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:50052666 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:50052799 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:50052119 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:50053646 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:50053682 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:50052403 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:50052432 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:50053677 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:50053688 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:50055607 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:50085205 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:50053137 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:50055607 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:50053583 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:50037905 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:50052843 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:50054195 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:50051904 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:50053329 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:50053392 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:50053925 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:50054195 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:50028197 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:50037980 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:50085251 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:50051846 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:50052166 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:50051793 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:50052432 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:50053432 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:50089728 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50052214 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50052781 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50053290 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50054273 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:50052074 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:50052194 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:50051789 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr23:50053707 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:50053046 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:50051775 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:50051864 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:50052213 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:50090764 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr6:99997423 C>T maps to NM_005190.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:99993052 G>A maps to NM_005190.3 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr11:69465984 G>T maps to NM_053056.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:69457917 C>T maps to NM_053056.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:4409087 C>G maps to NM_001759.3 Y261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:4385386 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:4398035 G>A maps to NM_001759.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:4398006 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:41908308 C>T maps to NM_001760.3 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:30303683 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:30311679 G>A maps to NM_001238.1 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:30303658 G>A maps to NM_001238.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:2493717 C>T maps to NM_001761.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:2485827 C>T maps to NM_001761.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:2505434 C>T maps to NM_001761.2 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:162868185 C>T maps to NM_199246.1 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:86707123 C>A maps to NM_001239.3 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:77969731 G>A maps to NM_006835.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:132086671 C>T maps to NM_001039780.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:132085047 G>A maps to NM_001039780.2 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:132084118 T>G maps to NM_001039780.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:97817913 T>G maps to NM_001134375.1 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr5:159682575 C>T maps to NM_024565.5 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:99968606 C>T maps to ENST00000437596 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:99959122 C>T maps to ENST00000437596 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:156870887 G>T maps to NM_020307.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:156866358 G>A maps to NM_020307.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:156868147 G>A maps to NM_020307.2 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:1334012 G>A maps to NM_030937.4 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:1333631 G>A maps to NM_030937.4 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:1325700 G>A maps to NM_030937.4 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:1325670 C>T maps to NM_030937.4 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr1:1323235 G>A maps to NM_030937.4 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:54527310 G>A maps to NM_021147.3 D315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:49110358 C>A maps to NM_001240.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:135711068 C>T maps to NM_058241.2 H348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:135710269 C>T maps to NM_058241.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:135712172 C>T maps to NM_058241.2 F716F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:135694490 A>G maps to NM_058241.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:135694461 C>T maps to NM_058241.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:135712127 C>T maps to NM_058241.2 H701H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:135676525 C>A maps to NM_058241.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:35854953 C>T maps to NM_145012.4 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:35858031 G>A maps to NM_145012.4 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:35819146 G>A maps to NM_145012.4 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:55652968 C>T maps to ENST00000442196 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:55652802 G>A maps to ENST00000442196 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr15:55652341 G>T maps to ENST00000442196 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:55657459 C>A maps to ENST00000442196 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:55652973 C>A maps to ENST00000442196 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:55664132 T>G maps to ENST00000442196 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:46245227 G>A maps to NM_001295.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:46399125 C>T maps to NM_001123041.2 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:46399584 C>T maps to NM_001123041.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:46399296 T>C maps to NM_001123041.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:46399383 C>A maps to NM_001123041.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:46307174 G>T maps to NM_178328.1 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:32995444 T>G maps to NM_005508.4 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:32995888 T>G maps to NM_005508.4 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:46414380 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:167550089 C>A maps to NM_004367.5 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:167550248 C>A maps to NM_004367.5 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:167550089 C>A maps to NM_004367.5 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:167550644 C>T maps to NM_004367.5 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:167550215 C>A maps to NM_004367.5 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:167550422 G>A maps to NM_004367.5 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:38711779 G>A maps to NM_001838.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:38715177 G>A maps to NM_001838.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:39374677 G>T maps to NM_005201.3 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:39374667 C>A maps to NM_005201.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:39374677 G>T maps to NM_005201.3 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:45943296 C>T maps to NM_031200.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:45942960 C>T maps to NM_031200.2 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:132319322 G>T maps to NM_178445.1 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:46449902 C>T maps to NM_001130910.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:69985879 C>T maps to NM_006431.2 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:69981761 C>T maps to NM_006431.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:69981997 G>A maps to NM_006431.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:69986772 A>G maps to NM_006431.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:69992133 T>C maps to NM_006431.2 Y456Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:69991467 G>T maps to NM_006431.2 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr12:69980552 C>T maps to NM_006431.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156305656 G>A maps to NM_005998.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:156288808 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:62099258 C>T maps to NM_006430.2 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:10256127 C>T maps to NM_012073.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:10262640 C>A maps to NM_012073.3 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:10256220 C>T maps to NM_012073.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:10258372 C>T maps to NM_012073.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:56125721 G>A maps to NM_001762.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr7:56130768 G>A maps to NM_001762.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:33257983 G>A maps to NM_006584.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:73475002 C>T maps to NM_006429.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:30434523 G>T maps to NM_006585.2 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:30434528 G>A maps to NM_006585.2 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:30439314 G>A maps to NM_006585.2 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:30432864 A>G maps to NM_006585.2 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:17072915 G>A maps to NM_014406.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:17073401 C>T maps to NM_014406.4 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr22:17072855 G>A maps to NM_014406.4 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:117561162 G>A maps to NM_004258.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:117552494 G>T maps to NM_004258.3 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:117552733 C>T maps to NM_004258.3 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:74407122 G>A maps to NM_133493.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:74440162 G>T maps to NM_133493.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:74481298 G>T maps to NM_133493.3 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:74524799 G>T maps to NM_133493.3 E1289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:74440162 G>T maps to NM_133493.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140011530 G>T maps to NM_001174105.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:145704265 C>A maps to NM_007053.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:7639098 G>T maps to NM_004244.4 C818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:7656280 G>A maps to NM_004244.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:7527242 G>A maps to ENST00000416109 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:7559320 G>A maps to ENST00000416109 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:7526063 G>A maps to ENST00000416109 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:7527242 G>A maps to ENST00000416109 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:7548799 G>A maps to ENST00000416109 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:7528344 A>G maps to ENST00000416109 H889H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:7586111 T>C maps to ENST00000416109 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:7586258 A>G maps to ENST00000416109 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr12:7556284 G>A maps to ENST00000416109 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:7528548 T>C maps to ENST00000416109 K821K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:7527892 G>T maps to ENST00000416109 V1005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:7585243 A>C maps to ENST00000416109 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr12:7531679 C>T maps to ENST00000416109 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:27706580 G>A maps to NM_207397.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:43858503 C>T maps to NM_020406.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:66479671 G>A maps to NM_005582.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:66479209 C>T maps to NM_005582.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:66479209 C>T maps to NM_005582.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:28944244 G>T maps to NM_001178098.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:28948661 C>T maps to NM_001178098.1 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:28946816 T>C maps to NM_001178098.1 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:28943907 C>A maps to NM_001178098.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:158225117 C>T maps to NM_001763.2 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:158299169 G>A maps to NM_001764.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:158263356 T>C maps to ENST00000368169 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr1:158261020 G>A maps to NM_001765.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:158260922 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:158262455 C>A maps to NM_001765.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr1:158262384 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:158263347 G>A maps to ENST00000368169 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr1:158259913 C>T maps to NM_001765.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:158152791 G>A maps to NM_001766.3 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:158324209 G>A maps to NM_030893.3 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:158326515 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:158325109 T>C maps to NM_030893.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:112063944 C>T maps to NM_001004196.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:112644020 T>G maps to NM_138806.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:112647834 C>T maps to NM_138806.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:112538668 G>T maps to NM_001008784.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:71060879 G>A maps to NM_015717.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:71058264 G>T maps to NM_015717.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr19:7806258 T>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:7807917 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7805480 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:7806082 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:7812455 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:7805364 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:7807825 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:7806215 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:7806646 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:7812203 T>A maps to NM_021155.3 K32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:7806672 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:35832836 C>T maps to NM_001771.3 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:35837482 C>T maps to NM_001771.3 N809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:35837567 G>T maps to NM_001771.3 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:35829215 A>G maps to NM_001771.3 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:67531603 C>T maps to NM_006566.2 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr18:67563236 C>A maps to NM_006566.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:160801180 G>A maps to NM_001166663.1 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:66082377 G>A maps to NM_020404.2 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:66083562 G>A maps to NM_020404.2 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:66083529 C>T maps to NM_020404.2 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:5456130 C>A maps to NM_014143.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:204591704 T>C maps to NM_006139.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:47548613 A>G maps to NM_012120.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:47544327 T>C maps to NM_012120.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:30364276 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:72469987 C>T maps to NM_007261.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:72469852 C>A maps to NM_007261.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:72613512 T>C maps to ENST00000426295 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:72691273 A>G maps to ENST00000412086 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:41931262 C>T maps to NM_145273.3 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:41926086 G>T maps to NM_145273.3 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr17:41931388 C>T maps to NM_145273.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:41925944 C>T maps to NM_145273.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:160636684 C>T maps to NM_001198759.1 A1741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:160639963 A>G maps to NM_001198759.1 T1669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:160639879 A>G maps to NM_001198759.1 C1697C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:160628523 C>T maps to NM_001198759.1 T1820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:160639923 C>A maps to NM_001198759.1 E1683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:51728510 G>T maps to NM_001772.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:208072455 G>A maps to NM_001025109.1 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:80292418 C>T maps to NM_001127444.1 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr19:49843515 C>T maps to NM_001774.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49841956 C>T maps to NM_001774.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:15842113 G>A maps to NM_001775.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:118209899 C>A maps to NM_000732.4 G165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:118211092 G>A maps to NM_000732.4 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:118209929 G>A maps to NM_000732.4 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:118183552 G>A maps to NM_000733.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:45912320 G>A maps to ENST00000423698 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:45912677 G>A maps to ENST00000423698 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:6909519 A>T maps to NM_000616.4 K33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:6925288 C>T maps to NM_000616.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr12:6924063 G>A maps to NM_000616.4 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr12:6927662 C>T maps to NM_000616.4 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:44757179 G>T maps to ENST00000372278 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr20:44751843 T>C maps to NM_001250.4 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135738535 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135741395 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135736564 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135736577 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:135732529 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:135736570 A>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:35218347 C>A maps to NM_000610.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:35226170 G>A maps to NM_000610.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:35198120 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:35227668 T>C maps to NM_000610.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:35227665 A>C maps to NM_000610.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:35226083 G>A maps to NM_000610.3 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:35243210 C>T maps to NM_000610.3 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:207934628 G>T maps to NM_172359.2 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:111434035 C>T maps to NM_000560.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:111434980 C>T maps to NM_000560.3 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:111437622 C>T maps to NM_000560.3 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:207504537 G>A maps to NM_001114752.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:207497931 T>C maps to NM_001114752.1 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:207510044 T>C maps to NM_001114752.1 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:117086942 A>C maps to NM_001779.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:117087139 C>A maps to NM_001779.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:117057252 A>C did not map to a codon.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr1:117078738 C>T maps to NM_001779.2 W159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:157805672 C>A maps to NM_005894.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:157809192 G>A maps to NM_005894.2 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr1:157805829 G>A maps to NM_005894.2 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:60777245 C>A maps to NM_006725.3 Y328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:60785339 G>A maps to NM_006725.3 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:60786759 C>T maps to NM_006725.3 N659N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:56119359 G>A maps to NM_001780.4 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7483612 C>T maps to NM_001251.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:7483612 C>T maps to NM_001251.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:9907002 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:9907008 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:9907628 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:9907002 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:9907195 C>A maps to NM_001781.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:9907413 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:9907101 A>C did not map to a codon.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr17:80274786 G>A maps to NM_006137.6 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:35616243 C>T maps to NM_001782.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:149785869 G>T maps to NM_001025159.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:149782804 G>A maps to NM_001025159.1 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:149784246 C>T maps to NM_001025159.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:149784246 C>T maps to NM_001025159.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:42383351 C>T maps to NM_001783.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:119246644 C>T maps to NM_005191.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr11:2417169 G>A maps to NM_004356.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:2416740 C>T maps to NM_004356.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:44626902 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:44626653 C>T maps to NM_002231.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:44640597 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:44616268 C>A maps to NM_002231.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:44626695 C>T maps to NM_002231.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:44639908 C>T maps to NM_002231.3 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr11:44626623 G>A maps to NM_002231.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:14133899 G>T maps to NM_004233.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:160519727 G>A maps to NM_001184879.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:160519727 G>A maps to NM_001184879.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:160535428 G>T maps to NM_001184879.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:121838341 G>A maps to NM_175862.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121822476 A>G maps to NM_175862.3 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:87017469 G>A maps to ENST00000456996 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:87016859 C>T maps to ENST00000456996 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:87049481 T>C maps to NM_172101.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:87085426 G>T maps to NM_172213.3 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr12:6344727 G>A maps to NM_001769.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:6345407 C>T maps to NM_001769.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:6346981 C>T maps to NM_001769.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr12:6346942 C>T maps to NM_001769.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:23065134 G>A maps to NM_012072.3 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:23065113 G>A maps to NM_012072.3 N572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:23066085 G>A maps to NM_012072.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:111263920 A>G maps to NM_198196.2 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:14508875 G>A maps to NM_078481.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:14516597 G>A maps to NM_078481.2 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:14512256 G>A maps to NM_078481.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:14517944 C>T maps to NM_078481.2 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:14507907 C>T maps to NM_078481.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:2656143 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:149937519 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:149944655 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:149944725 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:149945911 C>T did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:149963705 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:149944704 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:149999736 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:149944712 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr13:49829997 A>G maps to NM_030911.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:49841906 G>T maps to NM_030911.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr13:49854643 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:49842067 G>A maps to NM_030911.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr13:49841857 G>A maps to NM_030911.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:49842082 C>T maps to NM_030911.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr13:49848454 C>T maps to NM_030911.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:43016797 A>C maps to NM_138477.2 L1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:43017734 C>T maps to NM_138477.2 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr10:12259466 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:12291718 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr1:100964703 G>A maps to NM_033312.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:100843119 A>T maps to NM_033312.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:100843125 G>A maps to NM_033312.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:99296262 C>A maps to NM_033331.2 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:99285548 G>A maps to NM_033331.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr13:115028490 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:115037692 C>T maps to NM_003903.3 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:115030680 C>T maps to NM_003903.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:43826613 G>A maps to NM_001255.2 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:43826243 G>A maps to NM_001255.2 W276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:54424247 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:137542298 T>C maps to NM_004661.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:137534407 C>A maps to NM_004661.3 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:48200931 T>A maps to NM_001789.2 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:48226146 C>A maps to NM_001789.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:48200931 T>A maps to NM_001789.2 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:48205813 A>G maps to NM_001789.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:3782971 C>T maps to NM_021873.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:137661569 C>T maps to NM_001790.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:137622213 C>A maps to NM_001790.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:45214584 C>A maps to NM_001114091.1 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:45214584 C>A maps to NM_001114091.1 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr19:10504111 G>A maps to NM_007065.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:4702006 T>C maps to NM_017913.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr9:4684941 G>A maps to NM_017913.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr6:110530465 C>T maps to ENST00000439165 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:110540947 C>T maps to NM_015891.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:110531921 G>T maps to NM_015891.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:22413169 T>A maps to NM_001039802.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:22405197 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:227219122 C>T maps to ENST00000366766 V1217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:227222417 G>A maps to ENST00000366766 Y1138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:227333225 C>T maps to ENST00000366766 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:227333348 T>G maps to ENST00000366766 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:227307582 T>C maps to ENST00000366766 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:227216515 G>T maps to ENST00000366766 S1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:227221037 A>G maps to ENST00000366766 F1185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:227268639 C>A maps to ENST00000366766 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:227300592 G>A maps to ENST00000366766 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:227211021 T>C maps to ENST00000366766 S1519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:103410636 C>T maps to NM_006035.3 T1333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:19761301 G>T maps to ENST00000240700 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:103429463 T>G maps to NM_006035.3 R919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:103418910 G>A maps to NM_006035.3 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:103410363 A>G maps to NM_006035.3 F1424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:103452886 G>A maps to NM_006035.3 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:103406422 G>A maps to NM_006035.3 C1517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr14:103470315 G>A maps to NM_006035.3 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:64594856 G>A maps to NM_017525.2 F1388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:64597447 G>A maps to NM_017525.2 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:37964406 C>T maps to NM_152243.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:65088707 C>T maps to NM_006779.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:37873325 G>A maps to NM_006449.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:37873325 G>A maps to NM_006449.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr2:37872989 C>T maps to NM_006449.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr17:71282168 C>T maps to NM_012121.4 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr17:71282584 G>A maps to NM_012121.4 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:71281907 G>A maps to NM_012121.4 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:19502558 C>A maps to NM_001178010.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:19467736 T>G maps to NM_001178010.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:19496118 C>T maps to NM_001178010.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr22:19504135 C>T maps to NM_001178010.1 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:44361281 G>A maps to NM_001253.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:44394256 G>A maps to NM_001253.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:44413534 T>C maps to NM_001253.2 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr6:44371578 T>C maps to NM_001253.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:44371594 G>T maps to NM_001253.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:38457264 G>T maps to NM_001254.3 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:91989649 C>A maps to NM_001134420.1 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:193094337 A>G maps to NM_024529.4 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:193202159 C>T maps to NM_024529.4 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:193116995 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:193219826 G>A maps to NM_024529.4 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:193218933 G>T maps to NM_024529.4 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:193111166 C>T maps to NM_024529.4 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:193094328 T>C maps to NM_024529.4 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:193119483 C>A maps to NM_024529.4 Y293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:25364887 C>T maps to ENST00000434814 N903N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:25343329 C>A maps to ENST00000434814 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:25364999 G>T maps to ENST00000434814 E941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr8:25364161 C>T maps to ENST00000434814 C661C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:25319575 C>A maps to ENST00000434814 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:25364620 A>G maps to ENST00000434814 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:6958491 G>A maps to NM_031299.4 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:6959718 T>C maps to NM_031299.4 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:105478230 G>C maps to NM_145701.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:64847106 G>A maps to ENST00000404147 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr11:64846704 G>A maps to ENST00000404147 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:174231875 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:174231978 T>C maps to NM_031942.4 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:21942654 T>G maps to NM_018719.4 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:21945912 T>C maps to NM_018719.4 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:21951372 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:21945149 G>A maps to NM_018719.4 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:38171157 G>T maps to NM_018101.2 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:45136959 G>A maps to NM_022842.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:45127510 G>A maps to NM_022842.3 N710N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:45127152 C>A maps to NM_022842.3 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:68842744 A>G maps to NM_004360.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:68842324 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:68862191 C>T maps to NM_004360.3 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GE-01A-11W-A062-09 chr5:24487771 T>A maps to NM_006727.3 *789Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:24511480 G>A maps to NM_006727.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:24537527 C>A maps to NM_006727.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:24493010 T>C maps to NM_006727.3 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:24487842 G>A maps to NM_006727.3 R766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:24491904 A>G maps to NM_006727.3 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:24487889 G>T maps to NM_006727.3 S750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:24487996 A>G maps to NM_006727.3 I714I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:24487880 G>T maps to NM_006727.3 S753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:24537668 G>A maps to NM_006727.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:24488206 G>T maps to NM_006727.3 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:24487809 C>A maps to NM_006727.3 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:65032567 C>T maps to NM_001797.2 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:65025716 C>T maps to NM_001797.2 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr16:64984769 G>A maps to NM_001797.2 N598N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:65005955 G>A maps to NM_001797.2 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:65016135 C>T maps to NM_001797.2 P356P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BS-A0UJ-01A-12D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:65005551 T>G maps to NM_001797.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:65032486 G>A maps to NM_001797.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:65032561 C>T maps to NM_001797.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr16:64984700 G>A maps to NM_001797.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr16:64984748 G>A maps to NM_001797.2 N605N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:21751877 C>A maps to NM_004061.3 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:21765151 C>A maps to NM_004061.3 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr5:21802370 C>T maps to NM_004061.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:82660741 G>A maps to NM_001257.3 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:83065693 C>T maps to ENST00000268613 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:83251056 C>A maps to ENST00000268613 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:83520202 C>T maps to ENST00000268613 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:83251039 G>T maps to ENST00000268613 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:89251660 C>T maps to NM_004933.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:89261271 C>A maps to NM_004933.2 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:66946630 T>C maps to NM_004062.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:66944307 G>T maps to NM_004062.2 Y674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:66948187 G>T maps to NM_004062.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:66945908 G>T maps to NM_004062.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:95182730 A>C maps to NM_001144663.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:95172210 G>T maps to NM_001144663.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:95189940 G>T maps to NM_001144663.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr8:95188892 G>A maps to NM_001144663.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:95188799 G>A maps to NM_001144663.1 Y131Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:19483467 C>T maps to NM_004934.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:19520834 G>T maps to NM_004934.3 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:19473778 G>T maps to NM_004934.3 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr5:19571895 C>A maps to NM_004934.3 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr5:19747279 C>T maps to NM_004934.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:19838915 G>A maps to NM_004934.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr5:19571761 G>A maps to NM_004934.3 Y393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:64172158 C>A maps to NM_021153.2 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:64176385 C>T maps to NM_021153.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:64218333 C>A maps to NM_021153.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:64235725 C>T maps to NM_021153.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr18:64235734 G>T maps to NM_021153.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:64197180 C>T maps to NM_021153.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:64172425 C>A maps to NM_021153.2 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr18:64218358 A>C maps to NM_021153.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:64172258 G>A maps to NM_021153.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:64172413 C>A maps to NM_021153.2 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:64218472 T>C maps to NM_021153.2 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:64212120 G>T maps to NM_021153.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:64235713 G>A maps to NM_021153.2 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr18:64212015 C>T maps to NM_021153.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:64172540 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:25565607 G>T maps to NM_001792.3 S620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:25570082 G>A maps to NM_001792.3 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:25585810 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:25583056 G>A maps to NM_001792.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:25585923 G>A maps to NM_001792.3 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:59166444 C>T maps to NM_031891.2 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:59221636 C>T maps to NM_031891.2 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:59166617 C>A maps to NM_031891.2 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:44845579 G>A maps to NM_021248.1 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:44869815 G>A maps to NM_021248.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr20:44815500 G>A maps to NM_021248.1 Y503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:44841648 G>T maps to NM_021248.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:44841827 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr10:73330674 G>A maps to ENST00000398860 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:73405613 C>A maps to ENST00000398860 Y394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:73199650 C>A maps to ENST00000398860 C21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:73565699 C>T maps to ENST00000398860 S2675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:73447447 C>T maps to ENST00000398860 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:73538007 C>T maps to ENST00000398860 I1715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:73544099 C>T maps to ENST00000398860 L1814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:73545395 C>T maps to ENST00000398860 I1912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:73571086 C>T maps to ENST00000398860 I3036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:73539106 C>T maps to ENST00000398860 G1762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:73501683 C>T maps to ENST00000398792 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:73330636 C>T maps to ENST00000398860 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:73491981 C>T maps to ENST00000398860 Y1323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:73500626 C>T maps to ENST00000398860 L1518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr10:73464699 C>T maps to ENST00000398860 N927N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:73491804 C>T maps to ENST00000398860 D1264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:73558165 C>A maps to ENST00000398860 P2300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr10:73544092 C>T maps to ENST00000398860 D1811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr10:73563089 C>T maps to ENST00000398860 T2600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:73269899 G>A maps to ENST00000398860 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:73571144 C>T maps to ENST00000398860 Q3056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr10:73464765 C>T maps to ENST00000398860 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr14:23518466 G>A maps to NM_022478.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:23518887 G>T maps to NM_022478.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr14:23524529 G>A maps to NM_022478.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr20:58564002 C>T maps to NM_177980.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:58564158 C>T maps to NM_177980.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:58533810 G>A maps to NM_177980.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:58560183 C>T maps to NM_177980.2 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:58562545 C>T maps to NM_177980.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:58564029 C>T maps to NM_177980.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:58571803 C>T maps to NM_177980.2 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:58547123 C>T maps to NM_177980.2 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr16:68716323 C>T maps to NM_001793.4 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:68716311 C>A maps to NM_001793.4 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:68718592 C>T maps to NM_001793.4 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:60448925 C>T maps to NM_001794.2 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:60448925 C>T maps to NM_001794.2 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:60511802 C>T maps to NM_001794.2 R851R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr20:60427925 C>T maps to NM_001794.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:60348141 C>T maps to NM_001794.2 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr20:60485503 C>T maps to NM_001794.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:66426079 C>T maps to NM_001795.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:66420803 C>T maps to NM_001795.3 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:66430021 C>T maps to NM_001795.3 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:66424423 C>T maps to NM_001795.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:66423331 C>T maps to NM_001795.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr16:66436891 C>T maps to NM_001795.3 Y725Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:66430088 G>T maps to NM_001795.3 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:66420929 C>T maps to NM_001795.3 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:66424468 C>T maps to NM_001795.3 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:66434905 C>A maps to NM_001795.3 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:66420785 C>T maps to NM_001795.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:66426268 G>A maps to NM_001795.3 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:31299655 C>T maps to NM_004932.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:31297423 G>A maps to NM_004932.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:31316411 C>A maps to NM_004932.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr18:63547796 C>T maps to NM_004361.2 N675N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:63525075 C>T maps to NM_004361.2 D420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:63547730 C>T maps to NM_004361.2 Y653Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr18:63477234 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:63511226 G>A maps to NM_004361.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr18:63477089 C>T maps to NM_004361.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr18:63492034 G>T maps to NM_004361.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:63547713 G>T maps to NM_004361.2 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:63430077 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:63548087 C>T maps to NM_004361.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:61689625 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:61935362 C>T maps to NM_001796.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:61851531 C>T maps to NM_001796.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:61858970 C>T maps to NM_001796.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:61761183 C>A maps to ENST00000394178 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:61687934 G>A maps to NM_001796.2 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr16:61823295 T>C maps to NM_001796.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:61687748 G>A maps to NM_001796.2 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:61851492 C>T maps to NM_001796.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:61854904 G>A maps to NM_001796.2 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:61761123 G>T maps to ENST00000394178 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:26881280 G>A maps to NM_016279.3 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:26881721 C>T maps to NM_016279.3 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr5:26906079 G>A maps to NM_016279.3 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:26885846 G>T maps to NM_016279.3 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:26881671 G>T maps to NM_016279.3 S648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:26881367 C>T maps to NM_016279.3 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:26885831 G>A maps to NM_016279.3 C591C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:26906107 C>T maps to NM_016279.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr5:26881679 C>T maps to NM_016279.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:85968627 A>G maps to NM_033100.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:85956267 C>T maps to NM_033100.2 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr10:85974274 G>A maps to NM_033100.2 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:176008462 G>C maps to NM_001171976.1 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:176004398 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:175992691 G>A maps to NM_001171976.1 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:176004675 C>T maps to NM_001171976.1 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:176004533 G>A maps to NM_001171976.1 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:176002577 C>T maps to NM_001171976.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:176004669 C>T maps to NM_001171976.1 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:176005392 C>A maps to NM_001171976.1 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:105636731 C>A maps to NM_152750.4 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:105664849 G>A maps to NM_152750.4 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:105669000 G>A maps to NM_152750.4 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:105658314 C>T maps to NM_152750.4 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:105641910 G>A maps to NM_152750.4 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49832786 C>T maps to NM_001007540.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:49836784 G>T maps to NM_001007540.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:49832648 G>A maps to NM_001007540.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:49832744 C>T maps to NM_001007540.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:618995 G>T maps to NM_021924.4 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr11:618013 G>A maps to NM_021924.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:620065 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:620350 G>A maps to NM_021924.4 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr11:621817 C>T maps to NM_021924.4 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr11:619502 G>A maps to NM_021924.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:29873948 G>A maps to NM_006319.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:29874015 G>T maps to NM_006319.3 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:62539952 T>C maps to NM_001786.4 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:1647885 G>A maps to NM_024011.2 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:1634967 G>A maps to NM_024011.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:1647896 C>A maps to NM_024011.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:37618486 T>C maps to NM_016507.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:37681029 C>T maps to NM_016507.2 R1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:40134245 T>C maps to NM_003718.4 S1402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:40132606 G>A maps to NM_003718.4 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:40117615 G>A maps to NM_003718.4 G931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr7:40127781 G>A maps to NM_003718.4 K1029K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:40132606 G>A maps to NM_003718.4 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:90492544 C>A maps to NM_012395.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr7:90747377 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:90741907 T>C maps to NM_012395.2 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:202688451 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:202672676 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:202700372 C>A maps to ENST00000450471 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr2:202698629 C>T maps to ENST00000450471 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:47085409 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:47085747 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:47083884 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:47083885 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47082952 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:47085614 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47086250 C>T did not map to a codon.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr23:47086816 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:96707194 A>G maps to NM_002595.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:96679897 A>T maps to NM_002595.4 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr12:96704852 G>A maps to NM_002595.4 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:96674609 G>A maps to NM_002595.4 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:96676322 G>A maps to NM_002595.4 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr12:96680441 C>A maps to NM_002595.4 G406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:205496942 C>A maps to NM_212503.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:205499460 G>A maps to NM_212503.2 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205493454 G>A maps to NM_212503.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr9:90588878 C>T maps to NM_001039803.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:123749830 C>T maps to NM_004642.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:73997590 C>T maps to NM_001258.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:58145446 C>T maps to NM_000075.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:58143259 G>A maps to NM_000075.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:58144512 A>G maps to NM_000075.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:150751364 G>A maps to NM_004935.3 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr7:150753876 A>G maps to NM_004935.3 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:30814874 G>A maps to NM_003885.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:30814874 G>T maps to NM_003885.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:30815153 G>A maps to NM_003885.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr17:30815432 C>T maps to NM_003885.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:219825345 C>T maps to NM_003936.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:219825408 C>T maps to NM_003936.3 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr2:219825498 G>A maps to NM_003936.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:123215892 C>T maps to NM_018249.4 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:123210352 C>A maps to NM_018249.4 G949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:123230135 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:123232495 C>A maps to NM_018249.4 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:123201896 C>A maps to NM_018249.4 E1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:123177383 C>A maps to NM_018249.4 E1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:123177383 C>A maps to NM_018249.4 E1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:123291020 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:46051797 G>A maps to NM_176096.1 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:46052881 C>T maps to NM_176096.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:46058165 T>C did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:46052655 G>T maps to NM_176096.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:92247412 G>A maps to NM_001145306.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr7:92355007 C>A maps to NM_001145306.1 G157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:92354984 G>A maps to NM_001145306.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:68572952 A>G maps to NM_001799.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:68572517 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:68551327 C>A maps to NM_001799.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:68568858 G>A maps to NM_001799.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr13:26975439 C>T maps to NM_001260.1 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr13:26911751 C>A maps to NM_001260.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:21201393 C>A maps to NM_017774.3 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:21065311 C>A maps to NM_017774.3 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:20781473 G>T maps to NM_017774.3 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:20955719 C>T maps to NM_017774.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:20781493 C>T maps to NM_017774.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:20846375 G>T maps to NM_017774.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:20758842 T>C maps to NM_017774.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:50799071 C>A maps to NM_004196.3 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:76523347 A>C maps to ENST00000307465 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:76523385 C>A maps to ENST00000307465 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:133695616 G>A maps to NM_001113575.1 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:133702066 C>A maps to NM_001113575.1 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:133686004 C>T maps to NM_001113575.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:133702066 C>A maps to NM_001113575.1 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:39440539 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:39440540 G>A maps to ENST00000395035 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:18600027 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:18622141 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:18582615 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:18622692 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18593568 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18606143 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18613525 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18622912 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18627679 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:18616706 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18593494 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18600051 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18646588 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:18622314 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:18668531 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:18664195 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:18593494 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:18525250 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:18622692 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:18622811 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:18622683 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:18643345 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:18671654 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:18593492 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:18593503 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr12:12870836 G>T maps to NM_004064.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:12871796 G>T maps to NM_004064.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:21970979 G>A maps to NM_001195132.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:184367364 A>G maps to NM_017632.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr4:184367452 G>T maps to NM_017632.2 G206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:133745591 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:51439872 C>A maps to NM_078626.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:54866652 A>G maps to NM_005192.3 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:14870190 C>A maps to NM_001029954.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:115146945 T>C maps to NM_001801.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:115151935 G>A maps to NM_001801.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:115142132 A>G maps to NM_001801.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:125887117 C>A maps to ENST00000392693 G265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:125891386 C>T maps to ENST00000392693 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:125867195 G>A maps to ENST00000392693 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr11:125875683 G>A maps to ENST00000392693 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:139866321 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:139865904 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:139866336 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:139866494 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:139865904 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:139866204 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:139866105 A>G did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:139866495 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:139866369 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:22360661 C>T maps to NM_001802.1 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:22359077 A>G maps to NM_001802.1 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:22358878 G>A maps to NM_001802.1 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:73000135 C>T maps to NM_014603.2 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:72998243 C>T maps to NM_014603.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:15522424 C>T maps to ENST00000261644 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:15499874 G>A maps to ENST00000455584 R877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr17:14139187 G>A maps to NM_001007530.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:14139313 G>A maps to NM_001007530.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:85538808 A>G maps to NM_001263.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:85540645 T>A maps to NM_001263.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr6:31084617 G>A maps to NM_001264.4 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:88873738 G>A maps to NM_030928.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:88872462 G>A maps to NM_030928.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:133306016 G>T maps to NM_001134422.1 *214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr13:28537389 G>A maps to NM_001265.3 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:72673352 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:72667228 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:72667417 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:72667576 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:72673378 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:72674415 G>A did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:72674212 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:72673383 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:72674222 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:72674386 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:72667270 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr23:72667324 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:4954426 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:4935806 T>C maps to ENST00000328908 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:4943875 C>T maps to ENST00000328908 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:4716005 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:4937878 C>T maps to ENST00000328908 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:4952504 C>T maps to ENST00000328908 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:4716005 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:4954457 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:4716010 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:80646528 G>A maps to NM_152342.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:43016515 G>A maps to NM_001712.4 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr19:43031526 C>T maps to NM_001712.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:43023106 G>A maps to NM_001712.4 N413N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:45202698 T>C maps to ENST00000396750 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr19:45209133 C>T maps to ENST00000396750 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr19:51983767 G>A maps to NM_001080405.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:51983893 C>T maps to NM_001080405.1 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:51983668 T>C maps to NM_001080405.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:42083573 C>T maps to NM_001098506.1 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr19:42083747 C>T maps to NM_001098506.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:42128109 G>A maps to NM_001817.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:42221425 T>C maps to NM_004363.2 D337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:42221377 G>A maps to NM_004363.2 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:42213830 G>A maps to NM_004363.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:42218962 C>A maps to NM_004363.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:42266024 C>A maps to NM_002483.4 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:42265155 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:43093723 G>A maps to NM_001816.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:23586845 C>T maps to NM_001805.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr14:23586713 G>A maps to NM_001805.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:33870159 G>A maps to NM_001806.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr19:33870579 C>T maps to NM_001806.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:37449553 A>G maps to NM_005760.2 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:37441024 C>A maps to NM_005760.2 E843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:37454883 G>A maps to NM_005760.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:37428912 C>T maps to NM_005760.2 R1053R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:37450366 C>T maps to NM_005760.2 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:37458680 G>A maps to NM_005760.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr2:37455612 C>T maps to NM_005760.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr22:18021592 C>T maps to ENST00000400579 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:18020201 C>T maps to ENST00000400579 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:18016793 C>T maps to ENST00000400579 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr22:18027932 C>T maps to ENST00000400579 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr22:17629390 A>G maps to NM_033070.2 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:135942010 C>T maps to NM_001807.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:135942274 C>T maps to NM_001807.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:135944203 C>T maps to NM_001807.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:135942539 T>G maps to NM_001807.3 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr9:135939900 C>T maps to NM_001807.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:51736399 G>A maps to NM_001971.5 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JS-01A-11D-A10B-09 chr1:15788135 G>A maps to ENST00000375924 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:15792497 C>T maps to ENST00000375924 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:15808870 C>T maps to ENST00000442979 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:15808196 C>A maps to ENST00000442979 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:15813841 C>T maps to ENST00000442979 I271I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:22307554 G>A maps to NM_007352.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:47494691 G>A maps to NM_001172639.1 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr10:11299737 G>A maps to NM_006561.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr10:11299755 C>T maps to NM_006561.3 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:151677564 G>A maps to NM_007185.4 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:34853090 G>A maps to NM_020180.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr18:34833869 C>T maps to NM_020180.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:34854348 C>T maps to NM_020180.3 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr18:34839144 G>A maps to NM_020180.3 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:34833887 G>A maps to NM_020180.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:3282369 C>T maps to NM_021938.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr22:46860120 C>T maps to NM_014246.1 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:46773008 G>T maps to NM_014246.1 L2511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:46792521 G>A maps to NM_014246.1 Y1941Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr22:46859793 G>A maps to NM_014246.1 L1331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:46860189 C>T maps to NM_014246.1 T1199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:46930826 C>T maps to NM_014246.1 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:46780524 G>A maps to NM_014246.1 F2266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:46765588 G>A maps to NM_014246.1 I2624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr22:46794513 G>A maps to NM_014246.1 G1811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr22:46860105 G>A maps to NM_014246.1 F1227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:46761230 G>A maps to NM_014246.1 S2817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:46768798 G>A maps to NM_014246.1 G2580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr22:46930652 G>A maps to NM_014246.1 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr22:46930004 A>T maps to NM_014246.1 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr22:46930181 G>A maps to NM_014246.1 A962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr22:46805015 G>T maps to NM_014246.1 S1701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:46931447 G>A maps to NM_014246.1 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:109794533 C>A maps to NM_001408.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:109806290 G>A maps to NM_001408.2 S1631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:109804152 C>T maps to NM_001408.2 R1400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:109814988 G>A maps to NM_001408.2 S2672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr1:109814334 C>T maps to NM_001408.2 T2639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:109805836 C>T maps to NM_001408.2 D1594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:109808368 C>A maps to NM_001408.2 R1914R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:109801501 G>A maps to NM_001408.2 A1253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:109808787 C>T maps to NM_001408.2 F1991F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:48696362 G>A maps to NM_001407.2 D1235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:48697907 C>T maps to NM_001407.2 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:48679368 G>A maps to NM_001407.2 S2913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:48698429 G>A maps to NM_001407.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr3:48694536 C>T maps to NM_001407.2 S1331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:48692571 G>A maps to NM_001407.2 S1631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:48699932 G>A maps to NM_001407.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:48679839 A>T maps to NM_001407.2 A2872A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:48686246 G>A maps to NM_001407.2 R2228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr3:48697841 G>T maps to NM_001407.2 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:48696749 G>T maps to NM_001407.2 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:48698282 G>A maps to NM_001407.2 I595I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D1-A15X-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:27015673 A>G maps to NM_001809.3 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:68374790 C>A maps to NM_001812.2 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:68358652 C>A maps to NM_001812.2 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:104098173 G>A maps to NM_001813.2 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:104116318 G>T maps to NM_001813.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:104068791 A>C maps to NM_001813.2 L1285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:104061410 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:104081904 C>T maps to NM_001813.2 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:104053974 C>A maps to NM_001813.2 E2267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:104115810 C>A maps to NM_001813.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:104041445 A>G maps to NM_001813.2 S2396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:104061026 T>C maps to NM_001813.2 R2041R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:214814999 C>T maps to NM_016343.3 Q1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:214818843 G>T maps to NM_016343.3 L1977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:214830481 C>T maps to NM_016343.3 R2898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:214792494 G>T maps to NM_016343.3 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:214814422 A>G maps to NM_016343.3 Q914Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:214819669 G>T maps to NM_016343.3 E2253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:214792511 G>A maps to NM_016343.3 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:214802423 G>A maps to NM_016343.3 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:214815547 T>C maps to NM_016343.3 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:214791951 G>A maps to NM_016343.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:214811225 C>T maps to NM_016343.3 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:214814273 G>T maps to NM_016343.3 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:214818808 G>T maps to NM_016343.3 E1966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:214819104 G>A maps to NM_016343.3 E2064E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:214819404 G>A maps to NM_016343.3 Q2164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:214818328 G>T maps to NM_016343.3 E1806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:214795545 T>C maps to NM_016343.3 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:214818690 G>A maps to NM_016343.3 E1926E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:100381741 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100403129 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100375732 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100382137 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:100375408 T>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:100375727 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:100402761 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100400133 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:100381741 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:100387233 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:100382162 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100381741 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:100400144 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:100402750 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:100400133 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100356136 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100402773 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100401159 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:100364524 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr13:25480570 C>T maps to NM_018451.3 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:25458194 C>A maps to NM_018451.3 E1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:25480096 G>A maps to NM_018451.3 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr13:25479517 T>C maps to NM_018451.3 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:25486760 C>A maps to NM_018451.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:25484093 C>T maps to NM_018451.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:25457410 G>A maps to NM_018451.3 T1307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:25473675 G>A maps to NM_018451.3 R958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:25473684 C>A maps to NM_018451.3 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:25483969 C>A maps to NM_018451.3 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:64848334 G>A maps to NM_022145.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr5:64814372 G>A maps to NM_022145.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:173780308 A>G maps to NM_001127181.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:173776422 C>T maps to NM_001127181.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:42342500 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:42339618 G>A maps to NM_024053.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:42342458 G>A maps to NM_024053.3 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:81053856 G>A maps to NM_001100624.1 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:81066214 A>G maps to NM_001100625.1 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:95094559 G>A maps to NM_001012267.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:49459912 T>C maps to NM_018132.3 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:67866396 T>C maps to NM_025082.3 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:122722237 A>C maps to NM_153223.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:122734891 C>A maps to NM_153223.3 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:122700209 C>A maps to NM_153223.3 E854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:56883863 A>G maps to NM_025009.3 K951K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:56851493 T>G maps to NM_025009.3 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:56877963 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:56819386 G>T maps to NM_025009.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:56820393 C>A maps to NM_025009.3 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:56878133 G>T maps to NM_025009.3 E929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:56818313 G>A maps to NM_025009.3 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:56841102 G>T maps to NM_025009.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:56851517 T>C maps to NM_025009.3 N617N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:49030643 C>T maps to NM_001194998.1 T1645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:49073445 C>T maps to NM_001194998.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:49083445 G>T maps to NM_001194998.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:49031003 G>A maps to NM_001194998.1 R1525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:49076203 C>T maps to NM_001194998.1 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:49031003 G>A maps to NM_001194998.1 R1525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:49037165 C>A maps to NM_001194998.1 E1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:117279733 G>A maps to NM_014956.4 R1246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:117261928 G>T maps to NM_014956.4 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:117265846 C>A maps to NM_014956.4 T951T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:117261928 G>T maps to NM_014956.4 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:117265757 G>A maps to ENST00000375253 *842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:117267282 G>A maps to NM_014956.4 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:117232697 G>T maps to NM_014956.4 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:243303283 G>A maps to NM_014812.2 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:243319623 G>A maps to NM_014812.2 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:243332945 A>G maps to NM_014812.2 P609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:243328510 T>C maps to NM_014812.2 G917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:243349593 G>T maps to NM_014812.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:243362458 C>T maps to NM_014812.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr18:13096261 G>A maps to NM_032142.3 A2171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr18:13067921 T>C maps to NM_032142.3 H1527H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:13116475 C>T maps to NM_032142.3 R2464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:13042240 G>T maps to NM_032142.3 G659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr18:13056359 C>T maps to NM_032142.3 S1257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:13092455 G>T maps to NM_032142.3 E2062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:13059100 T>C maps to NM_032142.3 R1426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:13049565 G>T maps to NM_032142.3 E926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:34091279 C>T maps to NM_007186.3 R1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:34096827 G>A maps to NM_007186.3 G2321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:34065927 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:34092409 G>A maps to NM_007186.3 E2071E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:34067469 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr20:34067177 G>A maps to NM_007186.3 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:88508237 C>A maps to NM_025114.3 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:88514814 C>A maps to NM_025114.3 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:88465119 C>A maps to NM_025114.3 E1988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:88514814 C>A maps to NM_025114.3 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:88457892 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:88476853 C>A maps to NM_025114.3 E1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:88490730 C>A maps to NM_025114.3 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:88514026 G>A maps to NM_025114.3 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:88524170 A>G maps to NM_025114.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:88505109 C>A maps to NM_025114.3 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:88505547 C>A maps to NM_025114.3 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:88465128 C>A maps to NM_025114.3 E1985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:88465636 G>A maps to NM_025114.3 R1926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:88514814 C>A maps to NM_025114.3 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:179965741 C>T maps to NM_014810.4 H150H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:179983376 C>T maps to NM_014810.4 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:180010798 C>A maps to NM_014810.4 V1408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:180022188 C>A maps to NM_014810.4 S1626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr1:180013257 T>G maps to NM_014810.4 A1524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:180065276 T>G maps to NM_014810.4 Y3008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:179989650 C>T maps to NM_014810.4 G914G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:180012228 C>T maps to NM_014810.4 V1467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr1:179989164 T>C maps to NM_014810.4 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:180063215 C>A maps to NM_014810.4 S2659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:95287834 T>C maps to NM_018131.4 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:95555715 T>C maps to NM_014679.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:95546668 C>T maps to NM_014679.3 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr11:95546159 G>A maps to NM_014679.3 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:95560969 C>T maps to NM_014679.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:134267966 A>G maps to NM_025180.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:134268008 G>A maps to NM_025180.3 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:134267943 G>T maps to NM_025180.3 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:134265011 G>T maps to NM_025180.3 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:65300090 G>T maps to NM_015147.2 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:65309694 C>T maps to NM_015147.2 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:65299675 T>G maps to NM_015147.2 Y482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:138219238 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:138216876 G>T maps to NM_024491.2 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:138256146 C>A maps to NM_024491.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:653237 C>T maps to NM_018140.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:635628 G>A maps to NM_018140.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:12697312 C>T maps to NM_024899.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:12699092 C>T maps to NM_024899.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr18:12678359 A>G maps to NM_024899.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:12701087 C>A maps to NM_024899.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:12697282 C>T maps to NM_024899.2 W215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:12700973 C>A maps to NM_024899.2 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:12701087 C>A maps to NM_024899.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:80866887 G>A maps to NM_001098802.1 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:101484046 T>C maps to ENST00000327230 D776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:101476481 C>T maps to ENST00000327230 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:131198060 G>A maps to NM_016174.4 W555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:131191108 C>T maps to NM_016174.4 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:131186870 C>T maps to NM_016174.4 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:47108065 G>A maps to NM_022766.5 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:47095303 G>T maps to NM_022766.5 Y283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:47086067 G>A maps to NM_022766.5 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:47116084 G>A maps to NM_022766.5 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:182413467 G>A maps to NM_001030311.2 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:182438594 C>T maps to NM_001030311.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:182413309 T>G maps to NM_001030311.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:182430196 G>A maps to NM_001030311.2 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:182409424 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:182438594 C>T maps to NM_001030311.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:182430215 G>A maps to NM_001030311.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:55846937 G>A maps to NM_001025195.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:55846910 C>A maps to NM_001025195.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:55854337 G>A maps to NM_001025195.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:66977919 G>T maps to NM_003869.5 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:66969573 G>A maps to NM_003869.5 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:66974546 C>T maps to NM_003869.5 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:66975530 C>T maps to NM_003869.5 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:66995266 C>T maps to NM_024922.5 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:67006370 C>T maps to NM_024922.5 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr16:67006864 G>A maps to NM_024922.5 W543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr18:580800 C>T maps to NM_004066.1 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:151997150 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:151997788 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:151998254 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:151997760 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:151998192 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:151998195 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:89701604 T>C maps to NM_004365.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:89703583 C>A maps to NM_004365.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:89695216 G>A maps to NM_004365.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:89695216 G>A maps to NM_004365.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:89695330 C>A maps to NM_004365.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:57007265 C>A maps to NM_000078.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:131356287 G>A maps to NM_032545.2 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr16:75339061 G>A maps to NM_006324.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:75446453 C>T maps to NM_006324.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:75445777 C>A maps to NM_006324.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:196716389 C>T maps to NM_000186.3 R1215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:196709836 C>T maps to NM_000186.3 Y957Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:196706060 G>T maps to NM_000186.3 E841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:196714983 C>T maps to NM_000186.3 D1116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:196648768 C>T maps to NM_000186.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:196706137 T>C did not map to a codon.
Sequencing variant TCGA-BG-A186-01A-11D-A12J-09 chr1:196648906 G>A maps to NM_000186.3 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr1:196716319 G>A maps to NM_000186.3 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:196714945 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:196795983 A>G maps to NM_002113.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:196799812 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:196918741 C>T maps to ENST00000367421 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:196928110 A>G maps to ENST00000367421 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr1:196748358 C>A maps to NM_021023.5 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:196884269 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:196883707 G>T maps to NM_006684.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:196871647 C>A maps to NM_006684.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:196883706 C>T maps to NM_006684.2 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:196881924 C>T maps to NM_006684.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:196946776 C>T maps to ENST00000367414 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:196965191 C>T maps to ENST00000367414 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:196977751 C>A maps to ENST00000367414 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:196973932 A>G maps to ENST00000367414 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:196952156 G>A maps to ENST00000367414 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:110673656 C>A maps to ENST00000394635 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:110662138 C>T maps to ENST00000394635 E562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:110670692 G>A maps to ENST00000394635 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:65622869 G>T maps to NM_005507.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr14:35182458 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:202014535 C>T maps to NM_001127183.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:202028695 A>G maps to NM_001127183.1 *481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47486876 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:47485528 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47485783 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr23:47485774 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47487605 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:47486973 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:47489029 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:47486646 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:117199681 C>T maps to NM_000492.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:117230479 G>T maps to NM_000492.3 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:117180157 G>T maps to NM_000492.3 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:117243837 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:117232392 C>T maps to NM_000492.3 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:117267693 C>A maps to NM_000492.3 S1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr6:87797873 C>T maps to NM_000735.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:49539413 A>G maps to ENST00000391869 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:49539004 G>T maps to ENST00000391869 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:49557793 G>A maps to ENST00000377280 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:88105000 G>A maps to NM_001195308.1 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:151509749 C>T maps to NM_020770.2 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:151507516 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:151496744 C>T maps to NM_020770.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:151509749 C>T maps to NM_020770.2 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr1:151501905 C>T maps to NM_020770.2 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:151506587 G>A maps to NM_020770.2 R960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:57731268 G>T maps to NM_032866.3 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:57734609 C>T maps to NM_032866.3 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:27325437 A>G maps to ENST00000404694 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:55005088 G>A maps to NM_006568.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:90966536 C>T maps to NM_003956.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:90966293 C>T maps to NM_003956.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:90966722 G>A maps to NM_003956.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:41247665 C>T maps to NM_024111.3 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr15:41247911 C>T maps to NM_024111.3 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:54001364 C>T maps to NM_001008708.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:54001346 C>T maps to NM_001008708.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:48542757 G>A maps to NM_001267.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:48545877 C>T maps to NM_001267.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:48543158 G>A maps to NM_001267.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:4418030 C>T maps to NM_005483.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:4418030 C>T maps to NM_005483.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:4409032 T>C maps to NM_005483.2 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:37759894 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:50828617 C>A maps to NM_020549.4 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:50856564 C>A maps to NM_020549.4 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr10:50854704 C>T maps to NM_020549.4 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:50833584 C>A maps to NM_020549.4 Y273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:50835760 G>A maps to NM_020549.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:50856578 C>A maps to NM_020549.4 C436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:50873022 G>A maps to NM_020549.4 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:50856605 C>T maps to NM_020549.4 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:50856578 C>T maps to NM_020549.4 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:132481250 G>T maps to ENST00000448878 C209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr7:132659958 G>A maps to ENST00000448878 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:132709324 C>A maps to ENST00000448878 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:14154406 C>A maps to NM_144636.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:14154578 C>T maps to NM_144636.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:113343899 C>T maps to ENST00000409719 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:113343977 C>A maps to ENST00000409719 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:113343815 T>G maps to ENST00000409719 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:126633521 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:57127225 G>A maps to NM_001011668.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr8:57127227 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:98236641 C>T maps to NM_001270.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:98239612 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:98199283 C>A maps to NM_001270.2 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:98208172 C>A maps to NM_001270.2 E1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:98199148 C>A maps to NM_001270.2 E1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:98192206 A>C maps to NM_001270.2 A1670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr5:98215303 T>C maps to NM_001270.2 E1063E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:146766136 C>T maps to NM_004284.3 N851N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:146724357 G>T maps to NM_004284.3 G70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:146728208 C>T maps to NM_004284.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:93467574 G>A maps to NM_001271.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:93521487 A>C maps to NM_001271.3 R868R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:93482840 G>A maps to NM_001271.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:93486100 G>A maps to NM_001271.3 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:93489437 G>T maps to NM_001271.3 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr17:7812639 C>T maps to NM_001005271.2 N1917N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:7813830 C>T maps to NM_001005271.2 I1951I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:7797491 T>C maps to NM_001005271.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:7808416 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:7807782 C>A maps to NM_001005271.2 I1365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:7814818 G>A maps to NM_001005271.2 E2032E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:7793981 C>T maps to NM_001005271.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:7811273 C>T maps to NM_001005271.2 R1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:7809936 C>T maps to NM_001005271.2 A1534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:7803986 C>A maps to NM_001005271.2 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr17:7801814 G>T maps to NM_001005271.2 E744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:7805992 C>T maps to NM_001005271.2 I1165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:7806816 C>T maps to NM_001005271.2 N1300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:6691350 G>T maps to ENST00000309577 R1517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr12:6709723 G>A maps to ENST00000309577 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr12:6710103 A>G maps to ENST00000309577 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:6703797 G>A maps to ENST00000309577 R714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:6711663 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:6202295 G>A maps to NM_015557.2 Y776Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:6206793 A>G maps to NM_015557.2 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:6209114 C>T maps to NM_015557.2 W394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:6206804 C>A maps to NM_015557.2 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:6194220 C>T maps to NM_015557.2 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:6203921 G>A maps to NM_015557.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:6219494 A>G maps to NM_015557.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:6214771 C>T maps to NM_015557.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr1:6194861 G>A maps to NM_015557.2 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr20:40050150 A>G maps to NM_032221.3 Y1708Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr20:40045876 T>C maps to NM_032221.3 L2080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:40042149 G>A maps to NM_032221.3 V2315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:40050387 G>T maps to NM_032221.3 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:40076600 G>A maps to NM_032221.3 R1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:40126770 A>G maps to ENST00000373222 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:40049282 C>A maps to NM_032221.3 E1998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:40052237 G>T maps to NM_032221.3 I1483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:40126067 G>A maps to NM_032221.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:40050061 G>T maps to NM_032221.3 S1738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:40084586 G>A maps to NM_032221.3 D954D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:40081483 G>A maps to NM_032221.3 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:40085915 G>A maps to NM_032221.3 G939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:40086041 G>A maps to NM_032221.3 G897G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A0JY-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:40041978 A>C maps to NM_032221.3 V2372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr20:40162125 G>A maps to NM_032221.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:40085987 G>A maps to NM_032221.3 R915R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:61763074 C>T maps to NM_017780.2 R1810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:61654248 G>A maps to NM_017780.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:61773591 C>T maps to NM_017780.2 L2580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:61768592 G>A maps to NM_017780.2 W2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:61654248 G>A maps to NM_017780.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:61741317 G>T maps to NM_017780.2 E1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:61654506 G>A maps to NM_017780.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:61757545 G>A maps to NM_017780.2 E1658E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:61763085 C>T maps to NM_017780.2 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:61778113 A>G maps to NM_017780.2 G2872G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr8:61655145 G>A maps to NM_017780.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr8:61769104 G>A maps to NM_017780.2 E2422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:61654066 G>T maps to NM_017780.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:61777672 C>T maps to NM_017780.2 I2725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:61750315 C>T maps to NM_017780.2 F1425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr8:61729018 C>T maps to NM_017780.2 R858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr8:61765994 C>T maps to NM_017780.2 S2237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:21862612 G>A maps to NM_001170629.1 R1808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:21870168 G>A maps to NM_001170629.1 R1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:21897479 G>A maps to NM_001170629.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:21861297 C>T maps to NM_001170629.1 L2145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:21871805 G>A maps to NM_001170629.1 I1108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:21859747 G>A maps to NM_001170629.1 T2313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:21859989 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:21868727 G>A maps to NM_001170629.1 R1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr14:21860731 C>T maps to NM_001170629.1 A2235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr14:21878148 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:53307608 C>T maps to ENST00000219084 Q1597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:53358255 C>T maps to ENST00000219084 L2715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:53330903 T>C maps to ENST00000219084 V1849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:53191269 C>T maps to ENST00000219084 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:53243564 G>T maps to ENST00000219084 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:53358437 C>T maps to ENST00000219084 S2775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:53289550 C>T maps to ENST00000219084 R1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:53851899 G>A maps to NM_018397.4 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:125514003 C>T maps to NM_001274.4 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr22:29085121 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:29106016 C>A maps to NM_001005735.1 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr22:29115436 G>T maps to NM_001005735.1 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:29095872 C>A maps to NM_001005735.1 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:29095872 C>A maps to NM_001005735.1 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:16631230 C>T maps to NM_006387.5 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:16630059 G>A maps to NM_006387.5 G887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:16631685 G>A maps to NM_006387.5 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:16641585 G>A maps to NM_006387.5 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:133446259 G>T maps to NM_001161344.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:133438074 G>A maps to NM_001161344.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr12:133434123 C>T maps to NM_001161344.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:133428285 G>A maps to NM_001161344.1 H482H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:5903045 T>C maps to NM_001819.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:5903503 G>A maps to NM_001819.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:5904269 G>T maps to NM_001819.2 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:5904127 C>T maps to NM_001819.2 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:5903968 G>A maps to NM_001819.2 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:203155444 G>A maps to NM_001276.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:203154343 C>T maps to NM_001276.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:203148972 A>G maps to NM_001276.2 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:111773880 C>A maps to NM_004000.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:111860697 G>A maps to NM_201653.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:111860622 C>T maps to NM_201653.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:111863054 C>T maps to NM_201653.2 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:111854923 C>T maps to NM_201653.2 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:72804264 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:72797296 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:72900818 T>G did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:72783202 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:54880227 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:54930446 G>T maps to NM_012110.2 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:54930446 G>T maps to NM_012110.2 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:903006 G>T maps to NM_001142676.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:899389 G>A maps to NM_001142676.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr11:884141 G>A maps to NM_001142676.1 H268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:67842270 G>A maps to NM_001277.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:67837654 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr11:67832038 A>G maps to NM_001277.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:67864497 C>T maps to NM_001277.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:51018641 G>A maps to NM_005198.4 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:432750 C>A maps to NM_006614.2 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:423868 G>A maps to NM_006614.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:423961 C>T maps to NM_006614.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:370021 G>T maps to NM_006614.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:424185 G>T maps to NM_006614.2 E670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:369909 G>A maps to NM_006614.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr3:383607 C>T maps to NM_006614.2 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:370021 G>T maps to NM_006614.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:404983 C>T maps to NM_006614.2 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:440698 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:85166339 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:85212881 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:85213875 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:85218761 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:85302492 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:85218694 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:85282504 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:85156160 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:85211372 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:85166297 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:85218738 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:85166275 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:85218919 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:85282493 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:85233855 C>A did not map to a codon.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr23:85128069 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:241798618 G>A maps to NM_001821.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:241797850 T>C maps to NM_001821.3 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:241798571 G>T maps to NM_001821.3 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:32436327 C>T maps to NM_176812.4 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr20:32441323 C>T maps to NM_176812.4 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:32439903 G>T maps to NM_176812.4 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:78970841 C>T maps to NM_024591.4 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:23115895 G>A maps to NM_152272.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:23116592 G>A maps to NM_152272.3 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:175742696 G>A maps to NM_001822.4 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:175666469 G>A maps to NM_001822.4 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:175677106 C>T maps to NM_001822.4 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr2:175742669 T>A maps to NM_001822.4 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:175809618 G>A maps to NM_001822.4 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:29438090 G>A maps to NM_004067.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:29394236 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:29519909 C>T maps to NM_004067.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:29394236 C>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr7:29552332 C>T maps to NM_004067.2 N463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:19629430 C>T maps to NM_024944.2 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:19628910 G>A maps to NM_024944.2 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr11:89936499 G>A maps to NM_012124.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:89947196 T>G maps to NM_012124.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:89938723 G>T maps to NM_012124.2 Y191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:89936571 T>C maps to NM_012124.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr2:220405040 C>T maps to NM_024536.5 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr2:220404224 G>A maps to NM_024536.5 C736C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:150935181 C>T maps to NM_019015.1 D578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:150934653 C>T maps to NM_019015.1 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:150933658 G>T maps to NM_019015.1 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:102091899 G>A maps to NM_020244.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:141525532 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:141525424 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:184102806 G>A maps to NM_003741.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:184107197 C>T maps to NM_003741.2 A952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:184101194 C>T maps to NM_003741.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:109924821 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:110005969 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:109964677 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:110006034 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:109922647 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:109924858 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:109937478 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:109919587 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:109924734 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:109937557 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:110035351 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:109922562 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:109924715 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:109963073 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:74415555 G>A maps to NM_015424.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:30654987 G>A maps to NM_139320.1 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:62677417 C>T maps to NM_000738.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:136700187 T>C maps to NM_001006628.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:136699971 C>T maps to NM_001006628.1 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:136700640 C>T maps to NM_001006628.1 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:240070948 G>A maps to NM_000740.2 W66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:240070918 C>T maps to NM_000740.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:240071722 C>T maps to NM_000740.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:240071824 C>A maps to NM_000740.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:46406730 G>T maps to NM_000741.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:46406904 C>T maps to NM_000741.2 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:34355007 C>A maps to NM_012125.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:175624103 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:175612926 G>T maps to NM_001039523.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:175619033 G>A maps to NM_001039523.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:3687471 G>A maps to NM_020402.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:3690538 C>T maps to NM_020402.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr11:3687576 C>T maps to NM_020402.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr8:27327283 G>A maps to NM_000742.3 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr8:27327457 T>C maps to NM_000742.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:27321500 C>A maps to NM_000742.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr15:78894002 G>A maps to NM_000743.4 N327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr15:78894497 G>A maps to NM_000743.4 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:78893981 C>T maps to NM_000743.4 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:78894311 G>A maps to NM_000743.4 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:61982033 C>T maps to NM_000744.5 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:61987367 G>T maps to NM_000744.5 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:61982273 G>A maps to NM_000744.5 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:61981061 C>T maps to NM_000744.5 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:61982033 C>T maps to NM_000744.5 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:42612090 G>A maps to NM_004198.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:32450725 C>T maps to NM_001190455.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:32451809 C>T maps to NM_001190455.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:32450796 G>A maps to NM_001190455.1 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr15:32455505 C>T maps to NM_001190455.1 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:32460302 C>T maps to NM_001190455.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:32460253 T>C maps to NM_001190455.1 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:40351318 A>G maps to NM_017581.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7357646 G>A maps to NM_000747.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7352060 C>A maps to NM_000747.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr17:7357775 C>T maps to NM_000747.2 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:42587097 C>T maps to NM_000749.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:42587121 G>A maps to NM_000749.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:42587226 G>A maps to NM_000749.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr8:42586851 C>T maps to NM_000749.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:78923428 C>T maps to NM_000750.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr15:78921374 C>T maps to NM_000750.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr15:78921974 G>A maps to NM_000750.3 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:78927918 G>A maps to NM_000750.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr15:78921668 G>T maps to NM_000750.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:233394808 C>T maps to NM_000751.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:4805930 C>T maps to NM_000080.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr2:233407754 C>A maps to NM_005199.4 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:233404489 G>C maps to NM_005199.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:233406158 G>A maps to NM_005199.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr11:45671663 C>T maps to NM_003654.4 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr11:45671885 C>T maps to NM_003654.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:45672050 C>T maps to NM_003654.4 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:45672089 G>A maps to NM_003654.4 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:45672410 C>T maps to NM_003654.4 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:101009859 C>T maps to NM_004854.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:101009816 C>A maps to NM_004854.3 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:101010057 G>A maps to NM_004854.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:101010057 G>A maps to NM_004854.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:101009760 G>A maps to NM_004854.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:105151232 C>T maps to NM_018413.5 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:105151232 C>T maps to NM_018413.5 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:105151529 C>T maps to NM_018413.5 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr7:2472864 C>T maps to NM_018641.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:125804258 C>T maps to NM_015892.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:125771885 C>T maps to NM_015892.3 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:125780867 C>T maps to NM_015892.3 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:125804294 G>A maps to NM_015892.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:125805532 C>A maps to NM_015892.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr10:125769685 C>T maps to NM_015892.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr3:142840773 G>A maps to NM_004267.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:73765713 C>T maps to NM_004273.4 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:71571476 G>A maps to NM_001166395.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:71571458 C>T maps to NM_001166395.1 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr16:75563169 G>A maps to NM_024533.3 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:75512724 G>T maps to NM_021615.4 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:75513561 G>A maps to NM_021615.4 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:75512838 C>T maps to NM_021615.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:75513507 C>T maps to NM_021615.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:46433935 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:46434090 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:46433806 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:46433677 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:46433793 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:46434059 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:34180226 C>T maps to NM_022467.3 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:34263625 C>T maps to NM_022467.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:34263781 C>T maps to NM_022467.3 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr19:34263409 C>T maps to NM_022467.3 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:24496402 G>A maps to NM_031422.4 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:24496320 G>A maps to NM_031422.4 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:24496570 G>T maps to NM_031422.4 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:24496912 G>T maps to NM_031422.4 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:101775529 G>A maps to NM_014918.4 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:101717610 G>A maps to NM_014918.4 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr15:101719158 G>A maps to NM_014918.4 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:839657 G>A maps to ENST00000317063 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:842298 C>T maps to ENST00000317063 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:846779 G>A maps to ENST00000317063 T1049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:69154298 C>T maps to ENST00000306585 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:101953116 C>T maps to NM_001278.3 W682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:90774233 A>G maps to NM_006384.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:90774720 G>A maps to NM_006384.3 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:78401694 C>T maps to NM_006383.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:78401708 C>A maps to NM_006383.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:78398115 G>A maps to NM_006383.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:16275662 C>T maps to NM_054113.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:42791055 C>A maps to NM_015125.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:42798424 C>T maps to NM_015125.3 C1432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:42793223 G>A maps to NM_015125.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:42794091 G>T maps to NM_015125.3 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:42795133 C>A maps to NM_015125.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:12274153 C>T maps to ENST00000342845 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:12262854 C>T maps to ENST00000342845 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:10998610 G>A maps to NM_000246.3 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:11004116 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:11001574 G>A maps to NM_000246.3 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:11000893 C>T maps to NM_000246.3 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:10971204 A>G maps to NM_000246.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr16:11002909 G>A maps to NM_000246.3 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:10997630 C>T maps to NM_000246.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr15:65496642 C>A maps to NM_003613.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:65489520 G>A maps to NM_003613.3 R1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:65496737 G>A maps to NM_003613.3 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:65491228 G>A maps to NM_003613.3 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr15:65491255 G>A maps to NM_003613.3 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:65489833 G>A maps to NM_003613.3 N930N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:65491252 G>T maps to NM_003613.3 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr15:65489644 A>G maps to NM_003613.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:65489862 G>A maps to NM_003613.3 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:19654084 C>T maps to NM_153221.2 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:19654643 C>T maps to NM_153221.2 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:19650494 C>A maps to NM_153221.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:19656593 C>T maps to NM_153221.2 C1080C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:19656413 C>T maps to NM_153221.2 R1020R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:175243713 G>A maps to NM_004882.3 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:1270879 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:1272471 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:69184773 C>T maps to NM_032830.2 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:120171982 G>A maps to ENST00000392521 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:120135576 T>A maps to ENST00000392521 G1923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:120172962 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:120241119 C>T maps to ENST00000392521 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr12:120150420 G>T maps to ENST00000392521 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr12:120263004 G>T maps to ENST00000392521 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:120151010 C>A maps to ENST00000392521 E1526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:120150035 C>A maps to ENST00000392521 E1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:120156644 C>A maps to ENST00000392521 E1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11M-01A-11D-A122-09 chr12:120150411 T>C maps to ENST00000392521 A1556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:120260756 A>G maps to ENST00000392521 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:120214624 C>A maps to ENST00000392521 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:120139557 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:120142173 G>A maps to ENST00000392521 I1766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:120210696 C>T maps to ENST00000392521 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:120151297 G>A maps to ENST00000392521 L1488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr12:120150105 G>A maps to ENST00000392521 C1577C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:120135627 C>T maps to ENST00000392521 A1906A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71522666 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:71521766 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:71521944 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:71522079 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:130931357 G>A maps to NM_012127.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:130931405 G>A maps to NM_012127.2 F740F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:53049108 C>T maps to NM_001098525.1 R629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:53035752 G>T maps to NM_001098525.1 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:106633074 C>T maps to NM_006825.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr12:106634088 G>T maps to NM_006825.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:106632897 C>T maps to NM_006825.3 E571E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:106633700 C>A maps to NM_006825.3 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:46799006 T>G maps to ENST00000415402 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:46799691 G>T maps to ENST00000415402 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:46771887 G>A maps to ENST00000415402 V1887V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:46801836 G>A maps to ENST00000415402 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:46772781 G>A maps to ENST00000415402 I1789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:46837801 A>G maps to ENST00000415402 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:46802010 G>A maps to ENST00000415402 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:66592127 C>T maps to NM_016951.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:45818798 G>A maps to NM_001824.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:45810896 G>T maps to NM_001824.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:43990273 C>A maps to ENST00000424065 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:43988293 C>T maps to ENST00000424065 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:43988298 C>T maps to ENST00000424065 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:43988497 C>A maps to ENST00000424065 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:80550219 T>C maps to NM_001825.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:80555015 G>A maps to NM_001825.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:122120861 T>C maps to NM_015282.2 A1364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:122125233 G>T maps to NM_015282.2 A1272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr2:122205894 C>T maps to NM_015282.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:122220105 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:122204922 G>A maps to NM_015282.2 Y634Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:122227525 G>A maps to NM_015282.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:122162008 G>A maps to NM_015282.2 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:122120866 G>A maps to NM_015282.2 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:122273334 G>A maps to NM_015282.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:122285414 G>A maps to NM_015282.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:122120866 G>A maps to NM_015282.2 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:122220151 C>A maps to NM_015282.2 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:33580286 G>A maps to ENST00000359576 G1193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:33650118 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:33686513 C>T maps to ENST00000333778 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:33633913 G>A maps to ENST00000359576 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:33731376 G>A maps to ENST00000359576 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:33614615 A>G maps to ENST00000359576 N904N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:33728566 T>A maps to ENST00000359576 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:33648901 G>A maps to ENST00000359576 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:33738392 G>T maps to ENST00000359576 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr3:33661092 A>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:86954764 C>T maps to NM_001285.3 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:86952421 C>T maps to NM_001285.3 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:86965704 G>T maps to NM_001285.3 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:86890040 C>T maps to NM_006536.5 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:86904626 C>A maps to NM_006536.5 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:86898056 C>A maps to NM_006536.5 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:86921077 T>C maps to NM_006536.5 Y900Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:86921122 C>A maps to NM_006536.5 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:86905886 C>T maps to NM_006536.5 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:86913198 C>T maps to NM_006536.5 H574H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:86904647 C>T maps to NM_006536.5 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:87036797 A>G maps to ENST00000263723 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:87041049 G>A maps to ENST00000263723 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:87012891 C>A maps to ENST00000263723 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:87025976 C>T maps to ENST00000263723 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:87025935 G>T maps to ENST00000263723 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:87045766 C>A maps to ENST00000263723 I834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:87025751 A>G maps to ENST00000263723 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:87040224 C>T maps to ENST00000263723 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:87046113 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:87031040 T>G maps to ENST00000263723 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:87040230 T>C maps to ENST00000263723 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:87041097 T>G maps to ENST00000263723 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:87031049 A>G maps to ENST00000263723 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:109486117 C>T maps to NM_001048210.1 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:109479938 C>T maps to NM_001048210.1 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:67132978 C>T maps to NM_013246.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:143016865 G>T maps to NM_000083.2 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:184072043 G>A maps to NM_004366.4 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:170641137 T>C maps to NM_173872.2 N841N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:170610361 T>G maps to NM_173872.2 L196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:170628206 G>T maps to NM_173872.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:170628250 A>G maps to NM_173872.2 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:10176540 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:10176346 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:10182073 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:10176083 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:10181782 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:10188719 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:10176189 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:10163102 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:10181837 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:10201540 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:10180578 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:10188850 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:10176252 C>G did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:10180634 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:10176399 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:49856786 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49840521 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49850638 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49855487 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49846417 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49834542 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49851263 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49854796 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:49851168 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:49840502 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:49855335 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49851061 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49855006 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:49834630 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:49855468 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:49855334 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49837153 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49854986 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:49854897 C>T did not map to a codon.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr23:49854897 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:49840585 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:49851438 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:49855152 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:49851136 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:49851179 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:11894611 G>A maps to ENST00000376496 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:11888255 C>T maps to ENST00000376496 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:11898474 G>A maps to ENST00000376496 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr1:11894087 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:1510486 G>A maps to ENST00000382745 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:1498403 C>T maps to ENST00000382745 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:1499062 G>A maps to ENST00000382745 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:1506159 G>A maps to ENST00000382745 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:16354379 C>A maps to NM_004070.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:16358282 G>A maps to NM_004070.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:16359705 C>T maps to NM_004070.3 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:16378031 C>A maps to NM_000085.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:190039814 G>A maps to NM_021101.4 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr13:96205183 C>T maps to NM_006984.4 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr3:170140954 C>T maps to NM_005602.5 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:37833708 G>A maps to NM_001146077.1 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr21:37833543 C>T maps to NM_001146077.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:100880774 G>A maps to NM_014343.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:31538293 T>G maps to NM_012131.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:31538539 G>A maps to NM_012131.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr21:31538800 C>T maps to NM_012131.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr21:31538527 C>T maps to NM_012131.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr21:31538890 G>A maps to NM_012131.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:137749868 C>T maps to NM_016369.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:43201547 C>T maps to NM_001123395.1 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:43205554 C>T maps to NM_148960.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:43205584 G>T maps to NM_148960.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:106171618 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:106171871 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:106171558 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:184240948 G>T maps to NM_001111319.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:184240732 C>T maps to NM_001111319.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr8:8560180 G>A maps to NM_194284.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:73245548 A>G maps to NM_001305.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:73246050 C>T maps to NM_001305.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:3065860 G>A maps to NM_021195.4 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:7164212 C>T maps to NM_001185022.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr21:31587910 A>G maps to NM_199328.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr21:31587885 G>A maps to NM_199328.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr21:31587724 C>T maps to NM_199328.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr3:98237834 T>C maps to NM_001040182.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:6978435 G>T maps to NM_182906.2 C296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:6978689 C>T maps to NM_182906.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:6979400 C>A maps to NM_182906.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:10131977 A>G maps to ENST00000355690 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:10165441 C>T maps to NM_001129998.1 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr14:38724726 G>A maps to NM_175060.1 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr14:38723829 G>A maps to NM_175060.1 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:38724102 G>A maps to NM_175060.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:38724732 G>A maps to NM_175060.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:38724543 C>T maps to NM_175060.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr14:38724534 G>A maps to NM_175060.1 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:11260293 C>A maps to ENST00000409790 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:11076760 G>A maps to ENST00000409790 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:11260317 C>T maps to ENST00000409790 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr16:11260317 C>T maps to ENST00000409790 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:11097004 G>A maps to ENST00000409790 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr16:11076760 G>A maps to ENST00000409790 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:11066900 C>T maps to ENST00000409790 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:11272252 C>T maps to ENST00000409790 N956N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:74447526 G>A maps to NM_001011880.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:10224048 C>T maps to NM_016511.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:10010204 G>A maps to NM_005127.2 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:10007019 G>A maps to NM_005127.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:9822347 T>C maps to NM_001004419.3 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr7:139225184 C>T maps to NM_001080511.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:78064420 G>T maps to NM_005752.3 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:78064737 G>T maps to NM_005752.3 *198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:45077053 C>T maps to NM_003278.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr3:45077076 C>A maps to NM_003278.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:45077070 G>A maps to NM_003278.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:7882332 G>A maps to NM_130441.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:8692499 A>C maps to NM_014358.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:8688735 G>A maps to NM_014358.2 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:71043934 A>C maps to NM_173535.2 L193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr2:71044149 G>A maps to NM_173535.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:71043378 G>T maps to NM_173535.2 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:7794384 C>T maps to NM_198492.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:7828095 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:7834042 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:7833811 C>T maps to NM_014257.4 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7830962 G>A maps to NM_014257.4 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:7828083 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:7828143 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr19:7831668 C>T maps to NM_014257.4 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:7831499 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:141629903 T>C maps to NM_013252.2 *189W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:141643762 G>T maps to NM_013252.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr12:10280145 T>C maps to ENST00000422474 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:10277697 C>T maps to ENST00000354721 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:10280283 C>T maps to ENST00000422474 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:10280283 C>T maps to ENST00000422474 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:10205298 G>T maps to NM_207345.2 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:10217365 A>C maps to NM_207345.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr4:141313526 T>C maps to NM_004362.2 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:141311791 G>T maps to NM_004362.2 S581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:31698687 G>A maps to NM_001288.4 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:154528408 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:154563698 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:154507294 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr23:154508585 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:154528202 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:154563726 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154563708 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:154507295 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:154508586 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154528132 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:154528124 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:154509324 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:154508595 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr9:139889255 G>A maps to NM_004669.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:25124324 G>A maps to NM_013943.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:45870869 G>A maps to NM_001114086.1 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:45983234 C>T maps to NM_016929.3 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr21:36079681 G>A maps to ENST00000360731 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:157244511 G>A maps to NM_001195555.1 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:157214821 C>T maps to NM_001195555.1 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:157233010 C>A maps to NM_001195555.1 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:157241237 C>A maps to NM_001195555.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:157244524 G>A maps to NM_001195555.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:122794386 A>T maps to ENST00000302528 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:122801327 C>T maps to ENST00000302528 E1147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr12:122848582 G>A maps to ENST00000302528 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:122812588 G>A maps to ENST00000302528 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:122758592 A>G maps to ENST00000302528 N1361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:122826045 C>A maps to ENST00000302528 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr12:122757586 G>A maps to ENST00000302528 C1384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:122763690 C>A maps to ENST00000302528 E1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:122801386 C>A maps to ENST00000302528 E1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:122763405 G>A maps to ENST00000302528 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:122839718 C>T maps to ENST00000302528 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:122825787 C>A maps to ENST00000302528 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr12:122763613 G>C maps to ENST00000302528 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:73800908 C>T maps to NM_003388.4 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:73795146 G>A maps to NM_003388.4 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:73791028 C>T maps to NM_003388.4 Y766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:73791040 G>A maps to NM_003388.4 Q770Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:73790287 C>T maps to NM_003388.4 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:73774560 G>A maps to NM_003388.4 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr7:73803433 G>A maps to NM_003388.4 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:36510151 G>A maps to NM_015526.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:36518042 G>A maps to NM_015526.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:36517616 G>A maps to NM_015526.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:29404677 G>A maps to ENST00000379543 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:29404668 C>A maps to ENST00000379543 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:29356614 G>A maps to ENST00000379543 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:29356671 G>A maps to ENST00000379543 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:29390369 G>T maps to ENST00000379543 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:201718694 G>A maps to NM_001162407.1 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:201718640 G>A maps to NM_001162407.1 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:201722491 G>A maps to NM_001162407.1 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:155235677 G>A maps to ENST00000368361 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:155238118 G>T maps to ENST00000368361 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:155239488 C>T maps to ENST00000368361 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:155238111 G>A maps to ENST00000368361 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:155238501 G>A maps to ENST00000368361 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr1:155234211 C>T maps to ENST00000424156 W170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:155233071 G>A maps to ENST00000368361 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:74920374 G>T maps to NM_001130028.1 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr15:74922130 C>T maps to NM_001130028.1 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:74919992 G>A maps to NM_001130028.1 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:178040600 A>G maps to NM_020666.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:178045655 G>A maps to NM_020666.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:178043935 G>A maps to NM_020666.2 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:178045648 G>A maps to NM_020666.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:178045556 C>T maps to NM_020666.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:95670572 C>T maps to NM_024734.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:95670443 G>A maps to NM_024734.3 N414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:95690156 G>A maps to NM_024734.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:95662970 C>A maps to NM_024734.3 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:95679704 A>T maps to NM_024734.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:95670038 A>C maps to NM_024734.3 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:95670572 C>T maps to NM_024734.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:95670710 G>T maps to NM_024734.3 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:95669414 G>A maps to NM_024734.3 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:95670089 A>G maps to NM_024734.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:28502864 C>T maps to NM_000086.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr13:77574677 C>T maps to NM_006493.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr13:77574797 A>G maps to NM_006493.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr8:1728600 A>T maps to NM_018941.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:1719306 C>T maps to NM_018941.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:10599660 C>T maps to NM_052964.2 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:56345847 A>G maps to NM_004898.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr4:56319267 G>A maps to NM_004898.2 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:57428407 G>T maps to NM_006831.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:72013350 G>A maps to NM_030813.3 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:72114096 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:72013353 T>C maps to NM_030813.3 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:72040813 G>A maps to NM_030813.3 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:72084035 G>A maps to NM_030813.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:6364613 C>T maps to NM_006012.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr19:6366339 C>T maps to NM_006012.2 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:45490626 C>T maps to NM_001294.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:45477841 C>T maps to NM_001294.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr19:45490602 C>A maps to NM_001294.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:45491408 C>T maps to NM_001294.2 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:1335226 C>T maps to NM_030782.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr5:1341803 G>A maps to NM_030782.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:1331932 G>A maps to NM_030782.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:65456366 C>A maps to NM_006660.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:65477455 C>T maps to NM_006660.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr15:65451044 C>A maps to NM_006660.3 G254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr3:150645802 G>A maps to NM_001195794.1 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:17524647 C>T maps to NM_001079827.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:17528665 C>T maps to NM_001079827.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:129691030 C>T maps to NM_152311.3 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:129676610 G>A maps to NM_152311.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr10:129676684 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:36202589 T>C maps to NM_022111.3 R1278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:36202616 G>T maps to NM_022111.3 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:36212490 C>T maps to NM_022111.3 E910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:36226213 C>G maps to NM_022111.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:36204751 G>A maps to NM_022111.3 R1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:36212388 A>G maps to NM_022111.3 C944C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:36216871 C>T maps to NM_022111.3 E669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:9790628 G>A maps to NM_001009566.1 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:9793472 C>A maps to NM_001009566.1 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:9811714 G>A maps to NM_001009566.1 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:9804552 C>T maps to NM_001009566.1 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:9833381 G>A maps to NM_001009566.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr1:9794180 G>A maps to NM_001009566.1 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:9791314 G>A maps to NM_001009566.1 N899N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:9809932 C>A maps to NM_001009566.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:9833396 G>A maps to NM_001009566.1 N49N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:140123570 C>T maps to NM_022131.2 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:140251311 C>T maps to NM_022131.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:140265495 C>A maps to NM_022131.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:140277679 C>T maps to NM_022131.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:140185521 C>T maps to NM_022131.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:140282884 C>T maps to NM_022131.2 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:140123540 A>G maps to NM_022131.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:140122483 G>A maps to NM_022131.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:7288892 G>A maps to NM_014718.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:7288970 G>A maps to NM_014718.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:175819906 C>T maps to NM_007097.2 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:175823487 G>A maps to NM_007097.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:57728562 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:57738965 C>T maps to NM_004859.3 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:57760294 G>T maps to NM_004859.3 E1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:57743474 C>A maps to NM_004859.3 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:57768067 T>G maps to NM_004859.3 V1633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:57760151 G>T maps to NM_004859.3 E1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:57738934 A>G maps to NM_004859.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:57758331 G>A maps to NM_004859.3 K993K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr17:57762560 C>T maps to NM_004859.3 L1527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:19175546 G>A maps to NM_007098.3 N1460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:19209535 G>T maps to NM_007098.3 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:19220115 C>T maps to NM_007098.3 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr22:19170956 G>A maps to NM_007098.3 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:19188971 G>A maps to NM_007098.3 Y1211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:27463924 G>A maps to NM_001831.2 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:27457332 C>T maps to NM_001831.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:27462459 C>T maps to NM_001831.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:27462759 C>T maps to NM_001831.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:27462624 C>T maps to NM_001831.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:27457332 C>T maps to NM_001831.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr8:27462759 C>T maps to NM_001831.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:27456052 C>A maps to NM_001831.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:3586220 C>T maps to NM_015041.1 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:633430 T>C maps to NM_199167.1 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:627245 G>A maps to NM_199167.1 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr8:62212626 C>T maps to NM_173519.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:123377087 C>T maps to NM_001010852.2 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:123369780 G>A maps to NM_001010852.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:123332280 C>T maps to NM_001010852.2 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:100523295 G>T maps to NM_206808.2 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:100511123 C>T maps to NM_206808.2 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:100518603 C>T maps to NM_206808.2 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:100518530 C>T maps to NM_206808.2 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:22208468 C>T maps to NM_018686.3 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:22214320 G>T maps to NM_018686.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:10290712 C>T maps to NM_138809.3 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:10286523 A>C maps to NM_138809.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:81727073 C>T maps to NM_198390.2 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:81736237 C>T maps to NM_198390.2 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:81712032 C>T maps to NM_198390.2 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr16:81641293 G>A maps to NM_198390.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:81691378 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr16:81737564 C>T maps to NM_198390.2 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:81654498 C>T maps to NM_198390.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:108686442 G>A maps to NM_001142344.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:6991611 C>A maps to NM_207315.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:66603921 C>T maps to NM_052999.3 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:66611056 C>A maps to NM_052999.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:66612768 C>T maps to NM_052999.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:66621835 G>A maps to NM_144673.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:66621856 C>T maps to NM_144673.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr16:66643335 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:66642237 C>A maps to NM_181553.2 C58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:66657327 G>A maps to NM_178818.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:23847619 G>A maps to ENST00000339180 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr14:23848245 C>T maps to ENST00000339180 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:23847685 C>T maps to ENST00000339180 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:32491043 G>T maps to NM_138410.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:79027464 G>A maps to NM_153610.3 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:79028955 G>A maps to NM_153610.3 E1456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:79031475 C>T maps to NM_153610.3 G2296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:79031680 G>T maps to NM_153610.3 E2365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:79033560 C>T maps to NM_153610.3 L2991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:79028074 G>T maps to NM_153610.3 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:79025328 A>G maps to NM_153610.3 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:79029625 G>T maps to NM_153610.3 E1680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:79031901 C>A maps to NM_153610.3 S2438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr5:79030279 A>T maps to NM_153610.3 K1898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:79030237 G>T maps to NM_153610.3 E1884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:79031881 G>T maps to NM_153610.3 E2432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:79032883 G>T maps to NM_153610.3 E2766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:79033519 G>T maps to NM_153610.3 E2978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:79029762 G>A maps to NM_153610.3 S1725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:79032661 G>T maps to NM_153610.3 E2692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:79030827 A>G maps to NM_153610.3 E2080E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:79028386 G>T maps to NM_153610.3 E1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:88365862 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:88365862 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:128889343 G>A maps to NM_001127192.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:128890057 G>A maps to NM_001127192.1 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr18:72251795 T>C maps to NM_032649.5 *508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:72226604 G>A maps to NM_032649.5 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:72168697 A>G maps to NM_018235.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:72183480 C>T maps to NM_018235.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr18:72180884 C>T maps to NM_018235.2 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr18:72178112 C>T maps to NM_018235.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:42891560 G>A maps to NM_032488.3 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:47938563 C>T maps to NM_001142564.1 E718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:47939118 T>C maps to NM_001142564.1 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:150912736 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:150911738 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:150907327 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:150911737 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:150912577 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:150911751 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:150912675 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:150912621 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:150908061 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:150908163 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:150911102 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:150912844 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:150912170 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:150912370 C>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:150908082 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:150912710 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:99012778 C>T maps to NM_001298.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:99013138 G>A maps to NM_001298.2 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:99013273 C>T maps to NM_001298.2 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:99013408 C>T maps to NM_001298.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:98994213 G>T maps to NM_001298.2 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:6261770 C>T maps to NM_001037329.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:6261779 G>A maps to NM_001037329.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:6261927 C>T maps to NM_001037329.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:6262963 C>T maps to NM_001037329.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:6265270 C>T maps to NM_001037329.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:6262792 G>A maps to NM_001037329.2 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:6261780 C>T maps to NM_001037329.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr16:57983297 T>C maps to NM_001297.4 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:57974188 G>A maps to NM_001297.4 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:57945694 G>A maps to NM_001297.4 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:57950053 G>A maps to NM_001297.4 Y732Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:57954408 G>A maps to NM_001297.4 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:87588333 C>A maps to NM_019098.4 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:87738811 A>G maps to NM_019098.4 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr8:87588109 G>C maps to NM_019098.4 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:87679353 G>A maps to NM_019098.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr8:87680361 G>A maps to NM_019098.4 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:87656093 G>A maps to NM_019098.4 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:54898923 C>T maps to NM_005776.2 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:54897090 C>A maps to NM_005776.2 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:66050742 C>A maps to NM_182553.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:66050208 G>A maps to NM_182553.1 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:224922409 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:224553592 G>T maps to NM_014184.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:224544682 C>T maps to NM_014184.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:26514788 C>T maps to ENST00000374253 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:26515799 G>T maps to ENST00000374253 E642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:21619468 T>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:21534643 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:21488921 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:21550164 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:21609230 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:21627219 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:21609256 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:21534677 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:21545019 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:21627197 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:21544997 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:21627196 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:21393034 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:21550084 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:21627417 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr23:21458858 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:21550030 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr23:21545043 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:21444747 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:21550055 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:21579611 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:21667092 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:21627451 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:21627227 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:21450784 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:21508596 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:21667019 T>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:21519657 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:154727732 C>A maps to NM_173515.2 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:11660160 C>T maps to NM_001299.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:11660462 C>T maps to NM_001299.4 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:1031119 C>T maps to NM_004368.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:95367328 C>A maps to NM_001839.3 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:95367287 T>C maps to NM_001839.3 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:101090493 C>T maps to NM_020348.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr10:101147662 C>T maps to NM_020348.2 D809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:101124758 C>T maps to NM_020348.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:101090070 C>T maps to NM_020348.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:104809545 C>T maps to NM_017649.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:104679766 C>T maps to NM_017649.3 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:104816705 C>T maps to NM_017649.3 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr10:104836927 C>T maps to NM_017649.3 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr10:104678815 G>A maps to NM_017649.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:104809561 G>T maps to NM_017649.3 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:97490891 C>T maps to NM_017623.4 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:97427569 C>T maps to NM_020184.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:97427899 C>T maps to NM_020184.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:97427242 G>A maps to NM_020184.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr2:97427704 C>G maps to NM_020184.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:58570991 C>T maps to NM_016284.3 R1849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:58573745 G>A maps to NM_016284.3 R1640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:58573715 G>A maps to NM_016284.3 R1650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:58615419 C>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr16:58620652 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:58589810 C>T maps to NM_016284.3 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:32750179 G>T maps to NM_015442.1 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:32806207 C>T maps to NM_015442.1 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:70723290 C>T maps to NM_014515.5 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:70724237 T>C maps to NM_014515.5 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:54652016 C>T maps to NM_014516.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:54656699 G>A maps to NM_014516.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:54649464 C>T maps to NM_014516.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:54655997 G>A maps to NM_014516.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr7:135080545 C>A maps to NM_001190850.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:135078790 G>T maps to NM_001190850.1 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:179980413 C>T maps to NM_015455.3 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:179998395 C>T maps to NM_015455.3 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:78695784 A>G maps to ENST00000512485 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:17088264 C>T maps to NM_013354.5 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:155301792 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:155301641 C>A maps to NM_001103176.1 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:155299792 C>A maps to NM_001103176.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:42903326 C>T maps to NM_006586.3 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:42902333 G>A maps to NM_006586.3 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:88854903 G>A maps to NM_016083.4 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:88853736 C>T maps to NM_016083.4 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr6:88854285 C>T maps to NM_016083.4 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:88854252 G>A maps to NM_016083.4 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:88854201 G>A maps to NM_016083.4 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:24201213 G>A maps to NM_001841.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:24201119 C>A maps to NM_001841.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:24201831 C>A maps to NM_001841.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:68521062 G>A maps to NM_015463.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:246823593 C>T maps to NM_152609.2 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:246811239 C>A maps to NM_152609.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:246811212 C>T maps to NM_152609.2 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:246829134 C>T maps to NM_152609.2 D702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:246810456 C>T maps to NM_152609.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:58390263 T>C maps to NM_000614.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:58391857 C>T maps to NM_000614.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:17309142 C>T maps to NM_017738.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:17340913 G>A maps to NM_017738.2 E578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:17484375 C>T maps to NM_017738.2 D1313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:17226201 G>T maps to NM_017738.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:17226273 G>T maps to NM_017738.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:17394759 G>T maps to NM_017738.2 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:17342365 C>T maps to NM_017738.2 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:17366630 G>T maps to NM_017738.2 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:41312513 A>C maps to NM_001843.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:41422974 G>A maps to NM_001843.2 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:41323787 C>A maps to NM_001843.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:41318405 G>T maps to NM_001843.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:41312547 C>T maps to NM_001843.2 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr1:205022357 T>C maps to NM_005076.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:205031626 G>A maps to NM_005076.3 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:205031671 C>T maps to NM_005076.3 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:205033516 C>T maps to NM_005076.3 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205030459 C>T maps to NM_005076.3 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205039654 C>T maps to NM_005076.3 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:205042350 C>T maps to NM_005076.3 I1000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:74420382 G>A maps to NM_020872.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr3:74316437 C>T maps to NM_020872.1 E932E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:74313587 A>C maps to NM_020872.1 P1017P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:74334516 A>C maps to NM_020872.1 A881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:74411081 A>C maps to NM_020872.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:74413672 G>A maps to NM_020872.1 C386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:74350822 G>A maps to NM_020872.1 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:74383984 T>C maps to NM_020872.1 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:74414773 G>A maps to NM_020872.1 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr3:74347149 C>A maps to NM_020872.1 G787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr3:74344349 G>A maps to NM_020872.1 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:3067882 C>T maps to NM_175607.1 D528D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:3084755 C>T maps to NM_175607.1 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:3081794 C>A maps to NM_175607.1 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:3081827 C>A maps to NM_175607.1 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:3081794 C>A maps to NM_175607.1 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:2777911 G>A maps to NM_175607.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:2777933 G>T maps to NM_175607.1 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:2908472 C>A maps to NM_175607.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:2942426 C>A maps to NM_175607.1 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:2942426 C>A maps to NM_175607.1 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:3081893 C>T maps to NM_175607.1 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr3:3067957 A>T maps to NM_175607.1 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:2613201 G>A maps to NM_175607.1 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:99827718 G>A maps to NM_014361.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:100126591 C>A maps to NM_014361.2 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:100170016 C>T maps to NM_014361.2 R837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:100126537 A>G maps to NM_014361.2 E684E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:100169928 C>T maps to NM_014361.2 F807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:100141897 C>T maps to NM_014361.2 R747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:100064358 C>T maps to NM_014361.2 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:1337343 C>T maps to NM_014461.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:1414031 C>T maps to NM_014461.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:1369155 G>T maps to NM_014461.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:1424984 C>T maps to NM_014461.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:1363375 G>A maps to NM_014461.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:1369182 C>T maps to NM_014461.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:1425039 C>A maps to NM_014461.2 S822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:1443183 G>A maps to NM_014461.2 E924E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:1320143 G>T maps to NM_014461.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:1337343 C>T maps to NM_014461.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:1424808 G>T maps to NM_014461.2 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:1427321 G>T maps to NM_014461.2 E849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:40843866 A>G maps to NM_003632.2 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:40838992 G>T maps to NM_003632.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:40845525 G>A maps to NM_003632.2 T988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:40838134 C>T maps to NM_003632.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr17:40845483 C>T maps to NM_003632.2 C974C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:40837388 C>T maps to NM_003632.2 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:40839787 C>T maps to NM_003632.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:147600792 C>T maps to NM_014141.5 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:147844733 G>A maps to NM_014141.5 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:147926751 C>T maps to NM_014141.5 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:147869376 C>A maps to NM_014141.5 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:148080906 C>T maps to NM_014141.5 C1214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:147600792 C>T maps to NM_014141.5 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:147926861 C>A maps to NM_014141.5 I1124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:147600792 C>T maps to NM_014141.5 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:147336342 C>A maps to NM_014141.5 Y681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:147092833 C>T maps to NM_014141.5 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:147092833 C>T maps to NM_014141.5 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:147259299 T>C maps to NM_014141.5 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:147926751 C>T maps to NM_014141.5 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:39171503 G>A maps to NM_033655.3 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:39085784 G>T maps to NM_033655.3 S1130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:39102548 C>T maps to NM_033655.3 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:39171461 G>A maps to NM_033655.3 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr9:39176053 C>T maps to NM_033655.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:76532581 C>T maps to NM_033401.3 Q785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:76509934 C>T maps to NM_033401.3 C584C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:76501291 T>C maps to NM_033401.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:76573638 T>C maps to NM_033401.3 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:76311628 G>A maps to NM_033401.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:76483712 C>A maps to NM_033401.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:76483712 C>A maps to NM_033401.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:76572193 C>T maps to NM_033401.3 S1058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:76592517 C>T maps to NM_033401.3 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:76482081 A>C maps to NM_033401.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:76528936 C>A maps to NM_033401.3 C736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:76556146 C>T maps to NM_033401.3 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:76486527 C>T maps to NM_033401.3 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:76555147 C>A maps to NM_033401.3 S825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:76523649 G>A maps to NM_033401.3 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:76587178 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:76501294 T>C maps to NM_033401.3 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:76532532 A>G maps to NM_033401.3 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:124999867 G>A maps to NM_130773.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:125521375 C>T maps to NM_130773.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:125530595 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:125284880 C>T maps to NM_130773.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:125669090 C>T maps to NM_130773.2 R1234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:124999900 G>A maps to NM_130773.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A1DQ-01A-11D-A135-09 chr2:125555703 G>A maps to NM_130773.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:124999966 C>A maps to NM_130773.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:125530563 C>T maps to NM_130773.2 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:125521350 T>C maps to NM_130773.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:125671837 C>T maps to NM_130773.2 S1298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:125367441 C>T maps to NM_130773.2 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:125622998 G>T maps to NM_130773.2 E1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:125504944 C>T maps to NM_130773.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:125669090 C>T maps to NM_130773.2 R1234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:125405392 C>T maps to NM_130773.2 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:125530569 C>T maps to NM_130773.2 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:125405356 G>A maps to NM_130773.2 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:125627266 C>T maps to NM_130773.2 R1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:125367441 C>T maps to NM_130773.2 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:125530502 C>T maps to NM_130773.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:7840086 T>G maps to NM_001037144.4 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr17:7851916 G>A maps to NM_001037144.4 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr17:7840525 C>A maps to NM_001037144.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:40717750 C>T maps to NM_001042532.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:51096590 G>A maps to ENST00000395542 D816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:51261159 A>G maps to ENST00000395542 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:51203926 C>T maps to ENST00000395542 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:51111096 A>G maps to ENST00000395542 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:51096884 C>T maps to ENST00000395542 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:51261125 C>A maps to ENST00000395542 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:51287538 C>T maps to ENST00000395542 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:165551734 G>A maps to ENST00000392717 R799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:165557218 C>A maps to ENST00000392717 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:165550940 C>T maps to ENST00000392717 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:140151379 C>T maps to NM_015456.3 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:140166979 C>T maps to NM_015456.3 H503H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:31349941 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:31354787 G>T maps to NM_004086.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:31354711 C>T maps to NM_004086.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:230804443 T>C maps to NM_007357.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:230795286 G>A maps to NM_007357.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:230795217 C>T maps to NM_007357.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:46083906 C>T maps to NM_031431.2 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:46056514 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:70546140 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:70534992 C>A maps to NM_015386.2 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:70548333 A>G maps to NM_015386.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:106844025 C>A maps to NM_006348.3 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:107198434 C>A maps to NM_006348.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:106850984 C>T maps to NM_006348.3 R818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr7:106938786 C>T maps to NM_006348.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr7:106924104 G>A maps to NM_006348.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr13:40293482 T>C maps to ENST00000255468 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:40233611 G>T maps to ENST00000255468 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:23415062 G>A maps to NM_153603.3 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:23430068 G>A maps to NM_153603.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:23428364 G>A maps to NM_153603.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:23400294 G>A maps to NM_153603.3 G753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:23409429 G>T maps to NM_153603.3 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:23415062 G>A maps to NM_153603.3 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr16:23400366 C>T maps to NM_153603.3 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:23424886 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:69366785 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:69368576 C>T maps to NM_032382.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:55027900 A>G maps to NM_004645.2 G234G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr6:116442360 C>T maps to NM_000493.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:116441505 A>G maps to NM_000493.3 C591C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:103347307 G>T maps to NM_080629.2 S1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:103405986 C>A maps to NM_080629.2 E1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:103444293 G>A maps to NM_080629.2 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:103470040 C>A maps to NM_080629.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:103544224 G>A maps to NM_080629.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:103484390 C>A maps to NM_080629.2 G457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:103453236 T>C maps to NM_080629.2 R830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:103347272 C>A maps to NM_080629.2 E1686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:103544278 G>A maps to NM_080629.2 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:103440429 C>A maps to NM_080629.2 G934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:103488528 A>G maps to NM_080629.2 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:103491840 T>G maps to NM_001854.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:103352369 G>A maps to NM_080629.2 F1629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:103544242 G>T maps to NM_080629.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:103540263 C>T maps to NM_080629.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:103345391 C>T maps to NM_080629.2 R1719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr1:103471420 C>T maps to NM_080629.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr1:103477986 A>T maps to NM_080629.2 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr1:103573653 G>A maps to NM_080629.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:33141151 C>T maps to NM_080680.2 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:75797370 G>A maps to ENST00000322507 R3035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:75840676 C>T maps to ENST00000322507 T1986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:75834942 A>G maps to ENST00000322507 Y2169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:75884891 C>A maps to ENST00000322507 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:75902056 C>A maps to ENST00000322507 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:75831068 G>A maps to ENST00000322507 F2345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:75912466 C>T maps to ENST00000322507 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:75818822 C>A maps to ENST00000322507 E2671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:75898227 C>A maps to ENST00000322507 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:75814963 A>G maps to ENST00000322507 C2741C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:75806968 C>T maps to ENST00000322507 P2859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:75838102 C>T maps to ENST00000322507 Q2083Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr6:75866093 C>T maps to ENST00000322507 V1043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:75840655 C>T maps to ENST00000322507 R1993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:75827140 G>A maps to ENST00000322507 I2492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:75831016 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr6:75844499 G>T maps to ENST00000322507 T1822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:71690163 C>T maps to ENST00000356340 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr10:71690163 C>T maps to ENST00000356340 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:71662505 C>T maps to ENST00000356340 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:71685583 G>T maps to ENST00000356340 G441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr10:71654306 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:71681679 C>T maps to ENST00000356340 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:121293158 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:121279118 G>T maps to NM_021110.1 E1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:121262979 C>T maps to NM_021110.1 D909D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:121279136 G>T maps to ENST00000434620 E843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:121216029 C>T maps to NM_021110.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:121322265 G>T maps to NM_021110.1 G1474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:121220600 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr8:121256206 G>A maps to NM_021110.1 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:121210081 G>T maps to NM_021110.1 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr9:101765841 G>A maps to NM_001855.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:101812037 G>T maps to NM_001855.3 G954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:101829294 G>A maps to NM_001855.3 L1261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:101832066 C>T maps to NM_001855.3 L1356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:101818585 T>G maps to NM_001855.3 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:101782715 G>T maps to NM_001855.3 G565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:101748018 C>T maps to NM_001855.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:101806851 C>T maps to NM_001855.3 G859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:101787280 G>A maps to NM_001855.3 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr9:101804352 T>G maps to NM_001855.3 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:101747931 T>C maps to NM_001855.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:32148534 C>T maps to NM_001856.3 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:32127272 G>T maps to NM_001856.3 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:32148534 C>A maps to NM_001856.3 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:32158080 G>A maps to NM_001856.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:32167722 T>C maps to NM_001856.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:105813676 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:105831819 G>A maps to NM_000494.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:105819432 G>T maps to NM_000494.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:105803328 C>T maps to NM_000494.3 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:105831819 G>A maps to NM_000494.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:105831819 G>A maps to NM_000494.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:105795237 G>A maps to NM_000494.3 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:105803328 C>T maps to NM_000494.3 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:105831819 G>A maps to NM_000494.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:105813870 G>A maps to NM_000494.3 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:105831825 G>A maps to NM_000494.3 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:105831819 G>A maps to NM_000494.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:105812854 G>A maps to NM_000494.3 R625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr21:46907402 C>T maps to ENST00000359759 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr21:46888522 C>T maps to ENST00000359759 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:46888300 C>T maps to ENST00000359759 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:46916433 A>T maps to ENST00000359759 G1258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr21:46915321 T>C maps to ENST00000359759 D1243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr21:46876304 C>T maps to ENST00000359759 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:70866101 G>A maps to NM_001858.4 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:70639406 C>T maps to NM_001858.4 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:70856774 C>T maps to NM_001858.4 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:70589494 G>A maps to NM_001858.4 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:70873263 T>A maps to NM_001858.4 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:70877934 C>T maps to NM_001858.4 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:70608915 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:70646710 C>A maps to NM_001858.4 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr6:70859906 G>A maps to NM_001858.4 K669K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:70890358 A>T maps to NM_001858.4 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr6:70608915 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:70637858 C>T maps to NM_001858.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:70900039 G>T maps to NM_001858.4 E1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:70637858 C>T maps to NM_001858.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:70639315 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:48266594 C>T maps to NM_000088.3 Q957Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:48265266 G>A maps to NM_000088.3 F1113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:48275865 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:48269364 G>A maps to NM_000088.3 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:94057719 G>A maps to NM_000089.3 K1214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:94059570 G>T maps to NM_000089.3 E1323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:94057765 G>T maps to NM_000089.3 E1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:94059650 C>T maps to NM_000089.3 I1349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:94049914 C>T maps to NM_000089.3 N750N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:94041909 C>T maps to NM_000089.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:94058738 C>T maps to NM_000089.3 C1317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:94059557 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:94027071 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:61937320 G>T maps to ENST00000326996 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:61937240 C>T maps to ENST00000326996 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:61945176 G>A maps to ENST00000326996 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:61943788 C>T maps to ENST00000326996 N614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:61936859 C>A maps to ENST00000326996 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:55922543 G>A maps to NM_030820.3 Q929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:55929420 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:56032932 C>A maps to NM_030820.3 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:56044910 C>T maps to NM_030820.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:56044580 G>A maps to NM_030820.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr6:55925772 C>T maps to NM_030820.3 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:55923986 C>A maps to NM_030820.3 E888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:55924867 A>G maps to NM_030820.3 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr8:139838948 C>T maps to NM_152888.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:139727959 C>A maps to NM_152888.1 G828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:139838990 G>A maps to NM_152888.1 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:139688871 G>A maps to NM_152888.1 R1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:139706804 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:139774702 G>A maps to NM_152888.1 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:139601591 G>A maps to NM_152888.1 L1595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:139638479 C>A maps to NM_152888.1 E1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:139675945 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:139727974 C>A maps to NM_152888.1 E823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:139703090 G>A maps to NM_152888.1 P927P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr8:139788226 C>T maps to NM_152888.1 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr8:139618623 C>T maps to NM_152888.1 P1368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:139825226 C>T maps to NM_152888.1 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:139737653 G>A maps to NM_152888.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:139791760 G>A maps to NM_152888.1 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:139611126 G>T maps to NM_152888.1 I1400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:139825238 G>T maps to NM_152888.1 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:177689226 G>A maps to ENST00000390654 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:177689223 G>A maps to ENST00000390654 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:86210408 G>A maps to NM_152890.5 R1538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:86308066 C>A maps to NM_152890.5 G1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:86591028 A>G maps to NM_152890.5 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:86591139 G>T maps to NM_152890.5 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:86590827 A>G maps to NM_152890.5 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:86591613 T>C maps to NM_152890.5 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:116931157 G>A maps to NM_032888.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:117050996 C>T maps to NM_032888.2 R1354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:116958292 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:116930722 G>A maps to NM_032888.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:117063377 C>T maps to NM_032888.2 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:7413127 G>A maps to NM_001037763.2 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:7476036 G>A maps to NM_001037763.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:7415128 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:7476036 G>A maps to NM_001037763.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:7572414 G>T maps to NM_001037763.2 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:7476036 G>A maps to NM_001037763.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:7571089 A>C maps to NM_001037763.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:48369807 C>A maps to NM_001844.4 G1179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:48380214 G>A maps to NM_001844.4 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:48378777 G>A maps to NM_001844.4 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:48370614 G>A maps to NM_001844.4 Q1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:48372388 G>A maps to NM_001844.4 D962D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:48370696 A>C maps to NM_001844.4 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:48393798 G>A maps to NM_001844.4 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr12:48372130 G>A maps to NM_001844.4 I982I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:189854838 C>T maps to NM_000090.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:189875081 T>G maps to NM_000090.3 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:189867043 C>T maps to NM_000090.3 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:189856933 C>T maps to NM_000090.3 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:189873864 C>T maps to NM_000090.3 S1247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:189859058 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:189872636 C>T maps to NM_000090.3 I1130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr13:110853210 G>A maps to NM_001845.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:110822909 G>C maps to NM_001845.4 G1242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:110839482 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:110804775 C>T maps to NM_001845.4 A1611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr13:111102752 C>T maps to NM_001846.2 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:111160417 C>A maps to NM_001846.2 P1577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:111164402 C>T maps to NM_001846.2 Y1668Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:111164351 C>T maps to NM_001846.2 R1651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:111164366 C>T maps to NM_001846.2 I1656I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:111141853 C>T maps to NM_001846.2 F1090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:111009848 G>T maps to NM_001846.2 G44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:111160549 C>T maps to NM_001846.2 I1621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr13:111144498 C>T maps to NM_001846.2 G1179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:111154019 C>T maps to NM_001846.2 R1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:111117885 C>T maps to NM_001846.2 D637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr13:111141853 C>T maps to NM_001846.2 F1090F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:228128610 T>C maps to NM_000091.4 C422C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:228111435 G>A maps to NM_000091.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:228122320 A>G maps to NM_000091.4 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:228109043 A>G maps to NM_000091.4 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:228135524 G>T maps to NM_000091.4 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:228131139 C>T maps to NM_000091.4 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:228135661 C>T maps to NM_000091.4 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:228145306 G>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr2:228147126 C>T maps to NM_000091.4 G845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:228173955 C>T maps to NM_000091.4 A1559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr2:228167815 A>G maps to NM_000091.4 P1315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:228104926 G>A maps to NM_000091.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:74675209 G>A maps to NM_001130105.1 Y740Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:74675209 G>A maps to NM_001130105.1 Y740Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:74698865 C>G maps to NM_001130105.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:227907841 T>C maps to ENST00000396625 S1116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:227917119 C>A maps to ENST00000396625 G957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:227907877 C>T maps to ENST00000396625 E1104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:227924156 C>A maps to ENST00000396625 G783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:227872100 T>C maps to ENST00000396625 K1671K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:227985768 G>A maps to ENST00000396625 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:227895165 G>A maps to ENST00000396625 G1322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr23:107858228 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107811877 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107834301 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107858158 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107821569 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107841956 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107925042 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107938583 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107939579 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107834335 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107869458 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:107936061 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:107807156 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:107840789 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:107841941 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:107865958 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:107930791 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr23:107936001 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107821340 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:107838757 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:107866025 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr23:107910412 G>A did not map to a codon.
Sequencing variant TCGA-B5-A1MU-01A-11D-A13L-09 chr23:107938566 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr23:107834397 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107838786 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107924119 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107938583 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107939545 C>T did not map to a codon.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr23:107858224 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:107911613 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr23:107826157 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:107434697 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:107408206 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107418364 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107431745 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107420181 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107422482 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107430346 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107462952 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107464499 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:107408264 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107413897 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107457402 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107464566 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107553978 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:107418373 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:107420146 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:107407851 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107417802 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107422626 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107448920 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:107400306 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:107412769 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:107402839 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:107408659 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107402883 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107431784 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107437765 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:107418364 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107414691 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107418385 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:107434697 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:107418318 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:107422481 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:107431152 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:107554052 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:107413942 A>T did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:107422033 G>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:107420128 C>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:137622080 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:137630648 G>T maps to NM_000093.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:137582890 G>A maps to NM_000093.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:137701127 G>T maps to NM_000093.3 G1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:137734037 C>T maps to NM_000093.3 I1802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:137717680 C>A maps to NM_000093.3 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr9:137716564 C>T maps to NM_000093.3 D1606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr9:137593016 G>A maps to NM_000093.3 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:137582830 T>C maps to NM_000093.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:137622284 T>C maps to NM_000093.3 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:137630648 G>T maps to NM_000093.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:137701072 G>A maps to NM_000093.3 Q1137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:137653805 G>A maps to NM_000093.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:137716561 G>A maps to NM_000093.3 A1605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:137703183 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:189975077 G>A maps to NM_000393.3 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:189923573 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:189940156 G>A maps to NM_000393.3 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:189925479 T>C maps to NM_000393.3 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:189917698 C>A maps to NM_000393.3 G867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:189927990 C>T maps to NM_000393.3 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:189916189 C>T maps to NM_000393.3 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:189927762 T>C maps to NM_000393.3 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:189923152 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:189932993 A>G maps to NM_000393.3 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr2:189899878 G>A maps to NM_000393.3 F1372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:10114390 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:10108825 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:10116302 G>A maps to NM_015719.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:10080078 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:10089902 C>A maps to NM_015719.3 E927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:10089622 C>A maps to NM_015719.3 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:10106795 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr19:10077058 C>T maps to NM_015719.3 S1571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr21:47421197 C>T maps to NM_001848.2 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:47423749 C>T maps to NM_001848.2 F970F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr21:47404311 G>A maps to NM_001848.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr21:47407534 A>G maps to NM_001848.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr21:47423482 G>T maps to NM_001848.2 T881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr21:47421966 C>T maps to NM_001848.2 N683N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr21:47549155 G>A maps to NM_058174.2 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:47532286 C>T maps to NM_001849.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:47549401 C>A maps to NM_058174.2 C918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:47536578 C>T maps to NM_001849.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr21:47538999 C>A maps to NM_001849.3 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr21:47538547 A>G maps to NM_001849.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr21:47532434 C>T maps to NM_001849.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr21:47538941 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr21:47541468 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:238277695 G>A maps to NM_004369.3 P1470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:238275402 G>A maps to NM_004369.3 S1809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:238275810 G>A maps to NM_004369.3 G1673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:238303577 C>A maps to NM_004369.3 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:238303758 C>T maps to NM_004369.3 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:238296285 C>T maps to NM_004369.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:238303379 C>A maps to NM_004369.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:238303482 T>C maps to NM_004369.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:238267721 C>A maps to NM_004369.3 G2122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:238283544 G>A maps to NM_004369.3 D1063D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:238253448 G>T maps to NM_004369.3 A2404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:238257023 C>A maps to NM_004369.3 E2312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:238274453 C>A maps to NM_004369.3 E1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:238287543 C>T maps to NM_004369.3 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:238277289 C>A maps to NM_004369.3 E1606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:238303653 C>T maps to NM_004369.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:238303524 G>A maps to NM_004369.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:238275492 C>T maps to NM_004369.3 R1779R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:130202994 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:130174421 C>T maps to ENST00000312481 Y2234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:130095104 C>T maps to ENST00000312481 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:130095662 C>T maps to ENST00000312481 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:130104010 C>A maps to ENST00000312481 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr3:130110454 A>G maps to ENST00000312481 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:130107606 T>C maps to ENST00000312481 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:130141608 G>T maps to ENST00000312481 G1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:130107954 C>A maps to ENST00000312481 I798I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:130114087 T>C maps to ENST00000312481 S1116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr3:130189787 C>T maps to ENST00000312481 N2517N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr3:130187862 C>T maps to ENST00000312481 L2339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:130095473 G>A maps to ENST00000312481 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:130188095 C>T maps to ENST00000312481 G2416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:130107921 C>T maps to ENST00000312481 F787F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:130107628 G>T maps to ENST00000312481 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr3:130284241 C>T maps to NM_001102608.1 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:130289761 C>T maps to NM_001102608.1 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:130354550 T>C maps to NM_001102608.1 I1679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:130394105 C>T maps to NM_001102608.1 F2219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:130368270 C>T maps to NM_001102608.1 I1866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:130282024 G>T maps to NM_001102608.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:130300438 C>T maps to NM_001102608.1 V1194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:48613154 C>T maps to NM_000094.3 E1961E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:48607590 G>A maps to NM_000094.3 G2487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:48610468 A>G maps to NM_000094.3 G2245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:48611137 T>C maps to NM_000094.3 G2186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:48623267 C>A maps to NM_000094.3 E1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:48612268 G>A maps to NM_000094.3 L2103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:48603081 G>A maps to NM_000094.3 I2809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:48615777 G>A maps to NM_000094.3 G1836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:48603706 C>T maps to NM_000094.3 Q2800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:48625745 C>T maps to NM_000094.3 A893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr3:48623614 C>T maps to NM_000094.3 P1205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:99513093 C>T maps to ENST00000429802 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:99513072 G>T maps to ENST00000429802 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr6:71010026 G>A maps to NM_001851.4 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:70935712 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:70970386 G>A maps to NM_001851.4 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:71004244 C>T maps to NM_001851.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:70993223 C>A maps to ENST00000370499 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:71004055 C>T maps to NM_001851.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:70935712 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr6:70926688 C>A maps to NM_001851.4 G893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:70993471 C>A maps to NM_001851.4 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr6:70990529 G>A maps to NM_001851.4 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:40775612 G>A maps to NM_001852.3 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:40777360 C>T maps to NM_001852.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:40773875 C>T maps to NM_001852.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:40770483 C>T maps to NM_001852.3 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr20:61472014 C>T maps to NM_001853.3 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:61452860 C>T maps to NM_001853.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:61458172 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:120103459 G>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:3691533 C>T maps to ENST00000418971 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:3691461 C>T maps to ENST00000418971 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr2:3652001 T>C maps to ENST00000418971 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:3691338 G>A maps to ENST00000418971 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:3673666 G>T maps to NM_199235.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:346918 G>A maps to NM_130386.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:334751 C>T maps to NM_130386.2 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:333083 C>A maps to NM_130386.2 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:321739 A>G maps to NM_130386.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr18:335165 G>T maps to NM_130386.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:346313 C>T maps to NM_130386.2 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:15497427 G>A maps to NM_005677.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:15512077 C>A maps to NM_005677.3 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr3:149469120 A>G maps to ENST00000483708 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:22606834 C>T maps to NM_012071.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:75631413 C>A maps to NM_017828.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:75631380 G>A maps to NM_017828.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr15:75630423 C>T maps to NM_017828.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr8:146076198 G>A maps to NM_001081003.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:47455161 C>A maps to NM_017845.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:36296182 C>A maps to NM_014186.3 *199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:18901371 G>A maps to NM_000095.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:18901669 G>A maps to NM_000095.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:160265889 A>G maps to NM_001098398.1 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:14487882 A>G maps to NM_001144061.1 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:14512116 T>A maps to NM_001144061.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr11:14487924 G>A maps to NM_001144061.1 Y731Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:14515329 G>A maps to NM_001144061.1 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:139077107 A>G maps to NM_004766.2 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:139102213 G>A maps to NM_004766.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr3:139079975 C>T maps to NM_004766.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:139081248 C>T maps to NM_004766.2 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:139085574 A>C maps to NM_004766.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19015579 C>T maps to NM_007263.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:19021871 G>A maps to NM_007263.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:19021871 G>A maps to NM_007263.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:130147133 G>T maps to NM_012133.4 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:17168256 T>C maps to NM_003653.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:17174210 A>C maps to NM_003653.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:17174285 G>A maps to NM_003653.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:83996582 A>G maps to ENST00000503682 *439W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:83989592 G>A maps to ENST00000503682 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:67970422 G>A maps to NM_006837.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr7:99689079 C>A maps to NM_006833.4 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:99688569 G>T maps to NM_006833.4 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:99688213 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr12:6838537 G>A maps to NM_001164093.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:6840198 G>A maps to NM_001164093.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56662971 C>T maps to NM_144576.3 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:56662914 G>A maps to NM_144576.3 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:198338630 G>T maps to NM_025147.3 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:198324779 G>T maps to NM_025147.3 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:84185390 G>A maps to NM_015697.7 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:84188846 G>A maps to NM_015697.7 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:131094466 C>T maps to NM_016035.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr9:131095905 C>T maps to NM_016035.3 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr12:120966824 A>C maps to NM_032314.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:74425870 G>T maps to NM_182476.1 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:74422205 A>G maps to NM_182476.1 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr14:74428566 G>A maps to NM_182476.1 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:19089440 C>A maps to NM_016138.4 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:47645273 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr4:47605588 G>T maps to NM_006587.2 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:47628536 C>A maps to NM_006587.2 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:30198424 G>T maps to NM_007074.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:30198369 C>T maps to NM_007074.3 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:30199131 C>T maps to NM_007074.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:67208619 C>T maps to NM_020441.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:109055853 G>A maps to ENST00000420959 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:109042551 G>A maps to ENST00000420959 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:109046160 C>T maps to ENST00000420959 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr12:109046046 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:109055853 G>A maps to ENST00000420959 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:100919840 G>A maps to NM_052820.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:100888860 G>A maps to NM_052820.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:100892139 G>A maps to NM_052820.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr9:100895355 A>G maps to NM_052820.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:27945912 G>A maps to ENST00000345068 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:27943171 G>A maps to ENST00000345068 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:4411086 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:4408454 G>A maps to NM_024535.3 C790C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:4408100 C>A maps to NM_024535.3 E821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:4408025 G>A maps to NM_024535.3 Q846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:4411018 G>A maps to NM_024535.3 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:4410534 G>T maps to NM_024535.3 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:4458241 G>A maps to NM_024535.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:10510303 G>C maps to ENST00000377049 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:84600468 G>A maps to NM_021149.2 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:13980288 G>T maps to NM_001303.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr17:14005477 G>A maps to NM_001303.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:14110262 C>T maps to NM_001303.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:53045859 G>A maps to NM_004375.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr17:53045824 A>G maps to NM_004375.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:53045892 C>A maps to NM_004375.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:101483778 T>C maps to NM_078470.4 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:70809446 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr7:975070 G>A maps to NM_006869.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:85838558 C>T maps to NM_001861.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:85838589 C>A maps to NM_001861.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr16:85834874 C>T maps to NM_001861.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:85832868 G>A maps to NM_006067.4 Y11Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:85814025 G>A maps to NM_006067.4 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:85822653 A>G maps to NM_006067.4 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:98263557 G>A maps to NM_001862.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr12:120875951 C>A maps to NM_004373.2 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr19:55865139 C>T maps to NM_144613.4 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:36642591 G>A maps to ENST00000437291 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:36641889 C>T maps to ENST00000437291 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:77155083 C>A did not map to a codon.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr23:77158217 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:77158172 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:77160701 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:93814373 G>T maps to NM_182971.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:148923989 G>A maps to NM_000096.3 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:148927150 C>A maps to NM_000096.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:148899876 G>T maps to NM_000096.3 I823I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:148894138 C>A maps to NM_000096.3 E1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:148916183 C>T maps to NM_000096.3 K561K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:148897438 G>T maps to NM_000096.3 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:130021496 C>T maps to NM_001868.2 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:130021010 G>A maps to NM_001868.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr7:130027803 G>A maps to NM_001868.2 W404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:130021598 C>T maps to NM_001868.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:130027663 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr7:130021553 C>A maps to NM_001868.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:129912924 G>T maps to NM_001869.2 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:129909624 C>A maps to NM_001869.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:148603899 C>T maps to NM_001870.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:148601548 C>T maps to NM_001870.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:129950687 A>G maps to NM_016352.3 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:129933074 G>T maps to NM_016352.3 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:129999461 G>A maps to NM_080385.4 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:130007766 G>A maps to NM_080385.4 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr8:68346314 G>A maps to NM_020361.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:68396943 G>A maps to NM_020361.4 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:68419113 G>A maps to NM_020361.4 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:68340314 G>A maps to NM_020361.4 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:68334861 G>A maps to NM_020361.4 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:68421853 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:17122404 G>A maps to ENST00000443236 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:17122288 C>T maps to ENST00000443236 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:17015128 G>T maps to ENST00000443236 T1443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:17057908 G>A maps to ENST00000443236 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:17038882 G>T maps to ENST00000443236 A1159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:17056394 G>A maps to ENST00000443236 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:17068725 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:17088186 G>A maps to ENST00000443236 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:17100479 C>T maps to ENST00000443236 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:17056433 T>C maps to ENST00000443236 K963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:17039895 G>A maps to ENST00000443236 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:17010303 C>A maps to ENST00000443236 V1667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:17004056 C>T maps to ENST00000443236 P1897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:17014556 G>T maps to ENST00000443236 T1511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:148558520 C>T maps to NM_001871.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:148545842 C>T maps to NM_001871.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:148563313 C>A maps to NM_001871.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:148562486 C>T maps to NM_001871.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:148562466 C>T maps to NM_001871.2 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:148545809 C>T maps to NM_001871.2 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr13:46656595 G>A maps to NM_001872.3 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:46629968 C>A maps to NM_001872.3 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:46658397 G>A maps to NM_001872.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:28750600 G>T maps to NM_001304.4 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:28749992 G>T maps to NM_001304.4 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:28758862 T>C maps to NM_001304.4 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:166408730 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:166418678 G>T maps to NM_001873.2 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:166385566 G>A maps to NM_001873.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr4:166385677 T>C maps to NM_001873.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:166418699 G>T maps to NM_001873.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:83215189 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:83215198 G>A maps to ENST00000261723 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:83215934 G>A maps to ENST00000261723 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr15:83222256 C>T maps to ENST00000261723 W341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:83226508 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:83240226 C>T maps to ENST00000261723 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:15009083 G>A maps to NM_001177382.1 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:93999738 G>A maps to NM_014912.4 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:173372015 C>A maps to NM_030627.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:173377041 C>A maps to NM_030627.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:173317009 G>T maps to NM_030627.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:173380157 C>T maps to NM_030627.2 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:173372135 T>C maps to NM_030627.2 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr5:175307103 T>G maps to ENST00000393746 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr5:175306031 G>A maps to NM_001008220.1 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:56979967 T>C maps to NM_181654.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:69326589 G>A maps to NM_001874.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:69252801 T>G maps to NM_001874.4 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:101808526 C>T maps to NM_001308.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:194062288 G>A maps to NM_001080513.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:34220552 C>T maps to NM_003915.5 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr20:34220146 G>A maps to NM_003915.5 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr16:57149426 C>T maps to NM_152727.5 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:57153156 C>T maps to NM_152727.5 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:57180175 G>A maps to NM_152727.5 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:87568511 C>T maps to NM_003909.3 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:87568430 A>C maps to NM_003909.3 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:87568511 C>T maps to NM_003909.3 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:87544735 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr8:87568445 A>G maps to NM_003909.3 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:87543408 A>G maps to NM_003909.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:131261535 G>T maps to ENST00000502818 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:36710089 G>A maps to NM_020939.1 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:36742748 G>A maps to NM_020939.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:36711471 G>A maps to NM_020939.1 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:36712048 G>A maps to NM_020939.1 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24545079 C>T maps to NM_006032.2 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr14:24543333 G>A maps to NM_006032.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:89655090 T>C maps to NM_014427.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:89645275 G>A maps to NM_014427.4 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:39223233 A>G maps to NM_153634.2 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:39071289 G>T maps to NM_153634.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:9771207 C>T maps to ENST00000383832 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:9754740 C>T maps to ENST00000383832 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr3:9746604 C>T maps to ENST00000383832 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:9767647 C>A maps to ENST00000383832 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:207833910 G>T maps to NM_173077.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:207820236 A>G maps to NM_173077.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:207833951 C>A maps to NM_173077.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:98309955 G>A maps to NM_000097.5 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:98309484 C>A maps to NM_000097.5 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:12798556 G>A maps to NM_018340.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr16:12758859 G>A maps to NM_018340.2 H276H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:211473147 C>T maps to NM_001122633.1 N758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:211459299 G>A maps to NM_001122633.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:211442228 G>T maps to NM_001122633.1 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:211459299 G>A maps to NM_001122633.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:211469900 C>T maps to NM_001122633.1 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:211469900 C>T maps to NM_001122633.1 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:211460264 G>T maps to NM_001122633.1 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:211469885 G>T maps to NM_001122633.1 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:211460209 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr2:211540486 C>T maps to NM_001122633.1 N1405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:211464184 C>A maps to NM_001122633.1 Y489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:145624228 G>T maps to NM_013291.2 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:145619223 G>A maps to NM_013291.2 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:145619000 G>A maps to NM_013291.2 D1342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:145621890 G>A maps to NM_013291.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:145623258 G>A maps to NM_013291.2 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr8:145619641 C>T maps to NM_013291.2 S1232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr8:145619713 C>T maps to NM_013291.2 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:92624011 T>C maps to NM_017437.1 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:92621535 G>A maps to NM_017437.1 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:92620731 G>T maps to NM_017437.1 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:9580642 G>T maps to NM_016207.2 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:9571000 C>A maps to NM_016207.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:1250898 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:69652730 G>A maps to ENST00000266679 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:61183136 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:68530202 G>A maps to NM_001876.3 Y589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:68548125 G>A maps to NM_001876.3 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:68579969 C>T maps to NM_001876.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:68564341 G>A maps to NM_001876.3 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:51008772 G>A maps to NM_152245.2 F697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:51012827 C>T maps to NM_152245.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:51015399 G>A maps to NM_152245.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:51008730 G>T maps to NM_152245.2 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:51008046 C>T maps to NM_152245.2 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50200581 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50200596 C>T maps to NM_152359.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50204609 C>T maps to NM_152359.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50214038 C>A maps to NM_152359.2 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:50209589 C>T maps to NM_152359.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:50208310 G>A maps to NM_152359.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr19:50212044 G>A maps to NM_152359.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:50204752 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:50200581 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:53676197 C>T maps to NM_000098.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:53679116 C>T maps to NM_000098.2 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:53676884 T>C maps to NM_000098.2 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:29160508 C>A maps to NM_031311.3 G57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:88008975 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:88008448 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:88009013 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:88009115 G>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:88008594 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:88008937 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:88009228 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:88009061 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:88008630 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:88008717 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:2777048 G>A maps to NM_019609.4 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:2774976 G>T maps to NM_019609.4 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:2777269 G>A maps to NM_019609.4 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr20:2777925 C>A maps to NM_019609.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr20:2776717 C>T maps to NM_019609.4 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:2779153 G>A maps to NM_019609.4 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:2776024 A>G maps to NM_019609.4 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:125528197 A>G maps to NM_198148.2 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:125539748 G>A maps to NM_198148.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:125650995 C>T maps to NM_198148.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:125521466 C>T maps to NM_198148.2 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:125526633 C>T maps to NM_198148.2 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:125516830 G>A maps to NM_198148.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:125651049 G>A maps to NM_198148.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr10:125558681 C>A maps to NM_198148.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:8613887 A>G maps to NM_001014447.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:207787834 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:207749005 G>A maps to NM_000651.4 T1506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:207739181 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:207780599 C>T maps to NM_000651.4 R1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:207760773 G>A maps to NM_000651.4 T1858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:207785142 G>A maps to NM_000651.4 A2139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:207700390 C>T maps to NM_000651.4 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:207793369 G>A maps to NM_000651.4 A2404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:207785377 C>T maps to NM_000651.4 C2189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:207697064 C>T maps to NM_000651.4 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:207751540 C>A maps to NM_000651.4 C1643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:207753756 T>C maps to NM_000651.4 C1703C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:207857220 C>T maps to NM_175710.1 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:207857225 C>A maps to NM_175710.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:207890812 C>A maps to NM_175710.1 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:207850825 G>T maps to NM_175710.1 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:207850884 C>A maps to NM_175710.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:207640106 G>T maps to NM_001006658.2 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:207648362 C>T maps to NM_001006658.2 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:207639998 C>T maps to NM_001006658.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:207658860 G>T maps to NM_001006658.2 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:207658857 C>T maps to NM_001006658.2 R1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr16:1703128 C>T maps to NM_020825.3 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr16:1716119 T>C maps to NM_020825.3 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr16:1676043 G>A maps to NM_020825.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:1670666 G>A maps to ENST00000436138 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:131860345 C>T maps to NM_000755.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:131865329 G>T maps to NM_000755.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:197390964 C>T maps to NM_201253.2 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:197404418 C>A maps to NM_201253.2 V1142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:197404469 C>T maps to NM_201253.2 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:197390724 G>A maps to NM_201253.2 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr1:197297978 A>T maps to NM_201253.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:197398734 G>T maps to NM_201253.2 G945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:197403906 G>T maps to NM_201253.2 E972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:197390289 C>T maps to NM_201253.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:197325985 C>T maps to NM_201253.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:197404223 T>C maps to NM_201253.2 N1077N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:197404298 C>T maps to NM_201253.2 I1102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:197297714 C>A maps to NM_201253.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:197404610 C>T maps to NM_201253.2 Y1206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:197397004 C>A maps to NM_201253.2 G850G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:197404292 A>C maps to NM_201253.2 I1100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:197390379 C>T maps to NM_201253.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:197396605 C>T maps to NM_201253.2 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:197404463 C>T maps to NM_201253.2 I1157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:126125150 G>A maps to NM_173689.5 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:126133829 G>A maps to NM_173689.5 A803A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:6465592 G>A maps to NM_174881.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:3216891 T>C maps to NM_016302.3 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:3209329 C>T maps to NM_016302.3 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:208461647 C>T maps to NM_134442.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:35736044 G>A maps to NM_006368.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:46332667 C>A maps to ENST00000288400 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:46342293 T>C maps to ENST00000288400 *520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:137567315 G>A maps to NM_194071.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:137613004 C>T maps to NM_194071.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:137612935 C>T maps to NM_194071.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:137590552 C>T maps to NM_194071.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:28858790 C>T maps to NM_182898.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:28547315 C>T maps to NM_182898.2 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:28857777 G>T maps to NM_182898.2 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr7:28857729 C>T maps to NM_182898.2 Q433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:3786727 T>A maps to NM_004380.2 K1495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:3781240 G>A maps to NM_004380.2 N1708N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:3789607 G>T maps to NM_004380.2 Y1417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:3807983 C>T maps to NM_004380.2 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:3900363 C>T maps to NM_004380.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:3808902 C>T maps to NM_004380.2 E1107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr16:3777855 C>A maps to NM_004380.2 G2398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:3778606 A>C maps to NM_004380.2 A2147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:3900363 C>T maps to NM_004380.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr16:3820639 C>T maps to NM_004380.2 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr16:3777958 C>T maps to NM_004380.2 P2363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:85374943 C>A maps to NM_001039618.2 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:167515476 G>A maps to NM_003851.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:167511535 C>A maps to NM_003851.2 *221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:102000098 C>T maps to NM_153836.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr3:9979790 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50318068 C>T maps to NM_001135101.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:50313428 C>T maps to NM_001135101.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:50313827 C>T maps to NM_001135101.1 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:35467885 G>T maps to ENST00000429130 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:35500596 G>T maps to ENST00000429130 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:35467804 C>A maps to ENST00000495960 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:76264610 C>T maps to NM_001882.3 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:76251569 G>A maps to NM_001882.3 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:76248964 G>A maps to NM_001882.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:76249998 C>T maps to NM_001882.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:76264671 G>T maps to NM_001882.3 G311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:43910843 C>T maps to NM_001145146.1 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:43884239 C>T maps to ENST00000293493 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:30695571 C>T maps to ENST00000348438 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:30706879 G>T maps to ENST00000348438 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:30693189 C>T maps to ENST00000348438 W401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:36704087 C>T maps to NM_016441.2 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:36726407 A>C maps to NM_016441.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:36771568 C>T maps to NM_016441.2 R892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:36764576 C>T maps to NM_016441.2 C837C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:36706748 C>T maps to NM_016441.2 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:43274217 C>T maps to ENST00000449267 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:43273850 G>A maps to ENST00000449267 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:43275368 G>A maps to ENST00000449267 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:1388538 C>A maps to NM_175918.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:49819776 G>A maps to NM_001131.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:49819809 G>A maps to NM_001131.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:49666152 G>A maps to ENST00000211238 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:49666125 G>T maps to ENST00000211238 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:49665640 G>A maps to ENST00000211238 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:49700924 A>C maps to NM_001190986.1 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr6:49701490 C>T maps to NM_001190986.1 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:75937841 C>T maps to NM_031461.5 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:75925136 G>A maps to NM_031461.5 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr8:75941635 C>T maps to NM_031461.5 C445C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:84940323 C>T maps to ENST00000448503 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:84888373 G>A maps to NM_031476.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:1340344 C>A maps to NM_016823.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:21304087 G>A maps to NM_005207.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr22:21272306 C>T maps to NM_005207.3 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:1331520 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:1317568 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:1321381 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:1325328 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:1317422 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:1317569 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:29131038 G>A maps to NM_015986.3 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:29124345 C>T maps to NM_015986.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:5996116 C>A maps to NM_019095.4 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:6017752 T>G maps to NM_019095.4 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr4:5853143 G>A maps to NM_001014809.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:5844831 G>A maps to NM_001014809.1 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:5853194 G>A maps to NM_001014809.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:5841361 G>A maps to NM_001014809.1 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:5868444 G>A maps to NM_001014809.1 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr4:5838608 G>A maps to NM_001014809.1 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:20025981 G>T maps to NM_016652.4 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:20028411 G>A maps to NM_016652.4 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:20031196 C>A maps to NM_016652.4 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:20016859 G>A maps to NM_016652.4 D842D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:152382564 G>A maps to NM_016190.2 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:152382522 T>C maps to NM_016190.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:152384673 G>A maps to NM_016190.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:152382483 C>T maps to NM_016190.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:17250856 G>A maps to NM_014675.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:17292239 C>T maps to NM_014675.3 S1476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:17272008 C>T maps to NM_014675.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:17281812 G>T maps to NM_014675.3 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:17257067 G>A maps to NM_014675.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:17275002 G>T maps to NM_014675.3 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:17296296 C>T maps to NM_014675.3 A1773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr7:86991070 A>G maps to NM_001143935.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:86991112 T>G maps to NM_001143935.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:87011733 T>C maps to NM_001143935.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:159683854 C>T maps to NM_000567.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:159684221 G>A maps to NM_000567.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:159683895 C>A maps to NM_000567.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:159683890 C>T maps to NM_000567.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GE-01A-11W-A062-09 chr10:99667887 G>A maps to NM_018058.4 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:99640120 G>A maps to NM_018058.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:99770902 G>A maps to NM_018058.4 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:99640120 G>A maps to NM_018058.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:99655695 G>T maps to NM_018058.4 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:99656693 G>A maps to NM_018058.4 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:99640048 G>A maps to NM_018058.4 C592C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:99695930 G>A maps to NM_018058.4 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:99640120 G>A maps to NM_018058.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:122724669 C>A maps to NM_019604.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:122722399 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:122738132 T>C maps to NM_019604.2 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:122724708 A>G maps to NM_019604.2 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:18870862 C>T maps to NM_001098482.1 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:18879596 C>T maps to NM_001098482.1 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:18882346 C>T maps to NM_001098482.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr19:18886476 C>T maps to NM_001098482.1 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:18888012 G>T maps to NM_001098482.1 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:18885714 T>G maps to NM_001098482.1 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:153923927 G>T maps to NM_181715.2 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:153923810 G>A maps to NM_181715.2 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:91184352 C>T maps to NM_022769.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr15:91172637 C>T maps to NM_022769.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:91185345 G>T maps to NM_022769.3 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr15:91185366 C>T maps to NM_022769.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:107398926 C>A maps to NM_004075.3 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:107391314 G>A maps to NM_004075.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr11:45880391 G>A maps to NM_021117.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:45882557 C>T maps to NM_021117.3 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:45891358 C>T maps to NM_021117.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:45882560 C>T maps to NM_021117.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr11:45877631 G>A maps to NM_021117.3 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:44592188 C>T maps to NM_000394.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:111781107 G>T maps to NM_001885.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:27576224 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:219855054 G>A maps to NM_057094.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:27019223 C>T maps to NM_001886.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:27012127 C>T maps to NM_001887.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:27003927 G>A maps to NM_001887.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:25625491 C>T maps to NM_000496.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:97607299 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:97596358 C>T maps to ENST00000182096 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:97631112 C>T maps to ENST00000182096 R755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:97631112 C>T maps to ENST00000182096 R755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:209028008 G>A maps to NM_014617.3 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:209025778 G>A maps to NM_014617.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:208994238 G>A maps to NM_020989.3 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:208986453 G>A maps to NM_006891.3 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:208986519 G>A maps to NM_006891.3 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:21013755 C>T maps to NM_015974.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:21086682 G>T maps to NM_015974.2 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:75172128 G>A maps to NM_001889.3 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:34969700 A>C maps to ENST00000416217 L252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56676251 G>A maps to NM_004077.2 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:53567554 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:151904510 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:151909175 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:151908977 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:10871679 G>A maps to NM_003651.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr12:10862581 C>G maps to NM_003651.4 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:115263258 G>A maps to NM_001130523.1 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:115280597 G>A maps to NM_001130523.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:115276471 C>A maps to NM_001130523.1 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:115275286 G>A maps to NM_001130523.1 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:115267908 G>A maps to NM_001130523.1 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:115280615 C>A maps to NM_001130523.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:115262207 C>T maps to NM_001130523.1 W751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:115273260 A>G maps to NM_001130523.1 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:47707503 C>T maps to NM_001316.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:47691916 G>T maps to NM_001316.2 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:47704594 C>T maps to NM_001316.2 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:47682764 C>T maps to NM_001316.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr20:47711484 C>T maps to NM_001316.2 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:110466478 C>T maps to NM_000757.4 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:110466016 C>T maps to NM_000757.4 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:149441111 C>T maps to NM_005211.3 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:149435905 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:149459852 G>A maps to NM_005211.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:149456995 G>A maps to NM_005211.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:131409797 G>T maps to NM_000758.2 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:1407699 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:1401634 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:1409306 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:1424365 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:1407770 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:1413239 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:1404675 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:1413222 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:1424582 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:1407430 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:1409341 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:1428414 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:1401625 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:1407422 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:1409266 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:1407704 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:1401669 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:37331408 G>A maps to ENST00000262825 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:37325579 G>A maps to ENST00000262825 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:37334027 G>A maps to ENST00000262825 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:36933247 C>T maps to NM_156039.3 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:36941191 C>T maps to NM_156039.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:36941115 G>A maps to NM_156039.3 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr1:36931957 C>G maps to NM_156039.3 *864Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:36933801 G>A maps to NM_156039.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:36934790 G>A maps to NM_156039.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:36939177 G>A maps to NM_156039.3 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:36945073 G>A maps to NM_156039.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:19263254 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:19363210 C>A maps to NM_018371.4 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:19315132 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:19363276 G>T maps to NM_018371.4 C23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr8:19297443 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:19316060 G>A maps to NM_018371.4 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:19363407 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:43650710 T>G maps to NM_018590.3 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:43659442 C>A maps to NM_018590.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr10:43654301 C>A maps to NM_018590.3 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:61972414 C>T maps to NM_001317.3 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:61972886 G>A maps to NM_001317.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr17:61972741 T>A maps to NM_022640.2 K183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:61949924 C>T maps to NM_022644.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr17:61987682 A>G maps to NM_022579.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr15:75094107 G>A maps to NM_004383.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:75093082 C>T maps to NM_004383.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:75094065 G>A maps to NM_004383.2 E306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:75094140 C>T maps to NM_004383.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr15:75094838 C>T maps to NM_004383.2 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:75090957 C>T maps to NM_004383.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:3141765 G>A maps to NM_033225.5 S1351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:3165981 G>A maps to NM_033225.5 Y1225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:3265577 G>A maps to NM_033225.5 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:3224755 G>T maps to NM_033225.5 I971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:3351155 C>T maps to NM_033225.5 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:3443699 C>A maps to NM_033225.5 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:4495006 C>T maps to NM_033225.5 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:2857534 G>A maps to NM_033225.5 S2716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:3047536 G>A maps to NM_033225.5 F1765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:2876122 T>C maps to NM_033225.5 G2635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:3076849 G>A maps to NM_033225.5 S1533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:2910028 C>A maps to NM_033225.5 E2539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:3047541 G>A maps to NM_033225.5 R1764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:2855535 G>A maps to NM_033225.5 R2792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:2967696 G>A maps to NM_033225.5 N2197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr8:2976038 G>A maps to NM_033225.5 S2104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr8:3432487 G>A maps to NM_033225.5 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr8:3045397 G>A maps to NM_033225.5 S1871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:3165981 G>A maps to NM_033225.5 Y1225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr8:2820777 G>A maps to NM_033225.5 R3140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:2876020 G>A maps to NM_033225.5 S2669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:2886843 G>A maps to NM_033225.5 R2618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:3047536 G>A maps to NM_033225.5 F1765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:2815272 C>T maps to NM_033225.5 T3253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:4277527 C>T maps to NM_033225.5 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:2855535 G>A maps to NM_033225.5 R2792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:3008925 G>A maps to NM_033225.5 I2008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr8:2944676 G>A maps to NM_033225.5 T2472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr8:2811773 T>C maps to NM_033225.5 E3337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr8:2813246 C>G maps to NM_033225.5 V3286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:34123657 G>A maps to ENST00000373381 D1405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:34204903 G>A maps to ENST00000373381 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:34076779 G>A maps to ENST00000373381 P2028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:34204921 G>A maps to ENST00000373381 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:34209202 G>A maps to ENST00000373381 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:33998707 G>A maps to ENST00000373381 S3331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:34052715 G>A maps to ENST00000373381 V2263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:34090753 G>A maps to ENST00000373381 F1759F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:34554618 C>T maps to ENST00000373381 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:34076818 G>A maps to ENST00000373381 T2015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:33985440 C>T maps to ENST00000373381 A3529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:34015858 G>A maps to ENST00000373381 I2905I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:34070948 G>A maps to ENST00000373381 G2115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:34204921 G>A maps to ENST00000373381 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:34276441 G>A maps to ENST00000373381 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:34189815 G>A maps to ENST00000373381 I954I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:34291301 A>C maps to ENST00000373381 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:34181973 G>A maps to ENST00000373381 S1003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr1:33985237 G>A maps to ENST00000373381 H3552H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:33998829 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:34209070 G>A maps to ENST00000373381 N621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:34090741 G>A maps to ENST00000373381 S1763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:34190131 G>A maps to ENST00000373381 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:33990512 G>A maps to ENST00000373381 I3415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:34008404 G>A maps to ENST00000373381 C3024C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:34037276 C>T maps to ENST00000373381 W2564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:34204789 G>T maps to ENST00000373381 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:114186020 G>A maps to NM_198123.1 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:113599464 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:113697857 A>C maps to NM_198123.1 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:114186125 A>G maps to NM_198123.1 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:113314088 A>G maps to NM_198123.1 L2791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr8:113314055 T>C maps to NM_198123.1 S2802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr8:113694758 T>A maps to NM_198123.1 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:113697737 C>T maps to NM_198123.1 G793G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:113318304 C>A maps to NM_198123.1 E2668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:113353883 T>G maps to NM_198123.1 T2158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:113599316 A>C maps to NM_198123.1 L1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:113349921 G>A maps to NM_198123.1 R2231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:113519056 T>C maps to NM_198123.1 A1586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:114111123 C>A maps to NM_198123.1 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:113348939 G>A maps to NM_198123.1 G2320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:113276012 G>T maps to NM_198123.1 I3239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:113314115 G>T maps to NM_198123.1 I2782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:113392593 A>G maps to NM_198123.1 H2041H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr8:113418768 G>A maps to NM_198123.1 S1931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:113246688 C>A maps to NM_198123.1 E3549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:113649183 G>A maps to NM_198123.1 R1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:114031299 A>G maps to NM_198123.1 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:114326922 C>T maps to NM_198123.1 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:113349921 G>A maps to NM_198123.1 R2231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:113678545 C>A maps to NM_198123.1 E926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr8:113649178 G>A maps to NM_198123.1 I1194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr8:113277715 C>T maps to NM_198123.1 T3204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:113267611 C>A maps to NM_198123.1 E3303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:113318319 G>A maps to NM_198123.1 R2663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:113323348 G>T maps to NM_198123.1 I2581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:113331156 A>G maps to NM_198123.1 C2423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:113314019 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:113314115 G>T maps to NM_198123.1 I2782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:113275988 T>C maps to NM_198123.1 T3247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:113841996 C>A maps to NM_198123.1 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:113318319 G>A maps to NM_198123.1 R2663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr8:113317097 T>C maps to NM_198123.1 R2706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:113259258 A>G maps to NM_198123.1 P3404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:113317112 G>T maps to NM_198123.1 I2701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:113516135 C>A maps to NM_198123.1 G1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:114031325 G>A maps to NM_198123.1 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:70823381 C>T maps to NM_001891.2 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:70823065 C>A maps to NM_001891.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:70823065 C>A maps to NM_001891.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:71115127 G>A maps to NM_005212.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:71114773 T>G maps to NM_005212.2 Y49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:148897433 C>A maps to NM_001025105.1 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:148929645 G>T maps to NM_001025105.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:148891430 G>A maps to NM_001025105.1 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr13:37679198 C>T maps to NM_145203.5 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:37678625 G>A maps to NM_145203.5 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr13:37678766 G>A maps to NM_145203.5 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:80206675 G>T maps to ENST00000269361 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:80203900 G>A maps to NM_139062.1 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:1978656 C>T maps to NM_001319.6 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:1978628 T>A maps to NM_001319.6 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:122881528 C>T maps to NM_001044723.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:122893235 C>T maps to NM_001044723.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:58208381 G>A maps to NM_001896.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:58220656 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:75978009 G>A maps to NM_001897.4 I1274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:75968547 G>A maps to NM_001897.4 P2104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:75968547 G>A maps to NM_001897.4 P2104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:75968739 G>A maps to NM_001897.4 N2040N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:75970056 G>T maps to NM_001897.4 L1707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:75981911 G>A maps to NM_001897.4 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr15:75974768 G>C maps to NM_001897.4 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:75981847 G>A maps to NM_001897.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:75981758 G>T maps to NM_001897.4 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:75969492 G>A maps to NM_001897.4 G1789G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:47618885 G>A maps to ENST00000383738 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:47618828 T>G maps to ENST00000383738 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:47604224 G>T maps to ENST00000383738 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:68084680 T>C maps to ENST00000389042 F983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:68105797 C>T maps to ENST00000389042 R1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:68087595 G>T maps to ENST00000389042 E1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:68102897 G>A maps to ENST00000389042 E1108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:67998306 G>T maps to ENST00000389042 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:68049688 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:68007896 G>T maps to ENST00000389042 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:68044263 G>A maps to ENST00000389042 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr8:67976656 C>G maps to ENST00000389042 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:39186565 C>T maps to NM_033027.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:39185729 C>T maps to NM_033027.3 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:39185750 G>A maps to NM_033027.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr3:39184626 G>T maps to NM_033027.3 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:51467728 G>T maps to NM_030809.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr12:51461453 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:51457918 A>G maps to NM_030809.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:166532997 C>T maps to ENST00000409420 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:166535644 G>A maps to ENST00000409420 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:166535345 C>T maps to ENST00000409420 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:201459431 C>T maps to NM_001193572.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:201459365 G>A maps to NM_001193572.1 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:18123456 G>A maps to NM_020536.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:18143486 C>T maps to NM_020536.4 D523D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:18165370 C>T maps to NM_020536.4 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:18163835 C>T maps to NM_020536.4 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:18123369 G>A maps to NM_020536.4 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr20:18125925 G>A maps to NM_020536.4 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:18165370 C>T maps to NM_020536.4 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:23728512 G>A maps to NM_001898.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr20:23807135 C>T maps to NM_001322.2 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:23614558 G>A maps to NM_000099.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr20:23667796 G>A maps to NM_001899.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:23669456 G>A maps to NM_001899.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:23586495 C>T maps to NM_001008693.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:23586480 C>T maps to NM_001008693.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr20:23549009 G>T maps to NM_080610.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:23548871 G>A maps to NM_080610.2 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:54974177 C>T maps to NM_001033522.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr20:54978734 C>T maps to NM_001033522.1 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:100093335 A>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100087825 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:100075441 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:100088273 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:100078931 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:100081722 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100077363 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:100087825 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:100088262 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100088236 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100075617 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100075461 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100078980 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100081743 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100093316 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:53457764 T>C maps to NM_015235.2 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:53458691 C>T maps to NM_015235.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:53458637 T>A maps to NM_015235.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr11:33123810 A>C maps to NM_001326.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr20:23425442 C>T maps to NM_138283.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:23421108 C>T maps to NM_138283.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr20:23420999 G>A maps to NM_138283.1 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:23421108 C>T maps to NM_138283.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:134948046 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:120009192 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:120008940 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:120008938 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:120008972 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:120009263 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:120008831 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:120009281 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr23:120007854 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:120008783 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:120008812 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:120008795 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:120008907 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:120009294 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:120007854 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:120009410 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr23:120008792 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:120009075 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr23:153880707 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153880741 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153880407 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153880616 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:153880609 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:19995785 T>C maps to NM_172241.2 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr18:19997363 C>T maps to NM_172241.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:19997413 C>A maps to NM_172241.2 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:19996546 C>A maps to NM_172241.2 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:19996876 C>A maps to NM_172241.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V7-01A-21D-A122-09 chr18:19997765 G>A maps to NM_172241.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:19996984 C>A maps to NM_172241.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:39762579 G>T maps to ENST00000396158 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr7:143453989 G>A maps to NM_178561.4 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:1209937 G>T maps to NM_001328.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:126683157 G>T maps to NM_022802.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:126686668 G>A maps to NM_022802.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr10:126683109 G>A maps to NM_022802.2 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:126683166 G>A maps to NM_022802.2 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:126683225 G>A maps to NM_022802.2 R738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr10:126715845 G>A maps to NM_022802.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr10:126716052 G>A maps to NM_022802.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr1:85040032 T>C maps to NM_004388.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:85029017 C>T maps to NM_004388.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr16:67655478 C>T maps to NM_006565.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr16:67645290 C>T maps to NM_006565.3 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr16:67645516 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:67655478 C>T maps to NM_006565.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr16:67660615 C>T maps to NM_006565.3 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:67660563 A>G maps to NM_006565.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:67645269 G>T maps to NM_006565.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:67645068 G>T maps to NM_006565.3 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr16:67662322 C>A maps to NM_006565.3 Y523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:67645272 C>T maps to NM_006565.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:67655478 C>T maps to NM_006565.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr16:67644948 C>T maps to NM_006565.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr16:67655478 C>T maps to NM_006565.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr16:67645272 C>T maps to NM_006565.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr16:67645325 T>A maps to NM_006565.3 Y197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr16:67645326 C>T maps to NM_006565.3 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr16:67655478 C>T maps to NM_006565.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr16:67663366 G>T maps to NM_006565.3 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr16:67662337 C>A maps to NM_006565.3 C528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr16:67663299 G>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr16:67645167 G>T maps to NM_006565.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr16:67655478 C>T maps to NM_006565.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:67670645 G>T maps to NM_006565.3 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr20:56090776 C>T maps to ENST00000423479 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:56098277 G>T maps to ENST00000423479 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:56089747 G>A maps to ENST00000423479 S410S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AX-A0J1-01A-11W-A062-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:56073638 G>T maps to ENST00000423479 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr20:56094332 G>A maps to ENST00000423479 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:56090880 A>G maps to ENST00000423479 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:56073644 G>A maps to ENST00000423479 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:56099209 C>A maps to ENST00000423479 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr20:56094424 C>A maps to ENST00000423479 G255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:77472970 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr18:77464900 C>T maps to NM_004715.3 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:219269108 C>T maps to NM_021198.1 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr12:58217770 G>A maps to NM_005730.3 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:37988584 C>T maps to NM_001008392.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:38009354 C>T maps to NM_001008392.1 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr6:132271193 G>A maps to NM_001901.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:132270667 G>T maps to NM_001901.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:70896051 T>C maps to NM_001902.5 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:70899533 G>T maps to NM_001902.5 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:70883707 G>T maps to NM_001902.5 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:104388141 T>C maps to NM_138455.2 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:204736210 G>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:138145785 C>T maps to ENST00000355078 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:138223277 G>T maps to ENST00000355078 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:138147922 G>T maps to ENST00000355078 G174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:138163316 C>T maps to ENST00000355078 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr5:138269726 C>T maps to ENST00000355078 H913H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:138117610 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:138240091 C>T maps to ENST00000355078 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:138160458 G>T maps to ENST00000355078 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:138240091 C>T maps to ENST00000355078 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:80846322 G>A maps to ENST00000402739 P848P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:80808839 G>T maps to ENST00000402739 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:80136805 C>T maps to ENST00000402739 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:80136811 G>A maps to ENST00000402739 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:80874783 C>A maps to ENST00000402739 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:80874922 C>T maps to ENST00000402739 R930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:80874922 C>T maps to ENST00000402739 R930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:80874922 C>T maps to ENST00000402739 R930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:80801342 C>T maps to ENST00000402739 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:80874765 C>T maps to ENST00000402739 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:67748547 C>A maps to NM_013266.2 G723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:68040263 T>G maps to NM_013266.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:69366750 C>T maps to NM_013266.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr10:67680275 G>A maps to NM_013266.2 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:69366750 C>T maps to NM_013266.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:68138967 G>A maps to NM_013266.2 Y558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:111745571 G>A maps to NM_003798.2 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:111727765 T>A maps to NM_003798.2 K495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:111761527 C>T maps to NM_003798.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:111739243 C>A maps to NM_003798.2 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:111741631 C>A maps to NM_003798.2 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:41268791 C>T maps to NM_001904.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:41267192 C>A maps to NM_001904.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:41266526 G>A maps to NM_001904.3 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:41275177 G>A maps to NM_001904.3 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:41275150 C>T maps to NM_001904.3 C439C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:41277267 C>T maps to NM_001904.3 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:41280694 A>G maps to NM_001904.3 E736E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr20:36396409 G>A maps to NM_030877.3 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:36488302 C>T maps to NM_030877.3 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr20:36374972 C>T maps to NM_030877.3 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:36431391 C>A maps to NM_030877.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr20:36405791 C>T maps to NM_030877.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr20:36431371 T>C maps to NM_030877.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr20:36431374 C>T maps to NM_030877.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:36406089 C>T maps to NM_030877.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr11:57573394 T>A maps to NM_001085458.1 Y588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:57561553 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:57569303 C>T maps to NM_001085458.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:57574423 G>T maps to NM_001085458.1 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:57559066 G>A maps to NM_001085458.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:57576002 G>T maps to NM_001085458.1 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr11:57577602 C>T maps to NM_001085458.1 R820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:57577668 G>T maps to NM_001085458.1 E842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:57575860 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr5:11018171 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr5:11199623 G>T maps to NM_001332.2 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:10981911 C>T maps to NM_001332.2 A1130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:11346683 G>A maps to NM_001332.2 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:11117663 G>A maps to NM_001332.2 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:11364814 C>T maps to NM_001332.2 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr5:11098725 C>T maps to NM_001332.2 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:11117570 G>A maps to NM_001332.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:11411747 G>A maps to NM_001332.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr5:11082829 G>A maps to NM_001332.2 D922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:11411747 G>A maps to NM_001332.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:11384921 C>T maps to NM_001332.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr5:11346574 C>A maps to NM_001332.2 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:11082811 G>T maps to NM_001332.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr5:11022918 G>A maps to NM_001332.2 I987I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:3560043 G>A maps to NM_001031681.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:3563593 C>T maps to NM_001031681.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr17:3563641 G>C maps to NM_001031681.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:41463064 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:41467862 C>T maps to NM_001905.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:41454291 A>G maps to NM_001905.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:41463116 G>A maps to NM_001905.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:41471750 G>A maps to NM_001905.2 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:16717205 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:16657015 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:16635271 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:16707600 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:16717109 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:16717106 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:16701277 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:16709722 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:16711538 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:16657301 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:16685814 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:16696534 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:16711511 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:16717110 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:10785275 A>G maps to NM_014633.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:10788009 G>A maps to NM_014633.3 W553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr11:10797147 G>A maps to NM_014633.3 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:10789902 C>A maps to NM_014633.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:10774235 C>T maps to NM_014633.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:75252931 C>T maps to NM_001906.4 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:75238124 C>T maps to NM_001025200.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:75239657 C>T maps to NM_001025200.3 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:15771138 C>T maps to NM_007272.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:15764986 G>A maps to NM_007272.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:15768951 G>A maps to NM_007272.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:15769967 C>T maps to NM_007272.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr1:15770021 C>T maps to NM_007272.2 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:15767059 C>T maps to NM_007272.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:67965042 C>T maps to NM_001907.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:44520656 C>T maps to NM_000308.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:88033706 G>A maps to NM_001814.4 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:88033767 C>T maps to NM_001814.4 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr11:1782694 G>A maps to NM_001909.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:206319111 C>T maps to ENST00000361052 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:206317645 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:66333157 C>T maps to NM_003793.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:66335103 G>A maps to NM_003793.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:79220054 G>A maps to NM_004390.3 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:79215423 A>G maps to NM_004390.3 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:150769330 G>A maps to NM_000396.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:150776716 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:99795308 C>T maps to NM_001333.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr9:99799009 C>T maps to NM_001333.2 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:156858607 C>A maps to NM_001334.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:156864326 C>T maps to NM_001334.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:57572772 C>A maps to NM_001336.3 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr20:57571798 T>C maps to NM_001336.3 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:70281135 C>T maps to NM_001184740.1 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:70265909 C>T maps to NM_001184740.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:70269061 C>T maps to NM_001184740.1 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr11:70263162 C>T maps to NM_001184740.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr11:70279798 C>T maps to NM_001184740.1 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:70260673 G>A maps to NM_001184740.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:117365130 C>T maps to NM_033427.2 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:117501334 G>A maps to NM_033427.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr7:117364736 G>A maps to NM_033427.2 S1437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:117374986 G>A maps to NM_033427.2 R1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:117432673 G>A maps to NM_033427.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:117422917 G>A maps to NM_033427.2 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:117431530 C>T maps to NM_033427.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:117431605 T>C maps to NM_033427.2 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:112999001 G>A maps to NM_018704.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:112998950 T>G maps to NM_018704.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:112998695 C>T maps to NM_018704.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:112998575 G>T maps to NM_018704.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:112998845 C>T maps to NM_018704.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:88781327 G>A maps to ENST00000378384 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr10:16877010 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:17156068 A>G maps to NM_001081.3 C280C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:17113966 G>A maps to NM_001081.3 R769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:17156056 T>C maps to NM_001081.3 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:16883019 C>T maps to NM_001081.3 A3230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:17113892 A>G maps to NM_001081.3 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:16870881 T>G maps to NM_001081.3 G3562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:16882950 C>T maps to NM_001081.3 T3253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:17032428 G>T maps to NM_001081.3 I1418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:17153023 G>A maps to NM_001081.3 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr10:17153023 G>A maps to NM_001081.3 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr10:16996472 G>A maps to NM_001081.3 I1590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:17110270 C>A maps to NM_001081.3 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:16918914 C>T maps to NM_001081.3 K3029K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:16893410 T>C maps to NM_001081.3 T3162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:104183455 G>A maps to NM_024040.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr10:104183302 G>T maps to NM_024040.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:104183287 C>G maps to NM_024040.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:148495738 C>T maps to NM_003592.2 N702N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr7:148486914 A>G maps to NM_003592.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:148495741 C>T maps to NM_003592.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:148494941 G>A maps to NM_003592.2 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr10:35343421 C>T maps to NM_001198778.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:35327865 G>A maps to NM_001198778.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:35320511 T>C maps to NM_001198778.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:35360155 G>A maps to NM_001198778.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:35327919 G>A maps to NM_001198778.1 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:225368526 C>A maps to NM_003590.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:225422404 C>A maps to NM_003590.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:225379336 G>A maps to NM_003590.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:225422408 T>G maps to NM_003590.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr2:225376110 A>G maps to NM_003590.3 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:113898761 G>T maps to NM_001008895.1 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:113897448 A>G maps to NM_001008895.1 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:113887601 C>T maps to NM_001008895.1 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:119681007 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119664033 T>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:119680465 G>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:119668438 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:119664025 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:119694053 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:119677648 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:119674362 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:119678367 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:119694088 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:119672055 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119664036 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119670795 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119679337 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119680991 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:119678398 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:119691869 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:119677987 T>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:119691831 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:119672045 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:119677972 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:119691815 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:119694269 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:119675502 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr6:43015921 G>A maps to NM_001168370.1 C795C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:43008396 G>A maps to NM_001168370.1 N1382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:43020439 G>A maps to NM_001168370.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:43010620 C>T maps to NM_001168370.1 G1272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:43013765 G>A maps to NM_001168370.1 C992C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:43017321 G>A maps to NM_001168370.1 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:43018849 G>A maps to NM_001168370.1 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:43014722 T>C maps to NM_001168370.1 G848G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:43013125 C>T maps to NM_001168370.1 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:43006701 G>A maps to NM_001168370.1 R1524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:43192056 G>A maps to ENST00000354495 W2477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:43181574 C>A maps to ENST00000354495 L1871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:43154798 G>T maps to ENST00000354495 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:43155032 G>A maps to ENST00000354495 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:43166399 C>T maps to ENST00000354495 R953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:43153219 C>T maps to ENST00000354495 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr6:43180996 C>T maps to ENST00000354495 Q1775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:43190596 C>T maps to ENST00000354495 N2372N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:43189421 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr6:43153209 C>T maps to ENST00000354495 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:101870947 C>T maps to ENST00000360264 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:101845210 C>A maps to ENST00000360264 Y889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:101870947 C>T maps to ENST00000360264 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:101758500 C>T maps to ENST00000360264 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:101845021 C>T maps to ENST00000360264 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:101923409 C>A maps to NM_001913.2 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:101845198 G>A maps to ENST00000360264 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:101758500 C>T maps to ENST00000360264 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:101813740 C>T maps to ENST00000360264 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:101845339 G>A maps to ENST00000360264 K932K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:101870842 C>A maps to ENST00000360264 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr7:101459345 G>A maps to ENST00000360264 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:101840428 G>T maps to ENST00000360264 G591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:101758500 C>T maps to ENST00000360264 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:101821816 C>T maps to ENST00000360264 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:101758500 C>T maps to ENST00000360264 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:101747647 C>T maps to ENST00000360264 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:101758500 C>T maps to ENST00000360264 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:101758539 G>T maps to ENST00000360264 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:111731340 C>A maps to NM_015267.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:111785565 C>T maps to NM_015267.3 Q1300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:111747899 C>A maps to NM_015267.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:111749988 C>T maps to NM_015267.3 I662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:124596455 G>A maps to NM_022034.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:124598704 G>T maps to NM_022034.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:180837940 C>T maps to NM_020943.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:64077802 C>T maps to NM_005869.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr5:64081366 C>T maps to NM_005869.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:102019993 A>G maps to NM_018294.4 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:107197779 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:107309825 C>T maps to NM_152434.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:107299924 C>A maps to NM_152434.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr11:107312294 T>C maps to NM_152434.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:107197722 T>C maps to NM_152434.2 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:107326465 C>A maps to NM_152434.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:107299909 C>A maps to NM_152434.2 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:48990561 G>T maps to NM_025087.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr4:49005767 G>A maps to NM_025087.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:49005924 G>T maps to NM_025087.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:57416022 C>T maps to NM_002996.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:57413564 G>A maps to NM_002996.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr16:57416763 C>T maps to NM_002996.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr3:39307901 G>A maps to NM_001171174.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:18924065 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:18933713 G>A maps to NM_001338.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:18933713 G>A maps to NM_001338.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr21:18919423 C>A maps to NM_001338.3 C41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:44876227 G>A maps to NM_001178134.1 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:134914146 C>T maps to NM_004887.4 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:74904125 C>T maps to NM_002090.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr4:74863730 G>A maps to NM_002994.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:74864017 G>A maps to NM_002994.3 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:219029292 C>T maps to NM_000634.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:219029604 G>A maps to NM_000634.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:218999670 T>C maps to NM_001168298.1 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:218999757 C>T maps to NM_001168298.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70836419 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70836819 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70836482 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70837168 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70836765 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:136872636 G>A maps to NM_001008540.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr3:45988222 C>T maps to NM_006564.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:45988383 C>T maps to NM_006564.1 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:237489596 C>T maps to NM_020311.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:237489992 G>A maps to NM_020311.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:237489773 C>T maps to NM_020311.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr18:47810329 G>C maps to NM_001101654.1 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:47810827 G>A maps to NM_001101654.1 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:139060957 C>T maps to NM_016463.7 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:144909317 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:144909393 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:144909376 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:144909301 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:144909265 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:30577667 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:30577774 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:30577795 A>G did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:30578218 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:30578029 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:30578161 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:30578159 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:30578412 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:30578106 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:35944154 C>G did not map to a codon.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr23:35937959 G>C did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:35974223 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:35985906 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:35988962 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:35989994 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:36007509 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:35969452 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:35970049 A>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:36007544 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:35944224 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:35944256 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:35988962 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:35985782 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:35993331 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:35944220 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:35989838 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:35993379 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:35993953 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:35969314 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:19948030 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:19947946 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:19973527 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19954004 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19984508 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19984665 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:19983365 T>G did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:19948034 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:19983403 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:19947909 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:19968951 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:19983323 T>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:19971140 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:19984323 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:19984267 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:19953994 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:19984653 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:19973550 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:75395383 A>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:75393001 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:75397502 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr23:75393430 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:37850306 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:37850191 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:37850415 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:37850248 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:37850106 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:37850251 C>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:45010960 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:45059967 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:45017096 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:45059948 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:45059855 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:45016980 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:45011127 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:45059985 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:40495961 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:40496358 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:40495819 G>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:40496265 A>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:40506328 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:40506316 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:40498356 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:148627336 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:148628450 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:148627413 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:149100950 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:149101942 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:149100979 C>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:149101854 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:106486501 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:106482151 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:106482155 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:106462193 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134303683 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118694245 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118694272 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:118694250 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:118676495 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:118675326 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:105891581 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:105868321 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105855603 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105855825 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105868321 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105876235 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105905326 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105921475 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:105855621 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:105905497 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:105905512 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:105865978 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:105882827 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:105921400 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:105883928 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:105905369 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:105876194 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:105855560 G>A did not map to a codon.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr23:105921449 T>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105855797 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105876194 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105876202 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105881034 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105905267 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:105855314 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:105855549 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:105879860 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:105881005 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:105881010 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:105855562 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:105881027 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:105912551 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:105868403 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:105905389 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:105905402 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:105868418 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:105881242 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:105905502 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:23953451 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:23953446 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:23934379 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:23956733 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:23934435 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:23953311 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr23:23929943 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:23953416 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:23953496 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:36091443 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:36091427 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:36122750 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:36162888 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:36091375 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:36156139 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:36103567 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:36156103 A>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:36103593 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr23:36103589 A>G did not map to a codon.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr23:70323921 C>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70323842 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70324244 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:70324254 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70323891 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr23:70324226 A>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:70325978 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr23:139038877 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:139038643 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:139038862 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:139047630 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:139040346 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:139038148 T>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:139040284 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:139038330 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:71920857 G>A maps to NM_148923.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:7762001 C>T maps to NM_144607.4 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:4047150 C>A maps to NM_144611.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:7687715 G>A maps to NM_016229.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:43023623 G>A maps to NM_001171660.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:43026905 G>A maps to NM_001171660.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:84646063 C>T maps to NM_016230.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:84573932 C>T maps to NM_016230.3 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:84634261 T>C maps to NM_016230.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:84665136 C>T maps to NM_016230.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:84618768 C>T maps to NM_016230.3 C124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:84603247 T>G maps to NM_016230.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:84646048 C>T maps to NM_016230.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:54656536 G>A maps to NM_001031672.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:37655331 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:37655374 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:37655331 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:37665641 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr23:37660562 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:37641427 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:37664263 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:37664375 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:37641411 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:37658232 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:37663302 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:37668881 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:37664351 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:37658212 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:37641411 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:37670098 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:22958213 G>A maps to NM_014608.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:22947061 C>T maps to NM_014608.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:22999493 C>T maps to NM_014608.2 D1122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:22956139 G>A maps to NM_001033028.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:22962517 C>T maps to NM_014608.2 Y746Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr15:22947028 G>A maps to NM_014608.2 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:22929781 C>T maps to NM_014608.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:22956551 C>T maps to NM_014608.2 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:22947031 C>T maps to NM_014608.2 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:22935948 C>T maps to NM_014608.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:156742095 C>T maps to ENST00000442283 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:156816393 C>T maps to ENST00000442283 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:156731325 C>T maps to ENST00000442283 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:156746873 C>A maps to ENST00000442283 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:156752563 C>T maps to ENST00000442283 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:156809614 C>T maps to ENST00000442283 C1044C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:156752580 C>T maps to ENST00000442283 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:156747678 C>T maps to ENST00000442283 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:156766138 C>T maps to ENST00000442283 F845F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:156786059 C>T maps to ENST00000442283 F932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:156766114 T>C maps to ENST00000442283 C837C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:156752629 G>T maps to ENST00000442283 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr5:156736773 C>T maps to ENST00000442283 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:156788521 C>T maps to ENST00000442283 Y1010Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:156757851 C>T maps to ENST00000442283 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr5:156810345 C>T maps to ENST00000442283 I1087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:74524662 C>T maps to NM_134268.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:145678819 G>A maps to NM_138496.1 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr23:83128724 T>A did not map to a codon.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr23:83129491 G>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:83127950 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:83128849 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:83128049 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:83126481 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:83129607 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr23:83128278 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:83128869 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:83129528 G>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:83128319 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:83124909 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:83128545 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:83129149 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:83128834 A>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:83129221 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:83129599 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr23:83128233 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83128848 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83129559 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:83128585 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr23:83128424 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:83126507 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:83128295 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:83129418 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:83128139 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:83129110 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:83129552 G>T did not map to a codon.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr23:83129138 A>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:105767843 G>T maps to NM_001340.3 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:105767843 G>T maps to NM_001340.3 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:105767470 G>A maps to NM_001340.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:105767866 T>C maps to NM_001340.3 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:50827514 C>T maps to ENST00000311559 Y803Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:50815308 C>T maps to ENST00000311559 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:50788327 C>A maps to ENST00000311559 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:50818326 G>A maps to ENST00000311559 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:50826527 T>C maps to ENST00000311559 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:74631643 G>T maps to NM_000781.2 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:74635343 C>A maps to NM_000781.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:143956375 G>A maps to ENST00000377675 H536H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr8:143957665 G>A maps to ENST00000377675 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:143994843 C>T maps to NM_000498.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:143994101 G>A maps to NM_000498.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr8:143994294 G>A maps to NM_000498.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:143999217 C>T maps to NM_000498.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:143993987 C>T maps to NM_000498.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr8:143994059 C>T maps to NM_000498.3 W428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:104593879 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr10:104595134 G>A maps to NM_000102.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:51504630 G>A maps to NM_031226.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:51503043 G>A maps to NM_031226.2 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:51503190 G>A maps to NM_031226.2 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:51519993 G>A maps to NM_031226.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:51503244 A>G maps to NM_031226.2 Y424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr15:51503005 T>C maps to NM_031226.2 *504W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr15:51535147 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:51507952 C>A maps to NM_031226.2 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:51510852 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:51535061 G>A maps to NM_031226.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:51510841 G>A maps to NM_031226.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:51507429 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr15:51503147 G>A maps to NM_031226.2 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:51520006 G>T maps to NM_031226.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:75012937 C>A maps to NM_000499.3 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:75014697 G>T maps to NM_000499.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:75014766 G>A maps to NM_000499.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:75047404 G>A maps to NM_000761.3 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:75042294 C>T maps to NM_000761.3 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:75042138 C>T maps to NM_000761.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr15:75042756 C>T maps to NM_000761.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:75044589 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:204143339 C>T maps to ENST00000429815 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:204103793 C>T maps to ENST00000429815 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:204131376 C>A maps to ENST00000429815 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:32006261 C>T maps to NM_000500.5 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:32008269 C>T maps to NM_000500.5 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:52786191 G>T maps to NM_000782.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:94834663 G>T maps to NM_000783.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:94835696 C>T maps to NM_000783.3 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:94836453 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:94836751 C>A maps to NM_000783.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:94836818 C>T maps to NM_000783.3 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:94836760 C>T maps to NM_000783.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:94834925 C>A maps to NM_000783.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:94836902 G>T maps to NM_000783.3 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:72371270 C>T maps to NM_019885.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:72362545 G>T maps to NM_019885.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:72362422 C>T maps to NM_019885.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:94821196 C>T maps to NM_183374.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:219677435 C>T maps to NM_000784.3 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:219677692 G>A maps to NM_000784.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:219679180 C>T maps to NM_000784.3 N421N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:219677013 G>A maps to NM_000784.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:58157495 A>G maps to NM_000785.3 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:58158201 G>A maps to NM_000785.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:58157399 C>T maps to NM_000785.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:58157561 A>G maps to NM_000785.3 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:127944888 C>T maps to NM_001001665.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:127953002 C>T maps to NM_001001665.3 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr2:127957047 G>A maps to NM_001001665.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:41596348 C>A maps to NM_000766.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:41601806 G>A maps to NM_000766.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:41601773 C>T maps to NM_000766.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:41601806 G>A maps to NM_000766.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:41596372 C>A maps to NM_000766.3 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr19:41597680 A>G maps to NM_000766.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:41595952 C>T maps to NM_000766.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:41354258 G>A maps to NM_000762.5 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:41354519 G>A maps to NM_000762.5 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:41356316 C>T maps to NM_000762.5 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:41351384 G>A maps to NM_000762.5 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:41382432 G>A maps to NM_000764.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:41510242 C>T maps to NM_000767.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:41512846 T>C maps to NM_000767.4 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:41497255 T>C maps to NM_000767.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:96493101 G>T maps to NM_000772.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:96495179 G>A maps to NM_000772.2 Q484Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:96454722 G>T maps to NM_000772.2 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:96612637 G>A maps to NM_000769.1 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:96540334 C>T maps to NM_000769.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:96580251 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:96818109 G>A maps to NM_000770.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:96740961 A>G maps to NM_000771.3 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:96702082 T>C maps to NM_000771.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:96702069 C>T maps to NM_000771.3 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr10:96701612 A>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:42523475 G>A maps to NM_000106.4 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:42523523 A>G maps to NM_000106.4 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:135347315 C>T maps to NM_000773.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:135352425 T>C maps to NM_000773.3 C480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:135350580 G>T maps to NM_000773.3 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:41627950 C>T maps to NM_000774.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:41622224 G>A maps to NM_000774.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:41627441 C>T maps to NM_000774.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:41627429 C>T maps to NM_000774.3 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr19:41627959 C>T maps to NM_000774.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:41627441 C>T maps to NM_000774.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:60375466 C>A maps to NM_000775.2 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:14902248 G>A maps to NM_024514.4 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:14901945 G>A maps to NM_024514.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:14901868 C>T maps to NM_024514.4 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:41704376 C>T maps to ENST00000301173 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:108866285 C>A maps to NM_183075.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:108868530 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:1024865 C>T maps to NM_017781.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:46604149 A>G maps to NM_016593.3 C236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:46609956 G>A maps to NM_016593.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr6:46593167 C>A maps to NM_016593.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:99361561 G>T maps to NM_017460.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:99364821 C>A maps to NM_017460.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:99441835 G>T maps to NM_022820.3 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:99247698 T>C maps to NM_000777.3 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:99250279 G>T maps to NM_000777.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:99250279 G>T maps to NM_000777.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:99250279 G>A maps to NM_000777.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:99270240 G>A maps to NM_000777.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:99293366 A>G maps to ENST00000292414 *534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:99293454 C>T maps to ENST00000292414 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:100157468 C>T maps to NM_006668.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:100157429 A>C maps to NM_006668.1 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:100158179 G>A maps to NM_006668.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:100184454 C>T maps to NM_006668.1 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:47399669 G>T maps to ENST00000371904 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:47610364 C>A maps to NM_001010969.2 C347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:47611553 C>T maps to NM_001010969.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:47279203 C>T maps to NM_001099772.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr1:47264758 G>A maps to NM_001099772.1 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr19:16034636 C>T maps to NM_021187.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:16033228 C>A maps to NM_021187.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:16032883 C>A maps to NM_021187.3 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:16032911 G>A maps to NM_021187.3 Y350Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:15795878 C>T maps to NM_023944.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:15791166 C>T maps to ENST00000430608 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:15806986 C>T maps to NM_023944.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:15791262 C>T maps to NM_023944.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:15784425 G>A maps to NM_023944.2 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:15791203 G>T maps to NM_023944.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:15784392 A>G maps to NM_023944.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:15807843 C>T maps to NM_023944.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:16003354 G>A maps to NM_001082.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15989637 C>T maps to NM_001082.3 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15989715 C>T maps to NM_001082.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:16000448 T>C maps to NM_001082.3 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:16001216 C>T maps to NM_001082.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:15659952 C>A maps to NM_173483.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:15636254 C>T maps to NM_173483.3 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr19:15661568 T>A did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:15636257 C>A maps to NM_173483.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:15752389 G>A maps to NM_000896.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:15770098 C>T maps to NM_000896.2 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:15763420 G>T maps to NM_000896.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:15770176 G>A maps to NM_000896.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:15740053 G>A maps to NM_007253.3 A482A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:187130245 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:187118183 A>G maps to NM_207352.3 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:187115702 G>A maps to NM_207352.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:187131687 G>T maps to NM_207352.3 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:47501569 C>T maps to NM_178033.1 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:47505192 T>G maps to NM_178033.1 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:47550417 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:47533218 C>T maps to NM_178134.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:91755741 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:59404923 G>A maps to NM_000780.3 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:59409434 G>A maps to NM_000780.3 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr8:59409581 G>A maps to NM_000780.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:65527637 C>T maps to NM_004820.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr8:65537089 G>A maps to NM_004820.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:65537020 G>A maps to NM_004820.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:42916579 G>A maps to NM_004391.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:86048228 C>T maps to NM_001554.4 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:77528355 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:77528305 G>T did not map to a codon.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr23:77528546 C>T did not map to a codon.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr23:77528310 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:77528305 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:77528382 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:77528768 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:77528340 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:77528768 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:77528659 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:49281756 C>T maps to NM_020377.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:49281634 C>T maps to NM_020377.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr13:49281357 G>A maps to NM_020377.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:76694945 G>A maps to NM_004762.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:76705779 T>C maps to NM_004762.2 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:76696473 C>T maps to NM_004762.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr17:76705745 G>A maps to NM_004762.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:76672180 G>A maps to NM_004762.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:48981747 C>T maps to NM_017457.4 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr7:6205174 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:6217518 G>A maps to ENST00000396741 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:6213282 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:6210863 G>T maps to ENST00000396741 C177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:6210229 G>A maps to ENST00000396741 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:37705302 C>T maps to NM_013385.3 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:37707080 C>T maps to NM_013385.3 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:37690747 C>T maps to NM_013385.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:37705260 C>T maps to NM_013385.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:37690747 C>T maps to NM_013385.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr22:37688717 C>A maps to NM_013385.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:37695290 C>T maps to NM_013385.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:37707080 C>T maps to NM_013385.3 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:158290932 C>T maps to NM_004288.4 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:158272656 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:5016913 G>A maps to NM_018659.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr4:5021019 C>T maps to NM_018659.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:5016952 T>C maps to NM_018659.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:27945214 C>T maps to ENST00000435845 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:242695406 C>T maps to NM_152783.3 H428H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:242690742 C>T maps to NM_152783.3 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:242690745 G>A maps to NM_152783.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:242689644 G>A maps to NM_152783.3 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:242694717 C>T maps to ENST00000445308 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:4418990 G>A maps to NM_001040101.1 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:59827538 G>T maps to NM_014992.1 E895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:59814307 A>G maps to NM_014992.1 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:59830500 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr14:59798625 T>C maps to NM_014992.1 Y652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:59792770 C>T maps to NM_014992.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr14:59793360 A>G maps to NM_014992.1 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:39828730 C>T maps to ENST00000398904 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr6:39864592 C>T maps to ENST00000398904 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:39839296 C>T maps to ENST00000398904 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr1:57537314 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:57480661 G>T maps to ENST00000371231 Y479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:57481087 G>A maps to ENST00000371231 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:57602293 A>C maps to ENST00000371231 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:57480925 G>A maps to ENST00000371231 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:57602266 G>T maps to ENST00000371231 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:57536734 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:39383331 G>A maps to NM_001343.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:39383331 G>A maps to NM_001343.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:39390599 G>A maps to NM_001343.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:39377262 C>T maps to NM_001343.2 Q542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:39382758 T>C maps to NM_001343.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:39393353 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:39377025 C>T maps to NM_001343.2 Q621Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:39393353 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:39376970 A>G maps to NM_001343.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:39392517 G>A maps to NM_001343.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr9:124544690 C>T maps to ENST00000408936 Q1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:124543793 G>A maps to ENST00000408936 A1122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:124530908 G>A maps to ENST00000408936 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:124528907 G>A maps to ENST00000408936 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:124530833 C>T maps to ENST00000408936 F607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:124534909 G>A maps to ENST00000408936 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr9:124532971 C>T maps to ENST00000408936 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:72204775 T>C maps to ENST00000359684 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr13:72131219 G>T maps to ENST00000359684 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:72063206 T>C maps to ENST00000359684 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:72204835 G>A maps to ENST00000359684 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:86069813 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:86071062 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:85906094 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:85950159 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:85950178 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:86068033 A>G did not map to a codon.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr23:85994746 C>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:85403893 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:85404095 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:86067999 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:85769310 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:85994752 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:85403713 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:85994831 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr23:85769337 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:85969667 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:85994793 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:85994849 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:85403959 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:85906105 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:86067985 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr23:85969555 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:85404095 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:85769307 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:86067985 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:59113576 C>T maps to NM_016651.5 Q746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:59112996 G>A maps to NM_016651.5 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr14:59113011 C>T maps to NM_016651.5 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:59112126 C>T maps to NM_016651.5 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:59107452 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr14:59105201 G>A maps to NM_016651.5 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr14:59112423 C>T maps to NM_016651.5 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:47151909 G>A maps to NM_145056.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:23044070 G>A maps to NM_001344.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:49568960 G>T maps to NM_004393.4 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:61507976 C>T maps to NM_006133.2 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:61507115 C>T maps to NM_006133.2 H612H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:61504724 C>A maps to NM_006133.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:61511570 C>T maps to NM_006133.2 F913F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:61490400 C>T maps to NM_006133.2 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:61508003 C>A maps to NM_006133.2 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:6485656 G>T maps to NM_139179.3 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr7:6474419 C>A maps to NM_139179.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:6485716 C>T maps to NM_139179.3 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr7:6487452 G>A maps to NM_139179.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:6464451 C>T maps to NM_139179.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:6449536 G>A maps to NM_139179.3 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:61113016 C>T maps to NM_015533.3 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:61110817 C>T maps to NM_015533.3 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:61111617 G>A maps to NM_015533.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:61109939 C>T maps to NM_015533.3 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49053773 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:13080764 C>A maps to NM_152654.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr12:109292544 C>A maps to NM_001917.4 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:10748342 A>G maps to ENST00000432074 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr1:155697426 T>C maps to NM_004632.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr9:90321975 C>T maps to NM_004938.2 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:90322149 C>T maps to NM_004938.2 A1388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:90252869 C>T maps to NM_004938.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr9:90296404 G>A maps to NM_004938.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:90315134 C>T maps to NM_004938.2 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:90321474 C>T maps to NM_004938.2 G1163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr9:90263766 C>T maps to NM_004938.2 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr9:90321195 G>A maps to NM_004938.2 Q1070Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:90254709 C>T maps to NM_004938.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:90252977 C>T maps to NM_004938.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:90255342 A>C maps to NM_004938.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:90301580 G>A maps to NM_004938.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:90321726 G>A maps to NM_004938.2 E1247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:90322002 C>T maps to NM_004938.2 L1339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr9:90312006 G>T maps to NM_004938.2 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr15:64218225 C>T maps to NM_014326.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:64218249 T>C maps to NM_014326.3 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3964296 G>A maps to NM_001348.1 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:3964802 G>A maps to NM_001348.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:3964314 G>A maps to NM_001348.1 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:159175858 C>T maps to NM_001122951.2 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:159176128 G>A maps to NM_001122951.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:159175381 C>T maps to NM_001122951.2 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:159175867 C>T maps to NM_001122951.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:159176212 T>C maps to NM_001122951.2 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:136678116 A>G maps to NM_001349.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:136670054 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:136670076 G>T maps to NM_001349.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:173825847 T>C maps to NM_018122.4 Y573Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:173822992 C>T maps to NM_018122.4 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:173797500 C>T maps to NM_018122.4 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:173797500 C>T maps to NM_018122.4 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:173803638 G>A maps to NM_018122.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:173826728 C>T maps to NM_018122.4 F608F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr1:173808503 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:33287596 T>C maps to NM_001350.4 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:1418239 C>T maps to NM_018959.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:1421250 C>T maps to NM_018959.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:1418717 G>A maps to NM_018959.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:16638328 G>A maps to NM_001190811.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:16640062 C>A maps to NM_001190811.1 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:16639612 G>A maps to NM_001190811.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:122011300 G>A maps to NM_014618.2 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:121929448 G>A maps to NM_014618.2 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:121930363 G>A maps to NM_014618.2 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:121930270 G>A maps to NM_014618.2 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:121929448 G>A maps to NM_014618.2 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:121929910 G>A maps to NM_014618.2 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr9:121929406 C>T maps to NM_014618.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:121976400 C>A maps to NM_014618.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:121930339 G>A maps to NM_014618.2 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:87537117 T>G maps to NM_006716.3 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:87514368 T>C maps to NM_006716.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:87516681 G>A maps to NM_006716.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr7:87530114 A>G maps to NM_006716.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:87514426 C>A maps to NM_006716.3 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr7:87516166 A>G maps to NM_006716.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr7:87530093 C>T maps to NM_006716.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:42824478 C>T maps to NM_145663.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:42818793 G>C maps to NM_145663.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:42824543 C>T maps to NM_145663.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:42818787 C>T maps to NM_145663.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:136516805 C>T maps to NM_000787.3 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:136507510 C>T maps to NM_000787.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr9:136522344 C>T maps to NM_000787.3 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr9:136501570 G>T maps to NM_000787.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr9:136501720 C>G maps to NM_000787.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr9:136508629 C>T maps to NM_000787.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:176887451 C>T maps to ENST00000393565 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:176893958 C>T maps to ENST00000393565 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:176887487 G>A maps to ENST00000393565 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:176894493 G>A maps to ENST00000393565 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:44037484 C>T maps to NM_001048225.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr7:44092470 C>A maps to NM_001122956.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr19:49134210 C>T maps to NM_001352.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:137893550 C>T maps to NM_016216.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:137881150 A>G maps to NM_016216.3 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:100706416 T>C maps to NM_001918.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:20180779 G>A maps to ENST00000227256 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:20178226 G>A maps to ENST00000227256 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:20180779 G>A maps to ENST00000227256 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:20180779 G>A maps to ENST00000227256 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:20180779 G>A maps to ENST00000227256 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:45410402 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:37861175 C>T maps to NM_024345.3 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr9:37819290 G>A maps to NM_024345.3 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr9:37861384 G>T maps to NM_024345.3 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:24588954 C>A maps to NM_025230.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:24586200 A>G maps to NM_025230.4 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:34093292 G>A maps to NM_015397.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:125686022 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:125686435 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:125685910 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:125685724 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:125685929 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:125686009 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:125685937 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:125686196 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:125686339 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:125686450 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:125686088 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:125685419 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:125686026 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:125686196 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:125686188 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:125686553 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr23:125685919 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:125299368 G>C did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:125299579 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:125298630 T>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:125299120 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:125299240 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:125298868 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:125299012 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:125298810 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:125299765 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:125298578 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:125298987 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:125299058 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:125299550 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:125298550 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:125299113 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:125298969 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:125298774 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:125298904 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:125298867 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:104432547 A>C maps to NM_015420.6 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:104432504 T>C maps to NM_015420.6 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:14065240 C>A maps to NM_138353.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:14065246 A>G maps to NM_138353.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:17805503 G>A maps to NM_017741.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:17805493 G>A maps to NM_017741.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:17805493 G>A maps to NM_017741.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr4:17805218 C>T maps to NM_017741.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:172336549 T>G maps to NM_025000.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:172337623 A>C maps to NM_025000.3 *521Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:172330393 G>T maps to NM_025000.3 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:73409753 C>T maps to NM_015604.3 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:73418568 C>T maps to NM_015604.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr14:73404733 C>T maps to NM_015604.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:73409753 C>T maps to NM_015604.3 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:41983827 C>T maps to NM_001029955.3 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:41984888 G>A maps to NM_001029955.3 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr8:88885122 C>T maps to NM_152418.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:88885962 C>T maps to NM_152418.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr8:88885716 C>T maps to NM_152418.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:88885278 C>T maps to NM_152418.3 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr8:88885796 G>A maps to NM_152418.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:69521430 G>A maps to NM_003861.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr14:69558512 G>A maps to NM_003861.2 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:69521896 C>T maps to NM_003861.2 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:69522121 G>A maps to NM_003861.2 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr14:69588991 G>A maps to NM_003861.2 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:168032975 C>T maps to ENST00000367840 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:168044652 G>T maps to ENST00000367840 E946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:167956831 G>T maps to ENST00000367840 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:168032913 G>T maps to ENST00000367840 E786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:168007703 A>T maps to ENST00000367840 K569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:168035685 C>T maps to ENST00000367840 R890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:168037604 C>T maps to ENST00000367840 R899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:61656798 T>C maps to NM_005828.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:61662601 C>T maps to NM_005828.3 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:61662637 T>C maps to NM_005828.3 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:160209744 G>T maps to NM_015726.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:160209666 C>T maps to NM_015726.3 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:160194850 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:160213759 G>A maps to NM_015726.3 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:27998292 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:27997857 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:27998726 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:27997715 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:27998822 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr23:27998091 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:27999213 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:27998897 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:27998800 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:27997794 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27997947 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27998710 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27999213 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr23:27998031 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:27998087 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:27998340 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:27998991 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:27998725 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:27765977 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:27765126 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:27765879 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:27766834 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:27765612 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:27766229 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:27766782 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:27766899 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:27765667 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:27765640 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:27766220 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr23:27766139 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27766252 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27766548 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27766758 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27766885 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:27765997 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:27765257 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:27765468 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:27765666 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:27765578 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:27766292 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:27766442 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:27765777 G>T did not map to a codon.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr23:27765666 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:43111726 G>A maps to NM_001128631.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:117859846 G>A maps to ENST00000338728 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:117859876 G>A maps to ENST00000338728 W285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr6:117861856 G>A maps to ENST00000338728 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:117841010 G>T maps to ENST00000338728 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr6:117862089 C>G maps to ENST00000338728 S420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr3:98518305 G>A maps to ENST00000326857 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:98568434 G>T maps to ENST00000326857 Y147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:98568385 C>A maps to ENST00000326857 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:98600611 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:50432631 C>T maps to NM_005215.3 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:50866252 C>T maps to NM_005215.3 R779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr18:50734146 C>T maps to NM_005215.3 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:50977006 C>T maps to NM_005215.3 R1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr18:50734113 T>C maps to NM_005215.3 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr18:50731694 C>T maps to NM_005215.3 Y561Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:51013308 C>T maps to NM_005215.3 F1293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:51013308 C>T maps to NM_005215.3 F1293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:50832016 C>T maps to NM_005215.3 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr11:31349794 T>C maps to NM_181807.2 E11E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:31327805 G>T maps to NM_181807.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr6:24178635 C>T maps to NM_016356.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:24278331 C>T maps to NM_016356.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:32676881 C>A maps to NM_001099434.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr1:32681131 G>A maps to NM_001099434.1 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr11:6662450 G>A maps to NM_003737.2 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:6651014 G>A maps to NM_003737.2 D1641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:6646656 T>C maps to NM_003737.2 G2306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:6653361 G>T maps to NM_003737.2 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:6662313 G>A maps to NM_003737.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:6647296 C>T maps to NM_003737.2 A2195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:6662382 C>T maps to NM_003737.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6645385 T>G maps to NM_003737.2 T2507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6648416 G>A maps to NM_003737.2 R1951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6650770 G>A maps to NM_003737.2 S1691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6652891 C>T maps to NM_003737.2 T1210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6662010 G>A maps to NM_003737.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:6648491 G>T maps to NM_003737.2 T1926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:6654042 C>T maps to NM_003737.2 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:6655486 G>T maps to NM_003737.2 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:6651020 G>A maps to NM_003737.2 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:6654186 C>T maps to NM_003737.2 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11M-01A-11D-A122-09 chr11:6646539 G>A maps to NM_003737.2 Y2345Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr11:6645096 G>A maps to NM_003737.2 R2604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr11:6652301 G>A maps to NM_003737.2 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:6661413 G>A maps to NM_003737.2 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:6662430 G>A maps to NM_003737.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:155161727 G>T maps to NM_017639.3 V1985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:155242137 C>T maps to NM_017639.3 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:155254131 G>A maps to NM_017639.3 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:155219699 T>C maps to NM_017639.3 R1467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:155157838 T>C maps to NM_017639.3 V2200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:155157880 G>T maps to NM_017639.3 G2186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:155219750 G>T maps to NM_017639.3 C1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:155156776 G>T maps to NM_017639.3 I2554I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:155157355 A>G maps to NM_017639.3 H2361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:155410665 C>T maps to NM_001142552.1 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr4:155410551 G>A maps to NM_001142552.1 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:155156317 T>C maps to NM_017639.3 Q2707Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:155155885 C>T maps to NM_017639.3 P2851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:155180890 C>A maps to NM_017639.3 E1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:155237001 C>A maps to NM_017639.3 E1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:155278399 C>T maps to NM_017639.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:155157192 C>A maps to NM_017639.3 E2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:155219191 C>A maps to NM_017639.3 E1637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:71892390 C>T maps to ENST00000504952 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:36410233 G>A maps to NM_004734.4 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:36699986 C>T maps to NM_004734.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:36384990 C>A maps to NM_004734.4 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:36396898 G>A maps to NM_004734.4 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr13:36348799 G>A maps to NM_004734.4 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:151124989 G>A maps to NM_001040261.4 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:151141892 C>T maps to NM_001040261.4 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:151023772 G>T maps to NM_001040261.4 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:151153943 C>T maps to NM_001040261.4 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:151153556 C>T maps to NM_001040261.4 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:151169506 G>A maps to NM_001040261.4 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:151023639 C>T maps to NM_001040261.4 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr3:36779043 G>A maps to NM_033403.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr3:36779892 A>G maps to NM_033403.1 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:115612807 G>T maps to NM_014881.3 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:115596904 G>A maps to NM_014881.3 R960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:114453966 G>A maps to NM_022836.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:114453756 C>A maps to NM_022836.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:114454071 C>T maps to NM_022836.3 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:114454276 G>T maps to NM_022836.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:14950784 A>G maps to NM_001033855.1 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr10:14950637 A>G maps to NM_001033855.1 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:14950424 G>A maps to NM_001033855.1 C687C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:91572142 G>A maps to NM_133503.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:91550897 G>T maps to NM_133503.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:91540002 G>A maps to NM_133503.2 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:91540002 G>T maps to NM_133503.2 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:91558440 G>A maps to NM_133503.2 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:53322205 C>T maps to ENST00000480258 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:53346309 G>T maps to ENST00000480258 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:2058395 G>A maps to NM_152640.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:2062037 G>A maps to NM_152640.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr12:2062240 G>A maps to NM_152640.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr12:2102469 G>A maps to NM_152640.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:112343726 G>A maps to NM_152624.4 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:112346469 T>G maps to NM_152624.4 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:112327880 G>A maps to NM_152624.4 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:126174026 G>T maps to NM_014026.3 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:126215348 C>T maps to NM_014026.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:126208230 C>T maps to NM_014026.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:126208230 C>T maps to NM_014026.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:155007002 C>T maps to NM_152494.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05D-01A-11W-A027-09 chr1:155014045 G>A maps to NM_152494.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:155012970 C>A maps to NM_152494.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:155007013 C>T maps to NM_152494.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:155020628 C>T maps to NM_152494.3 R618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:155015883 C>A maps to NM_152494.3 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:154995638 C>A maps to NM_144622.2 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr1:155002999 G>A maps to NM_144622.2 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:95092216 G>A maps to NM_001129889.1 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:95118886 T>G maps to NM_001129889.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:95131485 A>G maps to NM_001129889.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:95092216 G>A maps to NM_001129889.1 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:183836130 G>A maps to NM_001012732.1 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:183836076 G>A maps to NM_001012732.1 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:183814197 G>A maps to NM_001012732.1 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:74590119 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:74597121 C>T maps to NM_004082.4 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:74595185 G>A maps to NM_004082.4 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:74590743 G>A maps to NM_004082.4 R1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:74601461 C>T maps to NM_004082.4 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:57927789 G>A maps to ENST00000434715 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:34613784 C>T maps to NM_007234.3 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr9:34617876 A>G maps to ENST00000447983 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr5:150110288 C>T maps to NM_001135643.1 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:30021656 T>C maps to NM_006571.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:182679116 G>T maps to NM_020640.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:182683355 C>T maps to NM_020640.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:182683538 G>A maps to NM_020640.2 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr3:182683523 C>T maps to NM_020640.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:114128569 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:114128538 A>G maps to NM_001014283.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr13:114128505 T>C maps to NM_001014283.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr16:20873794 A>G maps to NM_173475.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:102937030 C>T maps to NM_032299.3 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:102953481 T>C maps to NM_032299.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:110574208 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:110653393 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:110653394 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:110574139 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:110653382 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:110654139 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:110653576 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:110654010 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:110555888 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:110654029 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:110653421 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:110644243 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:17425149 C>T maps to NM_024050.5 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:85787230 G>A maps to NM_012137.3 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:61081955 G>T maps to NM_001923.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:61070093 T>C maps to NM_001923.3 T1024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:61094319 C>A maps to NM_001923.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:61068358 A>G maps to NM_001923.3 G1087G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:61070620 G>A maps to NM_001923.3 R947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:47259479 C>T maps to NM_000107.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:50537793 C>A maps to NM_000790.3 G373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:50611696 G>C maps to NM_000790.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:53529718 G>A maps to NM_001160148.1 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:53521253 G>T maps to NM_001160148.1 S780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:53522413 C>A maps to NM_001160148.1 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:53518562 G>A maps to NM_001160148.1 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:53539317 A>G maps to NM_001160148.1 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:53619597 G>A maps to NM_001160148.1 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:38091918 T>C maps to NM_001164232.1 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:38109480 G>T maps to NM_001164232.1 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:38109449 G>A maps to NM_001164232.1 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:38105319 C>T maps to NM_001164232.1 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr11:103908617 G>A maps to NM_001001711.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:103907762 C>T maps to NM_001001711.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:103907909 C>T maps to NM_001001711.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:103908726 C>T maps to NM_001001711.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:15953247 C>T maps to NM_032341.4 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:57910666 G>A maps to NM_001195056.1 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:101109121 C>T maps to NM_145244.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr4:101111092 T>A maps to NM_145244.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:110729609 C>A maps to NM_003649.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:110734611 C>T maps to NM_003649.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:20982213 C>T maps to NM_005216.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr6:30864798 G>A maps to NM_013994.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:30865855 A>G maps to NM_013994.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:30862314 G>A maps to NM_013994.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:30862383 G>A maps to NM_013994.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:162731236 C>T maps to NM_006182.2 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:162731095 C>A maps to NM_006182.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:162746001 C>T maps to NM_006182.2 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:162725487 G>A maps to NM_006182.2 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:162749997 G>T maps to NM_006182.2 E844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:15744593 C>T maps to NM_004939.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:15746296 C>T maps to NM_004939.1 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:15760381 C>T maps to NM_004939.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:108594075 G>T maps to NM_004398.2 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:108535927 G>A maps to NM_004398.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:108586615 G>T maps to NM_004398.2 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:108586678 G>T maps to NM_004398.2 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:31242048 C>T maps to NM_030653.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:31247734 C>T maps to NM_030653.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:31249808 A>G maps to NM_030653.3 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:31249576 G>T maps to NM_030653.3 G510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr12:31254801 C>T maps to NM_030653.3 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr12:31242865 G>A maps to NM_030653.3 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr12:31237968 G>T maps to NM_030653.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:118583084 A>C maps to NM_006773.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:118582184 A>G maps to NM_006773.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:118588171 G>T maps to NM_006773.3 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:118579627 C>T maps to NM_006773.3 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:70405368 C>T maps to NM_018332.3 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr16:70400724 C>T maps to NM_018332.3 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:70399021 C>T maps to NM_018332.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:70366964 C>T maps to NM_007242.4 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:112308659 T>C maps to NM_007204.4 C538C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:70734427 A>G maps to NM_004728.2 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:70723155 C>A maps to NM_004728.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:70719893 T>C maps to NM_004728.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:70719618 G>T maps to NM_004728.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:94517773 T>C maps to NM_020414.3 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:94546065 G>C maps to NM_020414.3 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:94528485 G>A maps to NM_020414.3 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr14:94526676 C>T maps to NM_020414.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:94545739 C>A maps to NM_020414.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:94545739 C>A maps to NM_020414.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:125788590 C>T maps to NM_013264.3 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:125787037 C>T maps to NM_013264.3 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:125781239 A>C maps to NM_013264.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:134713748 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:134711278 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:134714083 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:134680806 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:134680809 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:134706842 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:134709040 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:134713789 T>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:134680348 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:134681171 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:134683577 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134681112 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:134714071 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:134711319 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:134679449 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:134679383 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:134679392 A>C did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:134690174 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:134703352 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:47859140 A>G maps to NM_017895.7 Q740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:47860164 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:47846805 C>T maps to NM_017895.7 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:47858654 G>A maps to NM_017895.7 A707A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BS-A0UJ-01A-12D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:47839532 C>T maps to NM_017895.7 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:135470282 C>T maps to NM_022779.7 Q842Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:135537700 C>A maps to NM_022779.7 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:135538067 C>T maps to NM_022779.7 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:135493756 G>A maps to NM_022779.7 Y700Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:135521416 G>A maps to NM_022779.7 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr23:41206198 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:41203304 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:41206133 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:41203315 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:41204682 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:41201790 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:41202548 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:41204490 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:41201785 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41200735 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41205841 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:41202566 C>G did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:41206689 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:41205842 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:41201789 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:41203539 G>A did not map to a codon.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr23:41202520 G>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:55034776 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:55083778 C>T maps to NM_024415.2 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:55086458 C>T maps to NM_024415.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:55094263 G>T maps to NM_024415.2 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:55086458 C>T maps to NM_024415.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:55112313 T>G maps to NM_024415.2 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:55094337 C>T maps to NM_024415.2 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:176940721 G>A maps to NM_016222.2 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr17:61890660 G>A maps to NM_203499.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr17:61889429 G>T maps to NM_203499.1 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:61888506 C>T maps to NM_203499.1 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:61876951 T>C maps to NM_203499.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr17:61864560 C>A maps to NM_203499.1 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:61888506 C>T maps to NM_203499.1 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:74116157 A>G maps to NM_018665.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:74124376 C>T maps to NM_018665.2 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:134106674 G>T maps to ENST00000452510 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:134130541 C>A maps to ENST00000452510 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:134109384 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:134113267 C>T maps to ENST00000452510 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr12:12975621 C>T maps to NM_016355.3 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19038659 G>A maps to NM_019070.4 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:19033520 C>T maps to NM_019070.4 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr19:19035726 C>T maps to NM_019070.4 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:19038638 C>T maps to NM_019070.4 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:70696827 C>T maps to NM_024045.1 R578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:70666723 T>C maps to NM_024045.1 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:70666523 G>T maps to NM_024045.1 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr10:70661145 T>G maps to NM_024045.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:70706347 C>T maps to NM_024045.1 R726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:132625047 G>A maps to NM_175066.3 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:132626120 G>A maps to NM_175066.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:35986017 A>G maps to NM_007010.3 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:35981513 C>A maps to NM_007010.3 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:35986121 C>A maps to NM_007010.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:23018662 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:23019679 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:23019917 T>A did not map to a codon.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr23:23018494 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:23018858 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:23019023 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:23019982 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:23018617 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:23018990 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:23019820 C>T did not map to a codon.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr23:23018927 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:23018205 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:23018343 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:23019770 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:23018493 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:23019030 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:23019262 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:113614667 G>A maps to NM_001111322.1 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:113596743 G>A maps to NM_001111322.1 Q863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr12:113617796 C>T maps to NM_001111322.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr12:113612889 C>T maps to NM_001111322.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr12:124094494 C>T maps to NM_020936.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:124104129 G>A maps to NM_020936.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:32491419 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:32493844 C>A maps to NM_014314.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:32493844 C>A maps to NM_014314.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr9:32493800 C>T maps to NM_014314.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:32488793 C>T maps to NM_014314.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:32467808 G>T maps to NM_014314.3 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:32488886 T>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:118635986 T>C maps to NM_004397.4 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:118636039 C>A maps to NM_004397.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:118625471 G>A maps to NM_004397.4 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:169145441 C>G maps to NM_017631.5 L1592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:169196647 C>A maps to NM_017631.5 E718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:169197321 C>T maps to NM_017631.5 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:169201623 C>A maps to NM_017631.5 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr4:169229243 C>T maps to NM_017631.5 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:169204595 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:169190101 C>A maps to NM_017631.5 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:169343006 T>C maps to NM_001012967.1 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:169379041 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:169392896 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr4:169377256 G>T maps to NM_001012967.1 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:169336895 C>T maps to NM_001012967.1 E927E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:169362565 C>A maps to NM_001012967.1 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:169336567 C>T maps to NM_001012967.1 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:169343061 T>C did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr4:169341409 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:680972 C>T maps to NM_021008.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr11:674718 C>T maps to NM_021008.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:679757 C>T maps to NM_021008.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:691530 C>T maps to NM_021008.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr11:681020 G>T maps to NM_021008.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:91049093 T>C maps to NM_001359.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:91064095 G>T maps to NM_001359.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:457484 C>T maps to NM_020664.3 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:461487 C>T maps to NM_020664.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr16:460224 C>T maps to ENST00000439661 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:457489 G>A maps to NM_020664.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:161093689 G>A maps to ENST00000368005 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:161094033 G>A maps to ENST00000368005 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:35287455 C>T maps to NM_022047.3 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:90028253 G>A maps to NM_207514.1 W324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:6793609 C>A maps to NM_001925.1 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:6793541 T>C maps to NM_001925.1 *98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:6914174 C>T maps to NM_021010.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:7694053 A>G maps to NM_080389.2 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr8:7698676 A>G maps to NM_080389.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:7698670 T>C maps to NM_080389.2 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr11:71548472 A>G maps to NM_001002035.1 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:49928034 C>T maps to NM_001037499.1 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:29976827 C>A maps to NM_153323.3 *89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:207949 C>A maps to NM_080831.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:210315 C>T maps to NM_080831.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr8:11831627 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:224377744 G>A maps to NM_003676.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:224377615 C>T maps to NM_003676.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:18256631 C>A maps to NM_003472.3 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:18226452 A>C maps to NM_003472.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:40980497 G>A maps to NM_022774.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:126219681 G>A maps to NM_020946.1 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:126345510 C>A maps to NM_020946.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:126429349 A>C maps to NM_020946.1 Y154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:197522161 G>A maps to NM_001195215.1 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:197641192 T>A maps to NM_001195215.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:197509131 C>A maps to NM_001195215.1 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr19:6479009 G>A maps to NM_024898.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:6478967 C>T maps to NM_024898.2 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr19:6475305 G>A maps to NM_024898.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:6468352 G>A maps to NM_024898.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:6477126 G>A maps to NM_024898.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:140219459 G>A maps to NM_015689.3 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr7:140219503 G>A maps to NM_015689.3 R976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:140257963 G>A maps to NM_015689.3 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:140244476 G>T maps to NM_015689.3 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:140301450 G>A maps to NM_015689.3 N249N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:140273770 G>T maps to NM_015689.3 S428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:115168167 T>C maps to ENST00000393274 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:115137121 G>T maps to ENST00000393274 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:115166229 G>A maps to ENST00000393274 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:115147640 G>A maps to ENST00000393274 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:115142904 G>T maps to ENST00000393274 C675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:111734939 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:111731339 C>T maps to NM_024901.3 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:142202479 G>T maps to NM_014957.2 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr8:142148178 C>T maps to NM_014957.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:142151351 C>T maps to NM_014957.2 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:142178472 G>A maps to NM_014957.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:142202479 G>T maps to NM_014957.2 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:142151330 G>A maps to NM_014957.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:142202479 G>T maps to NM_014957.2 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:142195340 C>T maps to NM_014957.2 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:65956718 C>A maps to ENST00000443035 E1846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:66025155 C>T maps to ENST00000443035 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:65994167 G>A maps to ENST00000443035 R831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:153914692 G>T maps to NM_014856.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:153913385 G>A maps to NM_014856.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:153905225 G>T maps to NM_014856.2 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:153913033 G>A maps to NM_014856.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:153916682 T>C maps to NM_014856.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:19336363 C>T maps to NM_017925.4 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:19346882 A>G maps to NM_017925.4 S1087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:19328072 G>A maps to NM_017925.4 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr9:19346462 T>C maps to NM_017925.4 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:19336368 G>A maps to NM_017925.4 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:19350767 G>A maps to NM_017925.4 S1177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:19346105 G>A maps to NM_017925.4 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:19316742 G>A maps to NM_017925.4 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:19358035 C>T maps to NM_017925.4 R1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:19324396 C>T maps to NM_017925.4 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:19372158 G>A maps to NM_017925.4 A1670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:9173908 G>T maps to NM_015213.2 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:9164377 C>T maps to NM_015213.2 T1134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:9200559 C>A maps to NM_015213.2 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr11:9202352 C>T maps to NM_015213.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr11:9165752 C>T maps to NM_015213.2 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:31577570 G>A maps to NM_144973.3 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:31540647 G>A maps to NM_144973.3 S1238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:31605148 C>A maps to NM_144973.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:31577546 G>A maps to NM_144973.3 G771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:31562304 G>A maps to NM_144973.3 R899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:31579259 G>A maps to NM_144973.3 F735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:123253440 T>C maps to ENST00000455982 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:123249867 G>T maps to ENST00000455982 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:68943556 G>T maps to NM_001114120.1 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:68948515 T>G maps to NM_001114120.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:68944984 G>A maps to NM_001114120.1 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:59934661 G>T maps to NM_018369.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:59893587 G>A maps to NM_018369.2 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:59893587 G>A maps to NM_018369.2 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr5:59982946 C>T maps to NM_018369.2 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr22:32239087 G>A maps to NM_001136029.1 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:32160976 C>T maps to NM_001136029.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:32234730 A>G maps to NM_001136029.1 Q796Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:32206534 C>T maps to NM_001136029.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:32211097 C>T maps to NM_001136029.1 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:32270315 C>T maps to NM_001136029.1 S1198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:32150966 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:32217578 C>A maps to NM_001136029.1 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:32302044 C>T maps to NM_001136029.1 H1495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr22:32217605 T>C maps to NM_001136029.1 Y663Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:32293559 C>T maps to NM_001136029.1 G1423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:32198756 C>T maps to NM_001136029.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:32210984 C>T maps to NM_001136029.1 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:33047355 T>C maps to NM_001077242.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:33053038 G>T maps to NM_001077242.1 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:33047475 C>A maps to NM_001077242.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr11:33054457 T>C maps to NM_001077242.1 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:16185507 G>T maps to NM_015954.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:16185507 G>T maps to NM_015954.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:16135315 G>T maps to NM_015954.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:124027713 G>A maps to NM_024295.4 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:5384695 G>A maps to NM_016041.3 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:24180323 C>G did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr2:220284817 C>T maps to NM_001927.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:89074351 G>T maps to NM_017996.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:89056286 G>A maps to NM_017996.3 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:3789034 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:3775292 C>T maps to ENST00000430539 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:3782394 C>T maps to ENST00000430539 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:3800134 G>T maps to ENST00000430539 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:3782526 G>T maps to ENST00000430539 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:3775364 C>T maps to ENST00000430539 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:117188501 C>T maps to NM_015404.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:117240928 G>T maps to NM_015404.3 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr9:117170229 G>A maps to NM_015404.3 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr9:117240823 C>T maps to ENST00000374057 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:117166286 G>A maps to NM_015404.3 G769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:117240778 C>T maps to ENST00000374057 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179325878 G>T maps to NM_001042702.3 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr2:179320751 C>T maps to NM_001042702.3 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179325937 T>C maps to NM_001042702.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:75509343 C>A maps to NM_032564.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:69424178 C>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:69424882 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69424208 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69397510 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69424364 T>G did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:69424937 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69420291 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:69420155 C>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:19127525 C>A maps to NM_022719.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr22:19052395 C>T maps to NM_005137.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:19052431 C>T maps to NM_005137.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:19076896 G>A maps to NM_005137.2 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:19052452 G>A maps to NM_005137.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr22:20079117 C>T maps to NM_022720.6 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:20097556 C>T maps to NM_022720.6 R750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:20078961 C>T maps to NM_022720.6 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr22:20073662 C>T maps to NM_022720.6 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:20074812 G>A maps to NM_022720.6 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56332728 C>T maps to NM_201554.1 R144*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56345563 C>T maps to NM_201554.1 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:56346660 A>G maps to NM_201554.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:56335091 C>T maps to NM_201554.1 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:56332990 G>T maps to NM_201554.1 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:56346579 C>T maps to NM_201554.1 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:56330837 C>T maps to NM_201554.1 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:56334721 G>A maps to NM_201554.1 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr12:56346872 G>A maps to NM_201554.1 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:14733809 C>A maps to NM_004080.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:14733723 A>C maps to NM_004080.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr7:14669860 C>T maps to NM_004080.2 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:234346114 C>T maps to NM_152879.2 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:234371305 C>T maps to NM_152879.2 F1037F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:234343073 G>T maps to NM_152879.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:234363465 G>A maps to NM_152879.2 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:234299110 C>T maps to NM_152879.2 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:54923151 C>A maps to NM_003647.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr17:54939506 C>T maps to NM_003647.2 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:186015901 G>T maps to NM_001346.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr3:185997704 G>A maps to NM_001346.2 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:185993450 G>A maps to NM_001346.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr3:185867950 C>T maps to NM_001346.2 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr3:185990100 C>T maps to NM_001346.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:186038211 C>A maps to NM_001346.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:42763186 G>T maps to NM_178009.2 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr13:42734208 C>T maps to NM_178009.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:42803248 G>A maps to NM_178009.2 P1196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr13:42733429 T>C maps to NM_178009.2 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:137330259 C>T maps to NM_004717.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:137080352 C>T maps to NM_004717.2 T1024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:137237287 T>A maps to NM_004717.2 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:137330283 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:137363353 G>T maps to NM_004717.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:137257533 A>G maps to NM_004717.2 C604C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:137271875 C>T maps to NM_004717.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:137170134 C>T maps to NM_004717.2 Q804Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:137092734 C>A maps to NM_004717.2 E944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:137172426 G>A maps to NM_004717.2 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:137172400 G>A maps to NM_004717.2 D779D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:137266650 G>A maps to NM_004717.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:137269963 G>A maps to NM_004717.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50118056 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50127715 A>G did not map to a codon.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr23:50118057 T>C did not map to a codon.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr4:959939 C>T maps to ENST00000502309 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr4:961567 G>A maps to NM_001347.2 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:46367099 C>T maps to NM_201533.3 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:46393653 G>A maps to NM_001105540.1 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:74184305 C>T maps to NM_080916.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:55337259 G>A maps to NM_014762.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:55317976 G>A maps to NM_014762.3 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:71148914 G>A maps to NM_001360.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:71149990 G>A maps to NM_001360.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:71155983 C>T maps to NM_001360.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:71146426 G>T maps to NM_001360.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:71155947 G>A maps to NM_001360.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:71155071 G>A maps to NM_001360.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr11:71146861 G>A maps to NM_001360.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:71148914 G>A maps to NM_001360.2 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:71152376 G>A maps to NM_001360.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:26786592 C>T maps to NM_024887.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:26786592 C>T maps to NM_024887.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:26759440 C>A maps to NM_024887.2 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr19:49437064 C>T maps to NM_014475.3 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:79924971 A>C maps to NM_000791.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:79924929 A>G maps to NM_000791.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:79945253 G>A maps to NM_000791.3 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:93780274 C>T maps to NM_001195643.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:93780238 G>T maps to NM_001195643.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:93780307 G>A maps to NM_001195643.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr16:72057418 C>T maps to NM_001361.3 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:72055122 C>T maps to NM_001361.3 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:72057409 C>T maps to NM_001361.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:12788162 G>A maps to NM_001930.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:24766023 G>A maps to NM_001136050.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:27228257 G>A maps to NM_144683.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr17:27225677 C>T maps to NM_144683.3 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:27225749 A>T maps to NM_144683.3 Y281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24108390 C>T maps to NM_182908.4 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:24108386 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24520092 C>T maps to NM_001082488.1 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:60616121 C>T maps to NM_016029.2 W307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:21081628 G>T maps to NM_015510.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:21094372 C>A maps to NM_015510.3 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:9680561 G>A maps to ENST00000330255 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr17:9676237 G>A maps to ENST00000330255 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr17:9674903 G>A maps to ENST00000330255 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr2:169938247 G>T maps to NM_001142271.1 G53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:2161131 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11M-01A-11D-A122-09 chr23:2139253 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:12162220 G>A maps to NM_018706.5 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:12126728 G>A maps to NM_018706.5 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:12162226 G>A maps to NM_018706.5 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:12126728 G>A maps to NM_018706.5 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr4:24578162 G>A maps to NM_001358.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:24578096 C>A maps to NM_001358.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:24538676 G>A maps to NM_001358.2 Q636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:24578045 C>T maps to NM_001358.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr6:30630401 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:30622999 C>T maps to NM_003587.4 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr5:54589921 G>A maps to NM_019030.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:47891045 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:47882587 G>A maps to NM_138615.2 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:47888076 C>T maps to NM_138615.2 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:47868967 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:127548180 G>T maps to NM_018180.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:127542553 G>A maps to NM_018180.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:127527584 G>T maps to NM_018180.2 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:127569153 G>A maps to NM_018180.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr17:5347716 C>T maps to ENST00000457531 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:5347653 G>A maps to ENST00000457531 C724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:5347818 G>A maps to ENST00000457531 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:5364375 A>G maps to ENST00000457531 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:47884182 C>A maps to NM_014681.5 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:47870311 C>T maps to NM_014681.5 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:47883071 C>T maps to NM_014681.5 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:37653937 G>A maps to NM_021931.3 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:37662909 G>T maps to NM_021931.3 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:37623522 C>T maps to NM_021931.3 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:37601221 C>T maps to NM_021931.3 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr3:153993986 T>G maps to NM_020865.2 P1000P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:154022721 G>T maps to NM_020865.2 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:154041968 C>T maps to NM_020865.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr3:154021158 C>G maps to NM_020865.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:125441307 G>A maps to NM_032656.3 H794H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:125470671 T>C maps to NM_032656.3 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr12:125434539 C>T maps to NM_032656.3 T1094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr12:125438645 G>T maps to NM_032656.3 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr12:125470808 T>A maps to NM_032656.3 K37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:72142454 C>T maps to NM_014003.3 I1068I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:72134477 C>T maps to NM_014003.3 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:72137074 C>A maps to NM_014003.3 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr16:72133142 G>A maps to NM_014003.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:72141655 C>T maps to NM_014003.3 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:72139998 C>T maps to NM_014003.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:57679887 T>C maps to NM_024612.4 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:57682970 A>G maps to NM_024612.4 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr17:57682854 T>C maps to NM_024612.4 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:39046214 A>C maps to NM_198963.1 Y1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:39075456 C>T maps to NM_198963.1 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr2:39088339 C>T maps to NM_198963.1 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:39095403 G>A maps to NM_198963.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:39095403 G>A maps to NM_198963.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:39089346 G>C maps to NM_198963.1 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:39053704 G>A maps to NM_198963.1 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr2:39081293 G>A maps to NM_198963.1 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr2:39081248 T>C maps to NM_198963.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:40257047 G>T maps to NM_024119.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:40259721 G>A maps to NM_024119.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:41599549 C>A maps to NM_004941.1 V1133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:41594594 T>C maps to NM_004941.1 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:41599510 G>A maps to NM_004941.1 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:41585387 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:41561545 G>A maps to NM_004941.1 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:182852657 C>T maps to NM_001357.4 R1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:182835592 T>C maps to NM_001357.4 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:182845676 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:182841506 T>C maps to NM_001357.4 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:182827690 G>A maps to NM_001357.4 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:182852657 C>T maps to NM_001357.4 R1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:182828233 G>A maps to NM_001357.4 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:182852657 C>T maps to NM_001357.4 R1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:122693122 G>A maps to NM_019887.4 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:122701380 A>C maps to NM_019887.4 Y117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140958763 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140905949 G>A maps to ENST00000398557 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:140953361 A>G maps to ENST00000398557 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:96212987 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:96013170 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:96173601 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:96136622 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:96502802 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:96204002 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:96354731 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:96684715 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:96013170 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:96185752 A>C did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:96354691 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:96194340 C>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:96684735 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:96171472 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:96328001 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:96185754 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:96013170 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:96171472 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:96173583 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:96369889 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:96502835 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:96854312 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:95940137 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:95993591 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:96197086 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:96213043 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:96603182 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:96136600 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:96013200 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:96136631 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:96213130 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:95993626 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:95993633 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:96185768 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:96192342 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:96220103 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:96212928 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:96684720 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:96328001 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:96639031 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr13:60384964 G>A maps to NM_001042517.1 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:60240873 A>C maps to NM_001042517.1 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:60545029 C>A maps to NM_001042517.1 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:60348916 G>T maps to NM_001042517.1 A1068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:60498947 C>A maps to NM_001042517.1 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr13:60582728 G>A maps to NM_001042517.1 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:60348871 C>T maps to NM_001042517.1 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:60686209 C>T maps to NM_001042517.1 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:60485871 A>G maps to NM_001042517.1 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:60240930 G>T maps to NM_001042517.1 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr13:60407387 T>G maps to NM_001042517.1 A960A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:60384933 C>A maps to NM_001042517.1 E1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:95562459 C>A maps to NM_177438.2 R1599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:95577779 G>A maps to NM_177438.2 D710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:95577680 C>T maps to NM_177438.2 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:95592955 T>C maps to NM_177438.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:95590632 C>A maps to NM_177438.2 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:95560356 G>T maps to NM_177438.2 I1744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr20:61525430 C>T maps to NM_033081.2 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:61541128 G>A maps to NM_033081.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:61512117 G>A maps to NM_033081.2 G1730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:61541304 G>A maps to NM_033081.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:61527944 C>T maps to NM_033081.2 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:61511406 G>A maps to NM_033081.2 F1967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:61513032 G>T maps to NM_033081.2 A1425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr20:61510728 C>T maps to NM_033081.2 R2193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr20:61528070 C>A maps to NM_033081.2 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:61511907 G>A maps to NM_033081.2 F1800F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:61513327 G>T maps to NM_033081.2 S1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr20:61512168 G>A maps to NM_033081.2 S1713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:61511640 G>A maps to NM_033081.2 F1889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:61513206 G>A maps to NM_033081.2 F1367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:54360101 C>T maps to NM_000792.5 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:54360123 C>T maps to NM_000792.5 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:80669487 G>A maps to NM_001007023.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:80669199 G>A maps to NM_001007023.2 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:102028685 C>T maps to NM_001362.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:102028132 C>A maps to NM_001362.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:102028420 C>A maps to NM_001362.3 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:102028327 C>T maps to NM_001362.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr14:102028447 C>T maps to NM_001362.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr14:102027970 C>A maps to NM_001362.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr14:102028219 G>A maps to NM_001362.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr21:47910558 A>G maps to ENST00000318711 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:47970481 C>T maps to ENST00000318711 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:47957400 C>T maps to ENST00000318711 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:47954541 C>A maps to ENST00000318711 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr21:47957396 C>T maps to ENST00000318711 Y583Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr21:47931423 G>A maps to ENST00000318711 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr21:47965903 C>T maps to NM_206891.2 G808G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:47966844 C>T maps to ENST00000318711 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:47931447 C>T maps to ENST00000318711 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr21:47954583 G>A maps to ENST00000318711 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:47957420 C>A maps to ENST00000318711 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:47987489 C>T maps to ENST00000318711 F1558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:51133244 C>T maps to NM_173602.2 S1410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:51112507 C>T maps to NM_173602.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr12:51117072 G>A maps to NM_173602.2 T1085T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51080410 G>A maps to NM_173602.2 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51108287 C>A maps to NM_173602.2 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51126252 C>T maps to NM_173602.2 I1305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:51034529 G>T maps to NM_173602.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:329332 G>A maps to NM_014974.2 D1391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:465071 C>T maps to NM_014974.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:409202 G>A maps to NM_014974.2 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:430543 C>T maps to NM_014974.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:436260 C>T maps to NM_014974.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:436283 C>A maps to NM_014974.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr10:415436 C>A maps to NM_014974.2 G710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:355975 G>A maps to NM_014974.2 H1327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:436212 C>T maps to NM_014974.2 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:445152 G>A maps to NM_014974.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:93375521 G>A maps to NM_017594.3 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:68512866 G>A maps to NM_004675.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:68512578 G>T maps to NM_004675.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr3:122591310 C>T maps to NM_032839.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:122545808 T>C maps to NM_032839.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:73355066 G>T maps to NM_014953.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:73345071 C>T maps to NM_014953.3 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:73352345 C>A maps to NM_014953.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:73340167 G>A maps to NM_014953.3 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr13:73340126 C>T maps to NM_014953.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr13:73346413 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr13:73346013 A>G maps to NM_014953.3 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:73351614 C>T maps to NM_014953.3 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr13:73337627 T>C maps to NM_014953.3 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:66607395 C>T maps to NM_001143688.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:66625247 C>A maps to NM_001143688.1 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:66615116 C>T maps to NM_001143688.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:66606424 C>T maps to NM_001143688.1 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:66606429 T>G maps to NM_001143688.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:66607509 C>T maps to NM_001143688.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr15:66618333 A>G maps to NM_001143688.1 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:66607509 C>T maps to NM_001143688.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:66621406 G>A maps to NM_001143688.1 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:66599164 G>A maps to NM_001143688.1 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr15:66618427 C>T maps to NM_001143688.1 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:233194657 C>T maps to NM_152383.4 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:232952223 G>T maps to NM_152383.4 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:233199396 C>T maps to NM_152383.4 F782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr2:233201207 G>T maps to NM_152383.4 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:231829599 G>A maps to NM_001164537.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:231829851 G>A maps to NM_001164537.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:231830232 G>A maps to NM_001164537.1 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:231837747 T>C maps to NM_001164537.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:231931027 G>T maps to NM_001164537.1 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:231829851 G>A maps to NM_001164537.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:232162284 T>C maps to NM_001164537.1 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:223168325 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:223178518 C>T maps to NM_032890.2 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:223178104 C>T maps to NM_032890.2 F1122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:223176547 C>T maps to NM_032890.2 H603H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:223176277 T>C maps to NM_032890.2 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:223165372 G>A maps to NM_032890.2 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:223176629 C>T maps to NM_032890.2 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:223177975 G>A maps to NM_032890.2 V1079V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:223177192 C>T maps to NM_032890.2 I818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:223177597 T>C maps to NM_032890.2 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:40657440 C>T maps to NM_033510.1 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:40661975 C>T maps to NM_033510.1 H1221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:40661342 C>T maps to NM_033510.1 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:40662023 T>C maps to NM_033510.1 Y1237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr15:40661099 C>T maps to NM_033510.1 H929H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr11:111865795 G>A maps to NM_001037954.2 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr11:111864293 T>C maps to NM_001037954.2 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:154003506 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:154005090 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:153994555 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153997466 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153994630 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:154004540 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154001486 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153994648 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153993723 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:154003514 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153995315 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:54074790 C>T maps to NM_012242.2 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:107956664 G>A maps to NM_014421.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:107845737 G>A maps to NM_014421.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:107956619 G>A maps to NM_014421.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:42231803 C>T maps to NM_014420.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:111899360 C>T maps to NM_001931.4 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:12955993 C>T maps to NM_182643.2 Q1027Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:12957118 G>A maps to NM_182643.2 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:12957934 G>A maps to NM_182643.2 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:12952358 G>A maps to NM_182643.2 D1145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:13259112 G>A maps to NM_182643.2 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr8:12957013 C>T maps to NM_182643.2 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr8:13162748 G>A maps to NM_024767.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr8:12943905 G>A maps to NM_182643.2 R1453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:12952330 G>A maps to NM_182643.2 R1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr8:12952358 G>A maps to NM_182643.2 D1145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:107545401 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:38151773 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:38104097 C>T maps to NM_007335.2 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:38139318 C>A maps to NM_007335.2 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:38158001 G>A maps to NM_007335.2 E1305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:38151596 C>T maps to NM_007335.2 Q1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:38103774 C>T maps to NM_007335.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:38129839 G>A maps to NM_007335.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:38161955 A>G maps to NM_007335.2 S1574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:38139079 C>T maps to NM_007335.2 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:38139104 T>C maps to NM_007335.2 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:38139079 C>T maps to NM_007335.2 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:196869605 C>A maps to NM_004087.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr11:84865695 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:83252819 G>A maps to NM_001142699.1 H674H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:83173056 C>A maps to NM_001142699.1 E937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:83180408 C>T maps to NM_001142699.1 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:83173065 C>A maps to NM_001142699.1 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr11:83544656 C>A maps to NM_001142699.1 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:83252788 G>A maps to NM_001142699.1 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:84245767 G>A maps to NM_001142699.1 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69673641 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69712109 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69713226 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69699062 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69722043 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69699018 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69715298 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69719066 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69673550 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69699018 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69719054 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:69669660 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr23:69717041 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:69668800 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:69673523 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:69719834 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:69712092 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:69670544 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:69670610 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:69699017 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:69668800 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:7106869 G>A maps to NM_001365.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:7107069 T>C maps to NM_001365.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7106610 C>T maps to NM_001365.3 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7107078 A>G maps to NM_001365.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:7106568 G>A maps to NM_001365.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:7096995 C>T maps to NM_001365.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:79576334 C>T maps to NM_004747.3 A1333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr10:79590510 G>A maps to NM_004747.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr10:79593715 G>T maps to NM_004747.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:79588738 A>G maps to NM_004747.3 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:79567687 G>A maps to NM_004747.3 D1554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr18:3879897 G>A maps to NM_004746.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:3567516 G>T maps to NM_004746.2 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:3499341 C>T maps to NM_004746.2 A925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:3729345 G>A maps to NM_004746.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:3880002 C>T maps to NM_004746.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr18:3879768 G>A maps to NM_004746.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:3729345 G>A maps to NM_004746.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr18:3879681 C>T maps to NM_004746.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr18:3879375 C>A maps to NM_004746.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr8:1497272 C>T maps to ENST00000357934 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr8:1626511 C>T maps to ENST00000357934 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:1626511 C>T maps to ENST00000357934 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:1581033 C>T maps to ENST00000357934 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:1581153 C>T maps to ENST00000357934 D526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:1626784 C>A maps to ENST00000357934 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:1497533 C>T maps to ENST00000357934 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:1497518 C>T maps to ENST00000357934 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr8:1645369 C>T maps to ENST00000357934 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:1645404 C>T maps to ENST00000357934 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:35365763 G>A maps to NM_001080418.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:35365868 C>T maps to NM_001080418.1 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr1:35370534 G>A maps to NM_001080418.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:35370108 T>G maps to NM_001080418.1 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:35370006 C>T maps to NM_001080418.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:35068237 C>T maps to ENST00000339266 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:35060764 C>T maps to ENST00000339266 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:35154345 C>T maps to ENST00000339266 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:35127700 C>T maps to NM_014902.4 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:35060359 C>T maps to ENST00000339266 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:55636158 G>A maps to NM_014750.4 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:55646412 G>A maps to NM_014750.4 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:55625285 G>A maps to NM_014750.4 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:101201220 C>T maps to NM_003836.5 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr14:101201178 C>T maps to NM_003836.5 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:43419736 G>A maps to NM_206539.1 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:43418726 G>A maps to NM_206539.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:43419709 G>A maps to NM_206539.1 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:170592395 C>T maps to NM_005618.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:170592090 G>A maps to NM_005618.3 C717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:170594100 G>A maps to NM_005618.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:170597823 G>A maps to NM_005618.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:170597465 G>A maps to NM_005618.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:39995960 C>A maps to NM_016941.3 C321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:39994846 G>A maps to NM_016941.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:39994718 C>T maps to NM_016941.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr14:75355993 A>G maps to NM_001933.4 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:172951604 T>C maps to ENST00000409492 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:172950524 C>T maps to NM_178120.4 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:172952983 G>A maps to NM_178120.4 *256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:48070874 G>T maps to NM_005220.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:44684318 C>T maps to NM_019100.4 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:44685959 C>T maps to NM_019100.4 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:124389422 T>C maps to ENST00000368915 P1912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:124399908 G>A maps to ENST00000368915 V2432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr10:124402856 C>T maps to ENST00000368915 V2524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:124389462 G>T maps to ENST00000368915 E1926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:124343856 G>A maps to ENST00000368915 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:124348592 C>T maps to ENST00000368915 V639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:124341318 G>A maps to ENST00000368915 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:124354010 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:124361565 G>A maps to ENST00000368915 W1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:46976310 T>C maps to NM_147192.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:46976788 T>A maps to NM_147192.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:38934570 A>G maps to NM_007068.2 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:38917655 G>A maps to NM_007068.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:32663084 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:32519934 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:31279076 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:31279111 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:31792255 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:32361288 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:32383220 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:32382819 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:31165457 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:32235083 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:32361327 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:32382762 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:32398742 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:32404522 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:32482732 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:32503172 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:31164407 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:31164499 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:31697497 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:31747750 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:31341766 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:31838165 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:31950210 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:31950305 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:32459324 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:32486704 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:32632542 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:31838105 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:31196075 A>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:31792290 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:31950312 A>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:32360239 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:32503186 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:32583956 G>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:32591908 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:31201000 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:32235098 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:32364163 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:32613949 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:32867890 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:31514911 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:32456457 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:32632438 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:32663149 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:31496308 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:31144819 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:31164465 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:31227736 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:31792262 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:31893302 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:32328196 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:32328372 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:32380920 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:32398786 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:32456382 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:32486813 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:32563313 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:32613949 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:32834696 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:32430324 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:31165592 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:31196048 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:31645827 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:31747811 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:31986487 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:32404462 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:33229398 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11M-01A-11D-A122-09 chr23:31241178 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:31697696 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:31747749 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:31224778 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr23:32663251 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:32430166 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:32509515 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:31697651 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:32366527 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:32486678 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:32827691 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:31187716 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:31747822 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:31950303 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:32305758 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:32456458 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:32408251 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:32717322 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:31139978 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:31196785 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:31462731 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:31497159 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:31525435 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:31645950 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:32456459 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:32466745 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:32536098 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:32632487 T>G did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:31224763 C>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:31196877 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:31462696 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:31854891 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:32472912 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:32563386 G>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:32328346 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr23:31792188 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr23:31196793 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:32360239 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:32509456 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:32466718 C>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:32591964 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:31196836 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:31525457 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:31676191 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:32382734 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:32456458 G>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:32486646 C>G did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:32328212 C>T did not map to a codon.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr23:32328241 G>A did not map to a codon.
Sequencing variant TCGA-FI-A2D2-01A-11D-A17D-09 chr23:31525490 A>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:78338287 G>T maps to NM_013391.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:78329212 A>C maps to NM_013391.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:36004013 G>A maps to NM_033317.4 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr19:36004002 T>C maps to NM_033317.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:88580373 T>C maps to NM_004407.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:88583146 G>T maps to NM_004407.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:88583221 G>T maps to NM_004407.3 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:88584186 G>A maps to NM_004407.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr4:88583802 C>T maps to NM_004407.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:88583650 G>T maps to NM_004407.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:46280757 G>A maps to NM_004409.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:46280644 G>A maps to NM_004409.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:1053756 C>T maps to NM_181872.4 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:990503 G>A maps to NM_021240.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:22451496 G>T maps to NM_022160.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr19:42354537 T>A maps to ENST00000427618 L305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:42353012 G>T maps to ENST00000427618 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:42354751 C>T maps to ENST00000427618 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:86803943 G>T maps to NM_021145.3 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:86815273 C>T maps to NM_021145.3 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:86813854 T>C maps to NM_021145.3 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:86823162 C>T maps to NM_021145.3 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:46289691 G>T maps to NM_004943.1 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr19:46289925 C>T maps to NM_004943.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:46289883 G>A maps to NM_004943.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:118485682 G>A maps to NM_005509.4 Q1387Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:118465056 A>G maps to NM_005509.4 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:118485421 C>T maps to NM_005509.4 F1300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:118487670 C>T maps to NM_005509.4 R1548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:118574724 C>T maps to NM_005509.4 F2846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:118470056 A>G maps to NM_005509.4 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:118465080 A>G maps to NM_005509.4 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:118484612 G>T maps to NM_005509.4 E1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:118533561 C>T maps to NM_005509.4 I2552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:118582691 T>C maps to NM_005509.4 I2954I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:118451945 G>T maps to NM_005509.4 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:118450212 G>T maps to NM_005509.4 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr5:118552678 T>C maps to NM_005509.4 N2649N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:51773809 C>T maps to NM_001174116.1 K1831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:51791646 C>T maps to NM_001174116.1 G1258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:51791859 G>A maps to NM_001174116.1 V1187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:51792125 C>A maps to NM_001174116.1 E1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:51766564 G>A maps to NM_001174116.1 R2397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:51772261 C>T maps to NM_001174116.1 A2213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:51743894 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:51792159 C>T maps to NM_001174116.1 K1087K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:51742424 G>T maps to NM_001174116.1 L2935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:51778323 G>A maps to NM_001174116.1 R1810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:51856379 C>A maps to NM_001174116.1 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr15:51763590 A>G maps to NM_001174116.1 P2407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:51830520 G>A maps to NM_001174116.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:51743894 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:70196988 A>G maps to NM_001080449.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:70209958 G>A maps to NM_001080449.1 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:70190254 C>A maps to NM_001080449.1 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:70225445 C>A maps to NM_001080449.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:70178925 C>T maps to NM_001080449.1 R1030R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:52402762 C>T maps to ENST00000273600 D1924D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:52398967 G>A maps to ENST00000273600 T1817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:52428536 G>A maps to ENST00000273600 P3625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52404739 C>T maps to ENST00000273600 L2142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52404783 G>A maps to ENST00000273600 E2156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52409254 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52426626 C>A maps to ENST00000273600 S3464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52429442 C>T maps to ENST00000273600 F3760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52432118 C>A maps to ENST00000273600 A4074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:52397048 C>T maps to ENST00000273600 Y1711Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:52398883 C>T maps to ENST00000273600 N1789N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:52426552 C>T maps to ENST00000273600 L3440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:52391949 C>A maps to ENST00000273600 I1339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:52397078 C>A maps to ENST00000273600 S1721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:52422223 C>T maps to ENST00000273600 Y3015Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:52402831 C>T maps to ENST00000273600 F1947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:52428587 G>A maps to ENST00000273600 S3642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr3:52398697 G>A maps to ENST00000273600 S1763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:52409984 G>T maps to ENST00000273600 E2392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr3:52384030 C>T maps to ENST00000273600 S851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:52428567 C>T maps to ENST00000273600 R3636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:124274538 C>T maps to NM_207437.3 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:124382335 G>A maps to NM_207437.3 P2982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:124268576 A>G maps to NM_207437.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:124323214 C>T maps to NM_207437.3 C1587C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:124270318 C>T maps to NM_207437.3 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:124341775 C>T maps to NM_207437.3 Y2086Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:124356031 C>A maps to NM_207437.3 T2438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:124395179 C>A maps to NM_207437.3 Y3247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:124268666 C>T maps to NM_207437.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:124359987 G>T maps to NM_207437.3 E2599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:124330622 C>T maps to NM_207437.3 Y1794Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:124358172 T>C maps to NM_207437.3 N2500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:124332584 G>A maps to NM_207437.3 A1846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:124395195 G>T maps to NM_207437.3 E3253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:124284840 G>T maps to NM_207437.3 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:124297862 G>A maps to NM_207437.3 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:124408891 A>G maps to NM_207437.3 E3775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:124252190 G>T maps to NM_207437.3 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:124257388 G>A maps to NM_207437.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:124323052 C>T maps to NM_207437.3 A1533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:124352577 G>A maps to NM_207437.3 R2359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:124358139 G>A maps to NM_207437.3 T2489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:124411190 C>T maps to NM_207437.3 Q3859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:124358139 G>A maps to NM_207437.3 T2489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:124393956 C>A maps to NM_207437.3 S3204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:124311256 G>A maps to NM_207437.3 Q1283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:124345600 C>T maps to NM_207437.3 A2146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:124398941 C>T maps to NM_207437.3 C3355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:124335511 G>A maps to NM_207437.3 T1942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:124268495 T>C maps to NM_207437.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr12:124417927 T>C maps to NM_207437.3 P4331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr7:21747334 C>T maps to NM_003777.3 R2196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:21906269 G>A maps to NM_003777.3 T3900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:21908480 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:21654737 G>T maps to NM_003777.3 E1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:21847544 G>T maps to NM_003777.3 E3411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:21901559 C>A maps to NM_003777.3 I3771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:21924012 C>T maps to NM_003777.3 F4171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:21938986 C>T maps to NM_003777.3 L4368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:21655862 C>T maps to NM_003777.3 Q1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:21675656 C>T maps to NM_003777.3 R1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:21784597 G>A maps to NM_003777.3 T2816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr7:21603810 C>T maps to NM_003777.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:21627779 G>A maps to NM_003777.3 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:21893967 C>T maps to NM_003777.3 N3706N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:21940748 C>T maps to NM_003777.3 Y4483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr7:21847594 C>T maps to NM_003777.3 Y3427Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr7:21628210 C>T maps to NM_003777.3 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:21630553 G>T maps to NM_003777.3 E730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:21779216 G>T maps to NM_003777.3 E2621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:21654761 G>T maps to NM_003777.3 E1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:21778397 C>T maps to NM_003777.3 I2582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:21604016 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:21938972 C>T maps to NM_003777.3 R4364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:21678683 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:21628824 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:21630553 G>T maps to NM_003777.3 E730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:21906201 G>T maps to NM_003777.3 E3878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:21912929 G>A maps to NM_003777.3 E4009E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:21641061 G>A maps to NM_003777.3 Q1158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:21654842 G>T maps to NM_003777.3 E1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:21678628 C>T maps to NM_003777.3 F1635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:21760398 C>T maps to NM_003777.3 S2404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:21778400 C>T maps to NM_003777.3 D2583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:21906201 G>T maps to NM_003777.3 E3878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr7:21744218 G>A maps to NM_003777.3 L2154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:21654748 G>A maps to NM_003777.3 E1290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:21646078 C>T maps to NM_003777.3 I1228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:21640503 G>T maps to NM_003777.3 E1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:21779216 G>T maps to NM_003777.3 E2621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:21901538 C>A maps to NM_003777.3 I3764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:21603903 C>T maps to NM_003777.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:21641065 G>T maps to NM_003777.3 E1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:21654887 C>T maps to NM_003777.3 R1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:21924012 C>T maps to NM_003777.3 F4171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:21698459 G>A maps to NM_003777.3 T1718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:57326124 G>T maps to ENST00000295941 L2449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:57401217 C>A maps to NM_178504.4 E1911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:57391409 G>T maps to NM_178504.4 I2163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:57386221 G>A maps to NM_178504.4 R2321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:57419200 C>A maps to NM_178504.4 E1602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:57489843 C>A maps to NM_178504.4 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:57496582 C>A maps to NM_178504.4 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:57327967 G>T maps to NM_178504.4 A3040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:57454590 C>A maps to NM_178504.4 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:57343825 G>T maps to NM_178504.4 I2783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:57457254 C>A maps to NM_178504.4 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr3:57489922 A>G maps to NM_178504.4 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:57443892 C>A maps to NM_178504.4 E973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:57454594 C>T maps to NM_178504.4 K739K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:76420010 G>A maps to ENST00000389840 A4478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:76526516 G>A maps to ENST00000389840 C1064C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:76563078 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:76497853 C>T maps to ENST00000389840 R1753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:76449423 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:76471849 G>A maps to ENST00000389840 G2726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76435168 T>C maps to ENST00000389840 V3922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76471849 G>A maps to ENST00000389840 G2726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76503560 G>A maps to ENST00000389840 D1517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76567719 G>A maps to ENST00000389840 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:76567818 G>T maps to ENST00000389840 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:76475711 G>A maps to ENST00000389840 R2571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:76570845 G>A maps to ENST00000389840 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:76497354 G>A maps to ENST00000389840 C1784C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:76570943 G>A maps to ENST00000389840 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:76562710 G>A maps to ENST00000389840 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:76499006 C>T maps to ENST00000389840 E1677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:76445561 G>T maps to ENST00000389840 Y3701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:76511089 G>A maps to ENST00000389840 I1289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:76521210 G>T maps to ENST00000389840 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:76447685 G>T maps to ENST00000389840 Y3519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:76481032 G>A maps to ENST00000389840 D2508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr17:76457791 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:7643238 G>A maps to NM_020877.2 W453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:7680143 G>A maps to NM_020877.2 K1665K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:7646256 T>C maps to NM_020877.2 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7637902 C>T maps to NM_020877.2 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7668884 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7678611 C>T maps to NM_020877.2 G1591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7679454 G>A maps to NM_020877.2 E1645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7691191 T>C maps to NM_020877.2 F2206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7630597 C>T maps to NM_020877.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7678182 C>T maps to NM_020877.2 F1536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7708668 C>T maps to NM_020877.2 R3134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:7626946 G>A maps to NM_020877.2 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:7690245 C>T maps to NM_020877.2 F2166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:7735059 C>A maps to NM_020877.2 I4231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:7736531 C>T maps to NM_020877.2 S4374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:7696520 C>T maps to NM_020877.2 R2523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:7720726 C>T maps to NM_020877.2 I3338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:7734073 T>C maps to NM_020877.2 H4048H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:7700777 C>T maps to NM_020877.2 S2670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:7720880 C>A maps to NM_020877.2 I3341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:7721274 C>A maps to NM_020877.2 I3416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7678156 C>T maps to NM_020877.2 R1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7695251 C>T maps to NM_020877.2 G2306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr17:7695356 C>T maps to NM_020877.2 L2341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr17:7710588 C>T maps to NM_020877.2 R3188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr17:7667542 C>T maps to NM_020877.2 H1096H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:7719939 C>T maps to NM_020877.2 Q3261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:7678147 G>T maps to NM_020877.2 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:7696393 C>A maps to NM_020877.2 T2480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:7668872 C>T maps to NM_020877.2 F1167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:7678096 G>T maps to NM_020877.2 E1508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7664166 C>A maps to NM_020877.2 I965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7684101 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:7673644 T>C maps to NM_020877.2 I1339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:7674694 G>A maps to NM_020877.2 S1470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:20955879 G>A maps to NM_017539.1 L3817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:21147645 G>A maps to NM_017539.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:20946729 G>A maps to NM_017539.1 V3979V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:21145683 A>C maps to NM_017539.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:20990726 G>A maps to NM_017539.1 S2667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:20990816 G>A maps to NM_017539.1 L2637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:21011602 G>A maps to NM_017539.1 R2122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:21030982 G>A maps to NM_017539.1 S1995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:20986638 C>T maps to NM_017539.1 T2725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:21136605 G>A maps to NM_017539.1 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:21156604 G>T maps to NM_017539.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:20974858 G>T maps to NM_017539.1 I3449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:20975158 G>T maps to NM_017539.1 I3349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:21011582 G>A maps to NM_017539.1 F2128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:21078665 G>T maps to NM_017539.1 L1152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:20952754 G>A maps to NM_017539.1 T3874T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:21080839 G>A maps to NM_017539.1 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:21123342 C>A maps to NM_017539.1 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:20999361 G>A maps to NM_017539.1 I2209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:20996938 G>T maps to NM_017539.1 I2375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:20999157 G>A maps to NM_017539.1 L2247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr16:20955916 G>A maps to NM_017539.1 N3804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:20944759 C>A maps to NM_017539.1 E4023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:20986562 C>A maps to NM_017539.1 G2751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:20990816 G>A maps to NM_017539.1 L2637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:21008665 G>A maps to NM_017539.1 I2180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:21053360 G>A maps to NM_017539.1 P1542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:21049286 G>A maps to NM_017539.1 I1582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr16:20975299 G>A maps to NM_017539.1 A3302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:20974882 C>T maps to NM_017539.1 Q3441Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:20996988 G>A maps to NM_017539.1 R2359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:21011582 G>A maps to NM_017539.1 F2128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:13794110 C>T maps to NM_001369.2 A2648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:13752335 C>T maps to NM_001369.2 R3645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:13776653 C>T maps to NM_001369.2 S3089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr5:13727633 A>G maps to NM_001369.2 P4005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:13759059 G>A maps to NM_001369.2 L3438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:13769681 A>G maps to NM_001369.2 S3216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:13781038 T>C maps to NM_001369.2 G2950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:13901441 T>C maps to NM_001369.2 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:13914643 C>T maps to NM_001369.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:13719137 C>A maps to NM_001369.2 E4118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:13753428 C>A maps to NM_001369.2 T3595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:13769651 C>T maps to NM_001369.2 A3226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:13809248 C>T maps to NM_001369.2 P2552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:13871021 C>A maps to NM_001369.2 E1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:13900514 C>A maps to NM_001369.2 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:13701533 A>G maps to NM_001369.2 I4450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:13841847 C>A maps to NM_001369.2 E1813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:13870997 C>A maps to NM_001369.2 E1238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:13762973 C>A maps to NM_001369.2 E3380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:13776707 G>A maps to NM_001369.2 H3071H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:13770946 G>A maps to NM_001369.2 H3172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:13841193 C>A maps to NM_001369.2 E1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:13830726 C>A maps to NM_001369.2 G2014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr5:13824358 C>T maps to NM_001369.2 T2176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:13700880 C>A maps to NM_001369.2 E4531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:13716595 C>T maps to NM_001369.2 Q4303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:13754447 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:13701496 C>A maps to NM_001369.2 E4463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:13919296 C>T maps to NM_001369.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:13810219 C>T maps to NM_001369.2 P2519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr5:13901501 A>G maps to NM_001369.2 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr5:13867993 G>A maps to NM_001369.2 G1314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:13870925 C>A maps to NM_001369.2 E1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:13717497 C>A maps to NM_001369.2 E4211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:13829813 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:84851695 C>T maps to NM_001370.1 G1435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:84934720 C>T maps to NM_001370.1 R2977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:84771459 C>T maps to NM_001370.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:84774397 C>T maps to NM_001370.1 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:84930557 G>T maps to NM_001370.1 E2701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:84752745 C>T maps to NM_001370.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr2:84846940 C>T maps to NM_001370.1 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:84756153 G>T maps to NM_001370.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:84934720 C>T maps to NM_001370.1 R2977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:84932820 C>T maps to NM_001370.1 R2893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:84864467 G>A maps to NM_001370.1 A1596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:84921573 G>A maps to NM_001370.1 K2498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:84931282 C>T maps to NM_001370.1 D2774D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:84880700 A>G maps to NM_001370.1 E1779E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr2:85012775 C>T maps to NM_001370.1 R3666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:196689149 G>A maps to NM_018897.2 G3040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:196659100 C>T maps to NM_018897.2 P3559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:196749421 G>A maps to NM_018897.2 R1884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:196729052 G>T maps to NM_018897.2 R2442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:196852953 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:196659120 G>A maps to NM_018897.2 R3553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr2:196825023 G>A maps to NM_018897.2 R951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:196729106 G>T maps to NM_018897.2 L2424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:196729738 G>A maps to NM_018897.2 R2214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:196746695 T>C maps to NM_018897.2 P1928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:196749415 G>A maps to NM_018897.2 R1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:196642562 G>A maps to NM_018897.2 F3675F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:196659120 G>A maps to NM_018897.2 R3553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:196737011 C>A maps to NM_018897.2 E2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:196822169 C>A maps to NM_018897.2 E965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:196642673 G>A maps to NM_018897.2 G3638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:196681638 C>T maps to NM_018897.2 S3158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:196640692 G>A maps to NM_018897.2 I3693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:196746610 G>A maps to NM_018897.2 R1957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:196737150 G>A maps to NM_018897.2 I2152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:196749415 G>A maps to NM_018897.2 R1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:196877604 C>A maps to NM_018897.2 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:196682517 T>C maps to NM_018897.2 G3109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:196765185 A>G maps to NM_018897.2 P1456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:196825104 C>A maps to NM_018897.2 E924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:196723269 G>A maps to NM_018897.2 C2665C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:196746610 G>A maps to NM_018897.2 R1957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:196674543 G>A maps to NM_018897.2 C3271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:196642562 G>A maps to NM_018897.2 F3675F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr2:196822050 A>G maps to NM_018897.2 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr2:196729214 C>T maps to NM_018897.2 A2388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:196718093 G>A maps to NM_018897.2 L2918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:38866032 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:38771020 G>T maps to ENST00000327475 E978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:38747762 C>A maps to ENST00000327475 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:38939446 T>C maps to ENST00000449981 C4165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:38754598 C>T maps to ENST00000327475 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:38903430 G>T maps to ENST00000327475 E3829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:38704974 G>T maps to ENST00000327475 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:38813481 G>T maps to ENST00000327475 E1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:38825445 C>T maps to ENST00000327475 S1950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr6:38893828 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:38818122 G>T maps to ENST00000327475 E1754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:38840727 G>A maps to ENST00000327475 W2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:38821119 A>G maps to ENST00000327475 A1898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:38939366 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr6:38840724 C>A maps to ENST00000327475 I2415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:38754598 C>T maps to ENST00000327475 F806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:38810450 T>G maps to ENST00000327475 L1527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:38810579 C>A maps to ENST00000327475 I1570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:38820537 C>A maps to ENST00000327475 I1833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:38858446 C>A maps to ENST00000327475 Y2819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:38897406 G>T maps to ENST00000327475 E3735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:38941565 C>T maps to ENST00000327475 R4207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:38828261 C>T maps to ENST00000327475 D1984D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:38863866 G>T maps to ENST00000327475 E2924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:38810209 T>C maps to ENST00000327475 G1499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr17:11540094 G>T maps to NM_001372.3 E594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:11572793 G>A maps to NM_001372.3 Q1012Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:11648148 C>T maps to NM_001372.3 S2049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:11597207 C>T maps to NM_001372.3 I1546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:11865482 G>A maps to NM_001372.3 T4381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:11604467 T>C maps to NM_001372.3 G1685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:11650949 G>A maps to NM_001372.3 Q2159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:11774937 C>T maps to NM_001372.3 N3359N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:11696894 C>T maps to NM_001372.3 R2713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:11806134 G>T maps to NM_001372.3 E3836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:11837304 C>T maps to NM_001372.3 R4136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:11845738 C>T maps to NM_001372.3 G4260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr17:11783506 A>T maps to NM_001372.3 K3531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:11840724 C>T maps to NM_001372.3 N4182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:11651012 C>A maps to NM_001372.3 L2180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:11725367 C>T maps to NM_001372.3 R2947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr17:11556156 G>C maps to NM_001372.3 V811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr17:11696894 C>T maps to NM_001372.3 R2713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:11572943 C>T maps to NM_001372.3 I1062I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:11631148 C>A maps to NM_001372.3 I1908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:11660941 G>T maps to NM_001372.3 E2310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:11757423 G>A maps to NM_001372.3 K3204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:11833331 G>A maps to NM_001372.3 E4009E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:11572958 G>A maps to NM_001372.3 T1067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:11806205 C>T maps to NM_001372.3 P3859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr17:11772536 G>A maps to NM_001372.3 V3340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:11572543 G>A maps to NM_001372.3 R965R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:34506853 C>T maps to NM_012144.2 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:34491512 G>A maps to NM_012144.2 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:34459020 G>A maps to NM_012144.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:72297259 T>C maps to NM_023036.4 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:72308305 C>T maps to NM_023036.4 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72285852 C>T maps to NM_023036.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72306262 C>T maps to NM_023036.4 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72308245 C>T maps to NM_023036.4 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:72283117 C>A maps to NM_023036.4 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:72308221 G>A maps to NM_023036.4 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZP-01A-21D-A10M-09 chr17:72277979 C>G maps to NM_023036.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:72278078 C>T maps to NM_023036.4 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:33038708 C>A maps to NM_001539.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:33030481 C>T maps to NM_001539.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:33036572 C>T maps to NM_001539.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:46993024 G>A maps to NM_005880.3 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:47005303 G>A maps to NM_005880.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:4491407 C>T maps to NM_005147.4 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:78566743 T>C maps to NM_018602.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:78565440 G>A maps to NM_018602.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:14627331 G>T maps to NM_006145.1 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:74103247 G>A maps to NM_017626.4 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:74100755 G>A maps to NM_017626.4 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:73662140 C>T maps to NM_153614.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:73679424 C>A maps to NM_153614.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:100824912 G>A maps to NM_001031723.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:234652301 G>A maps to NM_001001394.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:234652169 C>T maps to NM_001001394.3 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:234652295 G>A maps to NM_001001394.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:78478892 G>T maps to NM_007034.3 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:34993341 G>T maps to NM_001135005.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:157155853 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:41257292 C>A maps to NM_145174.1 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:128181670 C>A maps to NM_153330.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:128181827 G>A maps to NM_153330.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:108213425 A>C maps to NM_012328.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:108212224 G>T maps to NM_012328.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:22209854 G>A maps to NM_022365.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:183584829 G>T maps to NM_018981.1 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:183621135 C>T maps to NM_018981.1 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:6697320 G>A maps to NM_018198.3 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:6727782 G>A maps to NM_018198.3 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:6697386 G>T maps to NM_018198.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:6704718 C>T maps to NM_018198.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr1:6741011 G>C maps to NM_018198.3 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:6705991 G>A maps to NM_018198.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:132179924 C>A maps to NM_015268.3 S530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:132235293 T>C maps to NM_015268.3 Y1838Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:132242497 G>T maps to NM_015268.3 E2001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:132209854 G>T maps to NM_015268.3 E1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:132201122 G>A maps to NM_015268.3 W976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:132209751 A>G maps to NM_015268.3 Q1160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:132172152 G>A maps to NM_015268.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:132176196 T>C maps to NM_015268.3 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:132219705 G>A maps to NM_015268.3 T1495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:132182619 G>A maps to NM_015268.3 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:56215919 G>T maps to NM_032364.5 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr13:43643081 G>A maps to NM_013238.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:15863052 G>A maps to NM_015291.2 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:15860794 C>T maps to NM_015291.2 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:15893704 G>A maps to NM_015291.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:15860734 T>C maps to NM_015291.2 H57H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:15863151 C>T maps to NM_015291.2 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:15873341 G>A maps to NM_015291.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:41065954 G>A maps to NM_018163.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:41068738 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-AP-A056-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:138749750 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:102953401 G>A maps to NM_014377.1 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:102953081 G>A maps to NM_014377.1 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:102962392 G>A maps to NM_014377.1 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:102968184 T>C maps to NM_014377.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:34937594 G>A maps to NM_194283.3 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:34937664 G>T maps to NM_194283.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:34945104 G>T maps to NM_194283.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:34936268 T>C maps to NM_194283.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:34937550 G>T maps to NM_194283.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:34954761 G>A maps to NM_194283.3 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:34945047 G>T maps to NM_194283.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:49745224 G>A maps to NM_024902.2 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:31392303 G>A maps to NM_181706.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr21:34860703 C>A maps to NM_001040192.1 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr21:34861097 T>C maps to NM_001040192.1 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:34861072 C>A maps to NM_001040192.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:34861549 C>A maps to NM_001040192.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:34861072 C>A maps to NM_001040192.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:96409924 G>T maps to NM_006260.4 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:96375599 T>C maps to NM_006260.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr20:62562310 C>T maps to NM_025219.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:66988893 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:27503032 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:27503295 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:65849986 G>T maps to ENST00000371069 G260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:65864505 G>A maps to ENST00000371069 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:65855266 G>A maps to ENST00000371069 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:65877063 G>T maps to ENST00000371069 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:40140848 T>C maps to NM_003315.3 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:75003168 C>A maps to NM_015190.3 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:75006582 G>A maps to NM_015190.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:74156178 G>T maps to NM_031427.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:38023320 G>T maps to NM_003462.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153633334 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153633336 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:153633184 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:153631617 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153631120 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153631131 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:2287040 C>T maps to NM_001374.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:58186794 C>A maps to NM_004944.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr2:230252979 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:230456318 C>A maps to NM_139072.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:230312256 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr11:6540894 C>T maps to NM_144666.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:6592589 C>T maps to NM_144666.2 G4616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:6593125 C>T maps to NM_144666.2 N4724N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:6550136 C>T maps to NM_144666.2 C711C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6567482 C>T maps to NM_144666.2 R1772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6568156 C>T maps to NM_144666.2 S1996S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6580461 C>A maps to NM_144666.2 T3156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6592488 C>T maps to NM_144666.2 L4583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:6585117 C>T maps to NM_144666.2 L3350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:6519558 C>T maps to NM_144666.2 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:6585808 C>T maps to NM_144666.2 L3511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:6588138 G>A maps to NM_144666.2 T3800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:6593182 G>A maps to NM_144666.2 R4743R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:6566209 C>T maps to NM_144666.2 S1347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr11:6568031 T>C maps to NM_144666.2 L1955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr11:6567731 C>T maps to NM_144666.2 L1855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr11:6554960 C>T maps to NM_144666.2 Y852Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr11:6593002 C>T maps to NM_144666.2 P4683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:6567853 G>A maps to NM_144666.2 P1895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:6569487 C>A maps to NM_144666.2 L2318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:6592568 G>A maps to NM_144666.2 S4609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:6591950 C>T maps to NM_144666.2 A4403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:6578769 C>T maps to NM_144666.2 L2749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:6530235 C>T maps to NM_144666.2 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr11:6567079 A>T maps to NM_144666.2 A1637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr9:131016983 C>T maps to ENST00000372923 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr9:130981010 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr12:32886653 T>C maps to ENST00000381000 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:32891218 G>T maps to ENST00000381000 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:32884002 G>T maps to ENST00000381000 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr12:32873729 G>C did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr12:32873711 T>C maps to ENST00000381000 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:10913004 G>A maps to NM_001005361.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:10906803 G>T maps to NM_001005360.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:10935827 C>T maps to NM_001005361.2 Y663Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:10887836 C>T maps to NM_001005361.2 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr19:10906061 G>A maps to NM_001005361.2 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr19:10940818 C>T maps to NM_001005361.2 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:10908169 G>A maps to NM_001005361.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:10930741 C>T maps to NM_001005361.2 F586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:172013548 C>T maps to ENST00000359070 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:172011169 G>A maps to ENST00000359070 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:172100367 C>G maps to ENST00000359070 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:172100370 G>A maps to ENST00000359070 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:172050997 C>T maps to ENST00000359070 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr10:101654734 G>A maps to ENST00000342239 R1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:101654767 G>A maps to ENST00000342239 R1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:101667761 G>A maps to ENST00000342239 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:101639599 C>A maps to ENST00000342239 E1530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:101716390 C>T maps to ENST00000342239 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:101716408 C>T maps to ENST00000342239 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:101639585 A>G maps to ENST00000342239 S1534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:10257085 G>A maps to NM_001130823.1 N945N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:10270428 C>T maps to NM_001130823.1 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:10260302 G>A maps to NM_001130823.1 N804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr19:10257085 G>A maps to NM_001130823.1 N945N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr19:10273405 G>A maps to NM_001130823.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:10291101 T>C maps to NM_001130823.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:10265275 G>A maps to NM_001130823.1 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:25463269 C>T maps to NM_175629.1 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:25464454 G>A maps to NM_175629.1 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:25464526 G>T maps to NM_175629.1 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:31383336 C>T maps to NM_006892.3 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:31375142 G>A maps to NM_006892.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:31375040 G>A maps to NM_006892.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:31369220 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:31394052 G>A maps to NM_006892.3 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:31383225 C>T maps to NM_006892.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:31379487 C>T maps to NM_006892.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:31372580 C>T maps to NM_006892.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:31372643 G>A maps to NM_006892.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:31383454 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr21:45671548 G>A maps to NM_013369.2 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:220251416 G>A maps to NM_012100.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr10:98064403 G>A maps to NM_004088.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:98078210 C>T maps to NM_004088.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr10:98087330 C>T maps to NM_004088.3 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:44431986 C>A maps to NM_052951.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:44421338 G>A maps to NM_052951.2 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:44424010 C>T maps to NM_052951.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:94342647 G>A maps to NM_014597.4 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:94335328 G>T maps to ENST00000436063 S790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:94342443 T>C maps to NM_014597.4 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:94337678 C>A maps to NM_014597.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:94335363 A>G maps to ENST00000436063 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:94335481 G>A maps to NM_014597.4 Y732Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:94342674 T>C maps to NM_014597.4 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:30017806 G>T maps to NM_003586.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr16:30018405 C>T maps to NM_003586.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:30018405 C>T maps to NM_003586.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:128821551 G>A maps to ENST00000398025 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:129231683 C>A maps to ENST00000398025 G1729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:128780219 G>A maps to ENST00000398025 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:128829957 C>T maps to ENST00000398025 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:129183157 C>A maps to ENST00000398025 Y1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr10:129202617 C>T maps to ENST00000398025 I1394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr10:128841416 G>A maps to ENST00000398025 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:128768997 G>T maps to ENST00000398025 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:129046279 C>T maps to ENST00000398025 F997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:129237359 C>T maps to ENST00000398025 D1755D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:129055660 C>T maps to ENST00000398025 F1049F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:129141971 G>A maps to ENST00000398025 E1107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr10:129152935 C>T maps to ENST00000398025 Y1121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr10:129179610 T>G maps to ENST00000398025 L1307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:129172082 C>T maps to ENST00000398025 V1202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:129183160 C>T maps to ENST00000398025 F1350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:129217982 C>T maps to ENST00000398025 I1627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:128923771 T>C maps to ENST00000398025 D865D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:225664957 G>A maps to NM_014689.2 I1472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:225717834 A>G maps to NM_014689.2 C631C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:225721590 T>C maps to NM_014689.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:225739029 G>A maps to NM_014689.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:225666729 G>A maps to NM_014689.2 G1432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:225669923 G>A maps to NM_014689.2 Y1350Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:225729338 G>A maps to NM_014689.2 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:225669779 G>T maps to NM_014689.2 I1371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:225672641 G>A maps to NM_014689.2 R1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr2:225729660 G>A maps to NM_014689.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:225666692 G>A maps to NM_014689.2 R1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:225659610 G>A maps to NM_014689.2 N1713N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:225761043 T>C maps to NM_014689.2 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:225662608 G>T maps to NM_014689.2 V1528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:225739029 G>A maps to NM_014689.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:225729365 A>G maps to NM_014689.2 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:225659688 G>A maps to NM_014689.2 S1687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:225670000 G>A maps to NM_014689.2 R1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:225670025 G>T maps to NM_014689.2 P1316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:225704713 G>A maps to NM_014689.2 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:225719698 G>A maps to NM_014689.2 N623N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:225669923 G>A maps to NM_014689.2 Y1350Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:225750386 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:117744325 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:117762163 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:117679321 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:117805039 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:117814500 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:117695358 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:117722185 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:117727244 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:117749565 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:117773494 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:117783057 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117676693 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117695437 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117706313 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117727300 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117770373 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117815109 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117815746 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:117700603 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:117702122 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:117731999 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:117772072 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:117773527 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:117782938 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:117706306 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:117785948 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:117815023 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:117743279 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:117817096 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:117700080 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117676739 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117712526 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117731475 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117773465 G>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:117788745 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:117714127 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:117722428 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:117788650 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:117805045 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr5:169122805 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:169116254 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:169230161 C>T maps to NM_004946.2 C885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:169108816 C>A maps to NM_004946.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:169125453 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:169494608 C>A maps to NM_004946.2 T1521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:169081455 C>T maps to NM_004946.2 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:169494543 G>T maps to NM_004946.2 E1500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:169494674 C>T maps to NM_004946.2 F1543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:169138991 A>G maps to NM_004946.2 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:169138989 C>T maps to NM_004946.2 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:169506137 G>T maps to NM_004946.2 S1718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:169139166 G>A maps to NM_004946.2 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:51198038 C>T maps to NM_004947.4 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:51264835 C>T maps to NM_004947.4 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:51266225 C>A maps to NM_004947.4 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:50971504 T>C maps to NM_004947.4 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:51127767 C>T maps to NM_004947.4 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:51386329 C>T maps to NM_004947.4 Y1321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:51395480 C>T maps to NM_004947.4 F1619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:51102025 G>T maps to NM_004947.4 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:51264763 C>A maps to NM_004947.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:51412014 A>G maps to NM_004947.4 G1803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:51196712 C>A maps to NM_004947.4 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:51264730 T>C maps to NM_004947.4 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:51413216 C>T maps to NM_004947.4 V1817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:51367624 C>T maps to NM_004947.4 D1153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:111517131 G>T maps to ENST00000428084 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:111449433 G>A maps to ENST00000428084 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:111382128 T>C maps to ENST00000428084 R1579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:111512548 C>A maps to ENST00000428084 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:111541815 C>A maps to ENST00000428084 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:111580246 G>A maps to ENST00000428084 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:111584866 G>A maps to ENST00000428084 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:111512548 C>A maps to ENST00000428084 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:111584866 G>A maps to ENST00000428084 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:111368575 C>T maps to ENST00000428084 P1894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:111535676 G>A maps to ENST00000428084 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:111503488 C>T maps to ENST00000428084 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:111580279 C>A maps to ENST00000428084 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:111580190 C>T maps to ENST00000428084 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:111503569 G>T maps to ENST00000428084 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:25203081 G>A maps to NM_024940.6 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:25265504 C>A maps to NM_024940.6 I1700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:25126364 G>A maps to NM_024940.6 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:25226165 G>A maps to NM_024940.6 R1121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:25234886 G>T maps to NM_024940.6 E1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:25249453 G>A maps to NM_024940.6 R1466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr8:25230227 C>T maps to NM_024940.6 N1226N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr8:25267714 T>C maps to NM_024940.6 T1835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr8:25166361 C>T maps to NM_024940.6 H371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr8:25158157 C>G maps to NM_024940.6 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr8:25234931 A>T maps to NM_024940.6 K1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:11312669 G>A maps to ENST00000319867 R1863R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:11313257 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:11353807 G>A maps to ENST00000319867 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:11332897 C>T maps to ENST00000319867 P1089P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:11348886 G>A maps to ENST00000252453 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:11348737 C>T maps to ENST00000319867 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr19:11333749 G>A maps to ENST00000319867 S996S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr19:11313382 G>A maps to ENST00000319867 R1748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:62941520 G>A maps to ENST00000371140 R1940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:62923375 C>T maps to ENST00000371140 R2071R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:63091069 G>A maps to ENST00000371140 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:62995107 T>C maps to ENST00000371140 G1207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr1:63084453 A>G maps to ENST00000371140 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:62940938 G>A maps to ENST00000371140 P2015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:63113404 C>A maps to ENST00000371140 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:62941818 G>A maps to ENST00000371140 Y1881Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:62993878 G>A maps to ENST00000371140 I1293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:63018422 G>A maps to ENST00000371140 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:63052295 C>A did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:62953083 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:62993827 C>T maps to ENST00000371140 T1310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:63009347 C>T maps to ENST00000371140 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:62961353 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:62954682 A>G maps to ENST00000371140 H1805H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:62971388 T>C maps to ENST00000371140 Q1525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:420537 G>A maps to NM_203447.3 R1326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:379891 C>T maps to NM_203447.3 Y854Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:379882 C>T maps to NM_203447.3 Y851Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:340297 A>G maps to NM_203447.3 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:99449491 A>C maps to ENST00000428223 A2025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:99554637 G>A maps to ENST00000428223 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:99520540 G>A maps to ENST00000428223 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:99515326 G>A maps to ENST00000428223 N1175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:99567595 G>A maps to ENST00000428223 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr13:99567640 G>A maps to ENST00000428223 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:99519784 G>T maps to ENST00000428223 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:99578103 G>A maps to ENST00000428223 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr13:99489816 T>C maps to ENST00000428223 E1392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:99446888 C>T maps to ENST00000339416 S2091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:99520540 G>A maps to ENST00000428223 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:74783472 A>G maps to NM_001381.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr8:21767295 C>T maps to NM_003974.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr8:21767295 C>T maps to NM_003974.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:176936547 G>A maps to NM_024872.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:57508715 G>A maps to NM_018110.3 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:53205224 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:3475166 G>A maps to ENST00000389653 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:131708577 G>A maps to NM_014908.3 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:131708118 A>G maps to NM_014908.3 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr9:131709536 G>A maps to NM_014908.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr9:131708811 G>A maps to NM_014908.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:131847513 C>T maps to NM_020438.4 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:34954502 C>T maps to NM_017613.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:83863318 G>A maps to NM_015018.2 V2073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:83872581 C>T maps to NM_015018.2 R2346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:83839123 C>A maps to NM_015018.2 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:83829561 G>T maps to NM_015018.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:83832635 C>A maps to NM_015018.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:83848696 C>T maps to NM_015018.2 R1646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:83877727 C>T maps to NM_015018.2 R2414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr6:83863646 C>T maps to NM_015018.2 Q2092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:83845373 C>T maps to NM_015018.2 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr21:37620743 C>T maps to NM_005128.2 R1626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:37602803 C>T maps to NM_005128.2 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:37617940 C>T maps to NM_005128.2 V1221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:37661366 G>A maps to NM_005128.2 T2126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:37597955 C>A maps to NM_005128.2 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:37572628 C>T maps to NM_005128.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:37626179 G>A maps to NM_005128.2 R1744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:37618921 C>T maps to NM_005128.2 N1548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:37617484 C>T maps to NM_005128.2 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:37661061 A>G maps to NM_005128.2 T2102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:37595580 C>T maps to NM_005128.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:37618096 G>A maps to NM_005128.2 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr21:37618894 A>G maps to NM_005128.2 T1539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:2180743 C>T maps to ENST00000221482 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:2211152 G>T maps to ENST00000221482 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:2193745 C>T maps to ENST00000221482 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:2225434 G>A maps to ENST00000221482 P1215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr19:2226431 C>T maps to ENST00000221482 D1304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:2185904 T>G maps to ENST00000221482 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:2216524 C>T maps to ENST00000221482 C723C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr11:118969159 G>A maps to NM_001382.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:103354445 C>T maps to NM_015448.1 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:30917749 A>G maps to NM_080870.3 Q503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:30919772 G>T maps to NM_080870.3 E1178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:30918056 G>T maps to NM_080870.3 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:30918697 A>T maps to NM_080870.3 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:30919856 G>T maps to NM_080870.3 E1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:30916475 G>T maps to NM_080870.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:30917341 G>A maps to NM_080870.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:30919439 G>T maps to NM_080870.3 E1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:89704324 G>A maps to NM_004413.3 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr16:89696826 C>T maps to NM_004413.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:89704333 C>T maps to NM_004413.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:68023260 G>A maps to NM_022355.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:68021653 C>A maps to NM_022355.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:68011840 C>T maps to NM_022357.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:68014145 G>T maps to NM_022357.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr19:38704352 G>A maps to NM_001135155.1 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:38713194 G>A maps to NM_001135155.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:65108958 C>T maps to NM_006268.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:73141065 T>C maps to NM_012074.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:73137951 C>T maps to NM_012074.3 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:73137873 C>T maps to NM_012074.3 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:73190388 C>T maps to NM_012074.3 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr14:73181176 G>A maps to NM_012074.3 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:44438204 C>T maps to NM_001384.4 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:16305691 G>T maps to NM_206831.2 C51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:16302332 G>A maps to NM_206831.2 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:49552687 G>A maps to ENST00000449701 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr1:155112590 G>C maps to NM_018973.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:116485480 T>A maps to NM_020868.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:116538521 T>C maps to NM_020868.3 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:116520161 A>C maps to NM_020868.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:116593773 T>C maps to NM_020868.3 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:116572516 C>T maps to NM_020868.3 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr2:116548693 A>G maps to NM_020868.3 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:116599879 G>T maps to NM_020868.3 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:116066929 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:116598351 G>T maps to NM_020868.3 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr11:66262678 C>T maps to NM_005700.3 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:66259217 G>T maps to NM_005700.3 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:66262732 C>T maps to NM_005700.3 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:162851882 C>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr2:162879282 A>G maps to NM_001935.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:162875360 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:162903516 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:154593072 A>G maps to NM_130797.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:154672633 C>T maps to NM_130797.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:154664395 C>T maps to NM_130797.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:154681007 C>T maps to NM_130797.2 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:154681004 C>A maps to NM_130797.2 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:154667654 C>T maps to NM_130797.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:154561154 C>T maps to NM_130797.2 H304H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:140006599 G>A maps to NM_013379.2 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:65771296 A>C maps to NM_197960.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:65771368 G>A maps to NM_197960.2 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:65782574 C>A maps to NM_197960.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr15:65792979 A>G maps to NM_197960.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr15:65782557 A>G maps to NM_197960.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:65793068 C>A maps to NM_197960.2 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:4702660 G>A maps to ENST00000357909 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:4702660 G>A maps to ENST00000357909 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:4676623 G>A maps to ENST00000357909 G956G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:4684773 G>A maps to ENST00000357909 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:4683626 G>T maps to ENST00000357909 I810I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:109028100 C>T maps to NM_138815.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:109056357 G>A maps to NM_018189.3 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:109049482 A>C maps to NM_018189.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:109049637 C>A maps to NM_018189.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:109050758 G>T maps to NM_018189.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr6:74063669 G>T maps to NM_001025290.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:74063915 C>T maps to NM_001025290.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:54140181 C>T maps to NM_001012728.1 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:54137908 G>A maps to NM_001012728.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:54140010 C>T maps to NM_001012728.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:168698376 T>C maps to NM_001937.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:168665804 A>G maps to NM_001937.4 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:34979906 A>G maps to NM_015283.1 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:35050096 T>A maps to NM_015283.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:35142526 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:63954417 G>A maps to NM_173812.4 I717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:63974504 C>A maps to NM_173812.4 G613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:64011137 A>G maps to NM_173812.4 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:63976190 G>A maps to NM_173812.4 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:63991611 C>A maps to NM_173812.4 E480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr12:64057597 A>G maps to NM_173812.4 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:32955656 A>G maps to NM_001172774.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:95777430 C>A maps to NM_181787.2 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:95774026 C>T maps to NM_181787.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:98186482 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:97770920 G>A maps to NM_000110.3 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:97564115 C>A maps to NM_000110.3 E899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:98144656 C>A maps to NM_000110.3 G282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:105405170 G>A maps to NM_001385.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:105405170 G>A maps to NM_001385.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:105463593 G>A maps to NM_001385.2 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:105405061 G>A maps to NM_001385.2 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:26509876 C>T maps to NM_001197293.1 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:146773636 C>T maps to NM_001197294.1 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:146775167 C>T maps to NM_001197294.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:146780395 G>A maps to NM_001197294.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:146795376 C>A maps to NM_001197294.1 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:146775200 G>A maps to NM_001197294.1 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:134010535 C>A maps to NM_006426.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:134013941 C>T maps to NM_006426.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:134014369 C>T maps to NM_006426.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:134018388 C>A maps to NM_006426.2 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:134014420 C>T maps to NM_006426.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:134006167 C>T maps to NM_006426.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:134016166 C>A maps to NM_006426.2 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:134006239 C>T maps to NM_006426.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:27150166 C>A maps to NM_020134.3 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:27156175 C>T maps to NM_020134.3 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr2:27121504 C>T maps to NM_020134.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:27165524 C>T maps to NM_020134.3 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:74746291 G>T maps to NM_133637.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:74745581 G>A maps to NM_133637.2 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:102314995 T>C maps to NM_018370.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:102315025 T>C maps to NM_018370.2 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:102302085 G>A maps to NM_018370.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:102313918 T>C maps to NM_018370.2 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:111663135 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:111667414 A>G maps to NM_178454.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:174870092 G>A maps to NM_000794.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:174868815 G>A maps to NM_000794.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:174869349 G>A maps to NM_000794.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:113295286 C>T maps to ENST00000355319 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:113283485 C>T maps to ENST00000355319 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr11:113287603 G>C maps to ENST00000355319 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:113295286 C>T maps to ENST00000355319 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:113858529 G>T maps to NM_000796.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:113858393 G>A maps to NM_000796.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:113847742 G>A maps to NM_000796.3 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:9783919 C>T maps to NM_000798.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:9784684 C>T maps to NM_000798.4 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:9784324 C>A maps to NM_000798.4 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:9784342 G>A maps to NM_000798.4 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:9784693 C>T maps to NM_000798.4 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:9784900 C>T maps to NM_000798.4 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:31816305 G>A maps to NM_004147.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:18001618 C>T maps to NM_001388.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:18010541 C>T maps to NM_001388.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:50574229 C>T maps to NM_001080520.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:50598232 G>T maps to NM_001080520.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100513424 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100509437 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100515046 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:100497443 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100486730 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100502117 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100509891 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:100507598 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100496666 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100513460 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:100513301 C>T did not map to a codon.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr23:100513383 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100496808 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100505980 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100509468 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100503522 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:100510194 A>C did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:100496666 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100503108 A>C did not map to a codon.
Sequencing variant TCGA-FI-A2D2-01A-11D-A17D-09 chr23:100486679 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:28736008 C>T maps to NM_024421.2 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:28720265 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:28719767 C>A maps to NM_024421.2 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:28728518 G>A maps to NM_024421.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:28736073 G>A maps to NM_024421.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:28648063 G>A maps to ENST00000438199 R888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:28660281 G>A maps to ENST00000438199 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:28662280 A>G maps to ENST00000438199 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:28605814 C>A maps to NM_001941.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:28586951 G>T maps to NM_001941.3 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:28609588 C>T maps to NM_001941.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:28588310 C>A maps to NM_001941.3 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:28576923 G>A maps to NM_001941.3 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:28609588 C>T maps to NM_001941.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr21:41385098 G>A maps to NM_001389.3 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr21:42064793 C>T maps to NM_001389.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr21:41648060 G>A maps to NM_001389.3 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:41385098 G>A maps to NM_001389.3 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:41465723 G>A maps to NM_001389.3 S1258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:41711076 G>A maps to NM_001389.3 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:41719804 G>T maps to NM_001389.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr21:41725647 G>C maps to NM_001389.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr21:41648129 C>T maps to NM_001389.3 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:41427706 G>A maps to NM_001389.3 I1660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:41457637 G>A maps to NM_001389.3 N1341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:41414597 G>A maps to NM_001389.3 R1796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:41446966 G>A maps to NM_001389.3 R1629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:41450635 G>A maps to NM_001389.3 F1563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr21:41450818 G>A maps to NM_001389.3 G1502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr21:41505883 G>A maps to NM_001389.3 D1153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:41452084 C>A maps to NM_001389.3 G1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr21:41385071 T>G maps to NM_001389.3 G1976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr21:41416155 G>A maps to NM_001389.3 N1744N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:41452099 C>A maps to NM_001389.3 E1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr21:41719669 G>A maps to NM_001389.3 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:117374632 G>A maps to NM_020693.2 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:117314719 G>T maps to NM_020693.2 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:117332196 C>T maps to NM_020693.2 R1187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:117651206 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:117389195 G>A maps to NM_020693.2 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:117375657 G>T maps to NM_020693.2 V781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:117303950 G>A maps to NM_020693.2 D1703D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:117301645 G>A maps to NM_020693.2 H1886H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:117387200 G>A maps to NM_020693.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:117340691 G>A maps to NM_020693.2 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:117651259 G>T maps to NM_020693.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:117651358 C>T maps to NM_020693.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:117403235 T>C maps to NM_020693.2 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:120862687 T>C maps to NM_024094.2 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr8:120855865 G>A maps to NM_024094.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:120850620 C>T maps to NM_024094.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr21:38600599 C>T maps to NM_006052.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:38600668 A>C maps to NM_006052.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:39493328 C>T maps to ENST00000398948 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr6:116757322 G>A maps to NM_013352.2 Q564Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:116720637 G>A maps to NM_013352.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:116758193 G>T maps to NM_013352.2 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr6:116757662 G>T maps to NM_013352.2 G678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr6:116720817 G>A maps to NM_013352.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:116757016 C>T maps to NM_013352.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr6:116747868 T>C maps to NM_013352.2 N183N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:65180378 G>T maps to NM_032160.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:65178776 C>T maps to NM_032160.2 S1033S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:65179154 G>A maps to NM_032160.2 I907I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:65180543 A>C maps to NM_032160.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:65181634 C>A maps to NM_032160.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:65180402 T>C maps to NM_032160.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:65178586 C>A maps to NM_032160.2 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr18:65180861 A>G maps to NM_032160.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:65178652 C>A maps to NM_032160.2 E1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:28926071 G>T maps to NM_001942.2 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:28934804 G>A maps to NM_001942.2 E882E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:28908286 G>T maps to NM_001942.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:28906913 C>T maps to NM_001942.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:28911706 G>A maps to NM_001942.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:28914114 G>T maps to NM_001942.2 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:28934327 C>T maps to NM_001942.2 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:28914120 G>T maps to NM_001942.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:28934289 G>T maps to NM_001942.2 G711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr18:29102103 G>A maps to NM_001943.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:29125766 G>A maps to NM_001943.3 S806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:29122788 G>T maps to NM_001943.3 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:29102121 C>T maps to NM_001943.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:29116234 A>C maps to NM_001943.3 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:29126622 G>T maps to NM_001943.3 E1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:29126690 G>A maps to NM_001943.3 Q1114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:29044103 A>T maps to NM_001944.2 K344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:29054117 G>A maps to NM_001944.2 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:29056027 G>A maps to NM_001944.2 E935E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:29041234 C>T maps to NM_001944.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr18:29045298 C>T maps to NM_001944.2 N430N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:29041234 C>T maps to NM_001944.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr18:29056169 C>T maps to NM_001944.2 R983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:29041207 G>T maps to NM_001944.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:28980877 A>T maps to NM_001134453.1 K438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr18:28983493 C>T maps to NM_001134453.1 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:28993482 C>T maps to NM_001134453.1 T1035T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr18:28991146 G>A maps to NM_001134453.1 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:35399323 C>A maps to NM_001145315.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr6:7580241 C>T maps to NM_004415.2 N1273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:7585417 C>T maps to NM_004415.2 I2641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:7584920 G>T maps to NM_004415.2 E2476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:7585432 G>A maps to NM_004415.2 T2646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:7581336 C>T maps to NM_004415.2 D1638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:7571678 G>T maps to NM_004415.2 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:7579783 G>T maps to NM_004415.2 E1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:7566695 A>G maps to NM_004415.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:7584592 C>T maps to NM_004415.2 R2366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:7579738 G>T maps to NM_004415.2 E1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr6:7582896 C>G maps to NM_004415.2 S1801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr6:7570708 C>T maps to NM_004415.2 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:7580073 G>A maps to NM_004415.2 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:7558437 C>T maps to NM_004415.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:7568072 G>A maps to NM_004415.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:7585256 G>T maps to NM_004415.2 E2588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:7583374 C>T maps to NM_004415.2 T1960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:7580323 C>T maps to NM_004415.2 Q1301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:7579644 G>A maps to NM_004415.2 A1074A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:88533937 T>C maps to NM_014208.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:88533706 A>C maps to NM_014208.3 G123G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:88534063 C>T maps to NM_014208.3 S242S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr4:88535226 T>C maps to NM_014208.3 S471S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BS-A0UV-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BS-A0UV-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BS-A0UV-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:88535706 C>T maps to NM_014208.3 S631S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A160-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr4:88535706 C>T maps to NM_014208.3 S631S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A17Q-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:56535536 C>T maps to ENST00000361203 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:56458646 G>A maps to ENST00000361203 F3969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:56480382 C>A maps to ENST00000281662 G3192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:56327948 G>A maps to ENST00000370754 L5512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:56347611 C>A maps to ENST00000361203 E6880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:56417082 C>A maps to ENST00000361203 E5292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:56470518 C>T maps to ENST00000361203 L2758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:56500437 A>G maps to ENST00000361203 C834C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:56507421 G>A maps to NM_015548.4 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:56338680 T>C maps to ENST00000361203 G7117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:56374626 G>A maps to ENST00000361203 I6064I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:56472305 G>T maps to ENST00000361203 R2163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:56480332 G>A maps to ENST00000281662 S3208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:56481316 G>A maps to ENST00000281662 S2880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:56481809 G>T maps to ENST00000281662 S2716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:56483427 C>A maps to ENST00000281662 E2366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:56485365 G>A maps to ENST00000281662 R1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:56716357 C>T maps to ENST00000370754 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:56492073 G>A maps to ENST00000361203 S1339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:56340979 G>A maps to ENST00000361203 I7066I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:56401725 C>A maps to ENST00000361203 E5330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:56469026 C>A maps to ENST00000361203 E3256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr6:56716266 C>A maps to ENST00000370754 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr6:56483446 A>G maps to ENST00000281662 L2359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr6:56471183 C>A maps to ENST00000361203 G2537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:56471700 A>C maps to ENST00000361203 T2364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:56472906 A>G maps to ENST00000361203 V1962V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:56483017 T>C maps to ENST00000281662 Q2502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:56336874 G>T maps to ENST00000370754 A5261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:56417412 C>A maps to ENST00000361203 E5182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:56417617 G>A maps to ENST00000361203 A5113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:56470239 T>C maps to ENST00000361203 V2851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:56473940 C>A maps to ENST00000361203 E1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:56481831 C>A maps to ENST00000281662 E2709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:56507222 T>C maps to ENST00000361203 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:56471616 T>C maps to ENST00000361203 G2392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr6:56473403 C>A maps to ENST00000361203 E1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:56468780 C>A maps to ENST00000361203 E3338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:56473287 G>A maps to ENST00000361203 D1835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:56484067 T>C maps to ENST00000281662 L2152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:56504318 C>A maps to ENST00000361203 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:56819309 G>A maps to ENST00000370754 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:56328520 A>G maps to ENST00000361203 L7363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:56489960 A>G maps to ENST00000361203 I1397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:56325024 G>A maps to ENST00000361203 R7425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:56422301 C>A maps to ENST00000361203 E4608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:56458601 T>G maps to ENST00000361203 T3984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:56380317 G>T maps to ENST00000361203 S5958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:56471502 G>A maps to ENST00000361203 Y2430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:56480604 G>A maps to ENST00000281662 R3118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:56716219 G>A maps to ENST00000370754 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:56327870 G>T maps to ENST00000370754 C5538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:56458516 C>A maps to ENST00000361203 E4013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:56496793 G>A maps to ENST00000361203 R1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:17585250 G>A maps to NM_006870.3 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:17585235 C>A maps to NM_006870.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:17585272 C>T maps to NM_006870.3 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:205138768 C>T maps to NM_015375.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:18576811 G>A maps to NM_080820.4 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:212273783 C>A maps to NM_016448.2 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:212254013 G>T maps to NM_016448.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:212276273 G>T maps to NM_016448.2 E729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:212273606 T>C maps to NM_016448.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr18:32374193 C>T maps to NM_001390.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:32455325 G>T maps to NM_001390.4 G596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:32431844 G>A maps to NM_001390.4 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr18:32457704 T>C maps to NM_001390.4 N615N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:32418102 T>C maps to NM_001390.4 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:32374064 C>T maps to NM_001390.4 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr18:32391969 C>T maps to NM_001390.4 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:32335964 G>T maps to NM_001390.4 G9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:32345947 C>T maps to NM_001390.4 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr18:32395925 G>A maps to NM_001390.4 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:32431826 C>A maps to NM_001390.4 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:25799718 C>T maps to NM_021907.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:15524781 C>T maps to NM_032122.4 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:15638031 A>G maps to NM_032122.4 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:15627594 C>A maps to NM_032122.4 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:49926881 C>T maps to NM_001144955.1 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr15:49935648 T>C maps to NM_001144955.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:49917403 G>T maps to NM_001144955.1 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:118280304 C>T maps to NM_173666.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:113531865 C>T maps to NM_004416.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:113532908 G>A maps to NM_004416.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr12:113531470 G>T maps to NM_004416.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZP-01A-21D-A10M-09 chr12:113534659 C>T maps to NM_004416.2 H593H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:113531865 C>T maps to NM_004416.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr7:76112068 C>T maps to NM_020892.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:76112074 G>T maps to NM_020892.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr7:76111930 A>G maps to NM_020892.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:122288286 G>T maps to NM_138287.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:122287406 A>G maps to NM_138287.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:122287505 G>A maps to NM_138287.3 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:122287739 G>A maps to NM_138287.3 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:122288249 C>T maps to NM_138287.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr11:58949672 G>T maps to NM_015177.1 G225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:45440613 C>T maps to NM_175940.1 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:45439828 C>T maps to NM_175940.1 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:45457047 C>T maps to NM_175940.1 L1535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr15:45437187 G>A maps to NM_175940.1 E744E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:45428766 C>T maps to NM_175940.1 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr15:45442848 C>T maps to NM_175940.1 V946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:45427398 C>T maps to NM_175940.1 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr15:45455872 G>A maps to NM_175940.1 R1464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:45391908 G>T maps to NM_014080.4 A1122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:45392299 A>G maps to NM_014080.4 C1044C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:45391943 C>A maps to NM_014080.4 E1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:45391588 C>A maps to NM_014080.4 V1169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:45392329 G>A maps to NM_014080.4 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:45405546 A>G maps to NM_014080.4 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:45389448 C>T maps to NM_014080.4 E1278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:45404058 G>A maps to NM_014080.4 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr15:45414401 G>A maps to NM_144565.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:45411396 A>G maps to NM_144565.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:45409501 C>T maps to NM_207581.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:80019497 G>A maps to NM_022156.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr16:68112415 C>T maps to NM_017803.3 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:68107938 G>A maps to NM_017803.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:68109408 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:5788367 C>T maps to NM_020175.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:5790183 C>T maps to NM_020175.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:5790315 T>C maps to NM_020175.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:107214230 G>A maps to NM_181581.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:172197161 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:172195923 C>T maps to NM_004417.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:221875918 C>T maps to NM_007207.3 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:221912392 C>A maps to NM_007207.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:221879662 G>A maps to NM_007207.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:221912555 G>A maps to NM_007207.3 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:221875828 G>A maps to NM_007207.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:221912918 C>T maps to NM_007207.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:221875888 G>T maps to NM_007207.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:74002126 C>T maps to NM_003584.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:74002107 G>A maps to NM_003584.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr1:161719794 G>T maps to NM_007240.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:30454956 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:12630938 C>A maps to NM_030640.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr12:12630803 C>A maps to NM_030640.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr12:12630317 G>A maps to NM_030640.2 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr12:12630251 G>A maps to NM_030640.2 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:12630141 C>T maps to NM_030640.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:44703599 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:44703846 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:44703566 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:44703760 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:44703761 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:44703389 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:44703877 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:44703748 A>G did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:44703623 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:44703877 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr6:335111 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:33454895 G>A maps to NM_024025.1 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:33449605 G>A maps to NM_024025.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:167095321 C>T maps to NM_001080426.1 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:167096116 C>T maps to NM_001080426.1 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:167097349 C>T maps to NM_001080426.1 H994H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:167095438 G>A maps to NM_001080426.1 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:167082967 A>G maps to NM_001080426.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:167097770 G>T maps to NM_001080426.1 E1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:167095562 C>T maps to NM_001080426.1 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:167095817 C>T maps to NM_001080426.1 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:167095912 G>A maps to NM_001080426.1 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:167096671 C>A maps to NM_001080426.1 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:41847045 G>A maps to NM_004090.3 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:41847096 G>A maps to NM_004090.3 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:29194614 G>A maps to NM_001394.5 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:29194752 C>T maps to NM_001394.5 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:29194806 G>A maps to NM_001394.5 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr8:29194923 G>A maps to NM_001394.5 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:29195982 G>A maps to NM_001394.5 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:29197740 G>T maps to NM_001394.5 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:112269829 C>A maps to NM_004419.3 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152915044 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:152915044 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152914981 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:152915044 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152915044 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:48626676 G>A maps to NM_001025248.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:57666656 G>A maps to NM_001012729.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:57669739 C>A maps to NM_001012729.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:57672039 C>A maps to NM_001012729.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:57666667 C>A maps to NM_001012729.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:57669724 C>A maps to NM_001012729.1 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:1277147 C>T maps to ENST00000378888 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:1273534 G>A maps to ENST00000378888 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:1275129 G>A maps to ENST00000378888 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JS-01A-11D-A10B-09 chr1:1274811 C>T maps to ENST00000378888 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:1273681 G>A maps to ENST00000378888 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:183887839 C>A maps to NM_004423.3 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr3:183888443 C>T maps to NM_004423.3 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:183885768 C>T maps to NM_004423.3 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:183888290 C>T maps to NM_004423.3 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr3:183885815 C>T maps to NM_004423.3 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr3:183887905 G>A maps to NM_004423.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:183887986 C>T maps to NM_004423.3 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:183882975 G>A maps to NM_004423.3 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:82098285 G>A maps to NM_138812.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:82098285 G>A maps to NM_138812.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:82102038 C>A maps to NM_138812.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:46906062 C>A maps to NM_017653.3 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:46798649 C>T maps to NM_017653.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:46645262 G>T maps to NM_017653.3 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:46645262 G>A maps to NM_017653.3 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:46906062 C>A maps to NM_017653.3 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:46645262 G>A maps to NM_017653.3 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr14:102484799 C>T maps to NM_001376.4 H2730H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:102515903 C>T maps to NM_001376.4 G4500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:102493588 C>T maps to NM_001376.4 V2950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:102498777 C>T maps to NM_001376.4 I3351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:102516830 C>T maps to NM_001376.4 F4624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:102452232 C>T maps to NM_001376.4 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:102476654 C>T maps to NM_001376.4 F2088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:102483492 C>T maps to NM_001376.4 C2639C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:102505425 G>A maps to NM_001376.4 T3765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:102442080 G>T maps to NM_001376.4 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:102449795 C>T maps to NM_001376.4 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:102489090 C>T maps to NM_001376.4 L2837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:102483796 T>A maps to NM_001376.4 A2711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:102505513 G>T maps to NM_001376.4 E3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:102452190 G>A maps to NM_001376.4 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:102452568 T>G maps to NM_001376.4 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:102472355 G>A maps to NM_001376.4 Q1855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr14:102477135 G>A maps to NM_001376.4 P2155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr14:102506034 C>T maps to NM_001376.4 L3886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:102478315 G>A maps to NM_001376.4 L2241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:102508811 C>T maps to NM_001376.4 R4123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:102476408 C>T maps to NM_001376.4 I2069I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr14:102471422 C>T maps to NM_001376.4 N1761N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr14:102452679 G>A maps to NM_001376.4 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr14:102499763 C>T maps to NM_001376.4 A3452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr14:102483835 A>G maps to NM_001376.4 S2724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:95614247 C>A maps to NM_004411.4 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:32576070 G>A maps to NM_016141.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:32586493 G>A maps to NM_016141.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:66783109 C>T maps to NM_006141.2 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr16:66768205 C>T maps to NM_006141.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr11:102984276 T>C maps to NM_001080463.1 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:102991710 G>T maps to NM_001080463.1 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr11:102980396 C>T maps to NM_001080463.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:103006638 C>T maps to NM_001080463.1 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:103055623 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:103092843 G>T maps to NM_001080463.1 E3065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:103191953 C>A maps to NM_001080463.1 S3981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:103325960 T>C maps to NM_001080463.1 L4175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:102984411 A>G maps to NM_001080463.1 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:103006506 G>T maps to NM_001080463.1 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:103014038 G>T maps to NM_001080463.1 E873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:103026058 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:103047130 G>T maps to NM_001080463.1 E1948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:103104761 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:102984345 T>C maps to NM_001080463.1 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:103031685 G>A maps to NM_001080463.1 E1468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:103031685 G>A maps to NM_001080463.1 E1468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:102986000 G>T maps to NM_001080463.1 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:102984956 T>C maps to NM_001080463.1 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:103178560 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:103349848 T>C maps to NM_001080463.1 D4271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:103041686 G>T maps to NM_001080463.1 E1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr11:103059233 G>A maps to NM_001080463.1 T2383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr11:103068671 C>T maps to NM_001080463.1 Y2573Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:44014331 A>G maps to NM_001193464.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:44023898 C>T maps to NM_001193464.1 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr2:44021769 G>T maps to NM_001193464.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:159057914 G>A maps to NM_006519.2 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:37700324 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr21:38853129 T>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr21:38877627 G>T maps to NM_001396.3 G428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr21:38868551 G>T maps to NM_001396.3 G411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr21:38877605 C>A maps to NM_001396.3 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:40321074 G>A maps to NM_004714.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:40318963 G>A maps to NM_004714.1 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:40317935 C>A maps to NM_004714.1 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:40317999 C>T maps to NM_004714.1 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:40321164 C>T maps to NM_004714.1 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:40319119 G>A maps to NM_004714.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:40319119 G>A maps to NM_004714.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:68051541 C>T maps to NM_006482.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:68051932 C>T maps to NM_006482.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:68051679 G>A maps to NM_006482.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:68051808 C>T maps to NM_006482.2 Y374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:206821625 C>T maps to NM_003582.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:206820830 A>G maps to NM_003582.2 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:206821557 G>T maps to NM_003582.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:206821625 C>T maps to NM_003582.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:4721738 C>T maps to NM_003845.1 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:4705361 C>T maps to NM_003845.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:4722720 C>T maps to NM_003845.1 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:4705880 C>A maps to NM_003845.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:4719363 A>G maps to NM_003845.1 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:4702174 A>C maps to NM_003845.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:71747338 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:71909752 C>T maps to NM_001130987.1 F2089F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:71755461 C>A maps to NM_001130987.1 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:71766337 G>A maps to NM_001130987.1 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:71780259 C>T maps to NM_001130987.1 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:71801449 G>A maps to NM_001130987.1 E1117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:71747312 C>T maps to NM_001130987.1 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:71825802 C>A maps to NM_001130987.1 I1228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:207528047 T>C maps to NM_001093730.1 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:207516542 C>A maps to NM_001093730.1 *579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:207527720 A>G maps to NM_001093730.1 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:207564523 A>G maps to NM_001093730.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:55789940 C>T maps to NM_130810.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:55783443 C>T maps to NM_130810.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:96293854 G>T maps to NM_198968.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:96242578 T>C maps to NM_198968.2 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:96239823 G>A maps to NM_198968.2 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:96242592 G>A maps to NM_198968.2 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:96241461 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:137811251 G>A maps to NM_173543.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:137807228 C>A maps to NM_173543.2 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:137811251 G>A maps to NM_173543.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr3:137787027 G>T maps to NM_173543.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:137783574 C>T maps to NM_173543.2 E679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:137783418 G>A maps to ENST00000486487 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:108363062 T>C maps to NM_014648.3 H398H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:108365496 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:108367790 G>A maps to NM_014648.3 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:32265136 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr20:32264597 G>A maps to NM_005225.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:32266143 T>A maps to NM_005225.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:32264612 G>A maps to NM_005225.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr1:23848405 C>T maps to NM_004091.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:20483133 G>A maps to NM_001949.3 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:20490606 C>T maps to NM_001949.3 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:67231532 C>A maps to NM_001950.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:67231532 C>A maps to NM_001950.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:86114380 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:86118438 C>T maps to ENST00000256117 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:86119718 G>T maps to ENST00000256117 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:77417806 G>A maps to NM_203394.2 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:77417950 C>T maps to NM_203394.2 V860V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:19251171 A>G maps to NM_024680.2 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:19251183 G>T maps to NM_024680.2 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:19256468 G>A maps to NM_024680.2 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr11:19251390 G>A maps to NM_024680.2 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:2284211 C>T maps to NM_004424.3 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:2283010 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr16:2285338 C>T maps to NM_004424.3 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:2285131 C>T maps to NM_004424.3 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:15477987 G>A maps to NM_033083.6 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:15473730 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121573587 G>T maps to NM_018456.4 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:121591462 A>G maps to NM_018456.4 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:121573664 A>G maps to NM_018456.4 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:121573610 T>C maps to NM_018456.4 H93H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:23535677 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:23546500 G>A maps to NM_001083614.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr8:110567110 C>T maps to ENST00000276658 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:110569181 G>T maps to ENST00000276658 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr5:158140131 G>A maps to NM_024007.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:158126148 C>T maps to NM_024007.3 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:158250202 C>T maps to NM_024007.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:158523396 C>T maps to NM_024007.3 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:158523369 A>G maps to NM_024007.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:158135077 G>A maps to NM_024007.3 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:158141166 C>T maps to NM_024007.3 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:158135110 G>T maps to NM_024007.3 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:25902321 C>T maps to NM_022659.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:25745359 C>A maps to NM_022659.2 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:25902327 C>T maps to NM_022659.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:25899736 C>T maps to NM_022659.2 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr10:131639150 C>T maps to ENST00000355311 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:131671848 C>T maps to ENST00000355311 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:131761783 G>A maps to ENST00000355311 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr10:131665495 C>G maps to ENST00000355311 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:4234763 C>T maps to NM_005755.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:4229594 G>A maps to NM_005755.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:73112026 A>G maps to NM_018029.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48382236 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48385381 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48386820 A>C did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:48382316 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48382227 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:50237311 A>C maps to NM_032565.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:74894302 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:21554506 G>A maps to NM_001397.2 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:21546453 G>T maps to NM_001397.2 V769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:21599297 G>T maps to NM_001397.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:21585332 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:183976236 C>T maps to NM_032331.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:184001758 C>T maps to NM_014693.3 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:183975339 C>T maps to NM_014693.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:184009971 C>T maps to NM_014693.3 F866F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:184008916 G>T maps to NM_014693.3 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:184005698 C>T maps to NM_014693.3 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:184008831 C>T maps to NM_014693.3 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:183975339 C>T maps to NM_014693.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:184008592 C>T maps to NM_014693.3 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:183994706 C>T maps to NM_014693.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr3:183975405 G>A maps to NM_014693.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:233345436 G>T maps to NM_004826.2 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:233348866 G>A maps to NM_004826.2 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:233348905 G>A maps to NM_004826.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:233349573 C>T maps to NM_004826.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:233348761 C>T maps to NM_004826.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:233349207 C>T maps to NM_004826.2 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:39308153 C>T maps to NM_001398.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:127652167 C>T maps to NM_001139510.1 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:127648253 C>A maps to NM_001139510.1 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:127648167 C>A maps to NM_001139510.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:127636019 C>T maps to NM_001139510.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:53377403 G>A maps to ENST00000371522 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:53377403 G>A maps to ENST00000371522 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:11791500 G>A maps to NM_024693.4 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:135178182 G>T maps to NM_004092.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:135182520 G>A maps to NM_004092.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150485876 C>T maps to ENST00000369049 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:150483379 C>T maps to ENST00000369049 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:150485242 C>T maps to ENST00000369049 C476C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:150484985 C>T maps to ENST00000369049 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:95277083 C>A maps to NM_001393.3 G295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:95263286 C>T maps to NM_001393.3 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:95272234 C>A maps to NM_001393.3 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:95272312 G>A maps to NM_001393.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:95272234 C>A maps to NM_001393.3 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:95277030 G>A maps to NM_001393.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:11618639 G>A maps to NM_016581.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr3:172523534 G>A maps to ENST00000392692 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:172523534 G>A maps to ENST00000392692 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr6:139135715 T>A maps to NM_001195037.2 L52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr6:139186208 G>A maps to NM_001195037.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:139164147 C>T maps to NM_001195037.2 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:139189334 G>T maps to NM_001195037.2 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:69247875 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:68840747 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69247721 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:69253327 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:69255290 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:69247829 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:65822578 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:65819473 T>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:65819381 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:65819462 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:65835849 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:65819448 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:65835773 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:109527528 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:109546647 G>A maps to ENST00000376651 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:74964021 G>T maps to NM_025083.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:74927792 C>T maps to NM_025083.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:74927864 G>A maps to NM_025083.3 N359N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:74948296 G>A maps to NM_025083.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr16:67917472 G>A maps to NM_014329.3 A1284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:67914623 T>C maps to NM_014329.3 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr16:67909956 T>G maps to NM_014329.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:67913643 C>T maps to NM_014329.3 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:67914115 C>T maps to NM_014329.3 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:67916230 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:67916200 G>T maps to NM_014329.3 E1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:67914656 G>A maps to NM_014329.3 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:21215868 G>T maps to NM_006683.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:21216047 C>T maps to NM_006683.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:21238526 G>A maps to NM_022360.4 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr14:21238404 A>G maps to NM_022360.4 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:21238341 C>A maps to NM_022360.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:21238698 C>T maps to NM_022360.4 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr3:5255167 G>A maps to NM_014674.2 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:33714065 C>T maps to NM_018217.2 W319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:184706770 G>A maps to NM_025191.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr1:184677467 G>C maps to NM_025191.3 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:184681638 G>A maps to NM_025191.3 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:184703758 C>A maps to NM_025191.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:184695460 A>G maps to NM_025191.3 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:184706770 G>A maps to NM_025191.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:83360548 G>A maps to NM_005711.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr5:83680183 G>A maps to NM_005711.3 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:83356292 C>T maps to NM_005711.3 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:83259122 A>G maps to NM_005711.3 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr1:41945138 G>A maps to NM_001956.3 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:41949788 G>A maps to NM_001956.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:57899379 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:148407150 C>T maps to NM_001957.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:148461552 C>T maps to NM_001957.3 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:78474735 G>T maps to ENST00000377211 C425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:78472379 G>A maps to ENST00000377211 H518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:78477407 G>T maps to ENST00000377211 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:78492729 C>T maps to ENST00000377211 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:78492426 G>A maps to ENST00000377211 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:78492684 G>A maps to ENST00000377211 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:78492243 G>T maps to ENST00000377211 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:93210002 C>T maps to NM_003566.3 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:93172977 C>T maps to NM_003566.3 E1189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:93213172 C>A maps to NM_003566.3 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:93221690 C>T maps to NM_003566.3 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:93205116 C>A maps to NM_003566.3 E713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:93244946 T>G maps to NM_003566.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:93219952 G>A maps to NM_003566.3 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:85989561 C>T maps to ENST00000351625 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:85961342 C>T maps to ENST00000351625 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:85988131 C>T maps to ENST00000351625 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:62124598 G>A maps to NM_001958.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr20:62121912 C>T maps to NM_001958.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:62129187 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:207027282 G>A maps to NM_021121.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:207027282 G>A maps to NM_021121.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:144663399 G>A maps to NM_032378.4 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:62338439 C>T maps to ENST00000378019 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62340136 G>A maps to ENST00000378019 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:62338514 C>T maps to ENST00000378019 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:62334326 G>A maps to ENST00000378019 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:62327558 G>T maps to ENST00000378019 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr11:62339343 G>A maps to ENST00000378019 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:3979937 C>T maps to NM_001961.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr19:3982299 C>T maps to NM_001961.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:3976617 C>T maps to NM_001961.3 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:3979937 C>T maps to NM_001961.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:22256033 A>G maps to NM_013302.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:22291668 C>T maps to NM_013302.3 Y680Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr16:22237172 C>A maps to NM_013302.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:22237178 G>A maps to NM_013302.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:128060257 G>A maps to NM_021937.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr3:128060155 C>T maps to NM_021937.3 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:36278592 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:36336764 G>A maps to NM_030636.2 W493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr7:36336722 C>T maps to NM_030636.2 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:36336743 G>A maps to NM_030636.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:60484398 C>T maps to NM_001144933.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:60483918 A>G maps to NM_001144933.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:60472538 G>T maps to NM_001144933.1 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:60484497 A>G maps to NM_001144933.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:60469294 C>A maps to NM_001144933.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:60493531 G>T maps to NM_001144933.1 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr12:3736872 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:3747478 G>T maps to NM_001144958.1 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:3749944 T>C maps to NM_001144959.1 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:3763379 C>T maps to NM_001144958.1 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:3768820 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:28407968 C>A maps to NM_198529.3 I1132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:28417654 C>T maps to NM_198529.3 G1300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:28414079 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:28323347 G>T maps to NM_198529.3 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:28407094 T>G maps to NM_198529.3 A1011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:28400721 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:43936087 G>A maps to NM_022785.3 D1266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:43976441 C>A maps to NM_022785.3 E1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:44073886 C>A maps to NM_022785.3 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:44074009 G>A maps to NM_022785.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:43926790 C>T maps to NM_022785.3 Q1429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:44074009 G>A maps to NM_022785.3 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:44151671 C>A maps to NM_022785.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:44178123 G>T maps to NM_022785.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr22:44068125 T>C maps to NM_022785.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr22:43950817 C>T maps to NM_022785.3 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:44168936 C>T maps to NM_022785.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:44031027 G>A maps to NM_022785.3 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:44107407 G>T maps to NM_022785.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr22:44031066 G>A maps to NM_022785.3 D671D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr22:44107497 C>T maps to NM_022785.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:44004440 G>A maps to NM_022785.3 R868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:64038142 C>T maps to NM_032437.2 R616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:63991309 C>T maps to NM_032437.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:56103764 G>A maps to NM_001039349.1 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:56098193 G>A maps to NM_001039349.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:56108798 G>T maps to NM_001039349.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:56144998 G>A maps to NM_001039349.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65638022 G>A maps to NM_016938.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65639777 C>T maps to NM_016938.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:22067417 G>T maps to NM_152726.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:22084146 G>A maps to NM_152726.2 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr13:22140934 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr8:16921705 G>A maps to NM_181723.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:16935363 G>T maps to NM_181723.2 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:16974064 G>T maps to NM_181723.2 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:16962958 G>T maps to NM_181723.2 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:16921652 C>T maps to NM_181723.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:16935351 C>T maps to NM_181723.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:19940337 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:19925940 T>C maps to NM_144715.3 T700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:19959748 C>T maps to NM_144715.3 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:19975021 G>A maps to NM_144715.3 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:19940960 C>A maps to NM_144715.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:19975303 C>A maps to NM_144715.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:52288770 C>T maps to NM_018100.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:52343938 C>A maps to NM_018100.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:52288823 C>T maps to NM_018100.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:44108060 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:44120446 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:44037635 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:44091780 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:44109469 T>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:44108081 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr23:44171992 C>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:44171908 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:44091864 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:44108075 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:44120402 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:44120318 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:44109507 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:44035606 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:44109507 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:44037674 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:44101386 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:233527634 C>T maps to NM_025202.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:233527640 C>T maps to NM_025202.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:15753728 C>T maps to NM_024329.5 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:155041627 C>A maps to NM_182689.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:107006302 C>T maps to NM_001962.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:106716955 C>T maps to NM_001962.2 *229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:68059897 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr23:68060231 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:68059563 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:68058622 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:68060193 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:68059542 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr23:68060378 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:68058491 C>T did not map to a codon.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr23:68060355 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:107145408 C>T maps to NM_004093.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:7611804 C>T maps to NM_001406.3 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7611771 G>A maps to NM_001406.3 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:7612878 C>A maps to NM_001406.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:132957060 C>T maps to NM_015137.3 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:132958774 T>G maps to NM_015137.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:132966203 G>T maps to NM_015137.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr8:132982721 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:132982783 C>T maps to NM_015137.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:132968093 G>T maps to NM_015137.3 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:132982783 C>T maps to NM_015137.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:132982822 C>T maps to NM_015137.3 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:132991255 C>T maps to NM_015137.3 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:23828093 C>T maps to NM_005864.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr14:23829013 G>A maps to NM_005864.2 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr14:23829933 G>A maps to NM_005864.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:82530760 C>T maps to NM_024580.5 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:82512524 T>C maps to NM_024580.5 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:82431175 G>T maps to NM_024580.5 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:82444714 C>A maps to NM_024580.5 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:82456239 G>A maps to NM_024580.5 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:82545088 C>A maps to NM_024580.5 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr15:82517537 A>G maps to NM_024580.5 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr17:42942388 C>T maps to NM_004247.3 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:42962637 C>T maps to NM_004247.3 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:42937314 G>A maps to NM_004247.3 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:42971859 C>T maps to NM_004247.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:110862108 A>G maps to NM_001963.4 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr4:110909857 C>T maps to NM_001963.4 H909H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:110929322 G>T maps to NM_001963.4 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:110834559 G>A maps to NM_001963.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:110897207 G>T maps to NM_001963.4 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:110904665 A>G maps to NM_001963.4 Q820Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:110908906 T>C maps to NM_001963.4 D833D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:110882146 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:110901287 A>G maps to NM_001963.4 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:110929322 G>T maps to NM_001963.4 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:110920909 C>T maps to NM_001963.4 H1027H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr4:110897222 C>T maps to NM_001963.4 Q629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:110862301 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:13651118 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:13621501 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:13588003 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:13636146 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:13636119 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13624595 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:13612961 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:13636146 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:13635869 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:13651187 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:13607701 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:13635863 C>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr6:32134573 G>A maps to NM_030652.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr5:38258882 C>A maps to ENST00000354891 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:38458479 C>T maps to ENST00000354891 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:38418223 C>T maps to ENST00000354891 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:38451480 C>T maps to ENST00000354891 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:38448427 G>A maps to ENST00000354891 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:38435339 C>T maps to ENST00000354891 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:38425120 C>T maps to ENST00000354891 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:38412737 A>G maps to ENST00000354891 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr5:38352397 C>T maps to ENST00000354891 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:55259422 C>A maps to NM_005228.3 Y827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:55231464 G>A maps to NM_005228.3 Q557Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:55241717 G>A maps to NM_005228.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr1:231557049 G>C maps to NM_022051.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:34419694 G>A maps to NM_022073.3 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:137801494 G>A maps to NM_001964.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:137802530 C>T maps to NM_001964.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:137803619 G>A maps to NM_001964.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:64573653 G>T maps to NM_001136178.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr10:64573184 G>A maps to NM_001136178.1 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:22548282 C>T maps to NM_004430.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr8:22548570 G>A maps to NM_004430.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:22548402 C>T maps to NM_004430.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:73519595 G>A maps to NM_001965.3 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:73518764 C>T maps to NM_001965.3 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:63169942 C>T maps to NM_015252.3 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:63176089 G>A maps to NM_015252.3 E738E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:63092095 G>T maps to NM_015252.3 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:63223863 G>A maps to NM_015252.3 A1093A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65350149 G>A maps to NM_001099409.1 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65350572 G>A maps to NM_001099409.1 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:65349714 G>A maps to NM_001099409.1 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:65349804 C>A maps to NM_001099409.1 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:65349943 G>T maps to NM_001099409.1 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr11:64645740 G>A maps to NM_006795.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:48221861 C>T maps to NM_014601.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:48229150 G>A maps to NM_014601.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:48229327 C>T maps to NM_014601.3 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:48239624 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:48244337 T>C maps to NM_014601.3 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:48229354 C>T maps to NM_014601.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr19:48244194 G>T maps to NM_014601.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:48244200 C>T maps to NM_014601.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:31489200 G>A maps to NM_014600.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:31483515 C>T maps to NM_014600.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:31457651 C>T maps to NM_014600.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:31489314 C>A maps to NM_014600.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:31457586 C>T maps to NM_014600.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:42235263 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:42193019 G>T maps to NM_139265.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:42193139 G>A maps to NM_139265.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:34673285 T>C maps to NM_012153.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr11:34668055 G>A maps to NM_012153.4 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:184922306 T>C maps to NM_001966.3 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr3:184971804 G>C maps to NM_001966.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:184935995 G>A maps to NM_001966.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:184910486 C>A maps to NM_001966.3 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:184910322 T>C maps to NM_001966.3 E621E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:140611615 G>A maps to NM_024757.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:140611198 T>C maps to NM_024757.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:140672501 G>A maps to NM_024757.4 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:31860606 G>T maps to ENST00000395728 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:125445187 T>C maps to ENST00000278903 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:49170771 G>A maps to NM_014335.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr19:40023165 G>A maps to NM_152361.1 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:104698015 G>T maps to NM_001008394.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:20156718 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:20152108 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:20156718 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:20150318 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:20150342 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:20159754 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr3:150299424 T>C maps to NM_032025.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:150281336 C>T maps to NM_032025.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:6077113 C>A maps to NM_014413.3 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr7:6082580 G>A maps to NM_014413.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:6066419 G>T maps to NM_014413.3 S568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:37368814 C>T maps to NM_001135651.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:37347266 G>A maps to NM_001135651.1 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:37336399 G>A maps to NM_001135651.1 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:37374084 C>A maps to NM_001135651.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:37334618 C>A maps to NM_001135651.1 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:37374084 C>A maps to NM_001135651.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:88874237 G>A maps to NM_004836.5 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:88874867 G>T maps to NM_004836.5 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:40309310 C>A maps to NM_001013703.2 V1311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:40269024 C>T maps to NM_001013703.2 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:40300267 C>A maps to NM_001013703.2 R1150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:40321630 G>C maps to NM_001013703.2 V1509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:40309412 C>A maps to NM_001013703.2 I1345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:40259645 C>T maps to NM_001013703.2 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr15:40284380 C>T maps to NM_001013703.2 D879D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr14:75473335 A>G maps to NM_014239.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:45363067 G>T maps to NM_020365.3 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:45363049 G>A maps to NM_020365.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:45392330 C>A maps to NM_020365.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:27592808 A>C maps to NM_172195.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:27592365 T>C maps to NM_172195.3 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:183855447 C>T maps to NM_003907.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:183859756 C>T maps to NM_003907.2 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:36359937 C>T maps to NM_012199.2 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:36354151 C>T maps to NM_012199.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:36358199 C>A maps to NM_012199.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:36354166 C>T maps to NM_012199.2 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:141567304 C>T maps to NM_012154.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:141566382 G>T maps to NM_012154.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:141542516 G>A maps to NM_012154.3 D823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:141545599 G>A maps to NM_012154.3 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:141570575 C>T maps to NM_012154.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:141542609 G>A maps to NM_012154.3 R792R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:141566018 C>T maps to NM_012154.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:141570578 G>T maps to NM_012154.3 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:141545599 G>A maps to NM_012154.3 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr8:141542163 C>T maps to NM_012154.3 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:141557712 G>A maps to NM_012154.3 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:36474545 G>A maps to NM_024852.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:36499872 T>C maps to NM_024852.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:36505934 C>T maps to NM_024852.2 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:36505934 C>T maps to NM_024852.2 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:36439107 C>T maps to NM_024852.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:36505934 C>T maps to NM_024852.2 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:36297436 C>T maps to NM_017629.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:36288534 C>T maps to NM_017629.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:36290939 C>T maps to NM_017629.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:36291651 G>T maps to NM_017629.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:36301435 G>A maps to NM_017629.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:36291026 C>T maps to NM_017629.2 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:67847475 C>T maps to NM_004094.4 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:67847475 C>T maps to NM_004094.4 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:32693351 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:32693351 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:32684601 G>A maps to NM_003908.3 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24080666 G>A did not map to a codon.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr23:24073091 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:24091278 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr23:24091291 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:24075831 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:24082444 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:24075779 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:24073732 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:120795558 G>A maps to NM_003750.2 R1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:120802267 C>A maps to NM_003750.2 E922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr10:120795672 G>A maps to NM_003750.2 R1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:120802172 G>A maps to NM_003750.2 D953D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:120795663 C>A maps to NM_003750.2 E1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:120801662 G>A maps to NM_003750.2 A1123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr10:120802001 A>G maps to NM_003750.2 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr10:120801731 C>T maps to NM_003750.2 R1100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:120810724 G>A maps to NM_003750.2 Q769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr10:120810134 A>G maps to NM_003750.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:2406668 C>A maps to ENST00000314800 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr7:2412410 C>T maps to ENST00000314800 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:2414169 C>T maps to ENST00000314800 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:2402722 C>T maps to ENST00000314800 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr7:2400399 G>T maps to ENST00000314800 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:36919228 G>T maps to ENST00000432675 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr22:36914915 G>A maps to NM_003753.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr8:109229598 C>T maps to NM_001568.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:32696724 C>T maps to NM_003757.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:32689633 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:44849796 C>T maps to NM_003758.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:39116666 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:39125693 C>A maps to NM_013234.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:39123129 C>T maps to NM_013234.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:32622376 C>T maps to NM_006360.3 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr11:32622233 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:7478536 G>A maps to NM_001416.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:7481735 C>T maps to NM_001416.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr17:7480413 C>T maps to NM_001416.2 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:7476180 C>T maps to NM_001416.2 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:186503751 T>C maps to ENST00000440191 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:186502818 C>T maps to ENST00000440191 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:186503752 G>T maps to ENST00000440191 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:78110132 G>A maps to NM_014740.3 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:78111285 C>T maps to NM_014740.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr17:78111189 G>A maps to NM_014740.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr17:78110073 G>A maps to NM_014740.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:99802208 G>A maps to NM_001130679.1 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:233431536 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:31843545 G>A maps to NM_019843.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:31859672 A>G maps to NM_019843.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:184038425 T>C maps to NM_001194947.1 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:184038426 C>T maps to NM_001194947.1 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:184038426 C>T maps to NM_001194947.1 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:184043160 G>A maps to NM_001194947.1 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:184049786 C>T maps to NM_001194947.1 L1518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:184039154 G>A maps to NM_001194947.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:10822543 G>A maps to ENST00000429377 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:10828866 C>T maps to ENST00000429377 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:10819385 C>A maps to ENST00000429377 E974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:21307561 C>A maps to NM_001198801.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:21188722 G>A maps to NM_001198801.1 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:21205829 G>A maps to NM_001198801.1 R850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:21296046 C>A maps to NM_001198801.1 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:21306901 G>A maps to NM_001198801.1 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:21137324 C>T maps to NM_001198801.1 P1530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:21212818 C>A maps to NM_001198801.1 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:21205994 G>A maps to NM_001198801.1 R795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:21268167 A>G maps to NM_001198801.1 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:21154189 C>A maps to NM_001198801.1 E1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:21268652 G>A maps to NM_001198801.1 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr1:21190989 G>A maps to NM_001198801.1 D975D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:73604021 C>T maps to NM_022170.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:103806787 G>T maps to NM_183004.3 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7212974 C>T maps to NM_001143760.1 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:170625562 A>G maps to NM_020390.5 D11D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:170612212 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:81272590 C>T maps to NM_001099692.1 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr10:81272497 G>T maps to NM_001099692.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:81272432 G>T maps to NM_001099692.1 G10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:81272749 T>C maps to NM_001099692.1 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr10:81272542 G>C maps to NM_001099692.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:100010861 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:100015221 C>T maps to NM_015904.3 I1135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:99999327 G>T maps to NM_015904.3 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:48510716 G>T maps to NM_018696.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:48513442 A>C maps to NM_018696.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:12903518 G>A maps to NM_018127.6 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:852348 C>T maps to NM_001972.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr19:8045965 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:8032674 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr19:8032491 G>A maps to ENST00000351593 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:8046029 C>T maps to ENST00000351593 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr19:8028621 G>A maps to ENST00000351593 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:50572034 C>T maps to NM_001144775.1 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr1:50659453 G>A maps to NM_021952.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:41517085 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:41525536 C>A maps to NM_172373.3 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:41517095 T>C maps to NM_172373.3 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr4:139983077 A>G maps to ENST00000379550 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:129203440 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129201261 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129208637 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129203475 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129205056 T>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:129206334 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:129208048 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:129206262 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:129215262 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:129206262 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:129208720 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:129208684 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:34503984 A>G maps to NM_198381.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:34504038 A>G maps to NM_198381.1 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr22:37770959 G>A maps to NM_052906.3 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr22:37771265 C>T maps to NM_052906.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:37771358 G>T maps to NM_052906.3 Y72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr22:37770695 C>T maps to NM_052906.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr22:37771001 G>A maps to NM_052906.3 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47498387 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47500662 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:47496465 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:96617427 G>A maps to NM_005230.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:96640821 C>T maps to NM_005230.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:18572618 G>A maps to NM_006532.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr19:18555600 G>A maps to NM_006532.3 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:18561308 G>A maps to NM_006532.3 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:18557220 G>A maps to NM_006532.3 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:18557130 G>A maps to NM_006532.3 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr19:18561592 G>T maps to NM_006532.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:95234142 G>A maps to NM_012081.5 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:95226944 G>A maps to NM_012081.5 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:95242390 G>A maps to NM_012081.5 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:95278737 G>A maps to NM_012081.5 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:95242390 G>A maps to NM_012081.5 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:37264524 C>T maps to NM_014800.9 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:37298952 A>G maps to NM_014800.9 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:37172815 G>A maps to NM_014800.9 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:37382246 G>A maps to NM_014800.9 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:37262252 C>T maps to NM_014800.9 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:37262258 A>G maps to NM_014800.9 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:37264563 C>T maps to NM_014800.9 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:37136253 G>A maps to NM_014800.9 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:45017801 G>A maps to ENST00000439931 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:45008942 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:45023109 C>T maps to ENST00000439931 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:45003264 T>C maps to ENST00000439931 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:107502334 C>T maps to NM_018712.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:107518313 C>T maps to NM_018712.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:107501286 C>T maps to NM_018712.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:107501244 C>A maps to NM_018712.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:141461344 G>A maps to NM_153702.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:141458655 T>C maps to NM_153702.3 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:141446705 C>T maps to NM_153702.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:73470730 C>T maps to ENST00000358929 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:73456974 G>A maps to ENST00000358929 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:73467562 C>T maps to ENST00000358929 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:73456947 C>T maps to ENST00000358929 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr7:73458248 A>G maps to ENST00000358929 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:73480060 C>A maps to ENST00000358929 Y745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:73449760 T>G maps to ENST00000416107 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:73467622 A>C maps to ENST00000358929 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr7:73480307 C>T maps to ENST00000358929 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:43830291 G>A maps to NM_022821.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:10984139 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:11011036 A>G maps to NM_017770.3 H3H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:10990004 G>A maps to NM_017770.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:11011015 T>C maps to NM_017770.3 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr6:10990625 G>A maps to NM_017770.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:103988813 G>A maps to NM_152310.1 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:103986352 G>A maps to NM_152310.1 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:103988318 G>T maps to NM_152310.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:103987499 C>T maps to NM_152310.1 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:80629238 G>T maps to NM_022726.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:53139936 C>T maps to ENST00000370918 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:53140016 C>A maps to ENST00000370918 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:53133990 A>G maps to ENST00000370918 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:110980893 G>A maps to NM_024090.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr4:110972772 C>T maps to NM_024090.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:111026738 G>A maps to NM_024090.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:60063693 G>A maps to NM_024930.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:60060156 G>T maps to NM_024930.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:33734887 G>T maps to ENST00000442325 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:28017927 T>C maps to NM_018091.5 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:27970631 C>T maps to NM_018091.5 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:27970631 C>T maps to NM_018091.5 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:27970610 G>T maps to NM_018091.5 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:31625361 A>G maps to ENST00000395934 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:48525448 C>A maps to NM_022142.4 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:48511930 C>T maps to NM_022142.4 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:79412079 G>T maps to NM_022159.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:79392575 G>A maps to NM_022159.3 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:79403948 C>A maps to NM_022159.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:79403922 G>T maps to NM_022159.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:49698141 C>A maps to NM_198449.2 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:49695698 T>C maps to NM_198449.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr5:49699123 C>T maps to NM_198449.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:101337094 G>A maps to NM_016242.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:101337094 G>A maps to NM_016242.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153609118 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153608310 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153609521 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153608712 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153608071 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153608699 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr17:48456817 G>A maps to NM_001166131.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:29621182 G>A maps to NM_133455.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:29611593 G>A maps to NM_133455.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr22:29627633 C>T maps to NM_133455.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:101063335 G>A maps to ENST00000397927 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:27308543 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:27306778 C>T maps to NM_007046.3 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:27305086 G>T maps to NM_007046.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27302011 C>T maps to NM_007046.3 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27303042 C>T maps to NM_007046.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:27306764 C>T maps to NM_007046.3 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:27308115 C>A maps to NM_007046.3 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:27303605 C>T maps to NM_007046.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:2891090 C>T maps to NM_032048.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:2891274 C>T maps to NM_032048.2 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:2891225 G>A maps to NM_032048.2 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:2908947 G>A maps to NM_032048.2 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr18:2892000 C>T maps to NM_032048.2 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:2890577 C>T maps to NM_032048.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:2909746 C>T maps to NM_032048.2 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:2891855 C>T maps to NM_032048.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:2909722 G>A maps to NM_032048.2 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr18:2891296 C>G maps to NM_032048.2 S391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:39991310 G>A maps to NM_052846.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:100405612 C>T maps to NM_001008707.1 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:100367270 G>A maps to NM_001008707.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:100405537 G>A maps to NM_001008707.1 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr14:100375725 C>T maps to NM_001008707.1 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:100404178 C>T maps to NM_001008707.1 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:100402648 C>T maps to NM_001008707.1 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:100363556 A>G maps to NM_001008707.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:100406397 C>A maps to NM_001008707.1 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:62371472 G>A maps to ENST00000278845 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:62378919 G>A maps to ENST00000278845 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr11:62374517 G>A maps to ENST00000278845 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:42515437 G>A maps to NM_019063.3 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:42557100 G>A maps to NM_019063.3 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:42490392 G>A maps to NM_019063.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:89148306 G>A maps to ENST00000380664 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:89154677 G>T maps to ENST00000380664 I893I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:89171222 G>A maps to ENST00000380664 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:89148261 A>G maps to ENST00000380664 C1032C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr14:89154749 T>A maps to ENST00000380664 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:89124729 C>A maps to ENST00000380664 G1226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:89171222 G>A maps to ENST00000380664 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:89171830 G>A maps to ENST00000380664 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:89172630 C>A maps to ENST00000380664 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:13366729 C>G maps to NM_001423.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:10626881 C>T maps to NM_001424.4 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:10637457 C>T maps to NM_001424.4 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:48830839 C>T maps to NM_001425.2 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:6906537 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:6921872 C>A maps to ENST00000381407 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:6906537 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:6897158 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:6916285 G>T maps to ENST00000381407 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:6897469 C>T maps to ENST00000381407 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:6916285 G>T maps to ENST00000381407 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:6908734 C>T maps to ENST00000381407 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:14863197 G>T maps to NM_013447.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:14877056 G>A maps to NM_013447.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:14865912 G>T maps to NM_013447.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:14863335 C>T maps to NM_013447.2 E531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:14877889 G>T maps to NM_013447.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:14876365 G>A maps to NM_013447.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:14752278 G>A maps to NM_032571.3 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:14749002 G>T maps to NM_032571.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:14765800 A>G maps to NM_032571.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:14736375 G>A maps to NM_032571.3 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:155255123 C>T maps to NM_001427.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:155255213 G>A maps to NM_001427.3 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:225705129 C>T maps to ENST00000284563 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:225695651 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:225706962 G>A maps to ENST00000284563 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:225707148 G>A maps to ENST00000284563 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr4:71510181 C>T maps to NM_031889.2 D1013D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:71507730 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:71510511 C>T maps to NM_031889.2 F1123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:71508663 T>G maps to NM_031889.2 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr4:71507895 G>A maps to NM_031889.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:71508798 C>T maps to NM_031889.2 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:71509908 C>A maps to NM_031889.2 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:71500176 A>G maps to NM_031889.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:71508606 T>C maps to NM_031889.2 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:73931011 G>A maps to NM_003633.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:73931355 C>A maps to NM_003633.2 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr5:73932187 C>T maps to NM_003633.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:94862577 C>T maps to NM_015036.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:94861920 C>A maps to NM_015036.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:94861563 T>C maps to NM_015036.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:48110704 C>T maps to NM_001172439.1 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr12:48110248 G>A maps to NM_001172439.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:48106307 G>A maps to NM_001172439.1 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:130578222 C>T maps to NM_001114753.1 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr9:130605435 G>A maps to NM_001114753.1 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr17:77076310 T>C maps to NM_001042573.1 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:77073796 G>A maps to NM_001042573.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:25304838 G>A maps to NM_145010.2 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:25279411 C>A maps to NM_145010.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:25279472 G>A maps to NM_145010.2 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:8931983 G>A maps to NM_001428.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr1:8927217 G>A maps to NM_001428.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:4860151 G>A maps to NM_053013.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:4856565 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:83369071 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:83375976 C>T maps to NM_021204.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:694277 C>T maps to ENST00000319815 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:685920 C>T maps to ENST00000319815 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:690587 C>T maps to ENST00000319815 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:43896592 G>A maps to NM_001127615.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:129837114 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:129771231 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129771325 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129771303 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129801654 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:129813518 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:129837097 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:129771276 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:129804064 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:129804064 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:129768983 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:111397617 G>A maps to NM_001977.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:111397812 T>C maps to NM_001977.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:111397843 C>T maps to NM_001977.3 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:111398052 C>T maps to NM_001977.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:111427816 C>T maps to NM_001977.3 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:111482587 A>G maps to NM_001977.3 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:111464030 C>A maps to NM_001977.3 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:111397731 G>A maps to NM_001977.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:132203594 C>T maps to NM_006208.2 Y737Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:132190589 C>T maps to NM_006208.2 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:132206137 C>T maps to NM_006208.2 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:120577195 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:120580413 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:120628548 G>A maps to NM_006209.3 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:120631536 C>T maps to NM_006209.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:120633723 C>A maps to NM_006209.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:120631536 C>T maps to NM_006209.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:120594792 C>T maps to NM_006209.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:120595978 A>G maps to NM_006209.3 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:120633708 C>A maps to NM_006209.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:120631536 C>T maps to NM_006209.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:132068062 G>A maps to NM_005021.3 K865K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:132054738 G>A maps to NM_005021.3 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:131996299 C>A maps to NM_005021.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr6:131962629 A>G maps to NM_005021.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:46107841 G>A maps to NM_014936.4 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:46108084 C>T maps to NM_014936.4 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:46135173 C>A maps to NM_021572.4 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr6:46135540 A>G maps to NM_021572.4 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:77709131 C>T maps to NM_178543.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:77709443 C>T maps to NM_178543.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150599921 G>A maps to ENST00000369009 Y68Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150600017 C>T maps to NM_207042.1 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:40161494 C>A maps to NM_152512.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:97583120 G>A maps to NM_001098175.1 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:97599459 C>T maps to NM_001098175.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr9:139944936 G>A maps to NM_203468.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:40442473 C>T maps to NM_001248.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:40453381 G>A maps to NM_001248.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:40453312 C>A maps to NM_001248.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:40456207 A>G maps to NM_001248.2 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:23294506 G>A maps to NM_004901.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:23305331 G>A maps to NM_004901.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr8:23290618 G>A maps to NM_004901.3 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr20:25204779 C>T maps to NM_001247.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:25190494 G>A maps to NM_001247.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:25198211 C>A maps to NM_001247.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:25187944 C>T maps to NM_001247.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr20:25193951 C>T maps to NM_001247.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:25187219 T>A maps to NM_001247.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:25204791 C>T maps to NM_001247.2 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr20:25205882 C>G maps to NM_001247.2 S429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:101448493 C>T maps to NM_020354.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr10:101455840 C>T maps to NM_020354.3 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:101460787 C>A maps to NM_020354.3 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:140329551 G>A maps to NM_001033113.1 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:140330218 G>A maps to NM_001033113.1 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:27761749 G>A maps to ENST00000449599 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:41547838 T>G maps to NM_001429.3 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr22:41562636 C>T maps to NM_001429.3 R1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:41513188 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:41562605 C>T maps to NM_001429.3 F1270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:41572403 C>T maps to NM_001429.3 R1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr22:41572484 G>T maps to NM_001429.3 E1672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr22:41574606 C>T maps to NM_001429.3 Q2298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:41564749 G>T maps to NM_001429.3 E1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:41568561 C>T maps to NM_001429.3 F1504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:41548328 G>A maps to NM_001429.3 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr22:41531814 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr22:41542812 A>G maps to NM_001429.3 P708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:41562648 G>T maps to NM_001429.3 E1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr22:41531830 G>T maps to NM_001429.3 G515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:132490714 G>A maps to ENST00000333577 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:132554089 C>T maps to ENST00000333577 Y3011Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:132534893 G>A maps to ENST00000333577 T2445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:132514700 C>T maps to ENST00000333577 Q1954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:132514660 C>A maps to ENST00000333577 T1940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:132498061 G>A maps to ENST00000333577 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:132514359 C>T maps to ENST00000333577 H1868H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:132472428 G>A maps to ENST00000333577 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr12:132512731 G>A maps to ENST00000333577 E1796E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr12:132446453 G>A maps to ENST00000333577 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr12:132547143 G>A maps to ENST00000333577 Q2780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:132446240 G>T maps to ENST00000333577 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:132562037 T>C maps to ENST00000333577 V3100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:132466815 G>A maps to ENST00000333577 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:132498055 C>T maps to ENST00000333577 I1247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr12:132530312 C>T maps to ENST00000333577 I2392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:132522339 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:46574170 C>T maps to NM_001430.4 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr2:46574122 T>C maps to NM_001430.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:46607832 C>A maps to NM_001430.4 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:46605045 C>T maps to NM_001430.4 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:46583906 C>T maps to NM_001430.4 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:46605833 C>T maps to NM_001430.4 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:46607727 G>A maps to NM_001430.4 W639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:46611732 C>T maps to NM_001430.4 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:46605854 T>C maps to NM_001430.4 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:29344856 G>T maps to NM_001166005.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:29385147 C>T maps to NM_001166005.1 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:29314318 G>T maps to NM_001166005.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:29365894 C>T maps to NM_001166005.1 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:34806862 G>A maps to NM_012156.2 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:34797777 G>A maps to NM_012156.2 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:131276415 T>C maps to NM_001431.3 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:131229988 A>G maps to NM_001431.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr6:131191020 G>A maps to NM_001431.3 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:5423512 G>T maps to NM_012307.2 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:5395146 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:5406874 G>T maps to NM_012307.2 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:5433963 G>T maps to NM_012307.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr18:5419889 A>G maps to ENST00000400111 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:5398064 T>A maps to NM_012307.2 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:5406831 G>A maps to NM_012307.2 R765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:5406894 C>A maps to NM_012307.2 E744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr18:5428398 C>T maps to NM_012307.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:5419805 C>T maps to NM_012307.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:111519798 C>T maps to NM_022140.3 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:111615980 C>A maps to NM_022140.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:111754708 C>A maps to NM_022140.3 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:112018714 C>T maps to NM_019114.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:112029804 G>A maps to NM_019114.3 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:111976098 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:112005905 T>C maps to NM_019114.3 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:120834819 A>G maps to NM_020909.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:120858390 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:120889209 A>C maps to NM_020909.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:120889269 C>T maps to NM_020909.3 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:43507413 G>T maps to NM_000119.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr15:43507314 C>T maps to NM_000119.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:43495431 G>A maps to NM_000119.2 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:21927801 C>T maps to ENST00000265800 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:21927807 C>T maps to ENST00000265800 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:21927729 C>T maps to ENST00000265800 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:32573737 G>T maps to NM_025209.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:32581996 T>C maps to NM_025209.2 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr10:32573761 T>C maps to NM_025209.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:149528401 A>G maps to NM_015630.3 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:149543943 T>C maps to NM_015630.3 *808Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:47604212 T>A maps to ENST00000426238 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:75174829 G>T maps to ENST00000413830 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:75178809 A>G maps to ENST00000413830 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr7:143094699 G>A maps to NM_005232.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:143092411 G>A maps to NM_005232.4 R695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:143092411 G>A maps to NM_005232.4 R695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:143092424 G>A maps to NM_005232.4 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:143098584 G>A maps to NM_005232.4 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:38227434 G>A maps to NM_001099439.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:38186094 G>A maps to NM_001099439.1 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:38227734 C>A maps to NM_001099439.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:38227200 C>T maps to NM_001099439.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:16459816 C>A maps to NM_004431.3 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:16459687 G>A maps to NM_004431.3 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:16464768 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:89259261 C>T maps to NM_005233.5 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:89259599 C>T maps to NM_005233.5 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:89498433 G>A maps to NM_005233.5 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:89528649 T>C maps to NM_005233.5 *984Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr3:89448532 C>G maps to NM_005233.5 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:89480457 C>T maps to NM_005233.5 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr3:89480424 C>A maps to NM_005233.5 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:222308300 A>G maps to NM_004438.3 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:222436880 C>A maps to NM_004438.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:222365880 C>A maps to NM_004438.3 G279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:222428880 G>A maps to NM_004438.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:222322588 C>T maps to NM_004438.3 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr2:222347410 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:66197713 G>A maps to NM_004439.5 D995D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:66201843 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:66217262 G>T maps to NM_004439.5 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:66280067 G>A maps to NM_004439.5 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:66201746 G>A maps to NM_004439.5 R919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:66217298 G>A maps to NM_004439.5 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:66217108 T>G maps to NM_004439.5 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:66467407 C>A maps to NM_004439.5 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr4:66242741 G>A maps to NM_004439.5 C610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr4:66197749 T>C maps to NM_004439.5 T983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:97454794 C>T maps to NM_001080448.2 Y987Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:96533481 G>A maps to NM_001080448.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:97167564 G>T maps to NM_001080448.2 G629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:93955044 G>T maps to NM_004440.3 S951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:93973599 G>A maps to NM_004440.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:93956552 G>A maps to NM_004440.3 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:93956552 G>T maps to NM_004440.3 R895R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:93973632 C>T maps to NM_004440.3 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:94068082 G>A maps to NM_004440.3 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:93953161 T>A maps to NM_004440.3 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:93973599 G>A maps to NM_004440.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:93956552 G>A maps to NM_004440.3 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:93969123 G>A maps to NM_004440.3 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:93955125 G>A maps to NM_004440.3 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:22928122 C>T maps to NM_020526.3 D969D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:22902939 C>T maps to NM_020526.3 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:22924313 C>T maps to NM_020526.3 D692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:22925488 C>T maps to NM_020526.3 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:22927918 T>C maps to NM_020526.3 A952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:22920022 G>T maps to NM_020526.3 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:134920467 C>T maps to NM_004441.4 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:134885782 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:134670763 C>T maps to NM_004441.4 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:134920467 C>T maps to NM_004441.4 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:134967180 C>T maps to NM_004441.4 D840D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr3:134967171 C>T maps to NM_004441.4 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:134911472 C>A maps to NM_004441.4 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:134851754 G>A maps to NM_004441.4 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:23111348 C>T maps to ENST00000400191 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:23101736 G>T maps to ENST00000374625 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:23233320 C>T maps to ENST00000400191 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:23232504 C>T maps to ENST00000400191 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:23234606 G>A maps to ENST00000400191 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:23234627 C>T maps to ENST00000400191 D773D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:23233420 G>T maps to ENST00000400191 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:23240245 A>G maps to ENST00000400191 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:23111075 C>A maps to ENST00000400191 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr1:23110964 G>A maps to ENST00000400191 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:23240242 C>T maps to ENST00000400191 D1016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:23239041 C>T maps to ENST00000400191 F934F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:184290764 C>T maps to NM_004443.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:184295579 C>T maps to NM_004443.3 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:184290536 A>G maps to NM_004443.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:184295486 C>T maps to NM_004443.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:184297349 C>T maps to NM_004443.3 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:184297346 C>T maps to NM_004443.3 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:100416162 G>A maps to NM_004444.4 Y467Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:100404062 G>A maps to NM_004444.4 Y821Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:100410756 G>A maps to NM_004444.4 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100401163 G>T maps to NM_004444.4 I961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:100410813 G>A maps to NM_004444.4 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:142568309 G>T maps to NM_004445.3 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:142566295 G>A maps to NM_004445.3 R695R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:142566104 C>A maps to NM_004445.3 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:142565465 C>A maps to NM_004445.3 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:142566057 G>T maps to NM_004445.3 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:226032855 C>T maps to NM_001136018.2 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:226032942 C>A maps to NM_001136018.2 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:226030146 C>T maps to NM_001136018.2 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:226026454 C>T maps to NM_001136018.2 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr8:27396186 C>T maps to ENST00000458037 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:27373266 C>T maps to ENST00000458037 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:27401306 C>T maps to ENST00000458037 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr8:27358478 A>C maps to ENST00000458037 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:27364408 C>T maps to ENST00000458037 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:27361206 C>A maps to ENST00000458037 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:92518155 T>C maps to NM_173567.4 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:92508472 T>C maps to NM_173567.4 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:92518158 C>A maps to NM_173567.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:37034307 G>A maps to NM_014805.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:37033499 C>A maps to NM_014805.3 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:37033506 T>C maps to NM_014805.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:37034226 G>A maps to NM_014805.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:37033013 C>A maps to NM_014805.3 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:56200685 C>T maps to NM_001130072.1 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:56204368 C>T maps to NM_001130071.1 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:56206140 G>A maps to NM_001130071.1 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:56206559 G>A maps to NM_001130071.1 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr19:56190211 C>T maps to NM_001130071.1 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:56204315 G>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:56204335 G>A maps to NM_001130071.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr19:56206691 G>A maps to NM_001130071.1 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:19213208 C>T maps to NM_014964.4 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:48618412 C>T maps to NM_017957.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:48618242 C>T maps to NM_017957.2 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:48618599 G>A maps to NM_017957.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr7:100319325 G>A maps to NM_000799.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr8:144946611 G>A maps to NM_031308.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr8:144942327 G>A maps to NM_031308.1 R1698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:144944811 C>T maps to NM_031308.1 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:144941103 C>T maps to NM_031308.1 E2106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:144941901 C>A maps to NM_031308.1 T1840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:144941463 C>T maps to NM_031308.1 T1986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:144942354 G>A maps to NM_031308.1 G1689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:220192393 A>G maps to NM_004446.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:220151973 G>A maps to NM_004446.2 R1333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:220156662 A>G maps to NM_004446.2 I1056I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:220151977 T>G maps to NM_004446.2 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:220178624 T>C maps to NM_004446.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:220193517 G>A maps to NM_004446.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:220208270 C>A maps to NM_004446.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:220195798 G>T maps to NM_004446.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:220192387 T>C maps to NM_004446.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:220174572 C>T maps to NM_004446.2 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:51860059 G>A maps to NM_001981.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:51829597 C>A maps to NM_001981.2 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:51873965 C>T maps to NM_001981.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:16495984 G>T maps to ENST00000455140 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:16472598 G>A maps to ENST00000455140 D859D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:16539569 G>T maps to ENST00000455140 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:16548589 C>T maps to ENST00000455140 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:16503189 G>A maps to ENST00000455140 D676D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:16536019 G>A maps to ENST00000455140 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:16539557 A>G maps to ENST00000455140 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:16536052 G>T maps to ENST00000455140 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr19:16524627 G>A maps to ENST00000455140 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:16497039 G>A maps to ENST00000455140 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:15823788 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:15813628 T>A maps to NM_004447.5 K286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:15803923 C>A maps to NM_004447.5 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:15818731 G>A maps to NM_004447.5 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr12:15777245 G>A maps to NM_004447.5 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:15784374 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:55598957 C>T maps to NM_133180.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:55593183 C>A maps to NM_133180.2 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:55593160 C>T maps to NM_133180.2 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:721348 G>A maps to NM_022772.3 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:724726 C>T maps to NM_022772.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:722522 A>G maps to NM_022772.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:110301934 G>T maps to NM_139053.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:110300102 G>A maps to NM_139053.1 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:110300102 G>A maps to NM_139053.1 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:110293380 G>A maps to NM_139053.1 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:43491706 C>T maps to NM_001002264.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:43491720 C>A maps to NM_001002264.1 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:43474495 C>T maps to NM_001002264.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:43528123 C>A maps to NM_001002264.1 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:26569132 G>A maps to NM_033505.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:26596457 G>T maps to NM_033505.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:56276964 G>T maps to NM_000502.4 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:56280665 C>A maps to NM_000502.4 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:56271398 G>A maps to NM_000502.4 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:56270881 G>A maps to NM_000502.4 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:56270884 G>A maps to NM_000502.4 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:56271111 G>A maps to NM_000502.4 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:56274529 C>T maps to NM_000502.4 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:91366662 G>A maps to NM_004950.4 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:27183339 A>G maps to NM_005702.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:27186289 G>T maps to NM_005702.2 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:96129594 C>A maps to NM_016442.3 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:96112227 C>A maps to NM_016442.3 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:96139389 C>T maps to NM_016442.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:96112227 C>A maps to NM_016442.3 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:96139389 C>T maps to NM_016442.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:96215742 G>A maps to NM_001130140.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:96249128 T>C maps to NM_001130140.1 F875F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:96248458 C>T maps to NM_001130140.1 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:96251472 G>A maps to NM_001130140.1 E913E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:96232434 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:96237301 C>T maps to NM_001130140.1 D555D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr5:96237331 C>T maps to NM_001130140.1 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr23:48687737 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48687841 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:48687821 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48687549 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48687919 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48688094 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:37879819 G>A maps to NM_004448.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:37866081 G>A maps to NM_004448.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:37881399 C>T maps to NM_004448.2 F864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:65338984 G>T maps to ENST00000506030 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:65334237 G>T maps to ENST00000506030 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:65349920 G>A maps to ENST00000506030 Q925Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr5:65319179 T>G maps to ENST00000506030 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:65320240 A>G maps to ENST00000506030 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr5:65372742 C>G maps to ENST00000506030 S1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:56495059 G>A maps to NM_001982.2 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:56495574 T>A maps to NM_001982.2 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:212537948 A>G maps to NM_005235.2 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:212248375 C>T maps to NM_005235.2 P1297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:212568833 G>A maps to NM_005235.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:212812334 G>A maps to NM_005235.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:212570070 G>A maps to NM_005235.2 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:212537909 G>A maps to NM_005235.2 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr2:212589908 C>T maps to NM_005235.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr2:212488691 C>T maps to NM_005235.2 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr12:1346067 C>T maps to NM_178040.2 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:1599362 G>A maps to NM_178040.2 E1106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:1250887 G>T maps to NM_178040.2 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:1192512 C>T maps to NM_178040.2 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:1553876 G>A maps to NM_178040.2 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:1137629 G>A maps to NM_178040.2 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr12:1137168 C>T maps to NM_178040.2 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:56468669 A>G maps to ENST00000460849 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:56183148 G>A maps to ENST00000460849 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:56468773 G>A maps to ENST00000460849 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:56114978 C>A maps to ENST00000460849 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:56026215 G>A maps to ENST00000460849 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:45923661 G>A maps to NM_202001.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:45922415 C>T maps to NM_202001.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:45912974 C>T maps to NM_001983.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:45860767 T>C maps to NM_000400.3 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:45872375 G>A maps to NM_000400.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:45855847 G>A maps to NM_000400.3 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:128044390 G>A maps to NM_000122.1 Y410Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:128051106 G>A maps to NM_000122.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:128038195 G>A maps to NM_000122.1 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr2:128051271 C>T maps to NM_000122.1 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:128044465 G>A maps to NM_000122.1 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:14029519 C>T maps to NM_005236.2 Y577Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:14041526 C>T maps to NM_005236.2 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr16:14014207 C>G maps to NM_005236.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:14042098 C>T maps to NM_005236.2 D882D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:14042071 C>T maps to NM_005236.2 I873I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:103524700 G>A maps to NM_000123.2 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:103515433 G>A maps to NM_000123.2 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr13:103514653 C>A maps to NM_000123.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:103514543 C>T maps to NM_000123.2 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:103515049 G>A maps to NM_000123.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:103525641 G>A maps to NM_000123.2 T971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:103514839 G>A maps to NM_000123.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:103528228 G>A maps to NM_000123.2 A1179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:103515211 G>A maps to NM_000123.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:50681041 C>T maps to NM_000124.2 T914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr10:50740605 C>T maps to ENST00000515869 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr10:50681553 G>T maps to NM_000124.2 S893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:50667075 C>A maps to NM_000124.2 E1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:71425355 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:71425165 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:71426403 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71424982 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71427125 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:71425952 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:71425525 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:71426725 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:71426901 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:71426261 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:71425308 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:71425837 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:71427102 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:71425280 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:71426539 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:71425359 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:71426485 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:71427162 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:71427392 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:71427501 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:71425832 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:71427451 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:75248493 A>C maps to NM_001432.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr4:75246854 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:75250453 C>T maps to NM_001432.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:42752958 C>T maps to NM_006494.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr21:39763611 C>A maps to NM_001136154.1 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:172324068 G>A maps to NM_001031711.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:29509340 T>C maps to NM_016570.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:29502072 A>G maps to NM_016570.2 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:29494749 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:29524559 G>A maps to NM_016570.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:29494148 A>G maps to NM_016570.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:34136357 C>A maps to ENST00000447986 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:69861566 G>A maps to NM_004450.2 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:69847353 G>A maps to NM_004450.2 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:8865586 G>A maps to NM_153332.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:20802173 A>G maps to NM_080663.2 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr16:20812682 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:20802178 C>A maps to NM_080663.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:20809417 A>C maps to NM_001142725.1 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:20809768 T>C maps to NM_001142725.1 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr1:44804989 T>C maps to NM_024066.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:44785407 G>A maps to NM_024066.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr1:44687310 G>A maps to NM_024066.1 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:623532 G>A maps to NM_207332.1 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:623433 C>T maps to NM_207332.1 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:623595 G>A maps to NM_207332.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr8:623568 G>A maps to NM_207332.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr2:54042065 T>C maps to NM_015701.3 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:37609198 G>A maps to NM_007175.6 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:37607999 C>A maps to NM_007175.6 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:43308308 C>T maps to NM_018538.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:158178084 C>A maps to NM_001009959.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:158178024 C>A maps to NM_001009959.1 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:5797932 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:62141505 G>A maps to NM_001433.3 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:62133037 C>A maps to NM_001433.3 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:62122797 G>A maps to NM_001433.3 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:23713989 G>A maps to NM_033266.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:23717684 G>T maps to NM_033266.3 Y233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:23702467 G>A maps to NM_033266.3 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:53128010 C>A maps to NM_014584.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:53133105 C>A maps to NM_014584.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:53119835 G>A maps to NM_014584.1 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:236389776 C>A maps to NM_019891.3 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr12:15068491 C>T maps to NM_152321.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:112457612 C>T maps to NM_006817.3 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:112457594 C>T maps to NM_006817.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr9:102768896 T>A maps to NM_015051.1 K303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:102769955 C>A maps to NM_015051.1 G260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:102784415 G>T maps to NM_015051.1 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:8073508 C>A maps to NM_018948.3 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:8073737 C>T maps to NM_018948.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:124624603 G>T maps to NM_138961.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr11:124623723 A>G maps to NM_138961.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:124626509 G>T maps to NM_138961.2 C126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:19153435 C>A maps to NM_052911.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:19110357 A>G maps to NM_052911.2 C823C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:19110414 T>C maps to NM_052911.2 E804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:19116044 G>A maps to NM_052911.2 D715D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:19153792 C>A maps to NM_052911.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:19154242 C>A maps to NM_052911.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr8:27645470 T>C maps to NM_001017420.2 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:47345583 G>A maps to NM_001984.1 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr13:47365502 G>A maps to NM_001984.1 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr20:13756596 C>T maps to NM_016649.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:13695802 G>A maps to NM_016649.3 N758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:13755839 G>T maps to NM_016649.3 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:13763471 G>A maps to NM_016649.3 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:54277938 C>A maps to NM_007036.4 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:54275224 C>A maps to NM_007036.4 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr12:53680491 C>T maps to NM_012291.4 A1324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:53686160 C>T maps to NM_012291.4 R1966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:53675313 G>A maps to NM_012291.4 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53663076 A>G maps to NM_012291.4 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53663544 C>T maps to NM_012291.4 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53677241 C>T maps to NM_012291.4 G999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:53673592 C>T maps to NM_012291.4 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr12:53663742 C>T maps to NM_012291.4 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr12:53677872 C>T maps to NM_012291.4 L1037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr12:53683908 C>T maps to NM_012291.4 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:53683989 G>A maps to NM_012291.4 Q1745Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:53664580 C>T maps to NM_012291.4 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr12:53677889 T>C maps to NM_012291.4 N1042N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:239039395 A>C maps to NM_194312.2 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:152382209 G>A maps to NM_001122741.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr6:152382233 C>G maps to NM_001122741.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr14:64727335 G>A maps to NM_001437.2 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:64716387 C>T maps to NM_001437.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:95658437 C>T maps to NM_017697.3 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:95680438 C>A maps to NM_017697.3 Y398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:95686697 C>T maps to NM_017697.3 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr8:95654197 C>T maps to NM_017697.3 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:95690533 G>A maps to NM_017697.3 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:95674531 C>T maps to NM_017697.3 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:95709136 G>T maps to NM_017697.3 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr8:95676967 C>T maps to NM_017697.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:95653674 G>A maps to NM_017697.3 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr8:95676981 G>A maps to NM_017697.3 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:95683794 C>T maps to NM_017697.3 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:95686697 C>T maps to NM_017697.3 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:68267736 C>A maps to NM_024939.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:68265483 G>A maps to NM_024939.2 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:76949043 C>A maps to NM_004452.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:76949043 C>A maps to NM_004452.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:76957943 C>T maps to NM_004452.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr14:76949100 A>G maps to NM_004452.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:216824366 G>A maps to NM_001438.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr1:216850595 C>T maps to NM_001438.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:103495395 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:103499130 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:103499461 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:103498875 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:103499159 C>T did not map to a codon.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr12:56522417 G>T maps to NM_001184796.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:56527422 C>T maps to NM_001184796.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr12:56532240 G>A maps to NM_001184796.1 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:158534266 G>T maps to NM_020728.2 I732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:138188300 T>G maps to NM_031913.3 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:138191203 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr3:138191380 C>T maps to NM_031913.3 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:138183257 C>T maps to NM_031913.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr3:138191605 C>T maps to NM_031913.3 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:138179466 C>T maps to NM_031913.3 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr3:138191324 G>T maps to NM_031913.3 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:138181012 C>T maps to NM_031913.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:67631289 C>T maps to NM_019002.3 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:67626325 G>A maps to NM_019002.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:137854379 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:137846285 C>A maps to NM_004730.2 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:137844487 C>T maps to NM_004730.2 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr15:76577984 T>C maps to NM_000126.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:51848614 G>A maps to NM_001014763.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:51857697 C>T maps to NM_001014763.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:51857487 G>A maps to NM_001014763.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:51848524 G>A maps to NM_001014763.1 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:159624621 T>C maps to NM_004453.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:159627393 G>T maps to NM_004453.2 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:44011054 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:22796698 C>A maps to NM_018638.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:22796737 C>T maps to NM_018638.4 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:22824228 G>T maps to NM_018638.4 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:22796813 G>T maps to NM_018638.4 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr12:22797149 C>G maps to NM_001039481.1 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:204115878 C>A maps to NM_018208.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:128360373 C>T maps to NM_001143820.1 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:128354816 G>A maps to NM_001143820.1 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr11:128354832 G>A maps to NM_001143820.1 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr11:128359284 A>G maps to NM_001143820.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:40185001 C>T maps to NM_005239.4 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr21:40194716 C>T maps to NM_005239.4 Y438Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:40185004 G>T maps to NM_005239.4 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:40194728 C>T maps to NM_005239.4 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:13949260 G>A maps to NM_004956.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:13975514 A>T maps to NM_004956.4 Y124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:13949260 G>A maps to NM_004956.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:13946089 G>A maps to NM_004956.4 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:13949260 G>A maps to NM_004956.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr19:36135600 C>A maps to ENST00000222279 Y320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:157095155 G>T maps to NM_001145312.1 S339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:157105446 G>A maps to NM_001145312.1 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:157068608 G>A maps to NM_001004341.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:157069063 G>A maps to NM_001004341.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:41607296 G>A maps to NM_001079675.1 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:41610694 T>C maps to NM_001079675.1 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:12006463 G>A maps to NM_001987.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:12037500 C>T maps to NM_001987.4 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:5735083 C>T maps to NM_153717.2 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:5785373 G>A maps to NM_153717.2 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:5733375 C>A maps to NM_153717.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:5586505 A>G maps to NM_147127.4 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:5624288 G>A maps to NM_147127.4 R826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr4:5630290 G>A maps to NM_147127.4 H627H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:5586358 C>T maps to NM_147127.4 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:5620243 G>A maps to NM_147127.4 F889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:5693009 A>T maps to NM_147127.4 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:5570208 G>A maps to NM_147127.4 S1173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:5624672 G>A maps to NM_147127.4 R698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:93142740 C>A maps to NM_005665.4 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:93170152 C>A maps to NM_005665.4 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:93170120 C>T maps to NM_005665.4 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:7914024 C>A maps to NM_001159944.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:7918173 C>T maps to NM_001159944.1 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:7913952 C>T maps to NM_001159944.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:7912616 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:7912758 C>T maps to NM_001159944.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:100563837 C>T maps to NM_016337.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:74018550 G>A maps to NM_001988.2 N183N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr17:74007957 A>G maps to NM_001988.2 Y821Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:74019390 G>A maps to NM_001988.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:74006621 C>T maps to NM_001988.2 K888K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:74017802 G>A maps to NM_001988.2 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:27284826 G>A maps to NM_001989.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:29696114 C>T maps to NM_013986.3 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:29669837 G>T maps to NM_013986.3 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr22:29668383 C>T maps to NM_013986.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:29692359 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:41483642 A>G maps to NM_152596.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:41482316 C>A maps to NM_152596.2 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:69704348 C>T maps to NM_001193363.1 H450H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:69697306 G>T maps to NM_001193363.1 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr9:140246631 C>T maps to NM_017820.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:140243726 G>A maps to NM_017820.3 D555D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:242016663 C>T maps to NM_006027.4 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:242030173 C>T maps to NM_006027.4 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:242042435 C>T maps to NM_006027.4 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr1:242015641 G>T maps to NM_006027.4 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:242042227 G>A maps to NM_006027.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:242020672 C>T maps to NM_006027.4 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:242042135 G>T maps to NM_006027.4 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:242042540 G>T maps to NM_006027.4 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:242042576 G>T maps to NM_006027.4 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:56770576 C>T maps to NM_018261.3 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:56726703 C>T maps to NM_018261.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr4:56759864 A>G maps to NM_018261.3 Q624Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:56762983 A>C maps to NM_018261.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:56750024 G>T maps to NM_018261.3 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:56744099 G>A maps to NM_018261.3 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:56757482 C>A maps to NM_018261.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:556013 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:619530 C>T maps to NM_018303.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:572543 G>A maps to NM_018303.4 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr6:598887 C>T maps to NM_018303.4 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr5:447745 C>T maps to ENST00000315013 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:462288 T>G maps to ENST00000315013 L517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:462137 C>A maps to ENST00000315013 C495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:447829 C>T maps to ENST00000315013 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:446349 G>A maps to ENST00000315013 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:45730999 C>T maps to NM_138568.3 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr19:45731254 G>A maps to NM_138568.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:132959851 G>T maps to NM_021807.3 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr7:133689778 C>T maps to NM_021807.3 I821I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:133059737 G>A maps to NM_021807.3 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:133602377 C>A maps to NM_021807.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:57675416 T>C maps to ENST00000340918 Q681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:57713451 G>A maps to ENST00000340918 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:57676388 G>A maps to ENST00000340918 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:57684764 T>C maps to ENST00000340918 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:57686113 G>A maps to ENST00000340918 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:57676476 G>A maps to ENST00000340918 Y584Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr14:57675340 G>A maps to ENST00000340918 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:57689053 A>G maps to ENST00000340918 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:94654713 C>T maps to NM_019053.4 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:94715464 T>G maps to NM_019053.4 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr10:94757349 C>T maps to NM_019053.4 N691N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:94818034 C>T maps to NM_019053.4 R780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:72945426 A>G maps to NM_015189.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:72740332 T>A maps to NM_015189.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:72406492 G>A maps to NM_015189.1 R803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:72802677 C>T maps to NM_015189.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:72725637 C>A maps to NM_015189.1 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:74085342 G>A maps to NM_001145297.2 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:231471625 T>C maps to NM_175876.3 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:38537966 C>T maps to NM_005107.3 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:38565429 T>G maps to NM_005107.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr10:99196960 G>T maps to NM_016046.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:99196981 G>A maps to NM_016046.3 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr1:11158134 G>A maps to NM_001001998.1 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:11158149 C>A maps to NM_001001998.1 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:11137470 G>A maps to NM_001001998.1 H610H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:11139787 G>A maps to NM_001001998.1 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:133573554 C>T maps to NM_014285.5 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:41898805 G>A maps to NM_020158.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:45048982 G>A maps to NM_015004.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:122734500 G>T maps to NM_001034194.1 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:122732752 A>T maps to NM_001034194.1 K252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:122723076 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr11:108380884 C>T maps to NM_015065.2 L1783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:108381247 G>A maps to NM_015065.2 N1662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:108385447 G>A maps to NM_015065.2 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:108382674 C>A maps to NM_015065.2 E1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:119122922 C>T maps to NM_000127.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr8:118847712 G>A maps to NM_000127.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:118834744 G>T maps to NM_000127.2 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr8:118825188 G>A maps to NM_000127.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:44129597 A>G maps to NM_000401.3 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:44228433 C>A maps to NM_000401.3 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:44130750 C>T maps to NM_000401.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:44129651 T>C maps to NM_000401.3 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:44129528 G>A maps to NM_000401.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:26355704 G>A maps to NM_004455.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:26349433 C>T maps to NM_004455.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:26349520 T>C maps to NM_004455.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:101343415 G>A maps to NM_001439.2 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:101339737 G>T maps to NM_001439.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:101343406 G>A maps to NM_001439.2 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:28588738 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:28574622 G>A maps to NM_001440.2 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:28574700 C>T maps to NM_001440.2 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:28575315 G>A maps to NM_001440.2 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr8:72128975 G>A maps to NM_000503.4 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:72123485 C>A maps to NM_000503.4 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr8:72182016 G>A maps to NM_000503.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:72123485 C>A maps to NM_000503.4 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:45797841 T>G maps to ENST00000360649 L350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:28315087 C>A maps to NM_001990.2 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:133846192 C>T maps to NM_172105.3 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:133777692 G>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:133804193 G>T maps to ENST00000452339 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:133783873 C>T maps to ENST00000452339 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr6:133789774 G>A maps to ENST00000452339 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:133802625 C>A maps to ENST00000452339 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:133844202 C>A maps to ENST00000452339 C548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:133827282 G>T maps to ENST00000452339 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:64430946 G>A maps to ENST00000370616 L3015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:64708979 G>A maps to ENST00000370616 S2274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:64430983 A>G maps to ENST00000370616 T3002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:64498112 G>A maps to ENST00000370616 I2536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:66205164 C>A maps to ENST00000370616 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:64694364 G>A maps to ENST00000370616 I2322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:65301088 T>C maps to ENST00000370616 A1557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:65301783 C>A maps to ENST00000370616 E1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:66115177 A>C maps to ENST00000370616 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:64431658 G>A maps to ENST00000370616 S2777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:66204813 G>A maps to ENST00000370616 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr6:65300638 A>C maps to ENST00000370616 Y1707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:65301639 G>A maps to ENST00000370616 R1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:65301247 C>T maps to ENST00000370616 Q1504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:65622592 C>A maps to ENST00000370616 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr6:65300467 A>G maps to ENST00000370616 I1764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:64516086 G>A maps to ENST00000370616 G2469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:65301487 C>T maps to ENST00000370616 T1424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:66094382 C>A maps to ENST00000370616 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:66205224 G>A maps to ENST00000370616 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:66044889 A>G maps to ENST00000370616 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr6:65612113 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:66200595 C>T maps to ENST00000370616 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr6:65149234 A>T maps to ENST00000370616 C1885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:40861955 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:40854582 G>A maps to ENST00000264646 Y740Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:40858128 G>A maps to ENST00000264646 R582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:40870043 C>A maps to ENST00000264646 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:40870043 C>A maps to ENST00000264646 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:40854917 G>A maps to ENST00000264646 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:40854573 G>A maps to ENST00000264646 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:40876418 C>T maps to ENST00000264646 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:40874815 C>A maps to ENST00000264646 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr7:148514367 G>C maps to NM_004456.3 Y452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:148507449 G>A maps to NM_004456.3 C668C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:148526819 C>A maps to NM_004456.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:148523716 C>A maps to NM_004456.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:148515007 C>A maps to NM_004456.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:148523585 A>G maps to NM_004456.3 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:148506426 C>T maps to NM_004456.3 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:159197490 G>T maps to NM_001111077.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr6:159206393 G>A maps to NM_001111077.1 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:113798204 G>A maps to NM_000504.3 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:113793761 C>T maps to NM_000504.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:113801763 G>A maps to NM_000504.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:113798390 C>T maps to NM_000504.3 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:187196991 G>A maps to NM_000128.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:187209668 G>A maps to NM_000128.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:187206879 G>T maps to NM_000128.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:187194255 G>T maps to NM_000128.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:187207629 C>T maps to NM_000128.3 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:187196991 G>A maps to NM_000128.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:187197533 G>T maps to NM_000128.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:187201164 G>T did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr4:187201164 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:160969738 A>G maps to NM_016946.4 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:160970427 G>A maps to NM_016946.4 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:176832967 C>T maps to NM_000505.3 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:176836062 A>C maps to NM_000505.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:6251103 G>A maps to NM_000129.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:6175062 C>A maps to NM_000129.3 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:6305752 G>A maps to NM_000129.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:197024881 G>A maps to NM_001994.2 C439C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:197019902 A>G maps to NM_001994.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:197026499 C>A maps to NM_001994.2 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:197030113 A>G maps to NM_001994.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:197029664 C>T maps to NM_001994.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:197030980 C>T maps to NM_001994.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:197026293 G>A maps to NM_001994.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:197031985 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:46745063 C>T maps to NM_000506.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:46748150 G>A maps to NM_000506.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr5:76028949 C>T maps to NM_001992.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:76129397 C>A maps to NM_005242.4 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:76129181 C>A maps to NM_005242.4 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:75913598 G>A maps to NM_004101.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:75919012 A>G maps to NM_004101.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:95005893 A>C maps to NM_001993.4 L44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:94996099 G>T maps to NM_001993.4 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:169521962 C>T maps to ENST00000367796 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:169519049 G>A maps to ENST00000367796 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:169519188 G>T maps to ENST00000367796 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:169528484 C>T maps to ENST00000367796 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:169511084 G>A maps to ENST00000367796 D1086D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:169510784 G>T maps to ENST00000367796 V1186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:169511450 G>T maps to ENST00000367796 I964I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:169505797 C>T maps to ENST00000367796 E1644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:169513612 G>T maps to ENST00000367796 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:169526088 G>A maps to ENST00000367796 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:169495211 C>T maps to ENST00000367796 W1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr1:169498897 T>C maps to ENST00000367796 R1794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:113771899 C>T maps to NM_000131.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:113772778 G>A maps to NM_000131.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr13:113772916 G>A maps to NM_000131.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:113768251 C>T maps to NM_000131.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:154128199 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:154159444 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:154176098 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:154221318 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:154124486 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:154132673 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:154157368 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:154159767 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:154185253 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:154134839 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:154182233 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:154250777 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:154132577 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:154157961 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:154158657 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:154158789 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:154159113 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:154194416 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:154158432 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:154185318 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:154225260 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154157053 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154158578 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154158675 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154159113 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154159726 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154159915 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:154132334 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:154176039 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:154194855 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:154185318 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:154185325 G>C did not map to a codon.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr23:154182235 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr23:154130382 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:154194755 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154156928 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154158020 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154158218 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154158737 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154182289 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154185253 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154194881 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:154157329 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:154158656 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:154185318 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:154227851 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:154157294 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:154157941 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:154159169 C>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:154159149 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:154157158 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:154158412 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:154194800 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:154158404 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:154088880 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:154091387 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:154132682 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:154185257 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:138642965 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:138623294 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:138642944 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:138643736 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:138643993 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:138623334 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:138643736 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:138633296 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:138644023 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:138643993 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:138633240 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:138619221 A>G did not map to a codon.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr23:138619302 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:138643010 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:138643957 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:74752909 G>A maps to NM_024306.4 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:74750488 G>A maps to NM_024306.4 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr16:74750272 G>A maps to NM_024306.4 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:46879174 G>A maps to NM_001441.2 W556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr23:57475069 G>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:57407424 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:57358181 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:57515325 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:57405175 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:57318938 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:57313439 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:57367775 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:57367769 G>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:57313276 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:57458374 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:57515325 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:88425855 C>A maps to NM_001443.1 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:82439298 C>A maps to NM_001105281.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:120241950 C>T maps to NM_000134.3 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:31842264 G>A maps to NM_004102.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:31845810 G>A maps to NM_004102.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:82391671 G>A maps to NM_001442.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:82196801 A>C maps to NM_001444.1 *136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:159661894 C>T maps to NM_001040442.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:159626054 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:82371437 C>A maps to NM_001080526.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:61578342 G>A maps to NM_013402.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:61624517 T>C maps to NM_004265.2 N260N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:61630801 C>T maps to NM_004265.2 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:61631195 C>T maps to NM_004265.2 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:72878807 C>T maps to ENST00000310226 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr17:72889585 G>A maps to ENST00000310226 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr17:72877284 G>A maps to ENST00000310226 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:72874540 C>T maps to ENST00000310226 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:50917799 G>A maps to ENST00000371778 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:51005292 G>T maps to NM_007051.2 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:51210447 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:51253789 C>T maps to NM_007051.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:175933840 C>T maps to NM_014613.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:175933840 C>T maps to NM_014613.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:80465357 C>T maps to NM_000137.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:96072905 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:96071506 G>A maps to NM_016044.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:96078672 G>T maps to NM_016044.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:97751481 G>T maps to NM_199336.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:138340350 A>G maps to NM_001033030.1 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:50284471 G>A maps to NM_012306.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:207087190 C>A maps to NM_005449.4 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:207078462 T>C maps to NM_005449.4 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:124798896 G>A maps to ENST00000389727 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:293242 G>A maps to NM_182705.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr17:295703 G>A maps to NM_182705.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:109171146 C>T maps to NM_001010883.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:109143229 C>T maps to NM_001010883.2 F60F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A056-01A-11W-A027-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AX-A0J1-01A-11W-A062-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:71205895 A>G maps to NM_001098832.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:55172606 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:55172585 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:55172670 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:14602333 C>T maps to NM_019018.2 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:14608931 C>T maps to NM_019018.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:14678859 A>G maps to NM_138348.4 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:14693037 G>T maps to NM_138348.4 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:14693048 A>G maps to NM_138348.4 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:14816251 C>T maps to NM_031453.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:14816464 G>A maps to NM_031453.2 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:1881307 G>A maps to NM_031213.3 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr9:74489859 C>T maps to NM_016014.2 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:74489839 G>A maps to NM_016014.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:74481810 A>G maps to NM_016014.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:81046632 G>A maps to NM_021214.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:81046584 C>T maps to NM_021214.1 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:42473728 G>A maps to NM_001002034.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr22:42473962 C>A maps to NM_001002034.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:42473764 C>A maps to NM_001002034.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr20:825657 C>T maps to NM_031424.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:59059109 C>T maps to NM_147189.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:59059265 C>T maps to NM_147189.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:59059115 C>T maps to NM_147189.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:59059487 C>T maps to NM_147189.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:59059593 C>T maps to NM_147189.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:59059061 C>T maps to NM_147189.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:59059823 C>T maps to NM_147189.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:59059235 G>A maps to NM_147189.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:59059412 C>T maps to NM_147189.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr11:58916407 C>T maps to NM_198847.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:58919863 A>G maps to NM_198847.2 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:58919581 C>T maps to NM_198847.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:58920028 C>T maps to NM_198847.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:58892856 G>A maps to NM_198947.3 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:58893621 T>A maps to NM_198947.3 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:58893084 G>A maps to NM_198947.3 W505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:58892670 G>A maps to NM_198947.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr11:58892886 A>G maps to NM_198947.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:2820433 C>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:2816137 A>G maps to NM_022760.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:2820476 G>A maps to NM_022760.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:2820456 G>A maps to NM_022760.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:47629980 C>T maps to NM_138371.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:38910244 G>A maps to NM_138389.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:38910316 G>A maps to NM_138389.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:38937389 G>A maps to NM_138389.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:153372559 G>A maps to ENST00000442256 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:153381905 G>T maps to ENST00000442256 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:153406869 C>A maps to ENST00000442256 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:153414287 C>A maps to ENST00000442256 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:143573386 G>A maps to NM_014719.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:143573566 G>A maps to NM_014719.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:143573677 G>A maps to NM_014719.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:143421489 G>A maps to ENST00000441159 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:57614072 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:57616181 A>T maps to NM_152678.2 L529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:57614591 C>T maps to NM_152678.2 Q547Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:57616517 C>A maps to NM_152678.2 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:50752272 G>A maps to NM_001001794.3 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:50754516 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50754614 G>A maps to NM_001001794.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50751925 C>T maps to NM_001001794.3 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:50754668 G>A maps to NM_001001794.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:47793543 A>G maps to NM_030802.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:47799862 C>A maps to NM_030802.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:47797765 C>T maps to NM_030802.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:47810065 C>T maps to NM_030802.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr22:45719233 G>T maps to NM_017911.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:96278416 G>A maps to ENST00000333936 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr9:96278458 C>T maps to ENST00000333936 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:96320200 G>A maps to ENST00000333936 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:96326644 G>A maps to ENST00000333936 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:96320197 G>A maps to ENST00000333936 P886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:170627636 C>T maps to NM_032448.1 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:170626673 G>T maps to NM_032448.1 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr6:170626882 A>G maps to NM_032448.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:170627240 G>T maps to NM_032448.1 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:170627599 G>A maps to NM_032448.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:170657245 G>A maps to NM_032448.1 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:170639603 G>A maps to NM_032448.1 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:54161389 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr23:54107764 G>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:54114296 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:54143173 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:54185824 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54159255 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54185905 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54107760 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54159280 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54162998 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54160248 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:54209308 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:54143173 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:54185830 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:54208944 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54117828 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54143201 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:54114218 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:71395910 A>G maps to NM_138333.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:133915874 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:133921557 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:133930187 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:133927878 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:133922823 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:133923149 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:133923140 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:133927884 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:133988255 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:133988147 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:133988176 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr23:133948870 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:133981411 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:133948871 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:133988189 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:133979419 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:25744197 G>A maps to NM_152704.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:25744404 G>A maps to NM_152704.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:25744740 G>A maps to NM_152704.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr13:25744272 C>G maps to NM_152704.2 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:63411642 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:63412634 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:63412688 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:63412029 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:63412463 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:63412792 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:63411271 T>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:63412572 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:63412633 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:63411056 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:63411365 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:63412040 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:63411549 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:63412710 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr23:63406009 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:63410873 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:63411446 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:63412636 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:63411409 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:63412581 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:63412097 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:63413147 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:63410348 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:63410817 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:63411782 C>A did not map to a codon.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr23:63412981 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:131520121 C>A maps to NM_001105195.1 C159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:131520871 C>T maps to NM_001105195.1 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr2:131520653 A>C maps to NM_001105195.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:131520781 C>T maps to NM_001105195.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:51855034 C>A maps to NM_145019.2 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr13:51805510 G>A maps to NM_145019.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:129246301 C>T maps to NM_033446.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:22999923 T>C maps to NM_032581.3 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:22985596 C>A maps to NM_032581.3 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:22985590 C>A maps to NM_032581.3 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:201862214 T>C maps to NM_173822.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:201846568 C>T maps to NM_173822.3 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:201846218 G>T maps to NM_173822.3 S456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:201857701 C>T maps to NM_173822.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr23:134166524 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:134166536 G>A did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:134166544 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:134186015 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:134186006 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:134186078 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:134186047 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:134185958 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:134156429 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134156202 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:134156315 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:134156425 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:134156308 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:184800983 G>T maps to NM_052966.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:184863256 G>A maps to NM_052966.2 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:184767325 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:184764665 A>G maps to NM_052966.2 N744N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:130270805 A>G maps to NM_022833.2 N443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:130279435 C>T maps to NM_022833.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:130279286 G>A maps to NM_022833.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr9:130271293 C>T maps to NM_022833.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:130271313 G>A maps to NM_022833.2 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:17654394 C>A maps to ENST00000335393 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:17643080 C>A maps to ENST00000335393 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:17657508 C>T maps to ENST00000335393 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:184062418 C>T maps to NM_144635.4 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:184059752 G>A maps to ENST00000310585 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:143056690 G>A maps to ENST00000452076 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:143054074 A>C maps to NM_001031690.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr7:143054502 C>T maps to NM_001031690.2 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:143054020 G>A maps to NM_001031690.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:1178289 G>A maps to NM_001014980.1 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:1179360 C>T maps to NM_001014980.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:92964552 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:92964817 A>T did not map to a codon.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr23:92964854 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:92965162 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr23:92964826 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:92964655 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:92195371 G>A maps to NM_152789.2 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:220046100 G>A maps to NM_024293.4 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:16483541 C>T maps to NM_001034850.1 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:16474906 T>C maps to NM_001034850.1 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:16565900 A>G maps to NM_001034850.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:40734097 C>T maps to NM_178126.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:40734722 C>T maps to NM_178126.3 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:71234983 C>T maps to NM_001162529.1 R733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:71185234 C>T maps to NM_001162529.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:71235786 T>C maps to NM_001162529.1 S1000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr6:71266480 A>G maps to NM_001162529.1 L1419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:71233776 C>A maps to NM_001162529.1 S404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:71237992 A>G did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr6:71235369 T>C maps to NM_001162529.1 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:139180156 G>A maps to NM_015912.3 Y413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr8:139144952 G>A maps to NM_015912.3 H1368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:139153552 C>T maps to NM_015912.3 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:139163741 G>A maps to NM_015912.3 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:139165013 G>A maps to NM_015912.3 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:139269002 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:139323089 G>A maps to NM_015912.3 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr8:139144969 G>A maps to NM_015912.3 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:139160912 C>A maps to NM_015912.3 E1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:139164854 T>C maps to NM_015912.3 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:139209842 A>G maps to NM_015912.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:89708997 C>A maps to NM_014883.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:89950688 C>A maps to NM_014883.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr4:89950785 C>T maps to NM_014883.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:89652541 C>A maps to NM_014883.2 E961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:89950703 C>A maps to NM_014883.2 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr4:89679903 C>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:89670942 G>A maps to NM_014883.2 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:137346762 G>A maps to NM_016603.2 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:137347508 C>A maps to NM_016603.2 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:137295431 A>G maps to NM_016603.2 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:137289149 G>A maps to NM_016603.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:137342824 A>C maps to NM_016603.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:137289149 G>A maps to NM_016603.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:61014092 A>G maps to ENST00000422313 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:61007450 C>A maps to ENST00000442566 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:61112176 C>T maps to ENST00000442566 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:61011368 C>A maps to ENST00000442566 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:61012572 T>C maps to ENST00000442566 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:187084063 G>A maps to ENST00000356371 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:187084670 A>G maps to ENST00000356371 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:55080532 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:55075024 A>G maps to NM_176782.2 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:55075357 G>T maps to NM_176782.2 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:55080443 C>T maps to NM_176782.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:55075348 C>A maps to NM_176782.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:175528584 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:177174764 C>T maps to ENST00000503567 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:177459828 C>T maps to ENST00000511856 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr9:18928943 G>A maps to NM_153707.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:18928783 C>A maps to NM_153707.2 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:82574610 C>A maps to NM_001008226.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:82575144 T>C maps to NM_001008226.1 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr13:108518527 G>A maps to NM_001080396.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:108518146 C>T maps to NM_001080396.2 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:68725609 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr23:68749537 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:68725596 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:68725596 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:68749483 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:68725268 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:68725819 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:68749608 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:68725596 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:53122564 G>A maps to NM_001042693.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr1:53122510 G>A maps to NM_001042693.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr11:6244357 G>T maps to NM_032127.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:6238726 C>A maps to NM_032127.3 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:6245213 C>A maps to NM_032127.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr11:6243761 G>C maps to NM_032127.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:6238807 C>A maps to NM_032127.3 G684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr10:116606407 G>T maps to NM_020940.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:116606012 G>T maps to NM_020940.3 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:116606337 A>C maps to NM_020940.3 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:21955095 C>T maps to NM_022749.5 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:21959292 C>T maps to NM_022749.5 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:62067078 G>A maps to ENST00000404929 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:62053726 C>A maps to ENST00000404929 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:62067000 G>A maps to ENST00000404929 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:62067334 C>T maps to ENST00000404929 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:62067352 G>A maps to ENST00000404929 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr2:62053628 C>T maps to ENST00000404929 E704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:62067192 C>A maps to ENST00000404929 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr2:62067439 C>T maps to ENST00000404929 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:62067078 G>A maps to ENST00000404929 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:74400973 G>A maps to NM_152445.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:122123103 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:122126161 C>T maps to NM_014367.3 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:117086374 G>A maps to NM_001085480.2 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:179782309 C>T maps to NM_173509.2 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:179783104 C>T maps to NM_173509.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:140139866 C>T maps to NM_001001710.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:140139956 C>T maps to NM_001001710.1 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:140139875 C>T maps to NM_001001710.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:32713147 A>G maps to NM_032648.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr11:73130925 C>T maps to ENST00000064778 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:73179450 C>A maps to ENST00000064778 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:73118641 A>C maps to ENST00000064778 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr2:131812926 C>T maps to NM_001009993.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr5:74077401 A>G maps to NM_015566.1 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:118968443 A>G maps to ENST00000420106 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:118970355 G>T maps to ENST00000420106 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:15255564 G>A maps to NM_001010924.1 N674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:15255146 G>A maps to NM_001010924.1 R814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:15255161 C>A maps to NM_001010924.1 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:15255387 G>A maps to NM_001010924.1 N733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:15255564 G>A maps to NM_001010924.1 N674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:15256371 G>A maps to NM_001010924.1 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:15325919 G>A maps to NM_001010924.1 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:15326033 G>T maps to NM_001010924.1 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:15255015 G>A maps to NM_001010924.1 H857H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:187627228 C>T maps to NM_177454.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:93410348 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:92956758 G>C maps to NM_032042.5 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:772355 C>A maps to NM_023933.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:10236718 C>T maps to NM_199133.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:93173516 G>A maps to NM_207446.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr15:93198571 G>T maps to NM_207446.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr15:93173571 C>G maps to NM_207446.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:84384688 G>A maps to NM_139076.2 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:84384688 G>A maps to NM_139076.2 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:126523197 G>A maps to NM_032182.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:126495402 G>T maps to NM_032182.3 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr1:222920027 G>A maps to NM_207468.2 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:102676646 C>T maps to NM_001136123.1 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:102706863 G>A maps to NM_001136123.1 Q1001Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:102689647 G>T maps to NM_001136123.1 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:102676960 T>G maps to NM_001136123.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:102678180 C>A maps to NM_001136123.1 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:102684372 A>T maps to NM_001136123.1 K539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:102685871 T>G maps to ENST00000370271 L713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:97587387 G>A maps to ENST00000417561 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:97626166 C>A maps to ENST00000417561 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:97568436 G>A maps to ENST00000417561 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:29245063 A>G maps to NM_199280.2 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:29234367 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:29237282 C>T maps to NM_199280.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:29222315 T>C maps to NM_199280.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:45431818 G>A maps to ENST00000361462 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr14:45431995 C>T maps to ENST00000361462 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:45523742 C>G maps to ENST00000361462 S1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:45542736 C>T maps to ENST00000361462 L1765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:45475278 C>T maps to ENST00000361462 R905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:45473351 T>C maps to ENST00000361462 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:45432434 G>T maps to ENST00000361462 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:45433453 G>A maps to ENST00000361462 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:45478298 G>T maps to ENST00000361462 E1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr14:94394865 C>T maps to NM_138344.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:94394669 C>T maps to NM_138344.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr14:94394669 C>T maps to NM_138344.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr14:94394612 G>A maps to NM_138344.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:119332596 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:49993718 G>A maps to NM_032130.2 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:49981393 G>A maps to NM_032130.2 D892D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:49993256 G>A maps to NM_032130.2 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:49993562 T>C maps to NM_032130.2 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:49994801 C>T maps to NM_032130.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:35718914 G>A maps to NM_152481.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:35719109 G>A maps to NM_152481.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr19:35719283 G>T maps to NM_152481.1 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:35715901 G>A maps to NM_152481.1 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:15883542 A>G maps to NM_024948.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:15821131 G>A maps to NM_024948.2 Y399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:30825569 C>T maps to NM_032222.2 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:30818143 G>T maps to NM_032222.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:30825415 G>A maps to NM_032222.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr9:72003182 G>A maps to NM_001127608.1 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:71992550 G>T maps to NM_001127608.1 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:71998635 G>A maps to NM_001127608.1 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:155217653 G>A maps to ENST00000368370 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:155224497 G>A maps to ENST00000368370 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:155224464 G>A maps to ENST00000368370 C68C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:155223523 C>A did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:155218264 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:10867972 T>G maps to NM_001079512.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:15449199 C>A maps to NM_145301.2 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:15458624 C>T maps to NM_145301.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr4:92520067 C>T maps to NM_001145065.1 Q855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:91234135 G>T maps to NM_001145065.1 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:91321218 G>T maps to NM_001145065.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:91234138 G>T maps to NM_001145065.1 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr10:86273356 C>T maps to ENST00000372088 H826H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:86131563 G>A maps to ENST00000372088 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:86131903 G>T maps to ENST00000372088 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:57206179 C>A maps to NM_024946.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:2632844 C>T maps to ENST00000324666 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr4:2692614 G>A maps to ENST00000324666 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:2632847 C>T maps to ENST00000324666 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:2701543 T>G maps to ENST00000324666 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr4:2696714 C>T maps to ENST00000324666 Y754Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:176951540 G>A maps to ENST00000442143 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:176951828 G>A maps to ENST00000442143 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:176959482 G>A maps to ENST00000442143 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:150377906 G>A maps to NM_152394.3 Y588Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:150396315 A>C maps to NM_152394.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:150403618 G>A maps to NM_152394.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:150384786 G>T maps to NM_152394.3 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:150403618 G>A maps to NM_152394.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr3:150421679 G>A maps to NM_152394.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:150396210 C>T maps to NM_152394.3 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:698180 C>T maps to NM_138418.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:128973600 C>T maps to NM_001039762.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:128973939 G>A maps to NM_001039762.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:128974188 C>T maps to NM_001039762.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:128973617 G>A maps to NM_001039762.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:159048639 G>A maps to NM_001128424.1 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:159091962 G>A maps to NM_001128424.1 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:159048588 G>A maps to NM_001128424.1 H510H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:159048597 G>T maps to NM_001128424.1 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:159048639 G>A maps to NM_001128424.1 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:159076894 G>A maps to NM_001128424.1 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:103434399 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:103434354 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:103434304 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:68466565 C>T maps to NM_213609.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr3:68055861 C>T maps to NM_213609.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:62148733 C>A maps to NM_178539.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:68802125 C>T maps to NM_182522.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:49103589 C>T maps to ENST00000336769 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:99144587 A>G maps to NM_145111.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:99145598 G>A maps to NM_145111.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:66533821 G>A maps to NM_017565.3 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:66538925 C>T maps to NM_017565.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:66539789 G>A maps to NM_017565.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:66548039 G>A maps to NM_017565.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:66536066 G>A maps to NM_017565.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:66538301 G>A maps to NM_017565.3 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:66536066 G>A maps to NM_017565.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:179019440 G>T maps to NM_014864.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:179041203 C>T maps to NM_014864.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:296992 C>T maps to NM_020223.2 Y462Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:208949 C>T maps to NM_020223.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr7:295866 C>T maps to NM_020223.2 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:195604 C>T maps to NM_020223.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:51853046 C>T maps to NM_001005751.1 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:51829401 C>T maps to NM_001005751.1 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:51889702 T>C maps to NM_001005751.1 D1204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr10:51829471 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:47945430 C>A maps to NM_018232.1 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:46280014 C>A maps to ENST00000399588 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:46254821 C>T maps to ENST00000399588 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:46280017 C>T maps to ENST00000399588 C828C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:46264958 A>G maps to ENST00000399588 E644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:46250492 C>A maps to ENST00000399588 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:89117987 C>T maps to ENST00000330762 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:89125939 G>A maps to ENST00000330762 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr9:97082831 G>A maps to NM_017561.1 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:97081921 C>T maps to NM_017561.1 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:97081115 C>T maps to NM_017561.1 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:97081091 G>A maps to NM_017561.1 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr9:99694091 C>T maps to NM_001170741.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:99700668 C>A maps to NM_001170741.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:124671218 G>A maps to NM_001029888.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:116878986 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:116833023 C>A maps to NM_153711.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:116836776 C>T maps to NM_153711.2 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:116837112 G>A maps to NM_153711.2 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr6:116836818 T>C maps to NM_153711.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:116784508 C>T maps to NM_001010919.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:116784862 T>C maps to NM_001010919.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153735635 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153735161 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:42710311 C>T maps to ENST00000398652 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr21:42694871 G>A maps to ENST00000398652 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:58622122 G>T maps to NM_138805.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:58620046 G>A maps to NM_138805.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:58631267 G>A maps to NM_138805.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:110594435 C>T maps to NM_033088.2 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:110581330 G>T maps to NM_033088.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr7:129091550 G>A maps to ENST00000450266 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:129079864 C>T maps to ENST00000450266 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:129100158 C>T maps to ENST00000450266 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:129107282 C>T maps to ENST00000450266 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:129125454 G>T maps to ENST00000450266 E823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:129096368 C>T maps to ENST00000450266 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:129100211 T>A maps to ENST00000450266 L551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:129125552 C>T maps to ENST00000450266 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:120867531 A>G maps to NM_207009.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:120871419 C>A maps to NM_207009.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr6:82459639 C>T maps to ENST00000369756 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:27333124 G>A maps to NM_052943.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:27333241 G>A maps to NM_052943.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:118166653 G>T maps to NM_017709.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:118166014 T>C maps to NM_017709.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:79698691 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:79698894 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:79698835 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:79698380 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:79699040 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:79699001 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:79698332 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:79699040 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:79698320 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:79698042 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:79699203 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:79699069 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:79699096 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:34149300 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:34148651 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:34149301 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:34148570 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:34150172 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:34150302 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:34148490 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:34148783 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:34148785 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:34149915 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:34148347 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:34148803 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:34150120 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:34149161 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:34148391 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:34148688 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:34149287 G>A did not map to a codon.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr23:34149263 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:34148780 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:34148207 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:34149160 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:34148341 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:34148043 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:34149476 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr23:34148800 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:34150212 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:34149536 T>C did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:34148213 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr23:34149570 G>A did not map to a codon.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr23:34149706 G>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:34962865 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:34960954 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:34961412 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:34961771 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:34962203 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:34961039 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:34961677 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:34962337 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:34962544 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:34961380 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:34962507 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:34962028 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:34962329 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:34962648 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:34962874 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:34961965 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:34962517 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr23:34961510 G>A did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:34962541 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:34962550 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:34961332 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:34962164 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:34962587 G>T did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:34961677 G>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:34961522 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:34961704 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:34962517 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:34962715 A>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:34962271 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:34962606 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:37028388 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:37027100 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:37029405 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:37027711 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:37028862 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:37027159 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:37026507 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:37027047 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:37028865 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:37029251 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:37029399 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:37027061 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:37026588 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:37027002 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:37028108 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:37029423 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:37026637 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:37028453 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:37028991 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:37029399 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:37028323 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:37029140 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:37028373 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:37028176 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:37028000 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:37026900 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:37027396 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:37028316 G>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:37028087 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:37614811 G>A maps to NM_001014286.2 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:37596173 G>A maps to NM_001014286.2 N545N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr13:37607712 A>G maps to NM_001014286.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr13:37622054 G>A maps to NM_001014286.2 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:24382952 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:24383533 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:24381585 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24381958 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:24383317 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:24381221 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:24381234 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:24381247 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:24381604 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:24382864 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:24383088 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:24382957 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr23:24330459 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:24330194 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:24331419 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:24329481 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:24329622 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24331034 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24331122 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:24330345 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:24330936 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr23:24329038 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:24329514 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:24329599 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:24329927 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:24330782 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:16736398 G>A maps to NM_030797.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:16742307 T>C maps to NM_030797.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:16743284 G>A maps to NM_030797.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:16745283 T>G maps to NM_030797.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:16742337 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:16734220 G>T maps to NM_030797.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:130861568 A>G maps to NM_016623.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153678254 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153678604 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153677291 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:153678572 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:153678064 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:3850482 C>T maps to NM_012135.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:3850188 G>A maps to NM_012135.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:3850878 C>T maps to NM_012135.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr6:3850440 C>T maps to NM_012135.1 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:3850203 C>T maps to NM_012135.1 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:3850773 C>T maps to NM_012135.1 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr4:1643214 G>A maps to NM_001174070.1 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:126384775 C>T maps to NM_014661.3 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr6:136560836 T>A maps to NM_138419.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:136564102 C>A maps to NM_138419.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:136562719 C>A maps to NM_138419.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:26156165 T>G maps to NM_001099626.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:114401366 T>C maps to ENST00000424269 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:114401417 G>A maps to ENST00000424269 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:114392968 G>A maps to ENST00000424269 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:114401501 G>T maps to ENST00000424269 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:114569314 C>A maps to NM_182495.5 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr11:114569353 A>G maps to NM_182495.5 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:101520221 C>T maps to NM_145037.2 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:101540611 C>T maps to NM_145037.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr3:101540725 G>A maps to NM_145037.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:114453517 G>A maps to NM_001077639.1 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:641253 G>A maps to NM_024792.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:152853729 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:152860070 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152853869 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152857993 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr23:152858166 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152861526 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:152860035 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:152853903 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152860120 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:152861583 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:29867557 G>A maps to ENST00000269209 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr18:29868042 G>A maps to ENST00000269209 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr18:29848073 G>A maps to ENST00000269209 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:29848073 G>A maps to ENST00000269209 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr18:29850247 C>T maps to ENST00000269209 K555K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:29848727 G>A maps to ENST00000269209 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:29867058 C>A maps to ENST00000269209 G501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:177245427 C>T maps to NM_021165.2 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:177226474 G>A maps to NM_021165.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:177226447 C>A maps to NM_021165.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:177249928 C>T maps to NM_021165.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:177250006 C>T maps to NM_021165.2 H565H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:177249656 C>T maps to NM_021165.2 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:177250474 T>C maps to NM_021165.2 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:190067929 G>A maps to NM_199051.1 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:190067918 G>T maps to NM_199051.1 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:190067579 C>T maps to NM_199051.1 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:190129922 G>A maps to NM_199051.1 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:190068002 G>A maps to NM_199051.1 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:190068224 G>T maps to NM_199051.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:190195305 G>A maps to NM_199051.1 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:190250767 G>A maps to NM_199051.1 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:190067519 G>A maps to NM_199051.1 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:190067780 C>T maps to NM_199051.1 Q556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:190067702 C>T maps to NM_199051.1 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11M-01A-11D-A122-09 chr1:190234171 G>T maps to NM_199051.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:190423927 C>T maps to NM_199051.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr1:150969843 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:150975078 C>T maps to NM_001163258.1 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:59102503 C>T maps to NM_001040450.1 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr15:59064435 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:59102503 C>T maps to NM_001040450.1 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:59064076 C>T maps to NM_001040450.1 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:6348471 G>A maps to NM_001195228.1 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:6352704 G>T maps to NM_001195228.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr16:67572664 C>T maps to NM_001193523.1 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:67573768 C>T maps to NM_001193523.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:67575778 C>T maps to NM_001193523.1 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:67579327 G>A maps to NM_001193523.1 R1047R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:24843332 C>T maps to NM_014722.2 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr6:24873111 G>A maps to NM_014722.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:24828517 G>A maps to NM_014722.2 R859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A1DQ-01A-11D-A135-09 chr6:24843368 C>T maps to NM_014722.2 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr6:24828517 G>A maps to NM_014722.2 R859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:24809983 C>A maps to NM_014722.2 E1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:24809983 C>A maps to NM_014722.2 E1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:49218959 G>A maps to NM_080829.2 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:49211098 G>A maps to NM_080829.2 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:49211904 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:49221268 C>T maps to NM_080829.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:49218674 C>T maps to NM_080829.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr20:49218764 G>A maps to NM_080829.2 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr20:49204375 G>A maps to NM_080829.2 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:49224990 C>T maps to NM_080829.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:93312916 C>A did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr9:139617827 C>T maps to NM_152421.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:139617772 C>T maps to NM_152421.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:72109249 A>G maps to NM_001044369.2 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr18:72113870 C>T maps to NM_001044369.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:72109230 G>A maps to NM_001044369.2 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:119419552 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119438333 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:119394784 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr23:119445138 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:119410873 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:119419525 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr13:114471914 C>A maps to ENST00000375348 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:114472079 G>T maps to NM_182614.2 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:114469088 A>G maps to NM_182614.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:212798350 G>A maps to NM_153606.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:212799685 G>A maps to NM_153606.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:156589790 G>T maps to NM_130899.2 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:156590215 C>A maps to NM_130899.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:156590264 G>T maps to NM_130899.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:67665006 T>G maps to NM_173526.3 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr14:67671517 C>T maps to NM_173526.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:67671310 G>C maps to NM_173526.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:50979468 G>A maps to ENST00000391816 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:50979134 G>A maps to ENST00000391816 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:128320095 C>T maps to NM_001012454.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:206141508 C>T maps to NM_001123168.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:206141508 C>T maps to NM_001123168.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr1:206141508 C>T maps to NM_001123168.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:206141508 C>T maps to NM_001123168.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:120842037 C>T maps to NM_001100910.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:143910091 G>A maps to NM_207418.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:78332066 A>G maps to NM_198549.2 Q518Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:78325056 C>T maps to NM_198549.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:131832165 G>A maps to NM_032809.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:131802776 C>T maps to ENST00000413435 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:131812154 C>T maps to NM_032809.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:43627780 A>T maps to NM_001145196.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:43624723 C>T maps to NM_001145196.1 P1321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:43625338 T>C maps to NM_001145196.1 K1116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:43625257 G>A maps to NM_001145196.1 G1143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:43626757 C>T maps to NM_001145196.1 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:90535526 C>T maps to NM_001145124.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:90537818 C>T maps to NM_001145124.1 G999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:90538301 C>A maps to NM_001145124.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:90538067 G>A maps to NM_001145124.1 S1082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr9:90535679 C>T maps to NM_001145124.1 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr9:90536783 C>A maps to NM_001145124.1 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:90535940 T>C maps to NM_001145124.1 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:90537365 C>T maps to NM_001145124.1 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:134136436 C>T maps to NM_033387.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:134151419 G>A maps to NM_033387.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:59752242 C>T maps to NM_152450.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:59752197 C>T maps to NM_152450.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:59808968 C>T maps to NM_152450.2 H304H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:94772514 C>A maps to NM_152548.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:94756011 C>T maps to NM_152548.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:38156690 G>T maps to NM_001170792.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:38179161 T>C maps to NM_144713.3 H268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:38156620 C>A maps to NM_001170792.1 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:38208471 A>G maps to NM_144713.3 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:38179323 T>G maps to NM_144713.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:38202432 G>T maps to NM_144713.3 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:41029327 C>T maps to NM_018145.1 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:41037246 G>A maps to NM_018145.1 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:41030767 C>T maps to NM_018145.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr8:124221768 C>T maps to ENST00000360681 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr8:124206355 G>A maps to NM_032899.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:54805206 C>T maps to NM_001010872.1 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:54735452 G>T maps to NM_001010872.1 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:54792311 C>T maps to NM_001010872.1 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:54735157 C>T maps to NM_001010872.1 H38H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr6:54805184 C>T maps to NM_001010872.1 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:54806652 G>T maps to NM_001010872.1 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:54804815 C>T maps to NM_001010872.1 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:54792418 C>T maps to NM_001010872.1 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr6:54806699 A>G maps to NM_001010872.1 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr20:33875516 C>T maps to NM_178468.4 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:33875354 G>T maps to NM_178468.4 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:33875621 C>T maps to NM_178468.4 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:37580706 G>A maps to NM_030919.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:37580706 G>A maps to NM_030919.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:37580266 C>T maps to NM_030919.2 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:49104611 C>T maps to NM_017708.3 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr17:18874815 G>T maps to NM_001039999.2 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:18874803 C>T maps to NM_001039999.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:144812671 G>T maps to NM_198488.3 Y27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:144812434 C>T maps to NM_198488.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr16:5145472 G>A maps to NM_201400.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:12040329 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:12286247 G>T maps to NM_001137610.1 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:231155812 C>T maps to NM_198552.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr1:231155818 G>A maps to NM_198552.2 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:17608569 A>G maps to NM_016255.2 *414W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:8374609 G>A maps to NM_018088.3 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr12:8377326 C>T maps to NM_018088.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:8376721 C>T maps to NM_018088.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:124787435 G>A maps to NM_144963.2 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:124798808 C>A maps to NM_144963.2 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:124796787 C>A maps to NM_144963.2 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:94730928 C>T maps to ENST00000452913 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:85135933 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:85138998 G>A maps to ENST00000393246 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:85143992 G>A maps to ENST00000393246 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:85135933 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:64373323 G>A maps to NM_032231.4 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:33810288 G>A maps to ENST00000395190 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:38762476 A>G maps to NM_173611.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr15:38766433 C>T maps to NM_173611.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:38776700 A>T maps to NM_173611.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:38897584 A>G maps to NM_174905.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:8763335 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:8767123 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:8767124 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:8763241 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:8763130 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:8763271 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:8763411 C>A did not map to a codon.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr23:8763174 C>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:8763126 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:8763411 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:8768124 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr23:8766462 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:8763151 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:8764349 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:8766188 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:8766430 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr23:8764375 C>G did not map to a codon.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr23:8763372 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:8764390 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:8763185 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:8764407 C>T did not map to a codon.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr23:8768147 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr23:9001022 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:9000451 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:9000440 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:8995940 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:8995914 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:8998325 G>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:9000487 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr23:9001029 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13056592 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:13056586 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:13057980 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:89831326 G>A maps to NM_000135.2 R917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:89824988 G>A maps to NM_000135.2 Q993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:14861706 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:14863025 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:14871175 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:14861761 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:14861990 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:14883517 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:14862070 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:14862677 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:14882851 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:14883282 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:14877437 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:14862649 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:14877445 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:14863361 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:14863191 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr23:14861926 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:14861759 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:14871186 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:14882850 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:14861830 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:14882703 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:14882685 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:14882985 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:14882996 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:14861698 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:14861999 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:14863160 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:10094112 C>T maps to NM_033084.3 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:10123088 C>T maps to NM_033084.3 Y1055Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:10108960 C>T maps to NM_033084.3 H818H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:10116323 G>A maps to NM_033084.3 T942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:10085212 C>T maps to NM_033084.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:10106494 C>T maps to NM_033084.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:10084271 G>A maps to NM_033084.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:10130578 G>T maps to NM_033084.3 E1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:10136906 A>G maps to NM_033084.3 E1329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:10081521 G>T maps to NM_033084.3 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:35423598 G>A maps to NM_021922.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr6:35430690 C>T maps to NM_021922.2 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35075721 G>T maps to NM_004629.1 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:35077396 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr15:89843576 T>C maps to NM_001113378.1 S950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:89838241 G>A maps to NM_001113378.1 Q851Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:58392949 G>A maps to NM_001114636.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr14:45667940 C>T maps to NM_020937.2 C1937C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:45658175 G>T maps to NM_020937.2 E1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:45642295 C>A maps to NM_020937.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:45644692 T>C maps to NM_020937.2 I912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:45665415 C>A maps to NM_020937.2 S1794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:45665505 T>G maps to NM_020937.2 G1824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:45636335 C>T maps to NM_020937.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:45665527 G>T maps to NM_020937.2 E1832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:45645466 G>A maps to NM_020937.2 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:45644491 C>A maps to NM_020937.2 I845I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:45644845 C>T maps to NM_020937.2 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:45667952 C>T maps to NM_020937.2 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr14:45645114 C>A maps to NM_020937.2 S1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:45645586 G>A maps to NM_020937.2 Q1210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:163044873 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:163081008 C>T maps to NM_004460.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:163055300 G>A maps to NM_004460.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:163070501 C>T maps to NM_004460.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr2:163075614 C>A maps to NM_004460.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:163076433 C>A maps to NM_004460.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:163039967 C>A maps to NM_004460.2 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:163076433 C>A maps to NM_004460.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:163059613 C>T maps to NM_004460.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:13743366 C>A maps to NM_032228.5 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:13716483 G>T maps to NM_032228.5 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:13734629 A>C maps to ENST00000355107 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:29423408 C>T maps to NM_018099.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:29450076 C>T maps to NM_018099.3 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:29486609 C>T maps to NM_018099.3 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:29464034 C>T maps to NM_018099.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr12:29446232 C>T maps to NM_018099.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:99091386 C>T maps to NM_005766.2 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:99064219 G>A maps to NM_005766.2 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:99092975 C>T maps to NM_005766.2 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:99099065 C>T maps to NM_005766.2 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:99099002 C>T maps to NM_005766.2 Y996Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr13:99098960 G>A maps to NM_005766.2 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:99099065 C>T maps to NM_005766.2 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:242344256 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:242401951 C>T maps to NM_014808.2 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:242381119 A>G maps to ENST00000413432 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:242432823 C>A maps to NM_014808.2 Y1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:242402027 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:5613463 C>T maps to NM_006567.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr6:5613463 C>T maps to NM_006567.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:13035618 C>T maps to NM_004461.2 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr19:13035582 G>A maps to NM_004461.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr2:223507594 G>A maps to NM_005687.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr2:223493603 G>T maps to NM_005687.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:90770294 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:90762943 T>C maps to NM_000043.3 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:90774068 G>A maps to NM_000043.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:90773999 C>A maps to NM_000043.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:172628520 G>A maps to NM_000639.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:80038254 G>T maps to NM_004104.4 A2346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:80042424 G>A maps to NM_004104.4 L1578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:80046679 G>A maps to NM_004104.4 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:80047242 G>A maps to NM_004104.4 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:80038643 G>A maps to NM_004104.4 I2250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:80046266 G>A maps to NM_004104.4 I864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:80045863 G>A maps to NM_004104.4 F944F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:80042434 G>A maps to NM_004104.4 R1574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr17:80041513 G>A maps to NM_004104.4 G1740G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr17:80037090 G>A maps to NM_004104.4 S2488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:80046166 A>G maps to NM_004104.4 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:150775155 G>T maps to NM_006712.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:170402873 C>A maps to NM_024622.3 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:170411646 C>A maps to NM_024622.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:170411656 C>T maps to NM_024622.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:170403006 C>T maps to NM_024622.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:207639119 G>T maps to NM_014929.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:207651462 C>T maps to NM_014929.3 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:7867935 G>A maps to NM_024091.3 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:7861279 G>A maps to NM_024091.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:7867437 C>T maps to NM_024091.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr5:7867848 T>C maps to NM_024091.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr5:7861279 G>A maps to NM_024091.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr5:7867080 G>A maps to NM_024091.3 C372C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:3127490 T>C maps to NM_021826.4 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:3128744 C>T maps to NM_021826.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr4:187524773 G>A maps to ENST00000260147 Q3639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:187518279 G>A maps to ENST00000260147 H4141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:187524888 G>T maps to ENST00000260147 G3600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:187541856 G>A maps to ENST00000260147 G1964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:187541874 G>A maps to ENST00000260147 S1958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:187628389 G>A maps to ENST00000260147 D864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:187532759 A>C maps to ENST00000260147 T3214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:187539936 G>A maps to ENST00000260147 Y2604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:187554939 T>C maps to ENST00000260147 G1407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:187509808 G>A maps to ENST00000260147 D4571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:187527289 G>A maps to ENST00000260147 I3431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:187557900 C>T maps to ENST00000260147 P1270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr4:187527265 G>A maps to ENST00000260147 N3439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr4:187509892 G>A maps to ENST00000260147 Y4543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:187509796 G>A maps to ENST00000260147 F4575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:187517874 G>A maps to ENST00000260147 F4276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:187539950 G>A maps to ENST00000260147 R2600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:187557283 C>A maps to ENST00000260147 E1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:187509972 C>A maps to ENST00000260147 E4517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:187584593 C>A maps to ENST00000260147 E1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:187524144 C>T maps to ENST00000260147 P3801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:187524686 G>A maps to ENST00000260147 R3668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:187584729 C>T maps to ENST00000260147 S1101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr4:187521279 G>A maps to ENST00000260147 Q3962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:187539689 C>A maps to ENST00000260147 E2687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:187542860 G>A maps to ENST00000260147 R1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:187521514 C>G did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr4:187521412 C>A maps to ENST00000260147 V3917V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr4:187540626 G>A maps to ENST00000260147 S2374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr4:187539090 G>C maps to ENST00000260147 Y2886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr4:187527259 G>A maps to ENST00000260147 P3441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr4:187517847 G>A maps to ENST00000260147 P4285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr4:187630041 C>A maps to ENST00000260147 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:187542794 C>A maps to ENST00000260147 E1652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:187554954 G>A maps to ENST00000260147 F1402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:187629399 C>A maps to ENST00000260147 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:187542224 C>A maps to ENST00000260147 E1842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:187521112 C>T maps to ENST00000260147 T4017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:187539950 G>A maps to ENST00000260147 R2600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr4:187524629 G>A maps to ENST00000260147 Q3687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:187539950 G>A maps to ENST00000260147 R2600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:187628407 C>T maps to ENST00000260147 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:187542066 T>C maps to ENST00000260147 P1894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr4:187539650 C>A maps to ENST00000260147 E2700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:187538990 G>A maps to ENST00000260147 R2920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:187549314 G>A maps to ENST00000260147 I1601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:187630312 G>A maps to ENST00000260147 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:150947661 G>A maps to NM_001447.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:150922047 G>A maps to NM_001447.2 H2880H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:150933921 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:150934009 G>A maps to NM_001447.2 S1286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:150948303 C>T maps to NM_001447.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:150923681 C>A maps to NM_001447.2 E2336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:150943167 C>A maps to NM_001447.2 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:150929030 G>A maps to NM_001447.2 F1538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:150914063 C>T maps to NM_001447.2 P3111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:150924258 G>T maps to NM_001447.2 V2143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:150946359 G>T maps to NM_001447.2 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:150947646 T>C maps to NM_001447.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:150901611 C>T maps to NM_001447.2 L3514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:150946796 C>A maps to NM_001447.2 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr5:150946214 C>A maps to NM_001447.2 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:150924606 C>T maps to NM_001447.2 A2027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:150922620 C>T maps to NM_001447.2 P2689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:150925304 C>A maps to NM_001447.2 E1795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:150920324 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:150948036 C>T maps to NM_001447.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:92623928 C>T maps to ENST00000298047 L4474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:92086976 C>T maps to ENST00000298047 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:92088307 G>A maps to ENST00000298047 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:92532622 C>T maps to ENST00000298047 D2148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:92539626 C>T maps to ENST00000298047 R3065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:92570869 C>T maps to ENST00000298047 G3422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:92568048 C>A maps to ENST00000298047 V3295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:92599959 C>A maps to ENST00000298047 I3904I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:92616095 C>T maps to ENST00000298047 I4158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:92531125 G>A maps to ENST00000298047 P1649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:92533024 C>T maps to ENST00000298047 D2282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:92533850 C>T maps to ENST00000298047 L2558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:92624182 C>T maps to ENST00000298047 S4558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:92533805 C>T maps to ENST00000298047 R2543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:92577371 C>T maps to ENST00000298047 S3613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:92599974 C>T maps to ENST00000298047 G3909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr11:92498154 G>A maps to ENST00000298047 P1365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:92085929 C>T maps to ENST00000298047 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:92534401 C>T maps to ENST00000298047 S2741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:92577515 C>T maps to ENST00000298047 F3661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:92577264 C>T maps to ENST00000298047 Q3578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr11:92086747 C>T maps to ENST00000298047 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:92498145 C>T maps to ENST00000298047 F1362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:92623912 C>T maps to ENST00000298047 P4468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:92538475 C>T maps to ENST00000298047 S3018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:92495337 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:92087767 T>C maps to ENST00000298047 V830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:92532332 C>T maps to ENST00000298047 L2052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:92532847 C>T maps to ENST00000298047 I2223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:92592328 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:92615942 T>C maps to ENST00000298047 C4107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr11:92577801 T>C maps to ENST00000298047 L3757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:92087077 C>A maps to ENST00000298047 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:92088266 G>T maps to ENST00000298047 E997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:92543009 C>T maps to ENST00000298047 G3083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:92086412 G>T maps to ENST00000298047 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:92495254 C>T maps to ENST00000298047 D1301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:92531780 G>T maps to ENST00000298047 E1868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:92495168 G>T maps to ENST00000298047 E1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:92577150 C>T maps to ENST00000298047 R3540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:92086171 C>T maps to ENST00000298047 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:92534059 C>T maps to ENST00000298047 P2627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:92531305 C>T maps to ENST00000298047 D1709D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr11:92613993 C>T maps to ENST00000298047 C4075C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr11:92533856 C>A maps to ENST00000298047 R2560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:92534953 G>A maps to ENST00000298047 A2925A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:92086874 G>T maps to ENST00000298047 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:92087083 G>A maps to ENST00000298047 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:92087887 C>A maps to ENST00000298047 V870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:92532847 C>T maps to ENST00000298047 I2223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr11:92085532 C>T maps to ENST00000298047 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr11:92543009 C>T maps to ENST00000298047 G3083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr11:92533420 C>A maps to ENST00000298047 T2414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:126411419 T>G maps to NM_024582.4 A4481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr4:126372808 T>A maps to NM_024582.4 Y3546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:126373180 C>A maps to NM_024582.4 S3670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:126373817 G>T maps to NM_024582.4 G3883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:126367492 G>A maps to NM_024582.4 S2413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:126241382 T>C maps to NM_024582.4 L1273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:126398513 T>C maps to ENST00000457801 C4131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:126240493 C>A maps to NM_024582.4 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:126336298 G>T maps to NM_024582.4 E2061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:126367549 T>G maps to NM_024582.4 T2432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:126372125 G>T maps to NM_024582.4 E3319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:126372541 G>A maps to NM_024582.4 P3457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:126397364 G>T maps to NM_024582.4 E4083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:126411470 C>A maps to NM_024582.4 I4498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:126329732 C>T maps to NM_024582.4 R1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:126412295 G>A maps to NM_024582.4 P4773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:126370700 C>T maps to NM_024582.4 R2844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:126328258 C>T maps to NM_024582.4 P1844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:126240400 G>A maps to NM_024582.4 K945K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:126412647 C>T maps to NM_024582.4 R4891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K0-01A-11W-A062-09 chr4:126370946 G>T maps to NM_024582.4 E2926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:126237934 G>A maps to NM_024582.4 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:126240605 C>T maps to NM_024582.4 R1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr4:126238897 C>T maps to NM_024582.4 Y444Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr4:126240667 C>A maps to NM_024582.4 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr4:126389665 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:126408687 C>T maps to NM_024582.4 F4335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:126370700 C>T maps to NM_024582.4 R2844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:126412181 T>C maps to NM_024582.4 G4735G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:126411630 G>T maps to NM_024582.4 E4552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:126238714 G>A maps to NM_024582.4 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:126241241 C>T maps to NM_024582.4 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:126337701 G>T maps to NM_024582.4 E2315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:126400928 C>T maps to NM_024582.4 S4169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:126411113 C>T maps to NM_024582.4 S4379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:126411740 C>T maps to NM_024582.4 N4588N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:126372319 T>A maps to NM_024582.4 G3383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:126372442 C>A maps to NM_024582.4 T3424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr4:126242534 A>C maps to NM_024582.4 R1657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr4:126337623 C>T maps to NM_024582.4 R2289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr4:126239980 C>T maps to NM_024582.4 N805N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr4:126238738 C>T maps to NM_024582.4 N391N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:126369688 G>A maps to NM_024582.4 S2506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:126370447 C>A maps to NM_024582.4 V2759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:126412860 G>T maps to NM_024582.4 E4962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:150889957 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:150891126 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr23:150885857 G>C did not map to a codon.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr23:150884675 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:150885864 G>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:150889906 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:64889276 G>T maps to NM_001997.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:73914244 C>T maps to ENST00000389570 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:40331281 G>A maps to NM_001436.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:40329692 G>A maps to NM_001436.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:40328354 G>T maps to NM_001436.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:16111125 T>C maps to NM_017556.2 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:45946456 C>A maps to ENST00000348697 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:45970447 T>C maps to NM_006486.2 D585D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:45929003 C>T maps to ENST00000348697 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr22:45938047 C>T maps to ENST00000348697 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:45914659 G>T maps to ENST00000348697 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr22:45960856 C>T maps to ENST00000348697 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr22:45937130 C>T maps to ENST00000348697 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:13659622 G>T maps to NM_001165035.1 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:13679274 C>A maps to NM_001165035.1 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr3:13661290 T>C maps to NM_001165035.1 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:92349412 G>A maps to ENST00000267620 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr14:92353549 G>A maps to ENST00000267620 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:92403519 G>A maps to ENST00000267620 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:92349334 T>C maps to ENST00000267620 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr14:92403396 C>T maps to ENST00000267620 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:112942776 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr15:48782150 G>A maps to NM_000138.4 C993C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:48797344 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:48707779 G>A maps to NM_000138.4 G2668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:48730114 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:48756144 A>G maps to NM_000138.4 C1672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:48703281 C>A maps to NM_000138.4 E2841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:48760623 G>A maps to NM_000138.4 R1523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:48776135 G>A maps to NM_000138.4 I1239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:48782077 C>A maps to NM_000138.4 E1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:48787749 C>A maps to NM_000138.4 G819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:48729256 C>A maps to NM_000138.4 E2133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:48737633 C>T maps to NM_000138.4 G1952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:48777578 G>T maps to NM_000138.4 S1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:48741072 C>A maps to NM_000138.4 E1855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:48720668 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr15:48764826 C>T maps to NM_000138.4 Q1419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:48762953 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:48766839 A>G maps to NM_000138.4 N1324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:48797344 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:48729256 C>A maps to NM_000138.4 E2133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr15:48797344 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:127668660 C>A maps to NM_001999.3 G1389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:127686617 A>G maps to NM_001999.3 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:127654577 G>A maps to NM_001999.3 N1529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr5:127595356 G>A maps to NM_001999.3 S2843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:127637080 G>A maps to NM_001999.3 N2013N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:127800597 C>T maps to NM_001999.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:127613620 G>A maps to NM_001999.3 C2474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:127712520 G>A maps to NM_001999.3 N625N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:127595365 G>A maps to NM_001999.3 N2840N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:127595479 G>A maps to NM_001999.3 P2802P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:127636611 G>A maps to NM_001999.3 V2021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:127674676 G>A maps to NM_001999.3 C1140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:127597538 G>A maps to NM_001999.3 V2751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr5:127681190 G>A maps to NM_001999.3 C1025C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:127615947 A>G maps to NM_001999.3 I2358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:8174204 G>A maps to NM_032447.3 A1508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:8162224 G>T maps to NM_032447.3 R1745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:8209851 G>A maps to NM_032447.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:8182068 G>A maps to NM_032447.3 D1190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:8152995 G>A maps to NM_032447.3 F2148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:8206887 G>A maps to NM_032447.3 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:8206610 G>A maps to NM_032447.3 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:8136976 G>T maps to NM_032447.3 L2681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:8152027 G>A maps to NM_032447.3 I2229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:8159444 G>T maps to NM_032447.3 T1930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:8152947 G>A maps to NM_032447.3 C2164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:8162289 C>A maps to NM_032447.3 E1724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:8207007 T>C maps to NM_032447.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:8190869 G>T maps to NM_032447.3 V879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:8181579 C>T maps to NM_032447.3 T1230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:8182411 G>A maps to NM_032447.3 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:8182459 G>T maps to NM_032447.3 C1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:8209800 G>A maps to NM_032447.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:97365683 A>G maps to NM_001127628.1 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:97329623 G>A maps to NM_003837.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:97346903 A>G maps to NM_003837.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:97321408 C>T maps to NM_003837.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:30680890 A>G maps to ENST00000356166 A956A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:30676628 G>A maps to ENST00000356166 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:9922033 C>T maps to NM_017703.1 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9921796 C>T maps to NM_017703.1 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr19:9922066 G>A maps to NM_017703.1 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:102517961 G>T maps to NM_145032.3 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr12:1702200 C>T maps to NM_152441.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:107197453 G>T maps to NM_001163315.2 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:107684212 C>A maps to NM_001163315.2 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:107559869 G>T maps to NM_001163315.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:5521468 G>A maps to NM_024963.4 H698H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr7:5540342 G>A maps to ENST00000312577 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr7:5521510 G>A maps to NM_024963.4 H684H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:5531016 C>T maps to ENST00000312577 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:30953774 G>A maps to NM_001099784.2 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:30958403 G>A maps to NM_001099784.2 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:33414829 C>T maps to NM_012157.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:33406173 T>C maps to NM_012157.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:33415406 C>A maps to NM_012157.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:33416901 G>A maps to NM_012157.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:33400457 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:33425650 C>T maps to NM_012157.3 Y374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:135276175 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:135272471 C>A maps to NM_012159.4 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:135277260 T>G maps to NM_012159.4 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:135276972 C>T maps to NM_012159.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:135277120 G>T maps to NM_012159.4 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:77595952 C>A maps to NM_012158.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:77581815 G>A maps to NM_012158.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:99353372 G>A maps to NM_012160.3 C344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:99374513 C>T maps to NM_012160.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr6:99322297 C>A maps to NM_012160.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:15640236 G>A maps to NM_012161.3 C159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:15627284 C>T maps to NM_012161.3 W480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:15613887 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:15627352 C>A maps to NM_012161.3 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:15627542 C>T maps to NM_012161.3 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:15626992 A>G maps to NM_012161.3 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:145580739 G>T maps to NM_012162.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr8:145580712 G>A maps to NM_012162.1 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:15928533 C>A maps to NM_012304.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:15937132 C>T maps to NM_012304.3 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:37537196 G>A maps to NM_012166.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:37537190 G>A maps to NM_012166.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:37515998 G>T maps to NM_012166.2 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:37537190 G>A maps to NM_012166.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:37537463 G>A maps to NM_012166.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:37515995 G>T maps to NM_012166.2 I867I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:37541342 G>A maps to NM_012166.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:37522822 G>A maps to NM_012166.2 Y643Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:37541342 G>A maps to NM_012166.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:48066804 C>T maps to NM_001190274.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:71797777 C>A maps to NM_001142958.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr18:71803100 T>G maps to NM_001142958.1 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:71796799 C>A maps to NM_001142958.1 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr18:71807495 A>G maps to NM_001142958.1 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr8:28314441 G>A maps to NM_172366.2 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:28314305 C>A maps to NM_172366.2 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:28286249 A>G maps to NM_172366.2 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:28321247 G>A maps to NM_172366.2 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:39433343 A>C maps to ENST00000448145 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:39435613 G>A maps to ENST00000448145 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:39439267 C>A maps to NM_148169.1 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:5957516 C>T maps to NM_032807.3 Y567Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:5958394 C>A maps to NM_032807.3 V639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:5957432 G>T maps to NM_032807.3 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:5948195 G>A maps to NM_032807.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:5979173 C>T maps to NM_032807.3 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:11710616 G>A maps to NM_012168.4 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:117612024 G>A maps to NM_033624.2 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:117627046 C>T maps to NM_033624.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr12:117603423 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:76225046 C>T maps to NM_147188.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:76225244 G>A maps to NM_147188.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:100187699 T>C did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr7:100187981 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:100190473 G>A maps to NM_012172.4 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:100187667 G>A maps to NM_012172.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr7:100198230 G>A maps to NM_012172.4 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:100189425 G>A maps to NM_012172.4 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr7:100193311 C>A maps to NM_012172.4 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:100187667 G>A maps to NM_012172.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:100187888 C>T maps to NM_012172.4 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:100187812 C>A maps to NM_012172.4 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:401396 C>T maps to NM_183421.1 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:385640 A>G maps to NM_183421.1 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:224345313 C>T maps to NM_015176.2 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:224340921 G>T maps to NM_015176.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:33777331 A>C maps to NM_012175.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:33790505 G>A maps to NM_012175.3 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr11:33792359 G>A maps to NM_012175.3 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:33770433 C>A maps to NM_012175.3 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:33768741 G>T maps to NM_012175.3 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:146125968 G>A maps to NM_032145.4 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:146127037 A>C maps to NM_032145.4 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:146126017 G>A maps to NM_032145.4 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr16:87376494 G>A maps to NM_024735.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:87380856 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:87377350 G>A maps to NM_024735.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:87393904 C>T maps to NM_024735.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:87364777 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr16:87376497 G>A maps to NM_024735.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:87377314 G>A maps to NM_024735.3 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:124525622 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:124547050 G>T maps to NM_058229.2 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr8:124526528 G>A maps to NM_058229.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:55817873 G>T maps to NM_152231.1 G256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:55817914 T>C maps to NM_152231.1 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:230841053 C>A maps to NM_174899.4 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:230875458 C>T maps to NM_174899.4 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr5:147807328 G>A maps to NM_205836.1 G824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:147774455 C>A maps to NM_205836.1 C39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:147781647 C>T maps to NM_205836.1 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:147805254 G>T maps to NM_205836.1 E637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:147795507 C>T maps to NM_205836.1 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:147774396 G>T maps to NM_205836.1 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr17:6683276 G>A maps to NM_153230.2 W30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:41929934 G>T maps to NM_012176.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:41941322 T>C maps to NM_012176.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:121340440 G>A maps to NM_016298.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:121341763 C>T maps to NM_016298.3 H496H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:121345714 C>A maps to NM_016298.3 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:121341803 C>T maps to NM_016298.3 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:121342180 C>T maps to NM_016298.3 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:73491551 G>A maps to ENST00000295133 R615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:73490372 G>A maps to ENST00000295133 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:16577347 C>T maps to NM_018994.1 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:16577761 G>A maps to NM_018994.1 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:101153092 T>C maps to NM_001029860.3 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:101153922 C>A maps to NM_001029860.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:101146118 C>A maps to NM_001029860.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr8:101153860 A>G maps to NM_001029860.3 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:11718435 C>T maps to NM_033182.5 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:196311116 C>A maps to NM_001105573.1 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:46216691 G>T maps to NM_001080469.1 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:46215151 G>A maps to NM_001080469.1 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:37111106 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:68691492 G>A maps to NM_001024680.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:153296400 T>C maps to NM_012177.3 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:153293426 G>A maps to NM_012177.3 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:153294180 G>A maps to NM_012177.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:153296496 T>C maps to NM_012177.3 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A186-01A-11D-A12J-09 chr6:153296655 A>T maps to NM_012177.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:153292540 C>T maps to NM_012177.3 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:153296105 G>A maps to NM_012177.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:153296352 G>A maps to NM_012177.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:11732026 C>T maps to NM_018438.5 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:32894333 T>C maps to NM_012179.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:32894501 G>A maps to NM_012179.3 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:32894168 G>A maps to NM_012179.3 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:175158730 G>A maps to NM_012180.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:175158654 G>A maps to NM_012180.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:52938286 C>A maps to NM_012347.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:52962582 C>T maps to NM_012347.4 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:18682559 G>A maps to ENST00000395665 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:18670127 C>T maps to ENST00000395665 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:18671956 C>T maps to ENST00000395665 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr17:18681917 G>A maps to ENST00000395665 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:18661635 C>T maps to ENST00000395665 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:18675853 C>A maps to ENST00000395665 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr17:18659389 C>T maps to ENST00000395665 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:18651251 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:18682406 C>T maps to ENST00000395665 F985F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:18673281 C>T maps to ENST00000395665 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:171326046 A>G maps to NM_012300.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr5:171303393 G>A maps to NM_012300.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:171337654 T>G maps to NM_012300.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr5:171337723 C>T maps to NM_012300.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:48414322 G>A maps to NM_207102.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:123550473 C>T maps to NM_012164.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:123526989 T>C maps to NM_012164.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr9:123535118 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:123526842 G>A maps to NM_012164.3 H453H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:123540778 G>A maps to NM_012164.3 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr10:103372158 A>G maps to ENST00000331272 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:103371149 C>T maps to ENST00000331272 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:103371164 G>T maps to ENST00000331272 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:103433324 C>T maps to ENST00000331272 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:139837070 G>T maps to NM_018998.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:139835487 G>A maps to NM_018998.2 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:153332915 G>A maps to NM_033632.2 R14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:153251900 C>A maps to NM_033632.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr4:153250882 G>A maps to NM_033632.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:153332918 G>A maps to NM_033632.2 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:153268096 C>T maps to NM_033632.2 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:153332523 C>T maps to NM_033632.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr4:153268137 G>A maps to NM_033632.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:117461993 G>A maps to NM_153348.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:117426487 T>C maps to NM_153348.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:117465276 C>T maps to NM_153348.2 N540N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:207133096 G>T maps to NM_001170631.1 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:207139158 G>A maps to NM_001170631.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:207134250 C>A maps to NM_001170631.1 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:55399545 C>T maps to NM_002000.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:55399593 C>T maps to NM_002000.2 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:55401210 A>G maps to NM_002000.2 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:159277608 G>T maps to ENST00000368115 G224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:159273838 C>T maps to ENST00000368115 H69H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A0JY-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:7755381 G>A maps to NM_002002.4 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:40424045 G>A maps to NM_003890.2 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:40424378 G>A maps to NM_003890.2 C608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:40370206 G>A maps to NM_003890.2 I4153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:40366421 C>T maps to NM_003890.2 A4604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:40382724 C>T maps to NM_003890.2 S3387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:40433476 A>G maps to NM_003890.2 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:40433704 G>A maps to NM_003890.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:40412111 G>A maps to NM_003890.2 C1172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:40392423 G>A maps to NM_003890.2 L2694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:40392667 G>A maps to NM_003890.2 N2612N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:40408593 G>A maps to NM_003890.2 F1415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:40434213 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:40377027 G>A maps to NM_003890.2 D3798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr19:40392057 G>A maps to NM_003890.2 N2776N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:149761784 C>T maps to NM_000566.3 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:120927285 C>A maps to NM_001017986.2 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:161476346 C>T maps to NM_001136219.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:161643020 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:161518211 G>A maps to NM_000569.6 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr19:50027782 G>A maps to NM_004107.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:50027854 G>A maps to NM_004107.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:17883491 C>T maps to NM_015122.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:17886897 C>T maps to NM_015122.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:17898629 G>A maps to NM_015122.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:17898530 G>A maps to NM_015122.2 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:17894971 C>T maps to NM_015122.2 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:72377613 C>A maps to NM_138782.2 S662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:141028985 G>A maps to ENST00000354789 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:72552499 G>A maps to ENST00000409314 N709N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:72560874 G>A maps to ENST00000409314 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:137809681 G>A maps to NM_002003.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:137804965 G>A maps to NM_002003.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:137779206 G>A maps to NM_004108.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:137777083 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:157771311 G>C maps to NM_052938.4 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:157771785 C>A maps to NM_052938.4 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:157746856 G>A maps to NM_030764.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:157740421 G>A maps to NM_030764.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:157740421 G>A maps to NM_030764.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:157669502 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:157660171 C>T maps to NM_052939.3 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:157668285 C>T maps to NM_052939.3 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:157667134 G>A maps to NM_052939.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:157665866 G>A maps to NM_052939.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:157659642 G>A maps to NM_052939.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:157667173 C>T maps to NM_052939.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:157660171 C>T maps to NM_052939.3 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:157665995 C>T maps to NM_052939.3 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:157557350 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:157545321 C>A maps to NM_031282.2 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:157548415 T>G maps to ENST00000438714 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:157516937 G>T maps to NM_031281.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr1:157488246 C>A maps to NM_031281.2 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:157512727 C>T maps to NM_031281.2 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:157488261 A>C maps to NM_031281.2 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:157512658 G>T maps to NM_031281.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr1:157485643 A>G maps to NM_031281.2 H944H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:159784011 G>A maps to NM_001004310.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:159778151 C>T maps to NM_001004310.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:159779354 T>C maps to NM_001004310.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:159779294 G>A maps to NM_001004310.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:159778097 C>T maps to NM_001004310.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161681070 G>A maps to NM_001184866.1 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:161680569 C>T maps to NM_001184866.1 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:161680547 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:161681931 G>C maps to NM_001184866.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr18:55221536 C>T maps to NM_001012515.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:55221566 C>T maps to NM_001012515.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:68583402 G>A maps to NM_015322.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:114860292 G>A maps to NM_020177.2 N522N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:114860957 C>A maps to NM_020177.2 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr5:114879070 A>G maps to NM_020177.2 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:61563790 C>T maps to NM_004111.4 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr11:61563825 C>T maps to NM_004111.4 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:108219115 G>T maps to NM_005246.2 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:108171462 G>T maps to NM_005246.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:108382828 C>T maps to NM_005246.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:108521922 C>T maps to NM_005246.2 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:108171462 G>T maps to NM_005246.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:97368123 C>T maps to NM_001113382.1 D1783D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:97335881 T>C maps to NM_001113382.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:97359387 G>A maps to NM_001113382.1 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:97368345 C>T maps to NM_001113382.1 Y1791Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:97365349 C>T maps to NM_001113382.1 F1585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:97369282 G>A maps to NM_001113382.1 E1941E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:97365293 G>T maps to NM_001113382.1 E1567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr2:97361394 A>G maps to NM_001113382.1 T1324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:97327508 C>T maps to NM_001113382.1 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:97355458 G>A maps to NM_001113382.1 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:124992804 G>T maps to NM_001039112.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:125058132 C>T maps to NM_001039112.2 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:125103804 C>A maps to NM_001039112.2 I1511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:125058132 C>T maps to NM_001039112.2 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:125072865 C>T maps to NM_001039112.2 C1021C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:125109589 C>T maps to NM_001039112.2 R1592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr8:124989700 T>C maps to NM_001039112.2 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr8:125072869 G>T maps to NM_001039112.2 G1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:125022854 T>C maps to NM_001039112.2 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:125083796 C>T maps to NM_001039112.2 S1339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:125110085 C>A maps to NM_001039112.2 I1615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:125072943 C>T maps to NM_001039112.2 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:19184586 G>A maps to NM_152898.2 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr7:19184846 G>A maps to NM_152898.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:6057984 G>A maps to NM_017671.4 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:6057831 G>A maps to NM_017671.4 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:6057963 A>G maps to NM_017671.4 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:6065922 G>A maps to NM_017671.4 Y461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:6077662 C>T maps to NM_017671.4 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:6075602 A>G maps to NM_017671.4 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:6100117 G>A maps to NM_017671.4 D28D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:63987446 C>T maps to NM_178443.2 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:63986814 G>A maps to NM_178443.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:63979167 C>T maps to NM_178443.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:63974955 G>A maps to NM_178443.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:63974964 C>T maps to NM_178443.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:91428410 G>T maps to NM_002005.3 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:91438727 G>A maps to NM_002005.3 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:186370279 G>T maps to NM_014375.2 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:186364078 G>T maps to NM_014375.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:186358247 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:125325667 G>A maps to ENST00000392709 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:125351529 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:125330510 C>A maps to NM_005103.4 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:125351485 C>A maps to NM_005103.4 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:121944332 C>T maps to NM_001024613.2 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:121943287 G>A maps to NM_001024613.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:121943768 G>A maps to NM_001024613.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:121942272 G>A maps to NM_001024613.2 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:121942967 A>G maps to NM_001024613.2 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:121943362 G>T maps to NM_001024613.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:121943912 C>T maps to NM_001024613.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:62356997 G>A maps to NM_018008.3 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:35843119 C>T maps to NM_005303.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:35941044 C>T maps to NM_005306.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr19:35941332 C>T maps to NM_005306.2 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:35863262 C>A maps to ENST00000246538 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:35862720 G>T maps to ENST00000246538 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:35862821 G>A maps to ENST00000246538 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:35849824 C>T maps to NM_005304.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:155505788 G>A maps to NM_000508.3 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:155509954 G>A maps to NM_000508.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr4:155505773 G>A maps to NM_000508.3 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:155507479 G>A maps to NM_000508.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:155507992 G>A maps to NM_000508.3 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr4:155508048 G>A maps to NM_000508.3 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:155490733 G>T maps to NM_005141.4 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:54492000 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:54482181 C>T did not map to a codon.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr23:54496763 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:54472578 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54475304 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54494299 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54496614 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54521575 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54496520 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54497158 C>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:54492140 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54482717 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:54482157 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:54497064 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54472808 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54491943 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54496661 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54497868 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:54475604 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:54496460 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:54496461 T>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:54494307 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:54475360 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:54475637 G>A did not map to a codon.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr23:54494262 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr6:36995821 G>A maps to NM_173558.3 Q617Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:36982771 C>A maps to NM_173558.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr6:36993701 G>T maps to NM_173558.3 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr6:36993650 C>T maps to NM_173558.3 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:36990097 C>A maps to NM_173558.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr6:36982458 C>A maps to NM_173558.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:95772574 G>A maps to NM_033086.2 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr9:95738786 C>A maps to NM_033086.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:95772640 C>T maps to NM_033086.2 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:95776150 C>A maps to NM_033086.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:95765247 C>T maps to NM_033086.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:95795190 C>T maps to ENST00000416701 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:32777595 C>T maps to ENST00000381025 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:32760901 C>A maps to NM_139241.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:32778685 G>A maps to NM_139241.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:32791806 C>A maps to ENST00000266482 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:32791770 G>T maps to ENST00000266482 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:14863052 C>T maps to NM_152536.3 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:14958760 C>T maps to NM_152536.3 N1137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:14861294 G>A maps to NM_152536.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:14861958 G>T maps to NM_152536.3 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:14922086 A>G maps to NM_152536.3 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:14861543 G>A maps to NM_152536.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:14863094 C>T maps to NM_152536.3 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr3:14861537 C>T maps to NM_152536.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:95486579 C>T maps to NM_018351.3 S1214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:95604528 G>A maps to NM_018351.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:95604849 C>T maps to NM_018351.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr12:95604390 C>T maps to NM_018351.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:44388711 A>G maps to NM_004465.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:44388499 G>A maps to NM_004465.1 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:7344856 C>T maps to NM_004112.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:191888348 G>A maps to NM_021032.4 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:191861893 C>T maps to NM_021032.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:192053205 C>A maps to NM_021032.4 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:191888259 C>T maps to NM_021032.4 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr3:191888253 A>G maps to NM_021032.4 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr23:137715054 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:137821413 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:137793105 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:137793031 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:137821410 C>T did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:137785187 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:137717638 A>C did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:137939731 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:102527533 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:76711874 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:21903674 C>T maps to NM_003867.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:170876178 C>T maps to NM_003862.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr4:123813544 G>A maps to NM_002006.4 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:49261236 C>T maps to NM_019113.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:49259627 G>A maps to NM_019113.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:4479820 G>A maps to NM_020638.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:4479907 C>T maps to NM_020638.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:69588178 C>T maps to NM_002007.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:81196070 G>T maps to NM_004464.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr4:81188028 C>T maps to NM_004464.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:81188262 G>A maps to NM_004464.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr4:81196106 C>T maps to NM_004464.3 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:4553298 C>T maps to NM_020996.1 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:4543526 C>A maps to NM_020996.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:22275366 C>T maps to NM_002010.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:22275366 C>T maps to NM_002010.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:22246296 C>A maps to NM_002010.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:15964248 C>T maps to NM_031950.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:15964284 C>A maps to NM_031950.3 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:38273432 G>A maps to NM_001174067.1 C634C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:167436090 T>C maps to NM_007045.2 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:27109490 C>T maps to NM_015633.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:27109583 G>T maps to NM_015633.2 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:27109484 G>T maps to NM_015633.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:27110532 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr10:123297910 T>C maps to ENST00000359354 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:123247584 C>A maps to ENST00000351936 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:123239493 A>G maps to ENST00000351936 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:123245036 G>A maps to ENST00000351936 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:123239529 G>T maps to ENST00000351936 Y789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:123279621 G>A maps to ENST00000351936 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:1807310 G>A maps to NM_000142.4 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:1808651 G>A maps to NM_000142.4 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr4:1808928 C>T maps to NM_000142.4 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr4:1806633 G>A maps to NM_000142.4 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:1807388 G>A maps to NM_000142.4 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:176517963 C>T maps to NM_213647.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:176518093 G>T maps to NM_213647.1 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr5:176517987 A>G maps to NM_213647.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:155531338 C>A maps to ENST00000407946 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:155533542 G>A maps to ENST00000407946 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr4:155529685 C>T maps to ENST00000407946 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:60228222 G>A maps to NM_001113411.1 Q565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:59812048 G>A maps to NM_001113411.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:60073503 C>T maps to NM_001113411.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:59922631 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:17739682 G>A maps to NM_201552.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr8:17726160 C>T maps to NM_201552.1 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:17731883 C>A maps to NM_201552.1 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:17731929 G>A maps to NM_201552.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr8:17739574 T>C maps to NM_201552.1 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:76828846 G>A maps to NM_006682.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:76826111 C>T maps to NM_006682.2 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:27948080 G>A maps to NM_005248.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:27939517 C>T maps to NM_005248.2 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:241667422 G>A maps to NM_000143.3 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:241675320 A>G maps to NM_000143.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:241661166 G>A maps to NM_000143.3 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:153897001 C>A maps to NM_033393.2 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:153897454 C>T maps to NM_033393.2 R1004R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:153896980 C>T maps to NM_033393.2 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:153881742 C>T maps to NM_033393.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:59999786 G>A maps to NM_002012.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr3:60522689 C>G maps to NM_002012.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135290786 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135290085 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:135290069 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr23:135289249 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:135290661 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135288731 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135290062 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135289251 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr23:135288595 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:135289979 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:135292105 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:38463733 C>T maps to NM_004468.3 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:97058495 G>T maps to NM_020482.4 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:97063515 A>G maps to NM_020482.4 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:97063605 C>A maps to NM_020482.4 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:97058578 C>T maps to NM_020482.4 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:67271472 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr18:34174814 C>T maps to NM_025135.2 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr18:34298470 C>T maps to NM_025135.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:33935536 C>T maps to NM_025135.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:34273180 C>A maps to NM_025135.2 Y502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:34322722 C>T maps to NM_025135.2 D1086D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:34324113 C>T maps to NM_025135.2 S1158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr18:34320731 C>A maps to NM_025135.2 S1055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:34297999 G>A maps to NM_025135.2 Q738Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:34174853 G>A maps to NM_025135.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:34289112 G>A maps to NM_025135.2 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:34289124 T>C maps to NM_025135.2 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:34298582 G>T maps to NM_025135.2 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:27016670 C>T maps to NM_203371.1 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:65655010 G>A maps to ENST00000426652 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:65655340 C>T maps to ENST00000442885 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr12:108912862 C>T maps to NM_007076.2 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:108912414 C>T maps to NM_007076.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:108912468 C>T maps to NM_007076.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:108910878 C>T maps to NM_007076.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:110112620 G>A maps to NM_014845.5 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:110064353 C>T maps to NM_014845.5 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:110037743 C>T maps to NM_014845.5 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:110112707 C>T maps to NM_014845.5 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15376305 T>G did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:15381341 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:15376293 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:15402025 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr23:15364358 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:164468182 G>T maps to NM_018086.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:164467309 T>C maps to NM_018086.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr2:164467735 T>C maps to NM_018086.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:50514087 C>A maps to NM_022116.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:76124489 G>A maps to NM_015687.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:76022796 G>A maps to NM_015687.2 D917D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:76024299 G>A maps to NM_015687.2 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:76024397 G>A maps to NM_015687.2 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr6:76072524 G>A maps to NM_015687.2 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:76024112 C>A maps to NM_015687.2 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:76063418 C>T maps to NM_015687.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:76024397 G>A maps to NM_015687.2 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:76063382 C>T maps to NM_015687.2 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:76124489 G>A maps to NM_015687.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:76024466 C>A maps to NM_015687.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:76024554 A>G maps to NM_015687.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:76023198 G>A maps to NM_015687.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:76024466 C>A maps to NM_015687.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:76063367 G>A maps to NM_015687.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:76024623 C>T maps to NM_015687.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:76124541 G>T maps to NM_015687.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:99568668 T>C maps to NM_001042459.1 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:99569204 G>A maps to NM_001042459.1 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:99569424 G>A maps to NM_001042459.1 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:99568173 C>T maps to NM_001042459.1 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:99568898 C>A maps to NM_001042459.1 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:99569453 C>A maps to NM_001042459.1 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:99569453 C>A maps to NM_001042459.1 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:99569891 C>A maps to NM_001042459.1 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:99569189 G>A maps to NM_001042459.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr3:99568911 A>G maps to NM_001042459.1 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:99569012 C>A maps to NM_001042459.1 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:99643128 C>A maps to NM_001042459.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:99567981 G>A maps to NM_001042459.1 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr4:54294282 T>C maps to NM_030917.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:54325595 G>T maps to NM_030917.3 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:54324840 C>T maps to NM_030917.3 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:54325594 C>T maps to NM_030917.3 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr7:100887351 G>A maps to NM_016068.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:56104886 G>A maps to NM_032836.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:56104853 G>A maps to NM_032836.2 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:35641209 C>T maps to NM_014344.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr17:39975642 C>T maps to NM_021939.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:39974765 C>T maps to NM_021939.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr17:39978632 C>T maps to NM_021939.3 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:39978050 C>T maps to NM_021939.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:115928417 C>T maps to ENST00000446284 P1225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:115928408 C>T maps to ENST00000446284 T1228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr9:115959315 G>A maps to ENST00000446284 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:24283682 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:2907921 C>T maps to NM_002014.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:2909013 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:2909215 T>C maps to NM_002014.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:35554822 G>A maps to NM_001145775.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:18643602 C>T maps to NM_012181.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:18642993 G>A maps to NM_012181.3 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:18643065 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:33014330 C>T maps to NM_007270.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:33014330 C>T maps to NM_007270.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:33039855 T>C maps to NM_007270.3 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:33016020 G>T maps to NM_007270.3 G205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr6:32096686 G>T maps to NM_022110.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:47258823 C>T maps to NM_024301.4 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:47258874 C>T maps to NM_024301.4 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:108370217 C>T maps to NM_006731.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:108397406 C>T maps to NM_006731.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:154965071 C>T maps to ENST00000405236 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:154960985 C>T maps to NM_025207.4 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:17125873 C>T maps to NM_144997.5 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:17124884 G>A maps to NM_144997.5 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:152275811 T>C maps to NM_002016.1 S3850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:152285585 G>T maps to NM_002016.1 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:152285557 G>A maps to NM_002016.1 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:152280809 T>C maps to NM_002016.1 S2184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:152282488 G>A maps to NM_002016.1 Q1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:152278733 T>C maps to NM_002016.1 G2876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:152276311 G>A maps to NM_002016.1 Q3684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:152287835 G>A maps to NM_002016.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:152275640 G>A maps to NM_002016.1 R3907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:152280545 C>T maps to NM_002016.1 Q2272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:152284103 C>T maps to NM_002016.1 V1086V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:152281621 G>A maps to NM_002016.1 Q1914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr1:152280890 C>T maps to NM_002016.1 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:152281253 G>A maps to NM_002016.1 H2036H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:152281865 C>T maps to NM_002016.1 S1832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:152287908 G>A maps to NM_002016.1 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:152280710 G>A maps to NM_002016.1 A2217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:152282167 G>A maps to NM_002016.1 Q1732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr1:152275826 G>A maps to NM_002016.1 S3845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:152282834 T>C maps to NM_002016.1 V1509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:152280011 G>A maps to NM_002016.1 S2450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:152285348 C>T maps to NM_002016.1 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:152326898 G>A maps to NM_001014342.2 G1121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:152329718 G>A maps to NM_001014342.2 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:152326871 T>C maps to NM_001014342.2 Q1130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:152327189 G>T maps to NM_001014342.2 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:152327771 G>T maps to NM_001014342.2 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:152323642 G>A maps to NM_001014342.2 R2207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:152324006 A>C maps to NM_001014342.2 S2085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:152326547 A>G maps to NM_001014342.2 T1238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:152327117 G>T maps to NM_001014342.2 S1048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:152326721 T>C maps to NM_001014342.2 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:152328944 G>T maps to NM_001014342.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:152328227 G>T maps to NM_001014342.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:152326459 G>A maps to NM_001014342.2 R1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:152327996 G>T maps to NM_001014342.2 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:128680465 C>T maps to NM_002017.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:128680645 C>T maps to NM_002017.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:128680759 C>A maps to NM_002017.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:128680759 C>T maps to NM_002017.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:18148670 G>A maps to NM_002018.2 C1224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:18151093 G>A maps to NM_002018.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr17:18157904 G>A maps to NM_002018.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:18156935 C>T maps to NM_002018.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:18157932 G>A maps to NM_002018.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:142498671 G>A maps to NM_207414.2 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:142498671 G>T maps to NM_207414.2 C243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:142446800 G>A maps to NM_207414.2 R1128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:142476519 G>A maps to NM_207414.2 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:142484236 G>A maps to NM_207414.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:142487989 G>A maps to NM_207414.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:142487904 G>A maps to NM_207414.2 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71379776 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:71379949 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:153593245 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153580766 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153590635 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153593613 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153595130 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153581290 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153581375 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr23:153577901 G>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153579298 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153586611 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153586673 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153590807 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153599397 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr23:153580008 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:153580956 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153580747 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr23:153593082 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153587373 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153593251 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153594807 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153596402 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:153581811 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:153583211 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:153578218 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:153587495 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:153581220 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr23:153596051 C>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:153590878 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:153580786 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:153578458 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:153582584 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153577250 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153590878 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153591040 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:153577917 C>G did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:153581454 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:153581455 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr23:153582382 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153578513 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153579377 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153582638 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153588138 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153588201 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153590358 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153594986 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153596325 T>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:153581678 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:153590868 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:153599477 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr23:153580677 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:153581419 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153586611 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153587851 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:58067393 C>T maps to NM_001164317.1 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:58109013 C>A maps to NM_001164317.1 Y1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:58109226 C>T maps to NM_001164317.1 A1178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:58132547 T>C maps to NM_001164317.1 G1883G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:58062899 G>A maps to NM_001164317.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:58081945 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:58107163 C>T maps to NM_001164317.1 Y1020Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:58116621 T>G maps to NM_001164317.1 V1459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:58080674 A>G maps to NM_001164317.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:57994482 C>T maps to NM_001164317.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:58132721 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:58133990 C>T maps to NM_001164317.1 D1960D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr3:58095042 C>A maps to NM_001164317.1 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:128489529 C>T maps to NM_001458.4 D1699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:128484713 C>A maps to NM_001458.4 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:128485211 C>T maps to NM_001458.4 G1231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:128488041 C>T maps to NM_001458.4 T1500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:128490436 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr7:128483353 C>T maps to NM_001458.4 G874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:128488683 C>T maps to NM_001458.4 N1550N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:128485076 G>A maps to NM_001458.4 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:128490932 G>A maps to NM_001458.4 R1825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:128477556 C>T maps to NM_001458.4 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:128498513 C>A maps to NM_001458.4 I2705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:128483927 C>T maps to NM_001458.4 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:128484974 G>A maps to NM_001458.4 V1152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr7:128478481 G>A maps to NM_001458.4 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:128491578 C>A maps to NM_001458.4 T1913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:128484109 C>T maps to NM_001458.4 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr7:128487997 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr7:128482672 C>T maps to NM_001458.4 Y770Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:128480650 C>T maps to NM_001458.4 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:30698877 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:30710007 C>T maps to ENST00000418160 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:27216018 T>C maps to ENST00000394906 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:27208317 G>A maps to ENST00000394906 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr17:27208260 C>T maps to ENST00000394906 Q404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:27209177 G>A maps to ENST00000394906 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:63884752 G>A maps to NM_013280.4 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:63884950 G>A maps to NM_013280.4 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:63883876 G>A maps to NM_013280.4 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:63883942 C>T maps to NM_013280.4 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:86089756 C>T maps to NM_013231.4 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:86088439 C>A maps to NM_013231.4 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:86089066 G>A maps to NM_013231.4 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr14:86089690 C>T maps to NM_013231.4 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:86089453 G>A maps to NM_013231.4 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:86089684 C>T maps to NM_013231.4 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr20:14306337 C>T maps to NM_198391.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:14306252 G>A maps to NM_198391.2 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:14306481 C>T maps to NM_198391.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:14307815 C>A maps to NM_198391.2 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:14306877 G>T maps to NM_198391.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:28877505 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:29041665 G>T maps to NM_002019.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:29004277 G>A maps to NM_002019.4 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:28931804 C>A maps to NM_002019.4 G712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:29041232 T>C maps to NM_002019.4 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:28903854 C>T maps to NM_002019.4 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:28919629 C>T maps to NM_002019.4 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:29004305 T>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:28893671 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:29001900 G>A maps to NM_002019.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:28622520 C>A maps to NM_004119.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:28631549 C>A maps to NM_004119.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr13:28592606 G>A maps to NM_004119.2 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr13:28636098 C>T maps to NM_004119.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:28611387 C>A maps to NM_004119.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:28608351 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:28589297 C>A maps to NM_004119.2 E917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:28623641 T>C maps to NM_004119.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:28608476 A>G maps to NM_004119.2 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:49979036 C>T maps to NM_001459.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:180040066 G>A maps to NM_182925.4 C1125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:180041137 G>A maps to NM_182925.4 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr5:180051061 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:180057233 C>T maps to NM_182925.4 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:180057257 C>T maps to NM_182925.4 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:180046743 G>A maps to NM_182925.4 F856F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:213068595 G>A maps to NM_014053.2 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:76088432 G>A maps to NM_017791.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:33300217 C>T maps to NM_001103184.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:33261396 G>T maps to NM_001103184.2 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:33359290 G>T maps to NM_001103184.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:33357276 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:33359541 C>A maps to NM_001103184.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:33359118 G>A maps to NM_001103184.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr15:33359119 C>T maps to NM_001103184.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:33359152 C>T maps to NM_001103184.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:33300231 C>A maps to NM_001103184.2 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:33359113 C>T maps to NM_001103184.2 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:240286510 C>T maps to ENST00000406993 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:240497470 A>C maps to ENST00000406993 S1712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:240341298 C>T maps to ENST00000406993 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:240371837 C>T maps to ENST00000406993 G1385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:240255882 G>A maps to ENST00000406993 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:240370259 A>C maps to ENST00000406993 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:240635678 G>T maps to ENST00000406993 E1833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:240635683 C>T maps to ENST00000406993 A1834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:43316398 G>A maps to NM_005892.3 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:43321220 G>A maps to NM_005892.3 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:43311013 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:153473603 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:153415313 C>T maps to NM_052905.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:153481979 G>A maps to NM_052905.3 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:50042122 G>A maps to NM_175736.4 N843N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:50043677 G>A maps to NM_175736.4 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:50045815 G>A maps to NM_175736.4 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:171236863 A>G maps to NM_002021.1 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:171251440 A>G maps to NM_002021.1 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:171250082 C>T maps to NM_002021.1 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:171247877 C>T maps to NM_002021.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:171174717 T>C maps to NM_001460.2 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:171178010 G>A maps to NM_001460.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:171083296 C>A maps to NM_006894.5 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:171076814 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:171289023 C>A maps to NM_002022.1 C20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:171302014 T>C maps to NM_002022.1 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:171300911 G>A maps to NM_002022.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr1:146687329 T>A maps to NM_001461.2 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:146661789 C>A maps to NM_001461.2 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:146684895 G>A maps to NM_001461.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:203317029 G>A maps to NM_002023.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:203317065 G>A maps to NM_002023.3 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:147014061 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:147014232 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:147024798 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:147027129 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:147030347 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:147014239 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:147027071 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:147024666 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:147030295 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:147018104 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:147026510 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr23:147024818 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:147014004 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:147014237 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:147026529 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:147010243 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:147022170 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr23:147018096 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:147014093 A>G did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:147026501 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:147030284 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:147084740 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:147063164 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:147090212 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:147063094 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:147106480 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr23:147106465 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:147090228 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:147106455 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:147063084 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:147063028 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:216230226 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:216230270 G>A maps to NM_212482.1 C2367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:216272024 C>T maps to NM_212482.1 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:216229640 G>A maps to NM_212482.1 L2404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:216272024 C>T maps to NM_212482.1 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:216271015 G>T maps to NM_212482.1 V977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:216245783 T>C maps to NM_212482.1 G1728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:216269198 G>A maps to NM_212482.1 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:216269252 G>A maps to NM_212482.1 Q1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:216240399 A>G maps to NM_212482.1 L1977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:216232745 G>A maps to NM_212482.1 N2286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:216269378 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:216240033 C>T maps to NM_212482.1 R2020R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:216243944 G>A maps to NM_212482.1 R1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:216271096 G>A maps to NM_212482.1 H950H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:216288199 G>A maps to NM_212482.1 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:216248132 T>C maps to NM_212482.1 S1656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:216262505 G>A maps to NM_212482.1 I1138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:216285396 G>A maps to NM_212482.1 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:216241230 G>A maps to NM_212482.1 Y1959Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:216296576 C>A maps to NM_212482.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:216269243 G>A maps to NM_212482.1 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:80699247 G>A maps to NM_022158.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:80706736 G>T maps to NM_022158.3 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:132740854 G>A maps to NM_015033.2 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr9:132662286 G>A maps to NM_015033.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:132671209 G>A maps to NM_015033.2 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:93965032 C>T maps to ENST00000370253 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:93988987 G>A maps to ENST00000370253 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr11:47744608 T>A maps to NM_015308.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr11:47746245 G>C maps to NM_015308.2 S698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:47765579 G>A maps to NM_015308.2 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:47772524 C>T maps to NM_015308.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:159653526 C>T maps to NM_032532.2 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr6:159687200 G>A maps to NM_032532.2 T1790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:159653676 T>C maps to NM_032532.2 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:159687140 C>T maps to NM_032532.2 F1770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:159646689 T>C maps to NM_032532.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:159653814 G>A maps to NM_032532.2 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:159653158 G>T maps to NM_032532.2 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr6:159660741 G>A maps to NM_032532.2 T1458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr6:159653394 G>A maps to NM_032532.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:49649472 G>T maps to NM_001079673.1 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr13:49705293 C>T maps to NM_001079673.1 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:49742747 G>T did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr13:49781437 G>A maps to NM_001079673.1 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:172048426 G>A maps to NM_022763.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:172048403 C>T maps to NM_022763.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:27715550 C>T maps to NM_022823.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:33333425 C>A maps to ENST00000291421 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:33330350 C>A maps to ENST00000291421 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:33333902 C>T maps to ENST00000291421 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:109256074 C>T maps to ENST00000271311 Y3Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:109270457 C>T maps to NM_001144937.1 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:109261552 T>G maps to NM_001144937.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:33454348 C>A maps to NM_017559.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:131039916 G>A maps to NM_133372.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:131007750 C>A maps to NM_133372.2 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:131007631 G>A maps to NM_133372.2 F835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:131039756 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:159747079 G>A maps to ENST00000379346 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:42932468 T>C maps to NM_002027.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:42914291 C>T maps to NM_002027.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:42932495 G>A maps to NM_002027.2 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr14:65499351 A>G maps to ENST00000448390 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:65511144 C>T maps to ENST00000448390 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr14:65499336 C>A maps to ENST00000448390 Y239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:49196522 G>A maps to NM_004476.1 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:89424314 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:89424165 A>G maps to NM_153696.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:94040782 C>T maps to NM_001080486.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:94039875 C>T maps to ENST00000328458 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:45973993 C>A maps to NM_006732.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:45973966 G>A maps to NM_006732.2 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:45976018 C>T maps to NM_006732.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:28634912 T>A maps to NM_005253.3 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:38061484 G>A maps to NM_004496.2 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:38061526 G>A maps to NM_004496.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:38061343 C>T maps to NM_004496.2 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05D-01A-11W-A027-09 chr20:22563344 G>A maps to NM_021784.4 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:22562493 G>T maps to NM_021784.4 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr20:22563131 C>A maps to NM_021784.4 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr19:46376054 C>T maps to NM_004497.2 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:79634635 C>T maps to NM_001013735.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:86601132 C>T maps to NM_005251.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:86601456 C>T maps to NM_005251.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:86601360 C>T maps to NM_005251.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr16:86601024 G>A maps to NM_005251.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:63789124 G>A maps to NM_012183.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:118038 G>A maps to NM_207305.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr2:114257093 C>T maps to NM_012184.4 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:114258023 C>T maps to NM_012184.4 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:114257906 G>A maps to NM_012184.4 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:1390652 C>T maps to NM_001452.1 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:1394946 C>G maps to NM_001452.1 Y396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:1395030 C>T maps to NM_001452.1 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:29237756 G>A maps to NM_005249.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:29237879 G>A maps to NM_005249.3 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:169535413 G>A maps to NM_012188.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZP-01A-21D-A10M-09 chr5:169533527 C>T maps to NM_012188.4 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:8205424 C>T maps to NM_018416.2 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:8200766 G>A maps to NM_018416.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:8205424 C>T maps to NM_018416.2 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:42647696 T>C did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:42657001 T>C maps to NM_001198850.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:42730850 G>A maps to NM_001198850.1 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:42657163 C>T maps to NM_001198850.1 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:42657344 G>T maps to NM_001198850.1 S327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:4799035 C>T maps to ENST00000450194 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:4794939 C>T maps to ENST00000450194 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:4799074 C>T maps to ENST00000450194 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:4800693 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr7:4800734 C>T maps to ENST00000450194 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:4800833 C>T maps to ENST00000450194 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:80559218 C>T maps to NM_004514.3 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:80529733 C>T maps to NM_004514.3 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:86612598 G>A maps to NM_005250.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:2968421 C>T maps to NM_202002.1 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:2973903 C>T maps to NM_202002.1 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:26861389 A>G maps to NM_003593.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:26851630 C>A maps to NM_003593.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:26864204 G>A maps to NM_003593.2 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:26864393 G>T maps to NM_003593.2 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr14:89878601 C>T maps to NM_001085471.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr14:89878373 C>T maps to NM_001085471.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:89629150 G>T maps to NM_001085471.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:109728090 C>T maps to NM_213596.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr6:108985778 A>G maps to NM_001455.3 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:70320827 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70321484 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70320824 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70321040 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70321260 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70321274 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70320734 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70316417 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70321051 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70321228 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr23:70316509 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70316564 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:70321172 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:70316775 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:71026153 C>A maps to NM_032682.4 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:71021727 G>A maps to NM_032682.4 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:71021321 G>A maps to ENST00000327590 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:71015129 G>A maps to NM_032682.4 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:71026982 C>T maps to NM_032682.4 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr3:71008526 G>C maps to NM_032682.4 V635V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D1-A17B-01A-22D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:114066707 G>T maps to NM_148898.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr7:114269984 A>G maps to NM_148898.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:114303568 T>C maps to NM_148898.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:114299665 G>T maps to NM_148898.3 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49111948 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49114019 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49109590 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr23:49107963 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49108004 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49110410 G>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:49110512 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49112256 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:41562612 C>T maps to NM_001012426.1 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr6:41557908 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr11:118849745 A>G maps to NM_181721.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:55650269 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:55650315 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:55650162 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:55650537 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:55650633 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:55650262 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:55650671 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:55650397 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:126146036 C>T maps to NM_017547.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:126143286 C>T maps to NM_017547.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr22:36886132 G>A maps to NM_001102371.1 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr22:36892245 C>T maps to NM_001102371.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:30432739 G>A maps to NM_004118.3 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr20:30432829 G>T maps to NM_004118.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:30432904 C>T maps to NM_004118.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:130575609 C>T maps to NM_004957.4 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:74670699 C>A maps to NM_003838.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:74670087 A>G maps to NM_003838.3 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:52249305 G>A maps to NM_002029.3 H314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:52272567 C>A maps to NM_001005738.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:52327117 C>T maps to NM_002030.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr19:52327702 T>A maps to NM_002030.3 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:95430575 C>A maps to NM_145246.4 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:95447190 G>A maps to NM_145246.4 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A186-01A-11D-A12J-09 chr10:95445036 C>T maps to NM_145246.4 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr4:79432435 C>T maps to NM_025074.6 D3263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:79308782 T>C maps to NM_025074.6 D1301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:79351536 G>A maps to NM_025074.6 K1645K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:79387501 C>T maps to NM_025074.6 D2390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:79410098 C>T maps to NM_025074.6 I2941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:79429970 C>A maps to NM_025074.6 V3197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:79158707 C>T maps to NM_025074.6 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:79166389 G>T maps to NM_025074.6 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr4:79462276 A>C maps to NM_025074.6 *4013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:79254555 T>C maps to NM_025074.6 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:79399012 C>A maps to NM_025074.6 V2632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr4:79402967 G>A maps to NM_025074.6 K2818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:14774071 G>A maps to ENST00000427623 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:14859179 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr9:14808126 C>A maps to ENST00000380880 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:14774112 C>A maps to ENST00000427623 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:14816795 C>A maps to ENST00000380880 E877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:14746977 G>A maps to ENST00000380880 I2030I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:14841515 C>A maps to ENST00000380880 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:14750209 G>T maps to ENST00000380880 V1827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:14823160 A>C maps to ENST00000380880 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:14859222 C>A maps to ENST00000380880 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:14863898 G>T maps to ENST00000380880 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr9:14746950 G>A maps to ENST00000380880 I2039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:39265290 C>T maps to NM_207361.4 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:39338571 G>T maps to NM_207361.4 E1799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:39448661 C>A maps to NM_207361.4 R2740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:39438676 C>T maps to NM_207361.4 F2639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr13:39262221 C>T maps to NM_207361.4 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:39438676 C>T maps to NM_207361.4 F2639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:39424214 C>T maps to NM_207361.4 S2140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr13:39263686 C>T maps to NM_207361.4 R736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:39424214 C>T maps to NM_207361.4 S2140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:39447012 C>T maps to NM_207361.4 Y2706Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:39448658 G>A maps to NM_207361.4 G2739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr13:39263337 T>C maps to NM_207361.4 H619H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:135438925 G>A maps to ENST00000443774 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:135438965 C>T maps to ENST00000443774 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:116381387 A>G maps to NM_002031.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:116264231 A>G maps to NM_002031.2 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:116263729 T>C maps to NM_002031.2 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:116325060 T>A maps to NM_002031.2 K149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:168457950 G>A maps to NM_024919.3 H492H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:168467457 G>A maps to NM_024919.3 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:85913714 C>A maps to NM_174938.4 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:85863360 C>T maps to NM_174938.4 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:85863194 C>A maps to NM_174938.4 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:85914033 G>A maps to NM_174938.4 R332*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BK-A0C9-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr10:13852875 A>G maps to NM_018027.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr10:13701372 C>T maps to NM_018027.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:13698768 C>T maps to NM_018027.3 K940K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:13693963 C>A maps to NM_018027.3 E1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:13708202 C>T maps to NM_018027.3 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:13702479 C>T maps to NM_018027.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:13699326 C>T maps to NM_018027.3 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:13852839 G>T maps to NM_018027.3 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:13716918 G>A maps to NM_018027.3 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:69299241 G>A maps to NM_015123.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:69244247 G>A maps to NM_015123.1 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:69247862 A>C maps to NM_015123.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:44175961 G>A maps to NM_032892.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:131219673 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:131211949 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:131211911 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:131212205 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:131212886 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:131231310 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:131234649 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:131212278 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:131218569 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:131212741 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:131212264 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:131212719 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:131212226 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:131212390 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:131231358 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:131234719 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:131261830 C>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:131234651 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:65172522 C>T maps to NM_031904.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:37733797 A>G maps to NM_014907.2 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:37745305 G>T maps to NM_014907.2 E1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:37733587 C>T maps to NM_014907.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:37740711 G>A maps to NM_014907.2 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:37744560 C>T maps to NM_014907.2 T844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr9:37740549 C>T maps to NM_014907.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:37745914 C>T maps to NM_014907.2 L1296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:37746072 G>A maps to NM_014907.2 Q1348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:37745191 G>T maps to NM_014907.2 G1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:37744837 C>T maps to NM_014907.2 R937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:37732428 G>A maps to NM_014907.2 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr9:37746495 C>T maps to NM_014907.2 A1489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:37729768 C>T maps to NM_014907.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:37745224 G>T maps to NM_014907.2 E1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:49381019 G>A maps to NM_001018071.3 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:49446048 C>T maps to NM_001018071.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:49371689 C>A maps to NM_001018071.3 E1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:49431307 C>A maps to NM_001018071.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:49430417 C>A maps to NM_001018071.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:49386160 C>A maps to NM_001018071.3 E942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:49365379 C>T maps to NM_001018071.3 S1305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:49371458 C>A maps to NM_001018071.3 E1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:49450284 C>T maps to NM_001018071.3 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:49457096 T>C maps to NM_001018071.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:49365379 C>T maps to NM_001018071.3 S1305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr10:49440296 G>A maps to NM_001018071.3 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:12734979 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:12627847 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:12720066 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:12708401 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:12728608 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:12734551 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:12736822 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:12734465 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:12734678 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12722575 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12736746 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr23:12627867 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:12692996 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:12736394 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:12734758 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:12735765 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:12734644 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:12736416 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:12734770 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr23:12632964 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:12516882 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:12692995 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:12734917 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:12692996 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:12722495 G>A did not map to a codon.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr23:12736730 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:12734689 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:12722532 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:12725709 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:100174537 G>A maps to NM_001013660.2 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:41738467 G>A maps to NM_006653.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr6:41738725 C>A maps to NM_006653.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:41738368 G>A maps to NM_006653.3 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:41738446 G>A maps to NM_006653.3 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr13:32821626 C>T maps to NM_023037.2 F2332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:32828497 C>T maps to NM_023037.2 F2461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:32768296 C>T maps to NM_023037.2 C1203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:32849121 C>T maps to NM_023037.2 A2760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:32761702 C>A maps to NM_023037.2 C1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr13:32783152 C>T maps to NM_023037.2 D1394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:32758751 G>T maps to NM_023037.2 E1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:32868674 C>T maps to NM_023037.2 L2917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:32709302 C>T maps to NM_023037.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:32759148 G>T maps to NM_023037.2 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr13:32653100 C>T maps to NM_023037.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr13:32783014 A>G maps to NM_023037.2 T1348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:32808877 G>T maps to NM_023037.2 E1899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:32783023 C>T maps to NM_023037.2 N1351N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:48548099 C>A maps to NM_015030.1 E1755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:48583535 C>T maps to NM_015030.1 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:48542829 A>G maps to NM_015030.1 S1945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:48559646 G>A maps to NM_015030.1 I1316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:48569346 T>C maps to NM_015030.1 E1029E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr4:48545844 C>T maps to NM_015030.1 G1857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr4:48514650 C>T maps to NM_015030.1 P2664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:48548277 G>A maps to NM_015030.1 N1695N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:48581083 C>A maps to NM_015030.1 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:48517067 T>C maps to NM_015030.1 E2638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:48542816 G>A maps to NM_015030.1 R1950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:48567553 C>T maps to NM_015030.1 A1108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr4:48514623 G>A maps to NM_015030.1 A2673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:44973988 G>T maps to NM_032135.3 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:44974441 C>T maps to NM_032135.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:44974785 C>A maps to NM_032135.3 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:44975793 G>A maps to NM_032135.3 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:44973759 C>A maps to NM_032135.3 E811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:44973915 C>A maps to NM_032135.3 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr17:79502117 C>T maps to NM_001077182.2 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:127235680 C>A maps to NM_020369.2 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:127235548 C>A maps to NM_020369.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:127235768 C>T maps to NM_020369.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:4306196 G>A maps to NM_024333.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:83455668 G>A maps to NM_001007122.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:83455640 C>A maps to NM_001007122.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr2:49190276 G>A maps to NM_000145.3 I561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:49247297 C>A maps to NM_000145.3 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:49189990 C>A maps to NM_000145.3 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:49295406 G>A maps to NM_000145.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:49190102 G>T maps to NM_000145.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:49190930 G>A maps to NM_000145.3 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:49190480 G>A maps to NM_000145.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:49190357 G>T maps to NM_000145.3 L534L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BS-A0UF-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:39893088 C>A maps to NM_152597.4 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:40057851 C>A maps to NM_152597.4 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:40057851 C>A maps to NM_152597.4 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:186669720 G>T maps to NM_173651.2 E5319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:186671429 C>A maps to NM_173651.2 I5888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:186671859 G>T maps to NM_173651.2 E6032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:186671118 G>T maps to NM_173651.2 E5785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:186697913 T>C maps to NM_173651.2 I6984I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:186670376 T>C maps to NM_173651.2 D5537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:186673523 T>C maps to NM_173651.2 F6586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:186672914 G>A maps to NM_173651.2 S6383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:186672402 G>T maps to NM_173651.2 E6213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:52779409 C>T maps to NM_013409.1 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:52779451 C>T maps to NM_013409.1 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:52778848 C>A maps to NM_013409.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:120123779 T>C maps to NM_007085.4 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:120115843 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:120123731 C>A maps to NM_007085.4 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:120129829 C>T maps to NM_007085.4 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:120130757 G>A maps to NM_007085.4 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:681701 C>T maps to NM_005860.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:681546 G>A maps to NM_005860.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:132569151 G>A maps to NM_015082.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:132560875 G>A maps to NM_015082.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:132535149 G>A maps to NM_015082.1 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:132560971 A>G maps to NM_015082.1 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:132556643 C>T maps to ENST00000360575 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:162307402 G>A maps to NM_020116.3 D680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:162402191 G>A maps to NM_020116.3 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr4:162841739 G>A maps to NM_020116.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:162459387 G>A maps to NM_020116.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:47570399 G>A maps to ENST00000397748 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:47557227 C>T maps to ENST00000397748 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:31089562 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:31089580 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:31089526 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:31089940 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr23:31089932 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:31089600 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:31089746 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:31089823 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:31089896 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr23:31089691 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:31089527 T>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:121187903 C>T maps to NM_177478.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:121188191 C>T maps to NM_177478.1 H178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr5:121187927 G>A maps to NM_177478.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:54145784 C>T maps to NM_001080432.2 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48339713 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48341095 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48341092 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:48337490 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48337471 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48340893 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:48340101 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:61899115 C>T maps to NM_017647.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:61898269 G>A maps to NM_017647.3 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:61898985 G>A maps to NM_017647.3 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:71318704 C>T maps to NM_018348.5 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:71318164 T>C maps to NM_018348.5 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:71318238 C>A maps to NM_018348.5 G529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:37418079 T>C maps to NM_015050.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:37429401 G>A maps to NM_015050.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:37440241 G>A maps to NM_015050.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:37429828 C>T maps to NM_015050.2 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:37440241 G>A maps to NM_015050.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:78425869 T>C maps to ENST00000436586 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:78432409 G>A maps to ENST00000436586 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:78426084 T>C maps to ENST00000436586 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:78422371 C>T maps to ENST00000436586 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:133491891 C>A maps to NM_003934.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr9:133491781 C>T maps to NM_003934.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:24172285 G>A maps to NM_000147.4 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:24180866 C>A maps to NM_000147.4 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:143816960 C>T maps to NM_032020.4 Q429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:143818582 C>T maps to NM_032020.4 W402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:70501787 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:70500903 G>A maps to ENST00000428974 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:44401344 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:44383467 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:44386559 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:44386487 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:154282909 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:154255273 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:154261709 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr15:91420240 T>A maps to NM_002569.2 L163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:91419525 G>A maps to NM_002569.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:91425098 C>T maps to NM_002569.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:31195691 T>A maps to NM_004960.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:31201373 C>A maps to NM_004960.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:49253821 G>A maps to NM_000148.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:49253821 G>A maps to NM_000148.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:33310932 A>G maps to ENST00000380081 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr8:33318925 G>A maps to ENST00000380081 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:33310998 C>T maps to ENST00000380081 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr19:49206443 C>T maps to NM_001097638.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:49206500 G>A maps to NM_001097638.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:5867544 G>A maps to NM_002034.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:5831616 C>T maps to NM_001040701.1 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:5831768 G>A maps to NM_001040701.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr19:5831792 G>A maps to NM_001040701.1 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:66028358 T>C maps to NM_178155.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:66083022 G>A maps to NM_178155.1 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:96652044 C>T maps to NM_006581.3 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:6503042 T>C maps to NM_012192.3 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:71687530 A>G maps to NM_000144.4 G162G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A11Y-01A-21D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:180675716 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:180671623 C>T maps to NM_005087.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:7497289 T>C maps to NM_004860.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:7496751 G>A maps to NM_004860.3 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:35655080 G>A maps to NM_001164605.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr19:35655080 G>A maps to NM_001164605.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:35646452 G>T did not map to a codon.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr19:35651660 G>T maps to NM_001164605.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:117713432 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:35639725 C>T maps to ENST00000439441 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:39203032 C>T maps to ENST00000263405 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:39202695 C>A maps to ENST00000263405 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:46008044 G>T maps to NM_024513.2 A927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:46005880 C>T maps to NM_024513.2 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:46007963 C>T maps to NM_024513.2 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:46014691 G>A maps to NM_024513.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:46009414 G>A maps to NM_024513.2 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:46003868 G>A maps to NM_024513.2 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:45972589 G>A maps to NM_024513.2 A1408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:46008781 G>A maps to NM_024513.2 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:112041007 C>A maps to NM_153047.1 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:112021363 C>A maps to NM_002037.3 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr6:112015623 G>A maps to NM_153047.1 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:90895821 C>T maps to NM_003505.1 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:90894671 G>A maps to NM_003505.1 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr12:130648443 C>T maps to NM_007197.3 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:130649127 G>A maps to NM_007197.3 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:130648134 C>T maps to NM_007197.3 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:42635697 G>A maps to NM_001466.3 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:42635949 C>T maps to NM_001466.3 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:42636006 G>A maps to NM_001466.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:42636579 G>A maps to NM_001466.3 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:42635703 G>C maps to NM_001466.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:42635325 C>T maps to NM_001466.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr8:28360562 G>A maps to NM_017412.3 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:28385039 G>T maps to NM_017412.3 G255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:86662420 G>T maps to NM_012193.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:86662288 C>T maps to NM_012193.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:86662932 C>A maps to NM_012193.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:86663407 G>A maps to NM_012193.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:208632173 G>A maps to NM_003468.3 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:104342107 C>T maps to NM_003506.3 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:202900161 C>T maps to NM_003507.1 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:202900407 C>T maps to NM_003507.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:202900491 C>T maps to NM_003507.1 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:202900143 C>T maps to NM_003507.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:202900641 C>T maps to NM_003507.1 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:202899384 C>T maps to NM_003507.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:202900782 C>T maps to NM_003507.1 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:202900986 C>T maps to NM_003507.1 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:202900491 C>T maps to NM_003507.1 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr10:35929592 G>A maps to NM_031866.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:72849725 C>T maps to NM_003508.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:72849026 C>T maps to NM_003508.2 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3533341 C>A maps to NM_001136198.1 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:3525879 G>A maps to NM_001136198.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr14:31055966 C>T maps to NM_017769.3 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:31081549 C>T maps to NM_017769.3 Y546Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:31061584 T>C maps to NM_017769.3 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:151169965 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr5:151183639 G>A maps to NM_198395.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr5:151175127 A>T maps to NM_198395.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr5:151175079 A>G maps to NM_198395.1 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:76580342 T>C maps to NM_203505.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr4:76572335 C>A maps to NM_203505.2 G312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:76570873 G>A maps to NM_203505.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:169764225 C>T maps to NM_021176.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr17:42152400 C>T maps to NM_138387.3 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153760975 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153762622 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153762347 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153762268 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:153762365 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153762302 C>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153774292 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:153760966 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:78081445 C>T maps to NM_001079804.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:78086493 C>T maps to NM_001079804.1 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:78087027 G>A maps to NM_001079804.1 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr4:144354722 C>A maps to NM_207123.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr4:144359328 C>T maps to NM_207123.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:77937595 T>C maps to NM_080491.2 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:77991677 G>T maps to NM_080491.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:77931373 G>A maps to NM_080491.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:77991781 G>A maps to NM_080491.2 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:77991695 G>A maps to NM_080491.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:77937754 G>T maps to NM_080491.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153924197 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153940974 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153941670 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153944310 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153928320 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:153924211 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:153925441 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153924240 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153927747 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153928295 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:153924246 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153927589 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153924197 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153925441 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153941541 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:153940544 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:153924242 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:153908407 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:153906508 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153944424 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:17443697 C>T maps to NM_001037814.1 Q550Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr22:17450935 C>T maps to NM_001037814.1 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr22:17443650 G>C maps to NM_001037814.1 S566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:75601984 G>A maps to NM_007285.6 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr6:29571042 G>A maps to ENST00000485026 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr6:29599212 G>A maps to NM_001470.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:29580346 C>T maps to NM_001470.2 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:29599356 C>T maps to NM_001470.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:101068621 G>A maps to NM_005458.7 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:101053031 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:101073403 G>A maps to NM_005458.7 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr9:101258724 G>A maps to NM_005458.7 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:101125025 G>A maps to NM_005458.7 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:101125026 C>T maps to NM_005458.7 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:27113921 G>T maps to NM_002040.3 E5*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr1:151065780 C>T maps to NM_144618.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:161324355 C>T maps to NM_001127648.1 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:161322684 G>A maps to NM_001127648.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:161322681 T>G maps to NM_001127648.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:161324317 C>T maps to NM_001127648.1 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:161317965 C>T maps to NM_001127648.1 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:161302641 G>T maps to NM_001127648.1 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:161309580 G>T maps to NM_001127648.1 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:161309604 G>T maps to NM_001127648.1 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:46305503 C>A maps to ENST00000507069 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:46252501 C>T maps to ENST00000507069 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:46305503 C>A maps to ENST00000507069 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:151358339 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:151453182 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:151514096 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:151358314 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:151514096 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:151337008 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr23:151514085 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:151336900 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr23:151358240 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:151336807 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:151514104 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:151376483 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:151336933 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:151533002 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:151393279 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:151336978 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:151366178 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:151376560 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:151376471 C>T did not map to a codon.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr23:151514096 C>T did not map to a codon.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr23:151532942 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr4:46979584 G>A maps to NM_000809.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr4:46930658 A>C maps to NM_000809.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:27126073 C>T maps to NM_000810.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:27114406 A>C maps to NM_000810.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:27182353 C>T maps to NM_000810.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:27193355 A>C maps to NM_000810.3 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:27128334 C>T maps to NM_000810.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:27128355 C>T maps to NM_000810.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:161113335 C>T maps to NM_000811.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:161119082 C>T maps to NM_000811.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:161116259 G>A maps to NM_000811.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:161117342 A>T maps to NM_000811.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:161116061 C>A maps to NM_000811.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:161119082 C>T maps to NM_000811.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:47034017 C>T maps to NM_000812.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:47163448 C>T maps to NM_000812.3 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr4:47163484 C>T maps to NM_000812.3 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr4:47405579 G>A maps to NM_000812.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr4:47405720 C>T maps to NM_000812.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr4:47163372 C>G maps to NM_000812.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:47034017 C>T maps to NM_000812.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:160886694 G>A maps to NM_021911.2 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:160973382 C>T maps to NM_021911.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr5:160753380 C>T maps to NM_021911.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:160721114 G>A maps to NM_021911.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:160761810 G>A maps to NM_021911.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A052-01A-11W-A027-09 chr15:26866465 C>A maps to NM_021912.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:1960628 C>A maps to NM_000815.4 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:1957150 C>T maps to NM_000815.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:1960556 G>A maps to NM_000815.4 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:151138726 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:151123214 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr23:151123938 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:151123978 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:151143071 A>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:151138739 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:151123556 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:151138846 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:151123938 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:151124008 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:151138729 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:46099216 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr4:46066479 G>T maps to NM_173536.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:46060508 C>T maps to NM_173536.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:46053438 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:46099314 G>T maps to NM_173536.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:161524708 C>A maps to NM_198903.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:161531030 C>T maps to NM_198903.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:161520893 C>A maps to NM_198903.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr5:161528291 T>C maps to NM_198903.2 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:161580181 C>T maps to NM_198903.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:161530982 C>T maps to NM_198903.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:27772696 C>T maps to NM_033223.4 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:27772696 C>T maps to NM_033223.4 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr5:170222321 G>A maps to NM_014211.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:151815614 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:151817794 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:151821091 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:151821371 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:151821262 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:151821638 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:151821201 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:151821313 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:151815610 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:151820161 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:151806757 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:151814011 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:151821526 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:151821512 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:151821186 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:151806717 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:151821551 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:151806757 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:151819992 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:89890124 C>A maps to NM_002042.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:89895098 C>T maps to NM_002042.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:89890094 G>A maps to NM_002042.3 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:89974214 G>A maps to NM_002043.2 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:89977511 G>A maps to NM_002043.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:97705640 T>C maps to NM_001105580.1 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:97744432 G>A maps to NM_001105580.1 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:97744432 G>A maps to NM_001105580.1 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:171710462 C>T maps to NM_000817.2 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:171713631 C>T maps to NM_000817.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:26513545 G>A maps to NM_001134366.1 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:26559669 C>A maps to NM_001134366.1 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr10:26507976 C>T maps to NM_001134366.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:26512879 G>A maps to NM_001134366.1 W195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:26559585 C>T maps to NM_001134366.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr10:26562594 C>T maps to NM_001134366.1 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:92220617 G>A maps to NM_006705.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:30885898 G>T maps to NM_207359.2 C237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:30896234 G>T maps to NM_207359.2 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr23:49368384 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49208290 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:49208299 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:890300 C>A maps to NM_005255.2 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr4:858937 C>T maps to NM_005255.2 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:870895 G>A maps to NM_005255.2 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:905554 C>T maps to NM_005255.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:68458442 C>T maps to NM_015973.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr22:30951446 G>A maps to NM_004861.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:65810562 G>A maps to NM_033036.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:88450794 G>A maps to NM_000153.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr14:88434713 A>G maps to NM_000153.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:24124346 G>A maps to NM_001008216.1 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:24123562 G>T maps to NM_001008216.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:73758962 G>A maps to ENST00000437911 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:73754365 C>T maps to ENST00000437911 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:49611852 G>A maps to NM_002044.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:49575812 A>G maps to NM_002044.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:38908498 C>T maps to NM_138801.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr2:38908465 G>A maps to NM_138801.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:38903138 G>A maps to NM_138801.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:88898498 G>A maps to NM_000512.4 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:88902224 C>T maps to NM_000512.4 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:33234694 C>T maps to NM_020474.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:33263416 C>T maps to NM_020474.3 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:33289622 C>T maps to NM_020474.3 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:33271037 G>A maps to NM_020474.3 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:153765929 C>T maps to NM_198321.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:153765899 C>T maps to NM_198321.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:153765887 C>T maps to NM_198321.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:151802421 C>T maps to NM_022087.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:151814457 A>C maps to NM_022087.2 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:151802348 A>G maps to NM_022087.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:151802421 C>T maps to NM_022087.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:101594052 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:101599405 C>T maps to NM_024642.3 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:101597632 C>T maps to NM_024642.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:155099386 G>T maps to NM_052917.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:155115620 G>A maps to NM_052917.2 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:154801060 G>A maps to NM_052917.2 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:155295127 G>T maps to NM_052917.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:155102354 G>A maps to NM_052917.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:155098575 A>C maps to NM_052917.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:155115636 G>T maps to NM_052917.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:155252588 G>T maps to NM_052917.2 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:155102454 G>T maps to NM_052917.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:155295238 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:155158058 T>G maps to NM_052917.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr2:31133838 G>A maps to NM_024572.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:31178826 C>T maps to NM_024572.2 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:31133910 A>C maps to NM_024572.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:31168706 G>A maps to NM_024572.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:31178799 G>A maps to NM_024572.2 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:230410204 G>A maps to NM_004481.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:230372098 C>T maps to NM_004481.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:230391030 C>T maps to NM_004481.3 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:230338998 C>T maps to NM_004481.3 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:230415062 C>T maps to NM_004481.3 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:230386268 C>T maps to NM_004481.3 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:166611441 G>A maps to NM_004482.3 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:166618395 T>C maps to ENST00000409882 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:158162325 C>T maps to NM_014568.1 C835C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:158115028 C>T maps to NM_014568.1 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:158116000 C>T maps to NM_014568.1 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:158157468 C>A maps to NM_014568.1 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:158153004 T>C maps to NM_014568.1 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51752036 G>A maps to NM_007210.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51758029 G>A maps to NM_007210.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:51773115 G>T maps to NM_007210.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:174219448 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:174235222 C>T maps to NM_017423.2 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:4853737 A>G maps to NM_017417.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:4854726 C>A maps to NM_017417.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:4830001 C>T maps to NM_017417.1 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:4853684 G>T maps to NM_017417.1 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:4854615 G>A maps to NM_017417.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:4848463 A>G maps to NM_017417.1 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:132685782 G>A maps to NM_001122636.1 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr14:69818848 C>A maps to NM_020692.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:69805437 C>A maps to NM_020692.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:69814802 T>A maps to ENST00000448469 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:69792089 G>A maps to NM_020692.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr14:69806318 C>T maps to NM_020692.2 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:16216834 G>A maps to NM_054110.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:16216906 C>T maps to NM_054110.4 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:16254225 G>T maps to NM_054110.4 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:16216750 G>A maps to NM_054110.4 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:16216807 G>A maps to NM_054110.4 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:11362476 G>T maps to NM_198516.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:11362395 G>A maps to NM_198516.2 H416H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:11454264 C>T maps to NM_198516.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:11292834 T>A maps to NM_198516.2 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:11362545 C>T maps to NM_198516.2 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:151664345 A>C maps to NM_145292.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:151711727 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:151680184 G>A maps to NM_145292.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:151699940 G>A maps to NM_145292.3 K267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:151668067 G>T maps to NM_145292.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:151680203 G>T maps to NM_145292.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:173804048 C>A maps to NM_001034845.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:173150915 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:173873282 C>A maps to NM_001034845.2 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:173734788 C>T maps to NM_001034845.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr9:34650406 C>T maps to NM_000155.2 H367H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:34647490 G>T maps to NM_000155.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr19:1399535 G>A maps to NM_138924.1 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr19:1399884 C>T maps to NM_138924.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:81398610 C>A maps to NM_022041.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:81397412 C>T maps to NM_022041.3 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:81390523 G>A maps to NM_022041.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:81391483 C>T maps to NM_022041.3 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:81398613 C>T maps to NM_022041.3 Y424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:81411176 C>T maps to NM_022041.3 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62398655 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:62398177 C>T maps to NM_198335.2 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:42621631 C>A maps to NM_198141.2 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:42621517 C>T maps to NM_198141.2 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:42632939 G>T maps to NM_198141.2 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:42635349 G>T maps to NM_198141.2 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:42603003 T>C maps to NM_198141.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:6647105 C>A maps to NM_002046.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:6647360 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:36029507 C>T maps to NM_014364.4 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:36034282 C>T maps to NM_014364.4 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:36027727 G>A maps to NM_014364.4 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:57790710 G>A maps to NM_152687.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:57790675 G>T maps to NM_152687.2 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:128083794 C>T maps to NM_015635.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:128099687 C>T maps to NM_015635.2 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr9:128113133 G>T maps to NM_015635.2 S1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:128064820 G>T maps to NM_015635.2 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:128112573 A>G maps to NM_015635.2 R1127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:128094283 G>A maps to NM_015635.2 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:128116969 C>T maps to NM_015635.2 R1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:128064547 G>T maps to NM_015635.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:128104529 G>T maps to NM_015635.2 E1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr9:128094804 T>C maps to NM_015635.2 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:110740320 G>A maps to ENST00000503671 *178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:110739246 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr9:130151330 G>A maps to NM_032293.4 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:130155397 C>T maps to NM_032293.4 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr9:130075771 C>T maps to NM_032293.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr9:130145789 C>T maps to NM_032293.4 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr9:130147339 C>T maps to NM_032293.4 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr7:30651838 C>T maps to NM_002047.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:30672004 C>T maps to NM_002047.2 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:30642706 A>G maps to NM_002047.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:30639570 G>A maps to NM_002047.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:34876556 G>A maps to NM_001136006.1 V969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:34889727 G>A maps to NM_001136006.1 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr21:34889431 C>T maps to NM_001136006.1 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:22770803 T>C maps to NM_005256.3 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr22:29708150 A>G maps to NM_152236.1 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr22:29704499 C>T maps to NM_152236.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:34072355 T>C maps to NM_139285.2 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:34072826 C>T maps to NM_139285.2 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr12:101017657 C>T maps to NM_174942.1 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:114531618 G>A maps to ENST00000357389 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr13:114530023 C>T maps to ENST00000357389 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:114531618 G>A maps to ENST00000357389 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr13:114523857 G>A maps to ENST00000357389 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:114523848 G>A maps to ENST00000357389 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr17:9820562 A>G maps to NM_201433.1 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:9843492 C>T maps to NM_201433.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:9862554 C>T maps to NM_201433.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:9843492 C>T maps to NM_201433.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:9885166 C>T maps to NM_201433.1 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:9837545 C>T maps to NM_201433.1 A274A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:90106745 C>A maps to NM_001481.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:39871856 C>T maps to NM_000805.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:48650525 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48650257 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr23:48651669 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48652241 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48650388 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:48649710 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:48650869 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48651631 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48649614 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:48650809 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48649665 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:128200709 G>A maps to NM_032638.4 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr10:8115823 G>A maps to NM_001002295.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:8100286 G>A maps to NM_001002295.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr20:61048635 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:19762800 C>A maps to NM_005257.3 C504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:19616153 C>T maps to ENST00000404158 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:19576354 G>A maps to ENST00000404158 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:19576390 C>T maps to ENST00000404158 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:120894896 C>T maps to NM_176818.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:45668828 G>T maps to ENST00000432007 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:99821543 G>A maps to NM_178831.6 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:30682295 G>A maps to NM_001037666.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:155204996 G>A maps to NM_001005742.2 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:155207268 G>A maps to NM_001005742.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:35748416 T>C maps to NM_020944.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:35738216 C>T maps to ENST00000378088 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:22749582 G>A maps to NM_020973.3 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:22749493 G>T maps to NM_020973.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:22749268 C>T maps to NM_020973.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:22749678 A>G maps to NM_020973.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:81586220 C>T maps to ENST00000264326 W548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:81640277 T>C maps to ENST00000264326 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr3:81630360 C>T maps to ENST00000264326 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:81539563 C>T maps to ENST00000264326 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:81548281 A>G maps to ENST00000264326 N677N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:104136896 C>T maps to NM_004193.2 D1497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:104136792 C>T maps to NM_004193.2 R1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr10:104136743 G>A maps to NM_004193.2 G1446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:104130494 C>T maps to NM_004193.2 R1179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:104136436 C>T maps to NM_004193.2 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr10:104139662 G>T maps to NM_004193.2 V1609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:104129478 C>T maps to NM_004193.2 F1053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:104129686 G>A maps to NM_004193.2 R1094R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:136029215 G>T maps to NM_021996.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:89522791 G>A maps to NM_002053.2 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:89522764 C>T maps to NM_002053.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr1:89521739 G>A maps to NM_002053.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:89585914 G>T maps to NM_004120.3 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:89573944 G>A maps to NM_004120.3 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:89579794 C>T maps to NM_004120.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:89585911 G>A maps to NM_004120.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:89578211 A>G maps to NM_004120.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:89486335 C>T maps to NM_018284.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:89486389 G>A maps to NM_018284.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:89486296 C>T maps to NM_018284.2 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:89651094 C>A maps to NM_052941.4 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:89659032 G>A maps to NM_052941.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:89651145 C>A maps to NM_052941.4 E572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:89657129 G>A maps to NM_052941.4 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:89652168 C>T maps to NM_052941.4 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:89657164 G>T maps to NM_052941.4 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:89662985 A>G maps to NM_052941.4 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:89727931 G>A maps to NM_052942.3 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:89732272 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:89849838 G>A maps to NM_198460.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:89846105 G>T maps to NM_198460.2 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:89848411 C>T maps to NM_198460.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:89843994 G>T maps to NM_198460.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:89613257 C>A maps to NM_207398.2 G453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:89607325 G>A maps to NM_207398.2 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr1:89630418 C>A maps to NM_207398.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:150846020 C>T maps to NM_001098834.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:237074796 T>C maps to NM_001485.2 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:163212990 T>C maps to NM_012198.3 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:38211724 G>A maps to NM_001171690.1 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:38211143 G>A maps to NM_001171690.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:127224375 T>G maps to NM_024523.5 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr7:127222556 A>G maps to NM_024523.5 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr7:127223057 C>T maps to NM_024523.5 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:127222757 C>T maps to NM_024523.5 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:127223255 G>A maps to NM_024523.5 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:109116050 C>T maps to NM_181453.3 R1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:109087090 G>T maps to NM_181453.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:109116103 C>T maps to NM_181453.3 F1626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:109124080 C>T maps to NM_181453.3 R1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:109104199 C>T maps to NM_181453.3 R1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:109099601 G>T maps to NM_181453.3 E1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:109087534 G>T maps to NM_181453.3 E584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:109100664 G>T maps to NM_181453.3 E1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:109068865 G>T maps to NM_181453.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:13007030 G>A maps to NM_000159.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:13010518 C>T maps to NM_013976.2 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr21:34110615 A>G maps to NM_016631.3 F783F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:34127648 C>A maps to NM_016631.3 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:34131545 G>T maps to NM_016631.3 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:34107337 G>A maps to NM_016631.3 R893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:34117903 C>A maps to NM_016631.3 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr15:41059513 C>T maps to NM_005258.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:44189603 G>A maps to NM_000162.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44190668 G>A maps to NM_000162.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44192978 G>A maps to NM_000162.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr7:44198689 G>T maps to NM_033507.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:27730612 C>T maps to NM_001486.3 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:53372323 G>A maps to NM_001498.3 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:53385598 A>C maps to NM_001498.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:53373403 G>A maps to NM_001498.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr1:94354608 C>T maps to NM_002061.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr1:94354617 C>T maps to NM_002061.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:10876134 G>A maps to NM_004752.3 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:10874563 C>T maps to NM_004752.3 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:10874512 C>T maps to NM_004752.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:10874512 C>T maps to NM_004752.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:120572100 G>A maps to NM_006836.1 H2437H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:120587476 G>A maps to NM_006836.1 H1493H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:120596419 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:120613555 G>A maps to NM_006836.1 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:120591043 G>A maps to NM_006836.1 I1345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:120616702 C>T maps to NM_006836.1 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:120602184 C>T maps to NM_006836.1 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:120587779 G>A maps to NM_006836.1 H1459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:120587830 G>A maps to NM_006836.1 F1442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:10586488 G>A maps to NM_145655.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:10621674 C>T maps to NM_145649.4 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:59911072 C>T maps to NM_004751.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:59911141 C>T maps to NM_004751.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:59910671 G>T maps to NM_004751.2 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:59910448 G>A maps to NM_004751.2 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:74325001 G>T maps to NM_016591.2 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:74324605 G>T maps to NM_016591.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr5:74325745 C>T maps to NM_016591.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:58004208 T>C maps to NM_001018090.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:75275245 C>T maps to NM_018972.2 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:75272400 G>T maps to NM_018972.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:42885866 G>A maps to NM_024034.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:42893228 C>T maps to ENST00000445952 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:42885839 C>T maps to NM_024034.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr20:42885845 C>T maps to NM_024034.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:118439542 G>A maps to NM_017686.3 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:118461245 A>G maps to NM_017686.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:118439576 A>G maps to NM_017686.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:19533211 C>T maps to NM_016641.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr16:19528399 G>A maps to NM_016641.3 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:48429099 C>T maps to NM_004962.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:48428835 G>A maps to NM_004962.2 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:48414021 G>A maps to NM_016204.1 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr10:48413997 G>A maps to NM_016204.1 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:48413859 G>A maps to NM_016204.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:7843190 C>T maps to NM_020634.1 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:7848273 A>C maps to NM_020634.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:7843049 T>C maps to NM_020634.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:7842982 T>A maps to NM_020634.1 K196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:7848138 C>T maps to NM_020634.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:7842974 G>A maps to NM_020634.1 F198F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-B5-A0JY-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BG-A0MQ-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D1-A103-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:34021967 G>A maps to ENST00000374375 S4S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A17A-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D1-A17Q-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:97172710 C>T maps to NM_001001557.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr8:97172578 A>G maps to NM_001001557.2 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:97156943 C>T maps to NM_001001557.2 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:132197316 G>A maps to NM_005260.3 Y443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:132197445 G>A maps to NM_005260.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr5:132197523 C>T maps to NM_005260.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:132197427 G>T maps to NM_005260.3 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153669505 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:153668810 A>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153667196 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153670981 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:5815879 G>T maps to NM_001494.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:5827951 G>A maps to NM_001494.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:5828008 T>C maps to NM_001494.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:57348303 G>T maps to NM_182569.3 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:57297999 C>T maps to NM_182569.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:57350185 C>T maps to NM_182569.3 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:69645914 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:69645623 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69649821 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69652916 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:69646792 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69646232 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69647033 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69649444 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:69644848 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:69646997 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr23:69644861 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:69649345 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:69649467 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:69645919 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:76980111 G>A maps to ENST00000376217 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:75155522 C>T maps to NM_030792.6 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr8:95272419 G>A maps to NM_181702.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:95272413 G>A maps to NM_181702.2 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:650448 C>T maps to NM_015721.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:648414 C>T maps to NM_015721.2 A956A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:648795 C>T maps to NM_015721.2 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:649239 G>A maps to NM_015721.2 N681N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr5:154316704 G>A maps to NM_015465.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:154308127 C>T maps to NM_015465.3 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:154278113 G>A maps to NM_015465.3 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:154281029 C>T maps to NM_015465.3 W961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:154271270 G>A maps to NM_015465.3 D1264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:154282159 A>C maps to NM_015465.3 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:39006474 C>T maps to ENST00000409566 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:45593626 T>C maps to NM_024707.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:14027160 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:14038641 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:14027100 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:14038254 T>G did not map to a codon.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr23:14038611 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:17953926 G>T maps to NM_001130009.1 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:17962212 C>T maps to NM_001130009.1 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:17955666 C>T maps to NM_001130009.1 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:17963128 G>T maps to NM_001130009.1 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:17946165 C>A maps to NM_001130009.1 C117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr17:42990696 C>T maps to NM_002055.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:42988009 G>A maps to NM_002055.3 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:42987857 G>A maps to ENST00000376990 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:42988019 G>T maps to NM_002055.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:2035968 C>T maps to NM_005262.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:135864539 C>T maps to NM_004188.4 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:135864470 C>T maps to NM_004188.4 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:158399903 C>T maps to ENST00000264263 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:158408049 C>T maps to ENST00000264263 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:158383127 C>T maps to ENST00000264263 N480N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:158376715 T>C maps to ENST00000264263 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:158399903 C>T maps to ENST00000264263 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:158364550 A>C maps to ENST00000264263 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:74041627 C>A maps to NM_032380.3 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:74021921 T>G maps to NM_032380.3 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:13365112 G>A maps to NM_018988.2 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:13470326 G>A maps to NM_033069.2 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:13365211 C>T maps to NM_018988.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr6:13365048 C>A maps to NM_018988.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:67719372 G>A maps to NM_030819.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:67709420 G>A maps to NM_030819.3 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:67709492 G>A maps to NM_030819.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:69569381 C>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:69590775 C>A maps to ENST00000357308 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:69556855 T>C maps to ENST00000357308 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:179745904 G>A maps to NM_005110.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:179755292 C>A maps to NM_005110.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:179743822 G>A maps to NM_005110.2 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:179743987 A>T maps to NM_005110.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:117849249 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:21551977 C>A maps to NM_001495.4 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr5:137593479 G>A maps to NM_001496.3 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:55216246 T>C maps to NM_207410.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:55266626 G>A maps to NM_207410.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:55196531 A>G maps to NM_207410.2 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr6:55216162 G>A maps to NM_207410.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:38019359 G>A maps to ENST00000381756 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr22:38017630 C>A maps to ENST00000381756 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:38014498 C>T maps to ENST00000381756 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:23507073 C>T maps to NM_015044.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:73240783 G>A maps to NM_138619.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:73237109 C>T maps to NM_138619.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:73235931 C>T maps to NM_138619.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:73235895 G>A maps to NM_138619.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:30540276 G>A maps to NM_024051.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:85777152 G>T maps to NM_000821.4 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:85788076 G>A maps to NM_000821.4 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:85779091 A>G maps to NM_000821.4 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr2:85785708 C>T maps to NM_000821.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:63930181 C>T maps to NM_003878.2 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:38877712 G>T maps to NM_152657.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:34912978 C>T maps to NM_024835.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr17:34945831 A>C maps to NM_024835.3 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:34934443 C>T maps to NM_024835.3 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:34935762 C>T maps to NM_024835.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:235505708 G>A maps to NM_001037277.1 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:235505795 T>C maps to NM_001037277.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr22:25019113 T>C maps to NM_005265.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:24620999 G>A maps to NM_001099781.1 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:24621549 G>A maps to NM_001099781.1 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:24622120 G>A maps to NM_001099781.1 H384H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:4461795 C>T maps to ENST00000414312 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:33442377 G>A maps to NM_178026.2 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr20:33447404 G>A maps to NM_178026.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:23966579 C>T maps to NM_178311.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:23966393 G>A maps to NM_178311.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:23967146 G>A maps to NM_178311.2 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:61994782 G>A maps to NM_000515.3 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:61958059 G>A maps to NM_022557.2 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:61958014 C>T maps to NM_022557.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:61957737 G>A maps to NM_002059.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:40342752 G>A maps to NM_032484.4 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:40342708 G>A maps to NM_032484.4 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:85903761 G>T maps to ENST00000436406 G84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:85904636 G>A maps to ENST00000436406 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:42719060 C>T maps to NM_000163.2 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:42719345 T>C maps to NM_000163.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:42713561 C>A maps to NM_000163.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:42695028 G>T maps to NM_000163.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:35882732 C>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:31018747 C>A maps to NM_000823.3 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:31018816 G>A maps to NM_000823.3 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr7:31013715 A>G maps to NM_000823.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:10327453 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:10331783 G>A maps to NM_016362.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:172166097 G>A maps to NM_198407.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:59610009 G>T maps to NM_005142.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr7:100281722 C>T maps to NM_022574.4 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:100279805 G>A maps to NM_022574.4 H938H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:100284395 G>A maps to NM_022574.4 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr2:233708862 G>A maps to ENST00000373566 T1021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:233625283 G>A maps to ENST00000373566 S158S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:233651951 G>T maps to ENST00000373566 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:233710594 T>C maps to ENST00000373566 D1175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:233709227 G>T maps to ENST00000373566 V1105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:233684607 G>A maps to ENST00000373566 Q836Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:233655825 G>T maps to ENST00000373566 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr2:233708928 G>A maps to ENST00000373566 Q1043Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:233660866 G>A maps to ENST00000373566 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:233712089 G>T maps to ENST00000373566 E1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:233613720 G>T maps to ENST00000373566 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:233671240 G>A maps to ENST00000373566 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:233709077 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:150417775 G>A maps to NM_130759.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:150269562 G>A maps to ENST00000430830 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr7:150269649 G>A maps to ENST00000430830 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:150325472 G>A maps to ENST00000438845 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:150324700 G>T maps to ENST00000477013 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:150324682 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:150325175 G>A maps to ENST00000438845 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:150217806 G>T maps to NM_153236.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:150171328 G>A maps to NM_175571.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:150171652 G>A maps to NM_175571.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:150164370 G>A maps to NM_175571.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:150174540 G>A maps to NM_175571.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr7:150174507 G>A maps to NM_175571.2 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:150163848 G>A maps to NM_175571.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:102432488 G>A maps to NM_017676.2 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:102440360 A>G maps to NM_017676.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:25394431 G>T maps to NM_021067.3 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:85721138 C>T maps to NM_016095.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:85712253 C>T maps to NM_016095.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr16:58437108 T>C maps to NM_001126129.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:41397255 T>G maps to NM_032336.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:41397470 C>T maps to NM_032336.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:41399359 C>T maps to NM_032336.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:41397470 C>T maps to NM_032336.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:47041682 C>T maps to NM_004123.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:14591506 G>A maps to NM_202470.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:78585101 A>C maps to NM_017655.4 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:3589486 G>A maps to NM_133261.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:46176121 C>T maps to NM_000164.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:27901773 G>A maps to NM_001085454.1 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:27908955 A>G maps to NM_001085454.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:110399166 C>T maps to NM_057169.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:110421245 T>C maps to NM_057169.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:110370836 G>A maps to NM_057169.3 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:121768643 C>A maps to NM_000165.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:121768293 C>T maps to NM_000165.3 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:90604483 G>A maps to NM_032602.1 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:90605200 T>C maps to NM_032602.1 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr6:90604243 C>A maps to NM_032602.1 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:90604303 G>A maps to NM_032602.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr6:90604915 T>C maps to NM_032602.1 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:90604378 C>A maps to NM_032602.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:20717373 G>T maps to NM_021954.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:20717412 G>A maps to NM_021954.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr13:20716980 G>A maps to NM_021954.3 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:20717019 G>A maps to NM_021954.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:20717130 G>A maps to NM_021954.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:147231019 C>A maps to NM_005266.5 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:147230815 G>T maps to NM_005266.5 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:147231304 T>C maps to NM_005266.5 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:147380741 C>T maps to NM_005267.4 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:147381155 G>A maps to NM_005267.4 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:147380444 C>T maps to NM_005267.4 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:147380903 C>T maps to NM_005267.4 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:147381050 C>T maps to NM_005267.4 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:39340689 C>A maps to NM_030772.4 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:39340656 C>A maps to NM_030772.4 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:39340267 C>A maps to NM_030772.4 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:39340267 C>T maps to NM_030772.4 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70443569 G>T did not map to a codon.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr23:70444033 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70443830 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70444120 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70443855 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:35227578 G>T maps to NM_153212.2 G242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:35227082 C>A maps to NM_153212.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:35226962 C>T maps to NM_153212.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:35223626 C>T maps to NM_005268.2 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:35223653 C>T maps to NM_005268.2 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:35223200 C>T maps to NM_005268.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:35223677 C>A maps to NM_005268.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:35223083 C>T maps to NM_005268.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:35223350 C>T maps to NM_005268.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:35223083 C>T maps to NM_005268.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:35223350 C>T maps to NM_005268.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:20796938 C>T maps to NM_001110221.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:87994099 C>T maps to NM_198568.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:42882585 G>A maps to NM_001080383.1 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:42882570 C>T maps to NM_001080383.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:42882783 G>A maps to NM_001080383.1 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:228346058 G>A maps to NM_020435.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr15:35044791 G>A maps to NM_020660.1 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr10:35897421 C>T maps to NM_153368.2 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:30726244 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:30738973 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:30714253 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:30671718 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:30686156 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:30686163 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr23:30739105 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:30683642 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:30712609 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:30714240 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:30738818 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:30712616 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:30671719 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:30712650 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:30714787 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:30719021 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:30719010 A>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr23:30709280 A>C did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:30726197 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:30739013 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:30714265 C>T did not map to a codon.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr23:30742279 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:80328184 A>G maps to NM_033214.2 C390C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:80329179 C>A maps to NM_033214.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:141884612 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:141891222 G>A maps to NM_001039547.2 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:141906609 T>C maps to NM_001039547.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:141934452 C>A maps to NM_001039547.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:86357483 A>G maps to NM_025211.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr9:86403524 C>T maps to NM_025211.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:69207070 A>G maps to NM_019617.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:69206013 A>G maps to NM_019617.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:69174361 G>A maps to NM_182536.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:69173562 G>A maps to NM_182536.2 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100662782 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100662846 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:100662698 T>C did not map to a codon.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr23:100658882 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:100653820 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100652898 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:100653430 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:100662731 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:100653404 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100652898 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100658903 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100662713 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:33055751 C>T maps to NM_000404.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:220107603 C>A maps to NM_024506.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:220102673 G>A maps to NM_024506.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:220107271 G>A maps to NM_024506.3 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:220104632 G>A maps to ENST00000440853 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:134240244 G>A maps to NM_138342.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:134241665 C>A maps to NM_138342.3 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:134217260 C>T maps to NM_138342.3 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:134244870 C>T maps to NM_138342.3 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr11:134240185 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:134181033 G>A maps to NM_001080407.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr11:134147713 C>T maps to NM_001080407.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr11:134151936 C>T maps to NM_001080407.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:134158720 G>A maps to NM_001080407.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr11:134188823 G>A maps to NM_001080407.2 K650K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:8062187 C>T maps to NM_138426.2 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr7:8124593 C>T maps to NM_138426.2 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:69560787 C>T maps to NM_015554.1 D353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:6588415 A>G maps to NM_000170.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:6533124 C>T maps to NM_000170.2 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:6553496 G>A maps to NM_000170.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:6592192 C>A maps to NM_000170.2 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:6553496 G>A maps to NM_000170.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:6554673 G>A maps to NM_000170.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:51687178 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:51693844 G>A maps to NM_181789.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:51696534 C>T maps to NM_181789.2 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr15:51669723 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:51696626 C>T maps to NM_181789.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:131285060 G>T maps to NM_001003722.1 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr9:131298670 C>T maps to NM_001003722.1 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr16:74525110 G>A maps to NM_012201.5 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:74486140 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr16:74486001 A>G maps to NM_012201.5 A1188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:74487013 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr16:74486875 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:74501662 G>A maps to NM_012201.5 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:74537530 C>T maps to NM_012201.5 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:74506452 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:74487010 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr16:74537503 T>C maps to NM_012201.5 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:57861832 G>A maps to NM_005269.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:57865379 G>T maps to NM_005269.2 G953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:57858941 G>A maps to NM_005269.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:57865426 A>G maps to NM_005269.2 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr12:57864805 T>G maps to NM_005269.2 Y761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:121729539 C>T maps to NM_005270.4 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:121708923 G>A maps to NM_005270.4 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:121555027 G>A maps to NM_005270.4 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:121554925 C>T maps to NM_005270.4 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:121732618 C>T maps to NM_005270.4 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:121708926 C>T maps to NM_005270.4 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr2:121747794 C>T maps to NM_005270.4 D1435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:121740293 C>T maps to NM_005270.4 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:42018305 G>A maps to NM_000168.5 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr7:42004665 C>T maps to NM_000168.5 P1335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr7:42088270 A>G maps to NM_000168.5 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:42007392 G>A maps to NM_000168.5 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:42007392 G>A maps to NM_000168.5 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr7:42004593 C>T maps to NM_000168.5 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:42018305 G>A maps to NM_000168.5 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:42065803 G>A maps to NM_000168.5 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr7:42006177 G>A maps to NM_000168.5 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:42012079 C>T maps to NM_000168.5 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:42018305 G>A maps to NM_000168.5 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:42004737 G>A maps to NM_000168.5 G1311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:42063090 G>A maps to NM_000168.5 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:42004785 G>A maps to NM_000168.5 F1295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr7:42004733 G>A maps to NM_000168.5 Q1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr7:42005918 G>A maps to NM_000168.5 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr7:42004377 C>T maps to NM_000168.5 P1431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:42004152 G>A maps to NM_000168.5 F1506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr8:144351571 A>G maps to NM_138465.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:75875801 C>T maps to NM_006851.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:75874698 T>G maps to NM_006851.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:75884217 C>T maps to NM_006851.2 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:75728561 A>G maps to ENST00000378695 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:75728660 C>T maps to ENST00000378695 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:75737519 G>A maps to ENST00000378695 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:75741427 C>T maps to ENST00000378695 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:75816690 C>T maps to ENST00000378692 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:53990491 G>A maps to NM_147193.2 H342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:53975573 C>T maps to NM_147193.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr1:54060494 C>T maps to NM_147193.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:4383408 C>T maps to NM_032575.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:3829448 G>A maps to NM_001042413.1 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:4125915 G>A maps to NM_001042413.1 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:4286284 C>T maps to NM_001042413.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:3879440 G>A maps to NM_001042413.1 D761D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:4117895 G>A maps to NM_001042413.1 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:3828385 G>T maps to NM_001042413.1 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:3898784 G>A maps to NM_001042413.1 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr1:92731982 A>G maps to NM_053274.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:92754609 G>A maps to NM_053274.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:92754607 T>C maps to NM_053274.2 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr1:92754481 T>C maps to NM_053274.2 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:38654684 A>G maps to NM_006708.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:673289 G>A maps to ENST00000397393 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:679018 C>T maps to ENST00000397393 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48629485 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48624306 C>T did not map to a codon.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr23:48631846 C>G did not map to a codon.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr6:39034025 C>T maps to NM_002062.3 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:39046922 C>T maps to NM_002062.3 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:39033593 C>T maps to NM_002062.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:39047366 C>A maps to NM_002062.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:9760823 C>T maps to NM_004246.1 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr17:9764495 T>A maps to NM_004246.1 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:151304088 G>A maps to NM_001146040.1 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:151235873 G>A maps to NM_001146040.1 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:151234712 G>T maps to NM_001146040.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:14592482 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:14627284 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:14599497 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:14550432 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:14748576 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:14625318 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:14548222 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:14748515 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:14748580 C>T did not map to a codon.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr23:14625252 T>G did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr4:175710000 T>C maps to NM_006529.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr23:102974095 C>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:102977096 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:102968473 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:102979100 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:102974044 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102979162 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:102983091 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:102979839 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:102979042 G>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:102977163 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:158074158 G>A maps to NM_001166060.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:158091771 G>A maps to NM_001166060.1 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:157999235 C>A maps to NM_001166060.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:158060030 C>A maps to NM_001166060.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:95158270 G>T maps to NM_002064.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:131965200 G>T maps to NM_006541.4 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:131977614 G>T maps to NM_006541.4 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:131943556 G>T maps to NM_006541.4 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:131958098 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:131969897 T>C maps to NM_006541.4 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:131977647 G>T maps to NM_006541.4 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:191760334 C>T maps to NM_014905.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:191792193 C>T maps to NM_014905.3 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:191760355 G>A maps to NM_014905.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:191785929 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:191788670 C>T maps to NM_014905.3 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:191792186 C>T maps to NM_014905.3 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr12:56873663 G>A maps to NM_013267.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:56866493 G>A maps to NM_013267.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:56865591 G>A maps to NM_013267.2 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr12:56865410 G>A maps to NM_013267.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:56874125 G>T maps to NM_013267.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr12:56881844 G>A maps to NM_013267.2 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:129360608 T>G did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr12:129373188 C>T maps to ENST00000442111 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:17691627 C>T maps to NM_024656.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:17692189 T>C maps to NM_024656.2 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:183908059 C>T maps to NM_015101.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:183914601 G>A maps to NM_015101.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:183938570 G>A maps to NM_015101.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:183933068 G>A maps to NM_015101.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:183938570 G>A maps to NM_015101.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr9:138516116 C>T maps to NM_182974.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:52729266 C>T maps to NM_018446.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:104408854 G>A maps to NM_031302.3 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:104396980 G>T maps to NM_031302.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:110295391 C>A maps to NM_016433.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:1263025 C>T maps to NM_001029885.1 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:48197733 C>A maps to NM_015711.3 S882S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:48202267 C>T maps to NM_015711.3 T1148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:48204762 G>A maps to NM_015711.3 S1258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:48259944 G>A maps to NM_015710.4 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:48258060 C>T maps to NM_015710.4 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:48259802 C>T maps to NM_015710.4 R439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:88817489 A>G maps to NM_005271.3 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr10:88854286 G>A maps to NM_005271.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:120181777 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:120181969 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:120182659 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:120181873 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:120181919 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr23:120183198 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:120182034 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:120182120 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:120182819 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr23:120181718 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr23:120182340 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:120182229 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:120182502 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:120182659 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:182353707 A>G maps to NM_002065.5 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:182356277 G>A maps to NM_002065.5 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:182354583 G>T maps to NM_002065.5 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:182354538 G>A maps to NM_002065.5 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:182356277 G>A maps to NM_002065.5 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:58491924 C>T maps to NM_201648.2 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:58714589 G>A maps to ENST00000317391 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:58711116 C>A maps to NM_080661.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:58722718 G>A maps to NM_080661.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:58605787 C>T maps to NM_145016.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:52326913 C>T maps to NM_145262.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:52325014 C>T maps to NM_145262.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:52324414 C>A maps to NM_145262.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:4855272 G>A maps to NM_032569.3 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr5:150646960 T>C maps to NM_000405.4 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr2:70070282 C>T maps to NM_178439.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:70106121 G>T maps to NM_178439.3 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:70070342 T>C maps to NM_178439.3 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:70064777 C>T maps to NM_178439.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:1930453 G>A maps to NM_001500.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr6:1726688 G>A maps to NM_001500.2 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:29040930 G>A maps to NM_006582.2 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:62229210 G>A maps to NM_012384.3 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:19746522 G>A maps to NM_016573.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:19745359 G>A maps to NM_016573.2 D680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:19740807 C>T maps to NM_016573.2 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:143928028 G>T maps to NM_002066.2 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:143928031 G>T maps to NM_002066.2 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:143921918 C>T maps to NM_002066.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr6:24785954 G>T maps to NM_015895.3 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:220369947 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:220371037 C>T maps to ENST00000373917 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:220370455 G>A maps to ENST00000373917 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr3:49759298 C>A maps to NM_013334.2 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:16274680 G>A maps to NM_006877.3 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr6:16247134 C>T maps to NM_006877.3 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24702773 C>T maps to ENST00000348719 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24707486 C>T maps to ENST00000348719 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:24706766 T>C maps to ENST00000348719 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr3:155639982 C>T maps to NM_003875.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:155633954 G>T maps to NM_003875.2 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr3:155611477 C>T maps to NM_003875.2 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:155628635 C>T maps to NM_003875.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:155611435 G>T maps to NM_003875.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr19:3113329 C>T maps to NM_002067.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:2771195 G>A maps to NM_007353.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr7:2771198 G>A maps to NM_007353.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:2834684 G>A maps to NM_007353.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:63010730 G>A maps to NM_006572.4 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:63049822 G>A maps to NM_006572.4 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:63052632 G>A maps to NM_006572.4 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:63049778 T>C maps to NM_006572.4 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:63052492 C>A maps to NM_006572.4 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:63010380 T>C maps to NM_006572.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:63049661 G>A maps to NM_006572.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:3155832 C>T maps to NM_002068.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:3148724 C>T maps to NM_002068.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:3163011 C>T maps to NM_002068.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:79840335 C>T maps to NM_002069.5 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:79842034 C>T maps to NM_002069.5 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:50290563 C>T maps to NM_002070.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:110128957 C>T maps to NM_006496.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:11753677 C>T maps to NM_182978.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:11753890 C>T maps to NM_182978.2 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:11868563 C>T maps to NM_182978.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:11868594 C>T maps to NM_182978.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:11868563 C>T maps to NM_182978.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr18:11867208 G>A maps to NM_182978.2 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:56385324 C>T maps to NM_020988.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:56385324 C>T maps to NM_020988.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:56388796 C>T maps to NM_020988.2 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:56370729 G>A maps to NM_020988.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:56370654 C>T maps to NM_020988.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:80430667 G>A maps to NM_002072.3 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr9:80409501 G>A maps to NM_002072.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:80336316 G>A maps to NM_002072.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:80409420 C>T maps to NM_002072.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:57415481 C>T maps to NM_016592.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:57430344 C>T maps to NM_080425.2 D675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:57428514 C>T maps to NM_080425.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:57430062 C>T maps to NM_080425.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:57428373 C>T maps to NM_080425.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:57429318 C>T maps to NM_080425.2 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:110155461 C>A maps to NM_005272.3 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:80117877 T>C maps to NM_001102386.1 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr22:23437996 C>T maps to NM_002073.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:23465440 C>A maps to NM_002073.2 Y297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:1737958 C>T maps to NM_002074.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr22:19789663 G>A maps to NM_053004.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:19776237 G>A maps to NM_053004.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:19776243 G>A maps to NM_053004.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:100275828 C>T maps to NM_005273.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr5:180665101 G>T maps to NM_006098.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr12:6952967 G>A maps to NM_002075.2 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:6954871 G>A maps to NM_002075.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:179138685 C>T maps to NM_021629.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:179132796 G>A maps to NM_021629.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:36233979 C>A maps to NM_001128227.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr9:36227403 G>C maps to NM_001128227.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr9:36217418 G>A maps to NM_001128227.2 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:36223466 A>G maps to NM_001128227.2 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:848768 G>A maps to NM_016541.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:848772 G>A maps to NM_016541.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:235715435 C>T maps to NM_004485.3 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:93540143 C>T maps to NM_021955.3 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr7:93540199 G>A maps to NM_021955.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:47284723 C>A maps to NM_001198754.1 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr6:30514091 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:52721603 G>A maps to NM_014366.4 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:52727693 C>T maps to NM_014366.4 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr23:54574746 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:54577463 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54578158 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54584944 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54587018 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54559004 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54585083 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:54574782 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:54577481 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr23:54570741 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr23:54570742 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:54574661 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:54570688 T>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54570678 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:54585065 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:54569403 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:54574756 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr2:85924687 C>T maps to NM_006433.3 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:85925685 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr2:85922518 C>T maps to NM_006433.3 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:42931363 C>T maps to NM_018960.4 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:231403516 T>C maps to NM_014236.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:231401048 A>G maps to NM_014236.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:231411229 G>T maps to NM_014236.3 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:231406609 G>A maps to NM_014236.3 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:141391504 C>T maps to NM_005471.4 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:44712971 C>A maps to NM_138335.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:53251322 C>A maps to NM_198066.3 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:102164826 C>A maps to NM_024312.4 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:102164296 G>A maps to NM_024312.4 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:102155099 C>T maps to NM_024312.4 T980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:102155012 A>G maps to NM_024312.4 N1009N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr12:102164826 C>A maps to NM_024312.4 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:102158197 C>A maps to NM_024312.4 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:102174051 C>A maps to NM_024312.4 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:102174051 C>A maps to NM_024312.4 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr12:102158900 G>A maps to NM_024312.4 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr12:102183789 A>G maps to NM_024312.4 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:3025458 C>T maps to NM_001501.1 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:68619941 G>A maps to NM_000406.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:68606318 C>T maps to NM_000406.2 W289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:65110562 G>A maps to ENST00000418919 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:65113863 C>A maps to ENST00000418919 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:65137013 C>T maps to ENST00000418919 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:127651788 G>A maps to NM_002077.3 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:127652753 C>A maps to NM_002077.3 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:127644206 G>A maps to NM_002077.3 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:127644206 G>A maps to NM_002077.3 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr9:131019782 C>A maps to NM_004486.4 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:133372629 G>A maps to NM_005895.3 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:133393231 G>A maps to NM_005895.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr12:133351714 G>A maps to ENST00000456883 P1385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:133378543 G>A maps to NM_005895.3 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:133398642 G>T maps to NM_005895.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:133350752 G>A maps to NM_005895.3 Q1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:133354392 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:133363361 G>A maps to NM_005895.3 F941F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:37363263 G>T maps to NM_001172713.1 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:37365197 C>A maps to NM_001172713.1 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:37365968 G>A maps to NM_001172713.1 Q886Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:37363232 A>G maps to NM_001172713.1 Q541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:37357086 A>T maps to NM_001172713.1 K493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:37357055 T>C maps to NM_001172713.1 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:37363257 G>T maps to NM_001172713.1 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:37340493 G>T maps to NM_001172713.1 E351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:93303794 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:93263972 C>A maps to NM_005113.2 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:93290965 G>T maps to NM_005113.2 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:93273265 G>T maps to NM_005113.2 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr14:93299561 G>A maps to NM_005113.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:72953837 C>T maps to NM_018652.4 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:72954930 C>T maps to NM_018652.4 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr15:34676170 G>A maps to NM_181077.3 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:121409629 G>A maps to ENST00000393667 R2861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:121413026 C>A maps to ENST00000393667 E2115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:121415985 C>T maps to ENST00000393667 Q1128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:121383777 G>A maps to ENST00000393667 R3224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:121415189 C>A maps to ENST00000393667 E1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:121415007 C>T maps to ENST00000393667 E1454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:121416395 C>A maps to ENST00000393667 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121383365 A>G maps to ENST00000393667 I3257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121417440 T>C maps to ENST00000393667 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121448818 C>A maps to ENST00000393667 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:121411333 C>A maps to ENST00000393667 E2293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr3:121413317 G>A maps to ENST00000393667 L2018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:121413815 C>A maps to ENST00000393667 E1852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:121414005 C>T maps to ENST00000393667 T1788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:121417266 G>A maps to ENST00000393667 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:167742798 C>A maps to NM_014498.3 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:167750469 C>T maps to NM_014498.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:167728166 G>A maps to NM_014498.3 R661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:167762636 A>G maps to NM_014498.3 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr3:167747022 C>A maps to NM_014498.3 G501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:88661458 G>A maps to ENST00000376023 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:204172022 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:204183022 G>T maps to NM_198447.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:155726769 G>A maps to ENST00000368331 I1832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:155735351 C>T maps to ENST00000368331 P1304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:117896452 C>A maps to NM_020399.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:28846980 T>C maps to NM_004871.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:28846975 G>T maps to NM_004871.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:45012642 T>C maps to NM_001012511.1 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:45009561 T>C maps to NM_054022.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:101163589 G>A maps to NM_002079.2 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr8:37795154 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:20335144 G>A maps to NM_001007240.1 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:20329676 C>T maps to NM_001007240.1 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:20334257 G>A maps to NM_001007240.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr16:20325988 A>G maps to NM_001007240.1 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:20331753 C>A maps to NM_001007240.1 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:194118246 C>T maps to NM_004488.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:194118510 C>T maps to NM_004488.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:194117961 G>A maps to NM_004488.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:55539186 C>T maps to NM_001083899.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr19:55525677 C>T maps to NM_001083899.1 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:167023596 C>A maps to NM_005814.1 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr8:145139944 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:113932064 C>T maps to NM_020918.4 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:113933572 A>G maps to NM_020918.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr10:113928679 G>A maps to NM_020918.4 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr10:113932004 G>A maps to NM_020918.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr10:113935424 G>A maps to NM_020918.4 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:96688914 C>T maps to NM_207328.2 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:96698043 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:96687924 C>A maps to NM_207328.2 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:96690382 C>T maps to NM_207328.2 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:96697879 C>T maps to NM_207328.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr2:96688769 C>T maps to NM_207328.2 E717E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:96687987 C>T maps to NM_207328.2 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:33597725 G>A maps to NM_018025.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:33586689 C>T maps to NM_018025.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:33608885 G>A maps to NM_018025.2 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:217604611 G>A maps to NM_018040.2 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:217665070 G>A maps to NM_018040.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:217784342 C>T maps to NM_018040.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:27219196 G>A maps to NM_022078.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:156565381 G>A maps to NM_015590.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:42512486 G>A maps to NM_001002909.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:42476222 T>C maps to NM_001002909.2 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr17:42541837 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:56531794 G>T maps to NM_001127236.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:46120973 G>A maps to NM_021639.4 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:46120873 G>A maps to NM_021639.4 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:241401803 C>A maps to NM_002081.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:241404519 C>T maps to NM_002081.2 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:99773227 G>T maps to NM_152742.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:99773839 T>C maps to NM_152742.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:99773397 G>A maps to NM_152742.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:132887967 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:132670182 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:132833929 G>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:132670252 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:132826498 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:133087202 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:132833995 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr23:133119400 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:132887944 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:132888182 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:132887752 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:133119460 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:132888171 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:133119362 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:132548923 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:132458476 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:132458552 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:132437268 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:132458452 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:132458391 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:132440051 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:132440114 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:132437079 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:132458411 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:132445385 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:132458184 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:92345834 C>T maps to NM_004466.4 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:92408549 G>T maps to NM_004466.4 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:92345717 G>T maps to NM_004466.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:92345669 C>T maps to NM_004466.4 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:92346015 G>T maps to NM_004466.4 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:95050869 C>T maps to NM_005708.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:95034786 C>T maps to NM_005708.3 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:94958322 C>A maps to NM_005708.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr13:95034747 C>T maps to NM_005708.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:5528402 C>T maps to NM_019593.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:5550810 A>T maps to NM_019593.3 C377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:50498377 C>T maps to NM_005276.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr12:50501423 G>A maps to NM_005276.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:32207338 C>T maps to NM_015141.3 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:32188172 C>T maps to NM_015141.3 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:157414014 A>G maps to NM_000408.4 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:157352681 G>T maps to NM_000408.4 G77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:1131549 G>A maps to NM_001505.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:64702301 G>A maps to NM_130769.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr14:63784384 G>A maps to ENST00000314140 C59C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr14:67578598 C>T maps to NM_020806.4 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:67631929 C>A maps to NM_020806.4 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:67647617 C>T maps to NM_020806.4 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:67147901 T>C maps to NM_020806.4 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:67579743 C>T maps to NM_020806.4 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:34859607 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:34859600 C>T maps to NM_000175.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48976107 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48972133 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48978818 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:48979896 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48976070 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:48970632 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:48978769 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:48973984 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:48980023 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:48976077 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr23:48976073 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48973403 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:24448418 G>T maps to NM_001503.2 Y488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:24467452 G>A maps to NM_001503.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:24450073 G>A maps to NM_001503.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:24447102 G>A maps to NM_001503.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:176561927 G>A maps to NM_005277.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:176594953 G>A maps to NM_005277.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:176733400 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:13834962 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:13798105 G>A did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:13798042 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13801611 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:13801509 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:13791102 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:13795480 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:27861837 C>A maps to NM_007266.3 Y233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:110893650 G>A maps to NM_001164373.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:110903016 G>A maps to NM_001164373.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:23299621 C>T maps to ENST00000435486 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:23299746 C>T maps to ENST00000435486 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:23313809 A>T maps to ENST00000435486 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:23286408 C>A maps to ENST00000435486 C25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:136113458 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:136113783 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr23:136112566 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:136112679 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:136112326 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:136112615 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:136113831 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:136112389 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:136112630 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr9:132853249 A>G maps to NM_001136557.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:132838689 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:6734314 G>A maps to NM_001080452.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:46993630 G>T maps to ENST00000283297 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr6:47647940 G>A maps to NM_153839.6 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:135431195 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:135455082 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:135429712 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:135445718 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr23:135430966 C>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:135429091 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:135429815 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:135432342 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135427606 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135429712 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135432562 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135441465 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135426786 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135427223 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135429113 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135455168 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135498630 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr23:135488085 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135426611 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135430372 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135431422 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135431460 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135432040 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135455093 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:135430302 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:135431838 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:135477569 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:135482222 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:135498648 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:135441528 A>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:135488110 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135405538 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135428663 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135428993 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135429707 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135435502 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135453579 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:135405498 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:135429140 G>A did not map to a codon.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr23:135445744 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135405099 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135426561 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135427321 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135430338 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135430339 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135431695 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135432463 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135426832 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135427048 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135432561 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135485423 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:135427081 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr23:135405544 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:135455145 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:135405034 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:135430576 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:135430847 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:135429184 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135405448 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135427537 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135429712 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135426976 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135427829 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135429316 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135430909 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135445656 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135453562 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135482211 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135488103 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135496376 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135405442 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135428745 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135429782 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135431010 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135431691 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135441573 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr23:135426786 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:135432518 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:135453674 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:135426791 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:135429005 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:135429359 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:135487990 G>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:135405498 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:135405288 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:135426669 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:135429706 A>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:135445719 G>T did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:135430052 G>C did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:135455202 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:26534792 G>A maps to NM_001145168.1 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:26534561 G>T maps to NM_001145168.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:26541848 G>A maps to NM_001145168.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr2:26534621 C>T maps to NM_001145168.1 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:26537450 C>T maps to NM_001145168.1 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:57601926 C>T maps to ENST00000349457 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:57596306 G>T maps to ENST00000349457 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:57600600 C>T maps to ENST00000349457 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:47682009 C>T maps to NM_153838.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:47685074 G>A maps to NM_153838.3 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:47681971 G>T maps to NM_153838.3 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:47682675 G>A maps to NM_153838.3 P565P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:47681541 T>C maps to NM_153838.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:47682912 G>A maps to NM_153838.3 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr6:46836764 G>A maps to NM_015234.4 C492C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:46851870 C>A maps to NM_015234.4 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:46821784 C>A maps to NM_015234.4 E1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:46824602 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:46847741 G>T maps to NM_015234.4 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:46832914 T>C maps to NM_015234.4 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:46847597 C>T maps to NM_015234.4 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:46834770 A>C maps to NM_015234.4 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:46849335 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129518823 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129518747 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:129518659 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:129518862 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:129518743 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:129518802 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:27333523 C>T maps to NM_005288.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr13:27333097 G>A maps to NM_005288.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:27333907 G>A maps to NM_005288.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:27333814 G>T maps to NM_005288.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:27333331 C>T maps to NM_005288.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:134906543 C>T maps to ENST00000368577 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:37693097 G>A maps to NM_032777.9 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr8:37688318 C>A maps to NM_032777.9 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:22389825 C>T maps to NM_145290.2 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:22390011 C>T maps to NM_145290.2 A1094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:22415373 C>A maps to NM_145290.2 E625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:22444478 C>T maps to NM_145290.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:22449124 C>T maps to NM_145290.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:22463421 T>G maps to NM_145290.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:22446629 T>G maps to NM_145290.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:142630716 G>A maps to NM_198569.2 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:142704963 C>T maps to NM_198569.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:142714134 C>A maps to NM_198569.2 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:142732440 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:142738464 C>A maps to NM_198569.2 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:142691385 C>T maps to NM_198569.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:100378594 C>T maps to NM_032787.2 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:100413628 C>A maps to NM_032787.2 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:100365441 C>A maps to NM_032787.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr3:100373720 G>A maps to NM_032787.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:100378645 C>A maps to NM_032787.2 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr3:100328733 C>T maps to NM_032787.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:100352193 T>C maps to NM_032787.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:105517471 G>A maps to NM_013345.2 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:105518272 C>T maps to NM_013345.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr14:105521733 G>A maps to NM_013345.2 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:131484926 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:131561347 A>G maps to NM_198827.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:131605454 C>T maps to NM_198827.3 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:131593321 C>T maps to NM_198827.3 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:131471727 G>A maps to NM_198827.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr12:131561342 C>T maps to ENST00000446583 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr14:59930846 C>T maps to NM_022571.5 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:59930653 G>A maps to NM_022571.5 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:59930653 G>A maps to NM_022571.5 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr11:64055321 C>T maps to NM_001170726.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:53066896 A>G maps to NM_001099652.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:53101670 A>G maps to NM_001099652.1 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:20043218 G>A maps to NM_001002911.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:20043734 G>A maps to NM_001002911.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:20084872 G>A maps to NM_001002911.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:20043416 G>T maps to NM_001002911.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:37780417 G>A maps to NM_181791.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72367985 C>T maps to ENST00000440684 F1175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:9707711 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:9714122 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:9728807 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:9714185 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:9714096 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:9727406 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:9727442 A>G did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr23:9728835 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr23:9727400 A>G did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:9709437 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:1097714 C>T maps to NM_138445.2 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:1097714 C>T maps to NM_138445.2 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:1098098 C>T maps to NM_138445.2 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:131487110 C>T maps to NM_207364.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:131487758 C>A maps to NM_207364.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr3:154146489 G>A maps to NM_001038705.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:154055906 G>A maps to NM_001038705.1 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:154146477 C>T maps to NM_001038705.1 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:154147080 A>C maps to NM_001038705.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:154055915 C>A maps to NM_001038705.1 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr3:154146618 C>T maps to NM_001038705.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:98251080 C>T maps to NM_005290.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:98251332 A>G maps to NM_005290.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:98251530 T>C maps to NM_005290.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:145895076 C>T maps to NM_194251.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:67219784 G>A maps to NM_206997.1 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:67219174 G>A maps to NM_206997.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:67219397 G>A maps to NM_206997.1 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:6314701 G>T maps to NM_207370.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:175311370 G>A maps to NM_152529.5 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:175301077 G>A maps to NM_152529.5 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:175326195 A>C maps to NM_152529.5 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:175337796 A>G maps to NM_152529.5 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:175337763 C>T maps to NM_152529.5 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:175330587 C>A maps to NM_152529.5 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:175335122 C>A maps to NM_152529.5 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:175346303 A>G maps to NM_152529.5 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr2:175330525 G>T maps to NM_152529.5 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:175346366 G>T maps to NM_152529.5 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:119886273 C>A maps to NM_153002.2 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:119887174 A>G maps to NM_153002.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:119912216 A>G maps to NM_153002.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:119905555 C>T maps to NM_153002.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:119886360 G>A maps to NM_153002.2 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:119886052 G>A maps to NM_153002.2 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:25877972 C>A maps to NM_020752.2 C597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:25887113 G>A maps to NM_020752.2 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:25887863 C>T maps to NM_020752.2 N1103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:25755614 G>A maps to NM_020752.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:25465116 C>T maps to NM_020752.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:25887408 G>T maps to NM_020752.2 E952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:25701315 C>T maps to NM_020752.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:25755614 G>A maps to NM_020752.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr10:25886792 G>A maps to NM_020752.2 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:25886792 G>A maps to NM_020752.2 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr10:25465029 G>A maps to NM_020752.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr10:25886882 C>T maps to NM_020752.2 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:168066469 G>A maps to NM_153832.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:168065998 G>T maps to NM_153832.1 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:168066277 C>T maps to NM_153832.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:168056927 G>A maps to NM_153832.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:168066064 G>T maps to NM_153832.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:6933885 C>T maps to NM_019858.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:6933606 T>G maps to NM_019858.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:128409052 C>T maps to NM_005291.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:128409019 C>T maps to NM_005291.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:150916345 C>T maps to NM_013308.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:150916563 G>A maps to NM_013308.3 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:150917065 G>T maps to NM_013308.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:150916333 A>G maps to NM_013308.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53106117 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53106286 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:53106058 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:53106383 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53105992 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53106711 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53106843 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:53106196 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:53106439 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:78426627 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:78426847 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:78427402 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:78427130 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:78427265 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:78427095 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr23:78426856 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:78426661 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:78426861 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0V7-01A-21D-A122-09 chr23:78427058 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:78426847 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:78426782 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:78427249 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:78427405 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:78427450 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr15:40093542 A>G maps to NM_007223.1 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr17:36483223 G>T maps to ENST00000398597 P2077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:36484669 G>T maps to ENST00000398597 P1595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:36489905 G>A maps to ENST00000398597 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:36483198 G>A maps to ENST00000398597 L2086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:36484564 G>A maps to ENST00000398597 I1630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:36484351 C>A maps to ENST00000398597 G1701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:36482575 G>A maps to ENST00000398597 I2293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:36484912 G>A maps to ENST00000398597 S1514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr17:36486427 G>T maps to ENST00000398597 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:36483730 G>T maps to ENST00000398597 S1908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:36482863 C>T maps to ENST00000398597 Q2197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:36484014 C>A maps to ENST00000398597 E1814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:36484515 C>A maps to ENST00000398597 E1647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:36483324 C>A maps to ENST00000398597 E2044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:36499281 G>A maps to ENST00000398597 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:36483073 C>T maps to ENST00000398597 K2127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:99907376 G>T maps to NM_005292.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:57389151 C>T maps to NM_007264.3 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:57389841 G>A maps to NM_007264.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:99947409 C>T maps to NM_004951.4 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:99948102 G>A maps to NM_004951.4 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:99947370 T>C maps to NM_004951.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:12815175 G>A maps to NM_006143.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:12814350 A>C maps to NM_006143.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr8:142367699 C>T maps to NM_005293.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:142366976 G>A maps to NM_005293.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:142367015 G>A maps to NM_005293.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr9:125797429 C>A maps to NM_005294.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:125797090 C>T maps to NM_005294.1 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:125797696 C>T maps to NM_005294.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:107114562 C>T maps to NM_005295.2 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:107115402 C>T maps to NM_005295.2 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:107115209 T>C maps to NM_005295.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:125434426 C>T maps to NM_153442.3 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr10:125434426 C>T maps to NM_153442.3 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr10:125426294 G>A maps to NM_153442.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:27720967 C>T maps to NM_005281.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:27720448 C>T maps to NM_005281.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:27720940 C>T maps to NM_005281.2 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr6:167571175 C>T maps to NM_005299.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:167570983 C>A maps to NM_005299.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr6:167570470 G>A maps to NM_005299.2 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:51274700 C>T maps to NM_001506.1 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:41555742 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:41554980 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:41555158 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:41555682 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:41555099 A>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:41555356 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:41555358 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41554984 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41555340 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:41555197 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:41555792 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:41554956 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:124386665 G>A maps to NM_005302.2 N585N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:124386653 C>T maps to NM_005302.2 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:124404499 G>A maps to NM_005302.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:124387097 C>T maps to NM_005302.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:124404208 G>T maps to NM_005302.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:202096930 G>A maps to NM_004767.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:202097566 G>A maps to NM_004767.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:202097122 C>A maps to NM_004767.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:133174980 G>A maps to NM_001508.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:133175067 G>A maps to NM_001508.2 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr2:133402827 G>A maps to NM_001508.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr2:133402881 C>T maps to NM_001508.2 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr2:133402851 G>T maps to NM_001508.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:46094086 C>T maps to NM_005282.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:46095037 G>A maps to NM_005282.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:105859133 C>T maps to NM_007227.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:150349090 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:150349266 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:150349680 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:150348828 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:150348306 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:150349722 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:150349723 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:150349105 C>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:150349119 T>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr23:150348763 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr23:150349034 G>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:150348838 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:150348964 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:150349093 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:150349743 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:110086750 G>A maps to NM_031936.4 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:110086144 G>A maps to NM_031936.4 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:110086768 C>A maps to NM_031936.4 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:97246791 A>G maps to NM_030784.2 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:19014253 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19014253 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:19017286 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:19017276 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:19017286 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:19026199 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:19031900 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:19021028 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:19022949 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:19031927 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:19014170 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:19025358 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:19045392 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:19055750 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:19014234 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:19021183 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:19025359 G>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:19049154 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:19058337 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:19031840 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:19031925 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:88477670 C>T maps to NM_003608.3 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:88477670 C>T maps to NM_003608.3 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:88478072 C>T maps to NM_003608.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr14:88477298 G>C maps to NM_003608.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:91700899 G>A maps to ENST00000238699 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:91701154 G>A maps to ENST00000238699 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:91701159 G>A maps to ENST00000238699 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:54081215 A>G maps to NM_006794.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:54081632 G>T maps to NM_006794.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr2:54081344 G>A maps to NM_006794.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41586828 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:41587143 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41586763 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41586924 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:41586677 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:94113734 C>T maps to NM_016540.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:54757335 A>C maps to NM_020370.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr12:54757110 G>A maps to NM_020370.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:112724181 G>A maps to NM_018970.6 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:112724142 G>A maps to NM_018970.6 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr3:151012691 G>A maps to NM_023915.3 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:151011992 C>T maps to NM_023915.3 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:151012744 G>A maps to NM_023915.3 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr3:151012382 G>A maps to NM_023915.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:151012415 T>A maps to NM_023915.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:151012144 C>A maps to NM_023915.3 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:101004692 G>A maps to NM_022049.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:145765404 G>T maps to NM_001097612.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:145818787 G>T maps to NM_001097612.1 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:145804267 G>A maps to NM_001097612.1 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:57719644 C>T maps to NM_170776.4 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:57712215 G>T maps to NM_170776.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:57719668 C>A maps to NM_170776.4 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr16:57712104 C>T maps to NM_170776.4 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:90073860 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:89949305 T>C maps to NM_032119.3 V1305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:89979785 A>G maps to NM_032119.3 A2016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:90101156 C>T maps to NM_032119.3 H4906H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:90106220 C>T maps to NM_032119.3 S5048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:89979965 C>T maps to NM_032119.3 I2076I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:90050960 G>T maps to NM_032119.3 E3847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:90106136 A>G maps to NM_032119.3 T5020T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:90368278 C>T maps to NM_032119.3 N6056N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:89918424 C>T maps to NM_032119.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:90077348 C>T maps to NM_032119.3 N4395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:90106106 C>T maps to NM_032119.3 S5010S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:89986684 C>T maps to NM_032119.3 R2260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:90074405 C>T maps to NM_032119.3 R4277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:90055240 G>T maps to NM_032119.3 E3986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:90449036 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr5:90007114 G>A maps to NM_032119.3 G3006G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:89923131 T>C maps to NM_032119.3 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:90136796 G>T maps to NM_032119.3 E5672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:89953749 G>T maps to NM_032119.3 G1469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:90070028 G>A maps to NM_032119.3 L4104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:89979950 C>T maps to NM_032119.3 S2071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:90004706 T>C maps to NM_032119.3 T2935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:89949443 A>G maps to NM_032119.3 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:89985765 C>A maps to NM_032119.3 I2193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:90087049 C>T maps to NM_032119.3 R4802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:90074405 C>T maps to NM_032119.3 R4277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:90106338 G>T maps to NM_032119.3 E5088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr5:89923206 T>C maps to NM_032119.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:89949104 C>A maps to NM_032119.3 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:89979776 C>A maps to NM_032119.3 V2013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:101912339 C>T did not map to a codon.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr23:101911724 G>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101908966 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101909126 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101911769 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101912184 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:101911586 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:101912838 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:101913020 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:101910741 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:101909433 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:101910934 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:101912262 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr23:101910264 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:101908927 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101909730 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101910147 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101910788 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101911017 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:101910195 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:101909730 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:101910538 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr23:101910399 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr23:101912775 A>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:101909835 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101909489 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101911868 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:101912905 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:101909217 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:101909007 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:101910526 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:101909251 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:101910538 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:101910579 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101969871 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101970082 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr23:101970793 G>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101972170 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:101971062 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101970305 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:101970996 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:101970122 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:101971699 C>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:101971347 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101970694 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101970938 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101971580 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:101972110 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:101969866 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:13065039 G>A maps to NM_003979.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr12:13061996 C>T maps to NM_003979.3 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:13061705 G>T maps to NM_003979.3 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:13061779 C>T maps to NM_003979.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr16:19883867 G>T maps to NM_016235.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:19883173 C>A maps to NM_016235.1 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:19883243 G>A maps to NM_016235.1 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:19883765 C>T maps to NM_016235.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:19884032 G>A maps to NM_016235.1 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:13103173 G>A maps to NM_018654.1 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:117113961 G>T maps to NM_148963.2 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:117113327 G>A maps to NM_148963.2 R920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:117114213 C>A maps to NM_148963.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:117130775 C>A maps to NM_148963.2 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:117121959 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:176026676 G>A maps to NM_052899.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:176025770 G>A maps to NM_052899.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr5:176025139 G>A maps to NM_052899.2 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:176025293 C>T maps to NM_052899.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:176026768 G>A maps to NM_052899.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:176026160 C>T maps to NM_052899.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:46999716 C>T maps to NM_014696.3 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr10:47000211 G>A maps to NM_014696.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr10:46999755 C>T maps to NM_014696.3 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:47000085 G>A maps to NM_014696.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:90169212 G>A maps to NM_198281.2 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:90170372 C>A maps to NM_198281.2 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:90169350 G>A maps to NM_198281.2 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:80014831 C>T maps to NM_212492.1 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:80011211 C>T maps to NM_212492.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr17:7216091 G>A maps to NM_004489.4 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr17:7216550 G>A maps to NM_004489.4 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr17:7218280 G>A maps to NM_004489.4 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:7217722 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:139231922 C>T maps to NM_001145638.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr9:139250947 C>T maps to NM_001145638.1 H589H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:109441518 G>T maps to NM_013296.4 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr8:145730783 C>T maps to NM_005309.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:46956213 G>A maps to NM_133443.2 Q366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr16:46952546 C>T maps to NM_133443.2 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:65406337 G>A maps to NM_002083.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:1105757 G>A maps to NM_002085.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:28478648 G>T maps to NM_182701.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:28473505 C>A maps to NM_182701.1 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:28473494 G>T maps to NM_182701.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:28473505 C>A maps to NM_182701.1 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:53072579 C>T maps to NM_015696.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:53072456 C>T maps to NM_015696.4 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:35506794 C>T maps to NM_020895.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:35512876 C>T maps to NM_020895.3 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:35514372 G>A maps to NM_020895.3 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:123484346 C>T maps to ENST00000456860 H600H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:123396873 C>A maps to ENST00000456860 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:123448101 G>A maps to ENST00000456860 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:123483480 G>A maps to ENST00000456860 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:123455030 T>C maps to ENST00000456860 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:123489386 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:123448269 C>T maps to ENST00000456860 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:113563453 G>A maps to NM_017577.4 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:113649559 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:113563348 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:113619972 G>A maps to NM_017577.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:72457720 C>A maps to NM_001012642.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr15:72458981 G>T maps to NM_001012642.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:72455725 C>T maps to NM_001012642.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:72455996 G>A maps to NM_001012642.2 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:72462231 G>T maps to NM_001012642.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:47061591 C>T maps to NM_015124.2 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:40364128 G>A maps to NM_004810.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:40356157 G>A maps to NM_004810.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:40364188 G>A maps to NM_004810.2 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr22:40364146 G>A maps to NM_004810.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:40362131 C>A maps to NM_004810.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:52404671 C>T maps to NM_181711.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:50673051 C>A maps to NM_005311.4 G442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:50737550 C>T maps to NM_005311.4 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:50685734 C>A maps to ENST00000428711 *109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:50694567 C>T maps to NM_005311.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:50686908 G>A maps to NM_005311.4 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:50663159 T>A maps to NM_005311.4 K538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:165476262 G>T maps to NM_004490.2 C86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:165353907 C>T maps to NM_004490.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:165383645 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:11741033 C>T maps to NM_014668.3 H814H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:11716656 C>A maps to NM_014668.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:11758552 G>A maps to NM_014668.3 G1184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:11780483 C>T maps to NM_014668.3 L1918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:11780423 G>A maps to NM_014668.3 T1898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:11770211 C>T maps to NM_014668.3 R1530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr2:11738968 G>A maps to NM_014668.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:11738968 G>A maps to NM_014668.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:11761032 C>T maps to NM_014668.3 I1349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr15:33023161 C>T maps to NM_013372.6 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr15:33023223 C>A maps to NM_013372.6 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr1:240656391 G>A maps to NM_022469.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:10136457 C>T maps to NM_198182.2 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:10098937 A>G maps to NM_198182.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:10136457 C>T maps to NM_198182.2 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:10105452 C>T maps to NM_198182.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:102570908 C>T maps to NM_024915.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:102676698 G>A maps to NM_024915.3 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr8:102644593 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:24664218 C>T maps to NM_021180.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:37430574 C>T maps to ENST00000377824 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:37424943 C>T maps to ENST00000377824 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:37424937 C>T maps to ENST00000377824 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr5:153054148 G>A maps to NM_001114183.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:153077647 C>T maps to NM_001114183.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:153190673 C>T maps to NM_001114183.1 G870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:153056609 C>T maps to NM_001114183.1 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:153065855 C>T maps to NM_001114183.1 H367H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:153065855 C>T maps to NM_001114183.1 H367H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:153026599 G>A maps to NM_001114183.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:158257899 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:158257014 G>T maps to NM_000826.3 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:158262532 C>T maps to NM_000826.3 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:158284072 G>A maps to NM_000826.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:158254050 C>A maps to NM_000826.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:158284177 C>T maps to NM_000826.3 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:158284076 C>T maps to NM_000826.3 R845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:158257527 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:122599628 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:122598814 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:122538762 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:122387347 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:122561850 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:122616783 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:122551431 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:122616685 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:122459977 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:122460030 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:122536913 G>A did not map to a codon.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr23:122599614 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:122387200 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:122528964 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:122536912 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:122561850 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:122319813 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:122319771 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:122387341 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:122460031 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr23:122318449 G>T did not map to a codon.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr23:122528924 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:122561819 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:122319704 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:122488768 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:122536912 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:122459978 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:122536944 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:122599619 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:122561850 C>A did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:122613915 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:105483046 C>T maps to NM_000829.3 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr11:105845251 C>T maps to NM_001077243.2 N875N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:105795444 C>A maps to NM_000829.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:105732915 T>C maps to NM_000829.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:105483046 C>T maps to NM_000829.3 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:105623905 C>T maps to NM_000829.3 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:105775931 C>T maps to NM_000829.3 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:105483016 C>T maps to NM_000829.3 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:87379673 G>A maps to NM_017551.2 Y770Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:87615931 G>A maps to NM_017551.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:87362311 C>T maps to NM_017551.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr10:87362284 G>A maps to NM_017551.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:94032023 G>T maps to NM_001510.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:94032001 C>A maps to NM_001510.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:94159635 C>T maps to NM_001510.2 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:94376817 C>T maps to NM_001510.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:94690540 C>T maps to NM_001510.2 F847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:94547442 C>T maps to NM_001510.2 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr4:94006428 C>T maps to NM_001510.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:94693572 C>A maps to NM_001510.2 S983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:30934170 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:30963545 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:31311716 C>T maps to ENST00000327783 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr21:30949472 C>T maps to ENST00000327783 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr21:30953853 G>T maps to ENST00000327783 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:31311716 C>A maps to ENST00000327783 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr6:102074348 A>G maps to NM_021956.4 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:102483388 A>C maps to NM_021956.4 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr6:102247566 G>T maps to NM_021956.4 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:102376359 C>T maps to NM_021956.4 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:37356572 G>T maps to NM_000831.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:37324816 G>A maps to NM_000831.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:37307342 G>A maps to NM_000831.3 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:37324831 G>A maps to NM_000831.3 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:37291208 G>A maps to NM_000831.3 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:37271816 G>A maps to NM_000831.3 Y734Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:120686168 C>T maps to NM_014619.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:120745921 C>A maps to NM_014619.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:120690558 C>T maps to NM_014619.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:120833253 C>T maps to NM_014619.2 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:120690495 C>T maps to NM_014619.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:120852857 T>C maps to NM_014619.2 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr11:120732717 C>A maps to NM_014619.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:42563647 G>A maps to NM_002088.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:42563515 G>A maps to NM_002088.3 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:42507498 T>C maps to NM_002088.3 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:42563670 G>A maps to NM_002088.3 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:42566664 G>A maps to NM_002088.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:140043498 C>T maps to ENST00000371546 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:140055533 C>T maps to ENST00000371546 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:140055593 C>T maps to ENST00000371546 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:140034093 G>A maps to ENST00000371546 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:9862749 G>A maps to NM_000833.3 G851G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:10274157 C>T maps to NM_000833.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:9857784 G>A maps to NM_000833.3 R1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:9916221 G>A maps to NM_000833.3 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr16:10274193 C>T maps to NM_000833.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:10031835 G>A maps to NM_000833.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr16:9862842 T>A maps to NM_000833.3 V820V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:9857866 A>C maps to NM_000833.3 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:9857665 G>T maps to NM_000833.3 L1245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:9857719 G>A maps to NM_000833.3 H1227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:13717234 G>A maps to NM_000834.3 N979N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:13906489 G>A maps to NM_000834.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:13764767 G>A maps to NM_000834.3 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:13768198 C>A maps to NM_000834.3 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:13716679 G>A maps to NM_000834.3 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:14018956 G>T maps to NM_000834.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:13906426 G>T maps to NM_000834.3 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr12:13715926 C>T maps to NM_000834.3 S1415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr12:13768201 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:14019049 G>A maps to NM_000834.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:13717237 G>A maps to NM_000834.3 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:13722884 G>A maps to NM_000834.3 C746C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:13764734 G>A maps to NM_000834.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:13716502 G>A maps to NM_000834.3 H1223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:72844039 G>A maps to NM_000835.3 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:72840564 G>A maps to NM_000835.3 D811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72843476 G>A maps to NM_000835.3 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr17:72844060 C>T maps to NM_000835.3 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:48917265 G>A maps to NM_000836.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:48917277 G>T maps to NM_000836.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:48945112 C>T maps to NM_000836.2 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:104375804 G>A maps to NM_133445.2 Y873Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:104433063 G>A maps to NM_133445.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:104432554 G>T maps to NM_133445.2 V713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:104449447 G>T maps to NM_133445.2 S245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:104449191 G>A maps to NM_133445.2 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:104499679 C>T maps to NM_133445.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:104432713 T>G maps to NM_133445.2 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:145066077 G>A maps to NM_001009184.1 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:66838439 G>A maps to ENST00000359742 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:66838439 G>A maps to ENST00000359742 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:66923623 A>G maps to ENST00000359742 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:66923613 G>A maps to ENST00000359742 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:66742963 G>A maps to ENST00000359742 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:66742821 G>A maps to ENST00000359742 R1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:14555182 G>A maps to ENST00000507975 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:14567391 G>A maps to ENST00000507975 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48847108 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48837665 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48846095 C>T did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:48855905 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:48858635 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48831683 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48844549 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:48853698 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:48853751 C>G did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:48832710 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48831641 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48837843 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48849957 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48846062 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:114322339 C>T maps to NM_002929.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:114436017 C>T maps to NM_002929.2 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:114426093 G>T maps to NM_002929.2 G345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:3037139 C>T maps to NM_182982.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr4:3021471 C>T maps to NM_182982.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:3029697 C>T maps to NM_182982.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:3009499 G>T maps to NM_182982.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:121201550 C>T maps to NM_005308.2 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:121196272 C>T maps to NM_005308.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:121214716 C>T maps to ENST00000457057 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:176862045 C>T maps to NM_002082.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr5:176859014 G>A maps to NM_002082.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:176860631 G>A maps to NM_002082.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:141497668 C>T maps to NM_139209.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr3:141497444 C>T maps to NM_139209.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr19:47423148 T>A maps to NM_004491.4 L406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:47422423 T>C maps to NM_004491.4 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:47425130 C>T maps to NM_004491.4 Q1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:47425246 C>T maps to NM_004491.4 Y1105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr19:47423228 C>T maps to NM_004491.4 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:47422066 G>A maps to NM_004491.4 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:47424920 C>T maps to NM_004491.4 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:47425364 C>T maps to NM_004491.4 R1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:47422256 C>T maps to NM_004491.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:47423228 C>T maps to NM_004491.4 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr19:47423372 C>T maps to NM_004491.4 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:47422930 C>T maps to NM_004491.4 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:47422256 C>T maps to NM_004491.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:47424604 C>T maps to NM_004491.4 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:47425582 T>C maps to NM_004491.4 N1217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:47423516 C>T maps to NM_004491.4 R529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:47424920 C>T maps to NM_004491.4 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:47503716 C>A maps to NM_004491.4 I1424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:47423780 C>T maps to NM_004491.4 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:47424920 C>T maps to NM_004491.4 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:47422138 T>C maps to NM_004491.4 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr19:47502648 C>T maps to NM_004491.4 V1375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr19:47421959 C>T maps to NM_004491.4 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:47424920 C>T maps to NM_004491.4 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:47424920 C>T maps to NM_004491.4 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr19:47425364 C>T maps to NM_004491.4 R1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:47424920 C>T maps to NM_004491.4 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:146755412 A>G maps to NM_000838.3 Q1022Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:146673402 G>T maps to NM_000838.3 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:146350982 G>A maps to NM_000838.3 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:146755634 C>T maps to NM_000838.3 D1096D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:146719938 G>A maps to NM_000838.3 W588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr6:146351081 C>T maps to NM_000838.3 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:146755478 G>A maps to NM_000838.3 A1044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:146351349 G>T maps to NM_000838.3 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:146755322 G>A maps to NM_000838.3 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:146747707 G>T maps to NM_001114329.1 E892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:146720181 G>A maps to NM_000838.3 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:146673440 C>A maps to NM_000838.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:51749288 C>T maps to NM_000839.3 C500C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:51746499 C>A maps to NM_000839.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:51750014 C>A maps to NM_000839.3 C742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:51752121 G>A maps to NM_000839.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr3:51746688 C>T maps to NM_000839.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:51749333 C>T maps to NM_000839.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr3:51749897 G>T maps to NM_000839.3 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:51746670 G>A maps to NM_000839.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:51746829 C>T maps to NM_000839.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:51747057 C>T maps to NM_000839.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr7:86416163 G>C maps to NM_000840.2 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:86394904 C>A maps to NM_000840.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:86469046 C>A maps to NM_000840.2 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:86394650 C>T maps to NM_000840.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:86415891 G>T maps to NM_000840.2 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:86394650 C>T maps to NM_000840.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:86394781 G>A maps to NM_000840.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:86468378 G>T maps to NM_000840.2 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr7:86415968 C>T maps to NM_000840.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:86416118 C>T maps to NM_000840.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:86394554 G>T maps to NM_000840.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr7:86416313 C>T maps to NM_000840.2 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:86416106 C>T maps to NM_000840.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:86493616 G>A maps to NM_000840.2 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:34008053 T>C maps to NM_000841.1 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:34004236 G>A maps to NM_000841.1 Y550Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr6:34003588 C>T maps to NM_000841.1 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:34101068 C>A maps to NM_000841.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:34004122 G>A maps to NM_000841.1 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr6:34101141 G>T maps to NM_000841.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:88300780 G>T maps to NM_001143831.2 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:88386431 G>A maps to NM_001143831.2 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:88242656 G>A maps to NM_001143831.2 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:88301130 G>A maps to NM_001143831.2 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:88301130 G>A maps to NM_001143831.2 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:88337959 G>T maps to NM_001143831.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:88301140 T>C maps to NM_001143831.2 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:88258555 G>A maps to NM_001143831.2 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:88338067 G>T maps to NM_001143831.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr5:178416068 C>T maps to NM_000843.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:178413397 C>T maps to NM_000843.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:178413682 C>T maps to NM_000843.3 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr5:178408804 C>T maps to NM_000843.3 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr5:178408731 G>A maps to NM_000843.3 R854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:178419153 G>C maps to ENST00000319065 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:178413547 C>T maps to NM_000843.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:178413559 C>T maps to NM_000843.3 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:7494417 C>T maps to NM_181874.2 Y433Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:6903449 G>A maps to NM_181874.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:7620309 C>T maps to NM_181874.2 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:7503378 C>T maps to NM_181874.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:7721812 G>A maps to NM_181874.2 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:7494327 G>A maps to NM_181874.2 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:7721827 C>A maps to NM_181874.2 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:6903500 G>A maps to NM_181874.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr3:6903317 G>A maps to NM_181874.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:6903488 C>T maps to NM_181874.2 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:7620680 C>A maps to NM_181874.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:7503405 C>A maps to NM_181874.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:126086177 A>G maps to NM_001127323.1 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:126746619 C>T maps to NM_001127323.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:126173175 C>A maps to NM_001127323.1 G754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:126542733 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:7062732 G>A maps to NM_025196.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:7064163 A>G maps to NM_025196.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:148730599 C>T maps to NM_152407.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:148730658 G>A maps to NM_152407.3 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:16168625 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:16142218 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:16168645 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:16170393 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:16168541 C>T did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:16170612 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:16142226 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:16168664 C>A did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:16142195 C>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:71691070 C>T maps to NM_002092.3 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:71691906 C>T maps to NM_002092.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:71691037 C>T maps to NM_002092.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:113979894 C>T maps to ENST00000375430 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:145246146 C>A maps to NM_001080516.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:145239451 A>G maps to NM_001080516.1 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:145252279 C>T maps to NM_001080516.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:95234881 C>T maps to NM_173849.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38130577 C>T maps to NM_178171.4 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr17:38122077 G>A maps to NM_178171.4 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:38062217 G>A maps to NM_001165958.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:130788447 C>A maps to NM_031415.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:130789710 C>T maps to NM_031415.2 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:144644660 G>A maps to NM_024736.6 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:13238100 C>A maps to NM_001080555.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:27818829 G>A maps to NM_001109763.1 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:27895900 G>A maps to NM_001109763.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr16:27974489 C>T maps to NM_001109763.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:27818829 G>A maps to NM_001109763.1 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:27895831 G>A maps to NM_001109763.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:3627969 C>T maps to NM_031965.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr17:3629016 C>T maps to NM_031965.2 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr17:3628866 C>T maps to NM_031965.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:3627684 G>A maps to NM_031965.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:3628866 C>T maps to NM_031965.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:42736212 T>C maps to NM_019884.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:119595265 C>T maps to NM_002093.3 W301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:119631581 G>T maps to NM_002093.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:119812192 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:119624628 A>G maps to NM_002093.3 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:119720936 C>A maps to NM_002093.3 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:119666149 G>A maps to NM_002093.3 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:119642288 C>T maps to NM_002093.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:124076246 C>T maps to NM_000177.4 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr9:124064371 C>T maps to NM_000177.4 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr9:124088905 C>T maps to NM_000177.4 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr9:124076301 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:124065294 C>T maps to NM_000177.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:11980449 C>T maps to NM_002094.3 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:11981522 G>A maps to NM_002094.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:51487301 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:51487854 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:51488493 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:51487903 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:51487449 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:51487365 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:51487542 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:51487830 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:51487529 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr23:51488295 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:51487066 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:51487679 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:51488602 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:51487903 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:51488104 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:51486910 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:51487440 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:51488279 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:51488024 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:51487125 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:51487529 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:51487235 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:51487802 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:30553989 G>A maps to NM_000637.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:30538551 C>A maps to NM_000637.3 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr6:52697701 C>A maps to NM_153699.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:52697704 G>A maps to NM_153699.1 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr6:52697737 C>T maps to NM_153699.1 W155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:106640255 T>C maps to NM_001031720.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr4:106763286 C>T maps to NM_001031720.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:142964765 C>T maps to NM_001143679.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:142961258 T>C maps to NM_001143679.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:142964765 C>T maps to NM_001143679.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:142965911 C>T maps to NM_001143679.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:110217455 T>C maps to ENST00000369830 *238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:110279595 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:110280988 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:110280786 G>A maps to NM_000849.4 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:110198932 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:110257639 G>A maps to ENST00000369812 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:110257849 C>T maps to ENST00000369812 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:67352639 C>T maps to NM_000852.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:67352612 C>A maps to NM_000852.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr11:67353637 C>T maps to NM_000852.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:67354011 C>T maps to NM_000852.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:67353645 G>A maps to NM_000852.3 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr11:67353975 G>C maps to NM_000852.3 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:77794295 G>A maps to NM_145870.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:77796096 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:28367823 C>T maps to NM_145657.1 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:28367892 G>A maps to NM_145657.1 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr4:54966537 G>A maps to NM_133267.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:144903215 G>A maps to NM_001164629.2 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:81658907 C>T maps to NM_015859.2 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:81662505 T>C maps to NM_015859.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:48848454 C>A maps to ENST00000437125 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:48960030 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:89323159 G>A maps to NM_001514.5 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:120500037 C>T maps to NM_005513.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr3:120489623 A>T maps to NM_005513.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:30469932 G>A maps to NM_002095.4 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:6387443 C>A maps to NM_002096.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:18359703 T>C maps to NM_005316.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:18357410 C>T maps to NM_005316.3 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:18359733 C>T maps to NM_005316.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:18362805 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:68874888 G>A maps to NM_001042490.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:124130036 G>A maps to NM_001516.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:30879921 G>A maps to NM_001517.4 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr6:30881096 G>A maps to NM_001517.4 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr7:74105435 A>T maps to NM_032999.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:74159107 G>T maps to NM_032999.2 G588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:74005274 C>T maps to NM_016328.2 Y855Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr7:73950542 G>A maps to NM_016328.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr7:73959112 C>G maps to NM_016328.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:73973314 C>T maps to NM_016328.2 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:73929870 C>T maps to NM_016328.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr7:73969766 G>T maps to NM_016328.2 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr7:74015503 C>T maps to NM_016328.2 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:74211960 C>T maps to NM_173537.2 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:74212341 G>A maps to NM_173537.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:74212065 G>T maps to NM_173537.2 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:74211843 G>A maps to NM_173537.2 H669H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr7:74211477 C>T maps to NM_173537.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:74212065 G>T maps to NM_173537.2 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:74211282 C>T maps to NM_173537.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:74234553 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:74212065 G>T maps to NM_173537.2 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:74564703 C>T maps to NM_001003795.2 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:74564502 C>T maps to NM_001003795.2 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:74552656 G>T maps to NM_001003795.2 G291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:74563987 G>T maps to NM_001003795.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:28009053 C>T maps to NM_002097.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:28006936 C>T maps to NM_002097.2 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:27472808 G>A maps to NM_001520.3 P2064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr16:27503656 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:27503961 C>A maps to NM_001520.3 T983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:27495631 A>G maps to NM_001520.3 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:27475815 G>A maps to NM_001520.3 P1899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:27480816 G>A maps to NM_001520.3 D1623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:27544640 C>A maps to NM_001520.3 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27560154 T>C maps to NM_001521.2 Q361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27549521 G>T maps to ENST00000431028 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27549628 G>A maps to NM_001521.2 A883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27565834 G>A maps to NM_001521.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27565939 G>A maps to NM_001521.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:197636475 C>T maps to NM_012086.2 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:197637709 C>A maps to NM_012086.2 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:197654094 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:197657733 G>A maps to NM_012086.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:197645293 C>A maps to NM_012086.2 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:197656091 C>T maps to NM_012086.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:197654674 C>A maps to NM_012086.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:197664287 G>T maps to NM_012086.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr2:197654702 A>G maps to NM_012086.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:135553527 C>T maps to NM_012204.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:135554621 T>G maps to NM_012204.2 L539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:135555033 C>T maps to NM_012204.2 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr9:135933231 C>T maps to NM_001122823.1 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr9:135919157 C>T maps to NM_001122823.1 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr9:135926247 C>A maps to NM_001122823.1 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:135917497 C>T maps to NM_001122823.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:39123306 C>T maps to NM_004286.4 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr22:39122109 G>A maps to NM_004286.4 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr22:39130402 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:39117782 G>T maps to NM_004286.4 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:89982284 T>C maps to NM_033107.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr6:43592646 G>A maps to NM_019096.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr6:43594045 C>T maps to NM_019096.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:43589778 G>A maps to NM_019096.3 N531N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr20:60775803 A>C maps to NM_015666.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:60776051 G>A maps to NM_015666.3 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:60772992 C>T maps to NM_015666.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:60775835 C>T maps to NM_015666.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:112714101 G>T maps to NM_014170.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:112714104 C>T maps to NM_014170.2 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:46704317 G>A maps to NM_016426.6 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:46704100 C>A maps to NM_016426.6 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:54854202 G>A maps to NM_144594.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:42355001 G>A maps to NM_176791.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:42355169 A>G maps to NM_176791.3 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:42355315 C>A maps to NM_176791.3 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr20:42355133 G>A maps to NM_176791.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:42162516 G>A maps to NM_002098.5 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr3:108635043 A>G maps to NM_005459.3 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:108627053 C>A maps to NM_005459.3 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:42629140 C>T maps to NM_033553.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:42628633 G>A maps to NM_033553.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:42620358 C>T maps to NM_007102.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:106849417 G>T maps to ENST00000282249 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:106849392 C>A maps to ENST00000282249 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:156651205 C>T maps to NM_001130684.1 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr4:156725804 C>T maps to ENST00000502959 R561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:156725861 G>T maps to ENST00000502959 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr4:156725761 C>T maps to ENST00000502959 H546H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:156698689 G>T maps to ENST00000502959 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:14825805 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:14822665 A>G maps to NM_004963.3 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:14836123 C>A maps to NM_004963.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr12:14772223 A>G maps to NM_004963.3 V932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:14792825 G>A maps to NM_004963.3 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:7915535 G>T maps to NM_000180.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:7915793 C>T maps to NM_000180.3 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7915502 G>T maps to NM_000180.3 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:108647677 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:108695264 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:108628471 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:108652273 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:108691389 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:108718888 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:108641881 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:108631812 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:108636150 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr23:108652308 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:108652345 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:108673605 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:108708625 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:108636231 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:108635276 A>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:108718935 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:108625434 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:108652340 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:108625402 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:108691389 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr23:108691387 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:108708415 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:108696905 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:108625441 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:108691352 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:108619184 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:108673540 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:108691388 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:108647604 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:108708670 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:44688040 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:44682714 A>G maps to NM_021927.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:44688622 C>T maps to NM_021927.2 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:44682858 G>T maps to NM_021927.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:228336129 C>T maps to ENST00000366720 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:228336391 C>T maps to ENST00000366720 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:189406035 C>T maps to NM_016315.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:189434798 A>G maps to NM_016315.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr2:189406035 C>T maps to NM_016315.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:189434063 C>T maps to NM_016315.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:189452777 C>T maps to ENST00000451191 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:65441100 C>T maps to NM_000181.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:65445279 C>T maps to NM_000181.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:65425945 C>A maps to NM_000181.3 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:42499642 G>A maps to NM_173601.1 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:73024211 C>T maps to NM_001080393.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:73016812 C>T maps to NM_001080393.1 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:73016824 C>T maps to NM_001080393.1 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr3:148744653 G>A maps to NM_004130.3 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:148714611 C>T maps to NM_004130.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr3:148714231 C>G maps to NM_004130.3 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:2772093 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:2795285 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:2773079 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:2761305 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:2772042 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:2774564 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:2777963 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:145061770 G>T maps to NM_002099.6 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:144922436 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:144921577 C>A maps to ENST00000283128 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:144826642 G>T maps to NM_198682.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:49488787 G>A maps to NM_002103.4 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:21757462 C>A maps to NM_021957.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:21693460 G>A maps to NM_021957.3 C564C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:21716177 G>A maps to NM_021957.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:21713408 G>T maps to NM_021957.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:21733334 C>A maps to NM_021957.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:21693496 G>A maps to NM_021957.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:21721828 C>A maps to NM_021957.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr20:23350332 C>T maps to NM_022482.3 C580C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:23350248 C>T maps to NM_022482.3 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:23346165 C>T maps to NM_022482.3 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:54404198 C>T maps to NM_006144.3 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:54405887 C>T maps to NM_006144.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:25101152 G>A maps to ENST00000382542 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:54320600 C>T maps to NM_002104.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:54329738 G>A maps to NM_002104.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:547337 G>A maps to NM_005317.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:549127 C>T maps to NM_005317.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:38201757 G>A maps to NM_005318.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:48723754 G>A maps to NM_181788.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr12:48723323 C>T maps to NM_181788.1 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:129266375 C>A maps to NM_153833.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:134686555 G>A maps to NM_138609.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:134670770 G>A maps to NM_138610.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:134696261 G>A maps to NM_138610.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:134670674 G>A maps to NM_138610.2 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr5:134696231 G>A maps to NM_138610.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:134670827 G>A maps to NM_138610.2 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:71835450 C>T maps to NM_018649.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:100870531 G>A maps to NM_002106.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr23:103267827 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:103267756 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:103268189 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:103267758 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr23:103268035 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:103268176 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:226259143 C>T maps to NM_002107.3 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr17:73775126 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:9323697 C>T maps to NM_004285.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:9305557 G>T maps to NM_004285.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:9324264 C>T maps to NM_004285.3 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:9324213 G>A maps to NM_004285.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:9324264 C>T maps to NM_004285.3 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:9324567 C>A maps to NM_004285.3 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:9323718 G>A maps to NM_004285.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:42995062 G>A maps to NM_012205.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:43015683 G>A maps to NM_012205.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:115337002 C>T maps to NM_004132.3 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:115345663 A>T maps to NM_004132.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:99252310 G>A maps to NM_014282.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:99252310 G>A maps to NM_014282.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr6:105178224 G>A maps to NM_020771.3 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:105177599 T>C maps to NM_020771.3 E889E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:105297080 C>A maps to NM_020771.3 G88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:105233197 A>G maps to ENST00000369127 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:105225078 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:105232048 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr4:108931030 A>T maps to ENST00000351726 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:26414142 G>A maps to NM_000182.4 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:26501518 C>T maps to NM_000183.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:26501605 C>A maps to NM_000183.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr2:26486332 G>A maps to NM_000183.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:26501518 C>T maps to NM_000183.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:1869158 G>A maps to NM_005326.4 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:96374581 T>C maps to NM_002108.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr12:96370473 G>A maps to NM_002108.2 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:119936433 C>T maps to ENST00000361035 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:119927402 C>A maps to ENST00000361035 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr5:82940460 G>A maps to NM_001884.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:156594140 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:89422303 C>T maps to NM_178232.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:46637544 G>T maps to NM_173811.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:46637142 A>G maps to NM_173811.3 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:46637622 C>T maps to NM_173811.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140054320 G>A maps to NM_002109.3 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140054386 G>A maps to NM_002109.3 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140075701 G>A maps to NM_012208.2 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:52217021 C>T maps to NM_001523.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:52217291 C>T maps to NM_001523.2 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:122641055 G>T maps to NM_005328.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:122626672 C>T maps to NM_005328.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:122641313 G>A maps to NM_005328.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:122626714 G>A maps to NM_005328.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:69148508 C>A maps to NM_005329.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr16:69143618 G>A maps to NM_005329.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:69143516 C>T maps to NM_005329.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:172841193 G>T maps to NM_003642.3 G308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:43685318 G>T maps to NM_138443.3 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:43685367 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:43708097 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:43708293 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:23420772 T>C maps to NM_017815.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:23416387 A>G maps to NM_017815.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:36109580 C>T maps to NM_015302.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36109809 T>G maps to NM_015302.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:36104781 G>A maps to NM_015302.1 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:19078268 T>G maps to NM_017645.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:19058867 C>A maps to NM_017645.3 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:19058901 C>T maps to NM_017645.3 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:19094393 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:19058867 C>A maps to NM_017645.3 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:19078224 C>T maps to NM_017645.3 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:152734671 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152722673 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152735988 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:152722092 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:152720501 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152721100 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:152722071 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:152721991 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr23:152719911 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152721961 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152722092 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr23:152722108 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:17170438 C>T maps to NM_033417.1 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:17163731 C>A maps to NM_033417.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:17169496 C>T maps to NM_033417.1 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:156479516 C>T maps to NM_001173393.1 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:156479611 G>A maps to NM_001173393.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:156522332 G>A maps to NM_032782.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:156533710 G>T maps to NM_032782.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:156533836 G>A maps to NM_032782.3 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:156533968 G>T maps to NM_032782.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:156533845 T>C maps to NM_032782.3 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:156515959 C>T maps to NM_032782.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:154246343 G>A maps to NM_006118.3 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:5247832 G>A maps to NM_000518.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:5247911 A>G maps to NM_000518.4 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr11:5290827 G>T maps to NM_005330.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:5290701 C>A maps to NM_005330.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:5269675 G>A maps to ENST00000440157 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:106822966 G>T maps to NM_012257.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:135317985 C>T maps to NM_006620.3 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:135358036 G>A maps to NM_001145207.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:135307888 C>T maps to NM_006620.3 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr6:135323933 C>T maps to NM_006620.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:135286418 A>C maps to NM_006620.3 *685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:135360725 C>A maps to NM_006620.3 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:135371729 C>T maps to NM_006620.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:110948949 A>C maps to NM_006402.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr1:110950281 G>C maps to NM_006402.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:11135416 G>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153217058 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:153219733 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153223311 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153220143 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153220616 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr23:153225791 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153218076 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153219957 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:153225347 T>C did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:153220731 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:153220865 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153216836 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153220850 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153225784 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153227716 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:153215748 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:153236188 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr23:153220132 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:153223661 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153216300 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153217603 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153229588 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:153225250 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:153220632 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153219911 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153220512 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153217993 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153219926 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153220609 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:153222766 G>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:153218061 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:153221674 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:153230036 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:153221853 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:153218219 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr23:153219156 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153215784 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:104490142 G>T maps to NM_013320.2 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:104496801 T>C maps to NM_013320.2 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:104492165 C>T maps to NM_013320.2 R596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:104492257 G>A maps to NM_013320.2 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr12:104487280 T>C maps to NM_013320.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:104481817 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:30676428 C>T maps to NM_002110.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:30671712 C>T maps to NM_002110.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:121355280 C>T maps to NM_005335.4 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:121354632 C>A maps to NM_005335.4 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121363759 C>A maps to NM_005335.4 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr3:121350797 G>A maps to NM_005335.4 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:121356005 G>A maps to NM_005335.4 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:121350734 G>A maps to NM_005335.4 H473H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:45262820 A>G maps to NM_021072.2 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:45396614 C>T maps to NM_021072.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr5:45262334 G>A maps to NM_021072.2 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:45262832 G>A maps to NM_021072.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:45353348 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:45267196 G>A maps to NM_021072.2 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:45267313 G>A maps to NM_021072.2 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:45262181 G>A maps to NM_021072.2 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:45353234 A>G maps to NM_021072.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr5:45262646 G>T maps to NM_021072.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:45267196 G>A maps to NM_021072.2 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:45462109 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:45645424 A>C maps to NM_021072.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:608109 C>T maps to NM_001194.3 Y455Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:603747 C>T maps to NM_001194.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:613885 G>A maps to NM_001194.3 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:73659957 G>A maps to NM_005477.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr15:73616474 G>A maps to NM_005477.2 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:73615822 G>A maps to NM_005477.2 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:73617683 G>A maps to NM_005477.2 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:73624576 G>A maps to NM_005477.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:73635794 C>T maps to NM_005477.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:73615568 C>T maps to NM_005477.2 P955P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:55145213 G>A maps to NM_001526.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:55147251 G>T maps to NM_001526.3 *445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:55039538 G>T maps to NM_001526.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:55145213 G>A maps to NM_001526.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:36394286 A>G maps to NM_014266.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:32797378 C>T maps to NM_004964.2 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:32782342 T>C maps to NM_004964.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr22:50686524 C>T maps to NM_032019.5 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:13522808 G>A maps to NM_024827.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:114277819 G>T maps to ENST00000398283 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:114264667 G>A maps to ENST00000398283 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:141005765 G>C maps to NM_003883.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:141007695 C>T maps to NM_003883.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:141008839 G>A maps to NM_003883.3 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:141005331 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:240005916 G>A maps to NM_006037.3 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:240078423 G>A maps to NM_006037.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:240066378 C>T maps to NM_006037.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:240003821 G>A maps to NM_006037.3 F871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:240002873 G>A maps to NM_006037.3 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:42162431 G>T maps to NM_001015053.1 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr17:42158129 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:42170787 C>T maps to NM_001015053.1 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:42157797 A>G maps to NM_001015053.1 I933I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:42169644 G>A maps to NM_001015053.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:42164977 G>T maps to NM_001015053.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48672892 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48674964 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48682636 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:48682666 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48681340 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48673822 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48673834 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48681637 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:48674999 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48681989 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48683252 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:48672930 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48661139 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48664813 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:48676757 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48674022 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48681419 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48661190 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48661281 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48673429 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48674905 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48681174 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:48681061 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:48676793 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:48674930 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48664869 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48672938 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48681857 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48681203 A>C did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:48676753 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48674976 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48675807 T>C did not map to a codon.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr23:48673380 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:71684359 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:71715033 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:71571646 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:71708852 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:18684313 C>T maps to NM_178425.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:18684358 C>A maps to NM_178425.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:18705843 G>A maps to NM_178425.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:18687596 C>T maps to NM_178425.2 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:18687587 G>T maps to NM_178425.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:18706066 G>T maps to NM_178425.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:18875115 G>A maps to NM_178425.2 Q831Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:50540518 G>A maps to NM_002112.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:125619919 G>A maps to NM_016063.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:156713984 C>T maps to NM_001126050.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:22570001 C>T maps to NM_138574.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:4475474 C>T maps to ENST00000301284 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:4488839 C>T maps to ENST00000301284 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:4499576 C>T maps to ENST00000301284 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:4491573 G>A maps to ENST00000301284 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:242174613 G>A maps to NM_005336.3 G1022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:242181873 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:242196044 G>A maps to NM_005336.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr2:242174928 G>A maps to NM_005336.3 I995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:242170329 G>A maps to NM_005336.3 Y1106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:242186271 G>A maps to NM_005336.3 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:242194838 G>A maps to NM_005336.3 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:242176061 C>A maps to NM_005336.3 E958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:242179435 A>G maps to NM_005336.3 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:242170209 G>A maps to NM_005336.3 R1146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:83616610 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:83724148 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:83724484 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:83730382 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:83723624 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr23:83723495 T>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:83581231 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:83723878 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:83723586 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:83599434 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:83581274 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:83723703 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:83588778 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:83723729 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83576978 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83588843 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83616531 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83723826 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:83724390 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:83723878 C>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:83599445 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:236719516 C>T maps to NM_018072.5 A1799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:236720518 G>T maps to NM_018072.5 P1777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:236730014 C>T maps to NM_018072.5 W1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:236716970 G>A maps to NM_018072.5 I2049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:236758864 G>A maps to NM_018072.5 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:236730116 G>T maps to NM_018072.5 I1379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:236749748 G>A maps to NM_018072.5 Y573Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:236762842 G>A maps to NM_018072.5 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:236718763 G>A maps to NM_018072.5 L1919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:769435 C>T maps to NM_017802.3 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:810216 C>T maps to NM_017802.3 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:803600 C>T maps to NM_017802.3 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr7:801457 C>T maps to NM_017802.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr7:796417 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:801457 C>T maps to NM_017802.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:50118057 C>T maps to NM_182922.2 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:50118043 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:50104186 G>A maps to NM_182922.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:50120146 A>G maps to NM_182922.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:50128614 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:50136288 G>A maps to NM_182922.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr14:73969642 C>T maps to ENST00000334988 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:73945406 G>A maps to ENST00000334988 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:73978788 G>A maps to ENST00000334988 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:73961943 C>A maps to ENST00000334988 E878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:73989319 A>T maps to ENST00000334988 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:31844079 G>A maps to ENST00000389961 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:31762741 A>T maps to ENST00000389961 T1964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:31813182 A>G maps to ENST00000389961 A1043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr14:31813161 C>T maps to ENST00000389961 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr14:31795406 C>T maps to ENST00000389961 W1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:31777218 G>A maps to ENST00000389961 S1560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:37286076 G>A maps to NM_019024.1 R635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:37241149 C>T maps to NM_019024.1 W1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:37208716 C>T maps to NM_019024.1 A2044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:37208730 G>A maps to NM_019024.1 R2040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:37229677 C>T maps to NM_019024.1 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:37286116 G>A maps to NM_019024.1 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:37268421 G>A maps to NM_019024.1 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr17:58132902 T>C maps to NM_022070.4 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:58143635 C>T maps to NM_022070.4 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:58147116 A>G maps to NM_022070.4 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr17:58134570 C>T maps to NM_022070.4 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:58120962 A>C maps to NM_022070.4 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:58134498 C>T maps to NM_022070.4 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr8:145235127 C>T maps to NM_032450.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr8:145246628 C>T maps to NM_032450.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:41054934 C>T maps to ENST00000296803 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:41015481 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:41004950 G>T maps to ENST00000296803 A1313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr5:41005725 G>A maps to ENST00000296803 H1258H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:41009402 G>A maps to ENST00000296803 I1134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:41054892 G>A maps to ENST00000296803 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:41058293 G>A maps to ENST00000296803 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr5:41015551 C>T maps to ENST00000296803 Q972Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr5:41058238 C>A maps to ENST00000296803 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:41000844 C>A maps to ENST00000296803 E1430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:41004913 G>A maps to ENST00000296803 R1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr5:41058233 G>A maps to ENST00000296803 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:13140126 G>A maps to NM_015987.4 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:31618222 C>A maps to NM_015382.2 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:31576351 C>T maps to NM_015382.2 T2242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:31618327 G>A maps to NM_015382.2 R732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:31647384 C>T maps to NM_015382.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:31578712 G>A maps to NM_015382.2 R2124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr14:31641302 A>G maps to NM_015382.2 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:93242758 C>A maps to ENST00000446394 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr10:93247525 C>T maps to ENST00000446394 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:93242743 A>G maps to ENST00000446394 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:93252195 G>T maps to ENST00000446394 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:45475780 C>T maps to NM_024602.5 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:45472632 G>T maps to NM_024602.5 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:45474271 G>A maps to NM_024602.5 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:45471737 G>A maps to NM_024602.5 C592C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:45475699 G>A maps to NM_024602.5 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:45475762 G>A maps to NM_024602.5 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:45469789 G>A maps to NM_024602.5 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:45469789 G>A maps to NM_024602.5 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr7:43484936 G>A maps to NM_015052.3 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:43483982 T>C maps to NM_015052.3 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:43436411 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:43581572 T>G maps to NM_015052.3 T1408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:43547614 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:43447269 T>C maps to NM_015052.3 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:197085626 G>T maps to NM_020760.1 I1395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:197106878 G>A maps to NM_020760.1 F1193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:197106878 G>A maps to NM_020760.1 F1193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:197122593 T>C maps to NM_020760.1 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:197183831 G>A maps to NM_020760.1 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:197105186 G>A maps to NM_020760.1 F1250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:197183831 G>A maps to NM_020760.1 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:197085593 G>A maps to NM_020760.1 I1406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:197105186 G>A maps to NM_020760.1 F1250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:197187307 C>A maps to NM_020760.1 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:197184344 G>A maps to NM_020760.1 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr3:124732421 G>A maps to NM_020733.1 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:124748126 G>A maps to NM_020733.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:124731646 C>A maps to NM_020733.1 E926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:124732832 G>A maps to NM_020733.1 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:124729355 G>A maps to NM_020733.1 C1000C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:124728654 G>A maps to NM_020733.1 C1029C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:66715759 G>T maps to NM_033647.2 E730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:66704270 T>C maps to NM_033647.2 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:66703944 G>T maps to NM_033647.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:66731873 G>T maps to NM_033647.2 E1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:96352270 C>T maps to NM_018063.3 N657N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:96317910 G>T maps to NM_018063.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:84376765 G>A maps to NM_133636.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:84348752 G>T maps to NM_133636.2 S880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:84339283 C>A maps to NM_133636.2 E1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:185941563 C>T maps to NM_001029887.1 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:65141981 C>T maps to NM_014877.3 E882E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:65110474 G>A maps to NM_014877.3 R1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:65157101 C>T maps to NM_014877.3 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:65163895 G>A maps to NM_014877.3 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr17:65105570 G>A maps to NM_014877.3 Q1384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:65132272 T>G maps to NM_014877.3 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr17:65134140 C>T maps to NM_014877.3 V953V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:65156375 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:65104744 G>A maps to NM_014877.3 S1529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:65104693 C>T maps to NM_014877.3 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:100692758 C>T maps to NM_018437.3 E306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:100692686 G>A maps to NM_018437.3 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:100693393 C>A maps to NM_018437.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:100692761 A>G maps to NM_018437.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:100689686 G>T maps to NM_018437.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr3:50609157 G>A maps to NM_016173.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:124793861 G>A maps to NM_152722.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:124793631 G>A maps to NM_152722.4 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:124792563 G>A maps to ENST00000374961 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr7:92848714 G>A maps to ENST00000453812 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:92848438 A>G maps to ENST00000453812 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr23:65413352 T>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:65392288 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:65423304 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:65423310 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:65423367 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:65474880 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:65390508 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:65413464 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr23:65409628 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:65393594 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:65408256 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:65478764 G>T did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:65423395 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:65417559 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:65392223 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:65414979 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:65478810 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:65393448 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:65414963 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:65418734 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:65476109 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:65478770 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:65418739 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:65420520 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr23:65474906 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:65428013 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:65413378 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:65476058 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:65474948 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:65423220 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:65423310 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:65486458 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:65479980 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:65390483 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:65392376 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:93815724 C>T maps to NM_001098672.1 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:93806268 T>C maps to NM_001098672.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:93796827 C>T maps to NM_001098672.1 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:93815697 G>T maps to NM_001098672.1 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:93797537 C>T maps to NM_001098672.1 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:93778856 C>T maps to NM_001098672.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:93844214 G>A maps to NM_001098672.1 T1064T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:93844856 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:63972915 C>T maps to ENST00000261887 W2095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr15:63986650 G>A maps to ENST00000261887 N1780N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr15:63986306 G>A maps to ENST00000261887 L1844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:63907989 G>A maps to ENST00000261887 R4691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:63918246 G>T maps to ENST00000261887 L4404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:63921011 G>A maps to ENST00000261887 L4323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:63970056 C>A maps to ENST00000261887 E2353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:64008585 T>C maps to ENST00000261887 E1355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:63967237 C>T maps to ENST00000261887 A2383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr15:63967149 G>A maps to ENST00000261887 R2413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:64021812 A>G maps to ENST00000261887 D968D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:63943488 G>A maps to ENST00000261887 G3503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:63964810 C>T maps to ENST00000261887 T2643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:63921014 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:63982783 G>A maps to ENST00000261887 L1965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr15:64039184 G>A maps to ENST00000261887 Q818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr15:28389093 C>T maps to NM_004667.4 L3781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr15:28389027 T>C maps to NM_004667.4 T3803T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:28356989 G>A maps to NM_004667.4 D4808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:28491984 C>T maps to NM_004667.4 T1098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:28389334 G>T maps to NM_004667.4 S3729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:28446667 C>T maps to NM_004667.4 T2550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:28459410 C>T maps to NM_004667.4 T2122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:28491886 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:28422638 C>T maps to NM_004667.4 T3060T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:28483762 C>A maps to NM_004667.4 G1245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:28517369 G>A maps to NM_004667.4 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr15:28377308 C>T maps to NM_004667.4 W4169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:28391469 C>A maps to NM_004667.4 E3641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:28482249 C>A maps to NM_004667.4 E1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:28502227 C>T maps to NM_004667.4 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:28436161 G>T maps to NM_004667.4 I2866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:28459290 G>T maps to NM_004667.4 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:28499627 C>A maps to NM_004667.4 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:28369218 G>A maps to NM_004667.4 F4384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:28436303 C>T maps to NM_004667.4 P2846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:28474703 T>C maps to NM_004667.4 T1674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr15:28360631 G>A maps to NM_004667.4 A4555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:28483808 G>A maps to NM_004667.4 D1229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr15:28502227 C>T maps to NM_004667.4 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:28377897 G>A maps to NM_004667.4 S4103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:28508146 G>T maps to NM_004667.4 S680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:28359942 A>G maps to NM_004667.4 D4576D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:28465763 G>A maps to NM_004667.4 R1893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:28474382 G>A maps to NM_004667.4 R1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V7-01A-21D-A122-09 chr15:28501280 G>A maps to NM_004667.4 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:28358366 G>A maps to NM_004667.4 I4694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:28375398 G>T maps to NM_004667.4 R4238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:28397856 G>A maps to NM_004667.4 D3622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:28437148 G>A maps to NM_004667.4 D2803D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:28508241 T>C maps to NM_004667.4 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr15:28517495 C>T maps to NM_004667.4 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr15:28408245 G>A maps to NM_004667.4 Y3580Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr15:28370292 G>A maps to NM_004667.4 D4283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr15:28422596 A>G maps to NM_004667.4 G3074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:28361876 G>A maps to NM_004667.4 R4515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr4:89574212 C>T maps to NM_014606.1 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:89574206 T>C maps to NM_014606.1 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:89579629 C>T maps to NM_014606.1 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr4:89527177 T>C maps to NM_014606.1 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr4:89574116 G>A maps to NM_014606.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:89599112 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:89601315 G>T maps to NM_014606.1 E757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr4:89628071 C>A maps to NM_014606.1 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:89597575 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:69750675 C>T maps to NM_022079.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:69692479 T>C maps to NM_022079.2 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:69714446 C>A maps to NM_022079.2 E756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:69832807 C>A maps to NM_022079.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:89407360 C>T maps to NM_016323.2 Y611Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:89415362 A>G maps to NM_016323.2 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:89425478 C>T maps to NM_016323.2 D893D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr4:89415461 A>G maps to NM_016323.2 E808E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:89421092 C>T maps to NM_016323.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:89408236 A>G maps to NM_016323.2 V623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr4:89389500 C>T maps to NM_016323.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:89358080 T>C maps to NM_017912.3 D814D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:89306692 C>A maps to NM_017912.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:89349827 C>T maps to NM_017912.3 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:89304512 G>T maps to NM_017912.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:89314670 A>G maps to NM_017912.3 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr4:89317267 C>T maps to NM_017912.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:89334368 A>G maps to NM_017912.3 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:56976049 C>T maps to NM_014685.2 H304H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:35673421 C>A maps to NM_022373.4 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:35674824 C>T maps to NM_022373.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:35734237 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:193855937 C>T maps to NM_005524.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:193854482 G>A maps to NM_005524.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:193854766 G>A maps to NM_005524.2 K74K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:57232812 G>A maps to NM_003865.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:57233868 G>T maps to NM_003865.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:57232323 C>A did not map to a codon.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr15:72668070 A>C maps to ENST00000457859 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:72638615 C>A maps to ENST00000457859 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:72640065 G>T maps to ENST00000457859 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr15:72648911 G>A maps to ENST00000457859 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:74012459 C>T maps to NM_000521.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:74009437 G>A maps to NM_000521.3 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr5:73981172 C>T maps to NM_000521.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:80398966 C>T maps to NM_173620.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:43246500 C>T maps to NM_144608.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:126080509 G>C maps to NM_012259.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:26091297 C>T maps to NM_000410.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:26093012 G>A maps to NM_000410.3 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:145415318 C>T maps to NM_213653.3 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:145415435 C>A maps to NM_213653.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:145415615 G>T maps to NM_213653.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:145415543 C>T maps to NM_213653.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:145415777 C>A maps to NM_213653.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:91781406 G>A maps to NM_001017975.3 D1035D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:91781508 C>T maps to NM_001017975.3 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:91784731 C>T maps to NM_001017975.3 K905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:91781508 C>T maps to NM_001017975.3 T1001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:91790315 T>C maps to NM_001017975.3 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:91818061 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:91844690 C>A maps to NM_001017975.3 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:91846512 C>A maps to NM_001017975.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:91861905 G>T maps to NM_001017975.3 S43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:91818158 T>G maps to NM_001017975.3 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:91788522 C>A maps to NM_001017975.3 E856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:91844690 C>A maps to NM_001017975.3 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:120357317 C>T maps to NM_000187.3 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:81334827 G>A maps to NM_000601.4 R630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:81372753 G>A maps to NM_000601.4 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:81386581 G>A maps to NM_000601.4 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr7:81355323 T>G maps to NM_000601.4 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:81346674 G>T maps to NM_000601.4 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:81388044 T>C maps to NM_000601.4 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:3446585 C>A maps to ENST00000511533 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:3449356 C>T maps to ENST00000511533 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:79653395 C>T maps to NM_004712.4 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr17:79655783 C>T maps to NM_004712.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:79654055 C>T maps to NM_004712.4 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr17:79667587 C>T maps to NM_004712.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:79668133 C>T maps to NM_004712.4 I732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:43054618 C>T maps to ENST00000458501 H633H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:43013803 C>T maps to ENST00000458501 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr8:43024315 T>C maps to ENST00000458501 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:210761331 G>A maps to NM_001170580.1 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:210560816 G>A maps to NM_001170580.1 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:210536251 G>T maps to NM_001170580.1 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:210577979 T>G maps to NM_001170580.1 L214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:42734296 C>T maps to NM_020707.3 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:42740544 G>A maps to NM_020707.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:94454327 G>T maps to NM_002729.4 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:94454303 G>T maps to NM_002729.4 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:94454497 C>T maps to NM_002729.4 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:94454330 G>T maps to NM_002729.4 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:94452230 C>T maps to NM_002729.4 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:145655946 T>G maps to NM_022475.1 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:145580933 G>T maps to NM_022475.1 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:145658913 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:100119030 G>A maps to NM_001127258.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:100134586 G>A maps to NM_001127258.1 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr14:100134577 G>A maps to NM_001127258.1 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:222695957 G>A maps to NM_024746.3 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:222715454 G>A maps to NM_024746.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:222705344 A>G maps to NM_024746.3 H562H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:100527432 G>T maps to NM_033055.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:100546116 G>T maps to NM_033055.2 G390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:97221465 G>A maps to NM_032558.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:97209145 C>A maps to NM_032558.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:191109611 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr22:21799355 C>A maps to NM_015094.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr22:21800635 C>T maps to NM_015094.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr22:21800950 C>T maps to NM_015094.2 Y589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:21799270 G>A maps to NM_015094.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:62207879 C>T maps to ENST00000394997 N690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr14:62193490 A>G maps to ENST00000394997 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:62188360 G>T maps to ENST00000394997 G122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:62200970 A>G maps to ENST00000394997 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr14:62200979 T>C maps to ENST00000394997 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:62211441 G>T maps to ENST00000394997 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:102304801 C>T maps to ENST00000442724 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:102300402 G>A maps to ENST00000442724 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:102296379 G>A maps to ENST00000442724 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:102296373 C>T maps to ENST00000442724 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr10:102305722 C>T maps to ENST00000442724 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:102304801 C>T maps to ENST00000442724 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:102296415 G>A maps to ENST00000442724 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:46823774 C>T maps to NM_152795.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr19:46834436 C>T maps to NM_152795.2 D579D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:46808598 C>T maps to NM_152795.2 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:46825081 C>T maps to NM_152795.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:46807289 C>T maps to NM_152795.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:42835681 G>A maps to NM_001099668.1 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:42927727 C>T maps to NM_016438.2 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr17:42925564 C>T maps to NM_016438.2 D15D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:175815936 C>T maps to NM_138820.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:119003604 C>T maps to NM_198971.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:119003929 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:119002691 C>T maps to NM_198971.1 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:130495000 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:130495032 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:130498167 G>A maps to ENST00000508488 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr5:130498369 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:35813290 A>G maps to NM_032593.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:35813655 G>T maps to NM_032593.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:126298819 T>C maps to NM_138571.4 *183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:75184824 G>A maps to NM_005338.4 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:75185446 G>A maps to NM_005338.4 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:75184732 G>A maps to NM_005338.4 C650C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:75192262 G>T maps to NM_005338.4 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:123332639 G>T maps to NM_003959.1 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:123340437 G>A maps to NM_003959.1 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:123346287 C>T maps to NM_003959.1 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr12:123343632 C>T maps to NM_003959.1 C728C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:114483871 C>G maps to ENST00000426820 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:114508828 C>T maps to ENST00000426820 N843N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:114483377 C>T maps to ENST00000426820 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:114483067 G>A maps to ENST00000426820 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:139416484 G>A maps to NM_022740.4 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:139311465 G>A maps to NM_022740.4 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:139316026 G>T maps to NM_022740.4 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:139268662 G>A maps to NM_022740.4 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:139416728 C>T maps to NM_022740.4 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:139281599 G>A maps to NM_022740.4 G860G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:139416053 G>A maps to NM_022740.4 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:139281656 G>A maps to NM_022740.4 R841R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:33358623 C>T maps to NM_005734.3 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:33358623 C>T maps to NM_005734.3 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:33360389 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:33363158 G>A maps to NM_005734.3 Q608Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr11:33308664 C>A maps to NM_005734.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:33360955 G>T maps to NM_005734.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr19:40886961 C>T maps to NM_144685.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:40885538 G>A maps to NM_144685.3 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:40889977 C>T maps to NM_144685.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:40889743 G>A maps to NM_144685.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:40886784 G>A maps to NM_144685.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:40885493 T>C maps to NM_144685.3 *617W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:40886691 C>T maps to NM_144685.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr22:19373147 G>A maps to NM_003325.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:19340906 G>A maps to NM_003325.3 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:19363251 G>A maps to NM_003325.3 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:19365411 G>A maps to NM_003325.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:19344539 G>A maps to NM_003325.3 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr22:19396039 A>T maps to NM_003325.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr16:30006662 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:30006496 G>T maps to NM_003609.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr6:26017618 C>T maps to NM_005325.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:27835001 A>C maps to NM_005322.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:26234993 G>A maps to NM_005320.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:26108248 G>A maps to NM_005323.3 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:25726745 G>A maps to NM_170745.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr6:26033450 G>A maps to NM_003513.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr6:26199363 G>C maps to NM_021065.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:26199344 G>A maps to NM_021065.2 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:26217492 T>C maps to NM_021052.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr6:27101173 C>T maps to NM_021064.4 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:27114960 C>A maps to NM_080596.1 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr6:27805886 G>A maps to NM_003510.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:27833518 C>T maps to NM_003511.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:25727309 G>A maps to NM_170610.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:26043702 C>T maps to NM_021062.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:26043672 G>A maps to NM_021062.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:26124039 C>T maps to NM_003526.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:26199854 G>A maps to NM_003522.3 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:26216817 A>G maps to NM_003518.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr6:26273259 G>A maps to NM_003525.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:26020785 T>C maps to NM_003529.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr6:26032030 C>T maps to NM_003537.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:26045832 G>A maps to NM_003531.2 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:26045859 A>G maps to NM_003531.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:26197294 G>A maps to NM_003530.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:27839883 G>A maps to NM_003533.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr6:26104306 C>T maps to NM_003542.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:26189064 C>T maps to NM_003539.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:26285580 G>A maps to NM_003543.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:27107332 C>T maps to NM_003495.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:27107296 C>T maps to NM_003495.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr6:27841159 G>A maps to NM_003546.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:149783764 G>A maps to ENST00000427880 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr1:149785070 G>A maps to NM_001123375.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:228645287 C>T maps to NM_033445.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:228646033 T>C maps to NM_175055.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:12120615 C>T maps to NM_002114.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:12164273 C>T maps to NM_002114.2 C2579C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:12123564 C>A maps to NM_002114.2 I1179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:12121950 G>A maps to NM_002114.2 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr6:12121941 C>T maps to NM_002114.2 H638H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:12163943 C>T maps to NM_002114.2 I2469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:12164504 A>G maps to NM_002114.2 Q2656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:12164222 C>T maps to NM_002114.2 A2562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:12120744 T>C maps to NM_002114.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:12124605 C>T maps to NM_002114.2 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr6:12122385 C>T maps to NM_002114.2 Y786Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr6:12124017 G>A maps to NM_002114.2 T1330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr6:12163907 G>T maps to NM_002114.2 V2457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:12164456 G>A maps to NM_002114.2 S2640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:143091557 G>A maps to NM_006734.3 R1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:143092152 G>A maps to NM_006734.3 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:143093193 G>A maps to NM_006734.3 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:143074762 G>A maps to NM_006734.3 D2274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:143092905 C>T maps to NM_006734.3 K990K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr6:143092439 G>A maps to NM_006734.3 L1146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:143094156 G>A maps to NM_006734.3 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr6:143092590 G>A maps to NM_006734.3 G1095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:143082655 G>A maps to NM_006734.3 C1855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:143091488 C>A maps to NM_006734.3 E1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:143094051 G>A maps to NM_006734.3 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:143093201 G>A maps to NM_006734.3 R892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:143095521 G>A maps to NM_006734.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:143082691 C>T maps to NM_006734.3 T1843T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:41990564 C>A maps to NM_024503.3 E1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:41978660 G>A maps to NM_024503.3 A2077A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:42046898 C>T maps to NM_024503.3 P1190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:41990469 G>A maps to NM_024503.3 I1773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:42045803 A>G maps to NM_024503.3 D1555D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:42050348 G>A maps to NM_024503.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:42048740 G>A maps to NM_024503.3 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:42048764 G>A maps to NM_024503.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:42049463 G>A maps to NM_024503.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:42046904 G>A maps to NM_024503.3 A1188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:42048494 G>C maps to NM_024503.3 Y658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:42041225 G>T maps to NM_024503.3 I1732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:42047654 G>T maps to NM_024503.3 V938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:41990568 G>A maps to NM_024503.3 N1740N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:234761225 G>A maps to NM_018410.3 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:234749871 G>A maps to NM_018410.3 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:234749576 G>A maps to NM_018410.3 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:234750255 G>A maps to NM_018410.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr10:71144658 G>A maps to ENST00000439900 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:71136804 C>T maps to ENST00000439900 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:71129036 C>T maps to ENST00000439900 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:71139842 G>A maps to ENST00000439900 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:71119665 C>T maps to ENST00000439900 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr10:71146122 C>T maps to ENST00000439900 C663C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:75117922 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:75109362 C>T maps to NM_000189.4 D612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:75118016 G>A maps to NM_000189.4 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:75116437 C>T maps to NM_000189.4 D814D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:75117941 T>C maps to NM_000189.4 H876H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:75106018 C>T maps to NM_000189.4 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:176318485 G>T maps to NM_002115.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:176318106 C>G maps to NM_002115.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr5:176310837 A>G maps to NM_002115.2 N662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:176323124 C>T maps to NM_002115.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:71002995 C>T maps to NM_025130.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:71018550 C>A maps to NM_025130.3 C684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:71005960 C>T maps to NM_025130.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:70992620 C>T maps to NM_025130.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:71003076 C>T maps to NM_025130.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr10:70998833 C>A maps to NM_025130.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:71025374 C>T maps to NM_025130.3 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr10:70980232 G>C maps to NM_025130.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:37854289 A>G maps to NM_181786.2 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:37854238 G>A maps to NM_181786.2 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:29910630 C>T maps to ENST00000376806 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:32975298 G>A maps to NM_002119.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:32782370 T>G maps to ENST00000452392 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr6:32783046 G>A maps to NM_002120.3 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr6:32782827 C>A maps to ENST00000452392 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:33053611 C>T maps to NM_002121.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:32629969 G>A maps to ENST00000374943 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:30457512 C>A maps to NM_005516.5 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:29692902 C>T maps to NM_001098479.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:29691980 C>T maps to NM_001098479.1 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:29796590 C>T maps to ENST00000376828 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:38269245 G>T maps to NM_000411.5 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr21:38139567 C>T maps to NM_000411.5 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:38302734 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:53398077 C>T maps to NM_002126.4 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:148802506 T>G maps to NM_003071.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:148778578 C>T maps to NM_003071.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:148759285 C>T maps to NM_003071.3 Q789Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:148802584 C>A maps to NM_003071.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:148789387 A>G maps to NM_003071.3 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr3:148786077 A>G maps to NM_003071.3 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr3:148781309 G>A maps to NM_003071.3 D356D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:221055539 G>A maps to NM_021958.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:221057694 C>T maps to NM_021958.3 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:221057748 C>T maps to NM_021958.3 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:30136877 C>T maps to NM_178581.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:30137092 C>T maps to NM_178581.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr20:30126011 C>T maps to NM_178581.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:28906492 T>C maps to ENST00000444075 H350H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:186113785 C>T maps to NM_031935.2 C4739C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:186023118 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:186113320 C>T maps to NM_031935.2 S4647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:185878512 C>T maps to NM_031935.2 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:186143644 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:186010191 C>T maps to NM_031935.2 S2076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:186043883 C>T maps to NM_031935.2 S2717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:186141263 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:185834940 T>C maps to NM_031935.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:185931677 G>A maps to NM_031935.2 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:186014853 C>T maps to NM_031935.2 V2113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:186082068 T>C maps to NM_031935.2 F3705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:186134267 C>T maps to NM_031935.2 S5094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:186082063 G>T maps to NM_031935.2 E3704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:186158715 C>T maps to NM_031935.2 L5538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:185902936 A>C maps to NM_031935.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:186039796 G>T maps to NM_031935.2 E2683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:185939557 C>T maps to NM_031935.2 G768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:186014934 C>T maps to NM_031935.2 D2140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:186099822 C>T maps to NM_031935.2 G4408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:185891512 C>T maps to NM_031935.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:185985348 C>A maps to NM_031935.2 I1723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:185976349 C>T maps to NM_031935.2 R1522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:186017960 C>A maps to NM_031935.2 V2189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:186043907 G>A maps to NM_031935.2 A2725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr1:186113407 G>A maps to NM_031935.2 A4676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:185985298 C>T maps to NM_031935.2 R1707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:185984478 C>T maps to NM_031935.2 R1607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:186082063 G>T maps to NM_031935.2 E3704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:186062645 T>C maps to NM_031935.2 D3347D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:186141229 G>T maps to NM_031935.2 G5261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr1:186039801 G>A maps to NM_031935.2 V2684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:185934979 T>C maps to NM_031935.2 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:186134305 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:186045695 G>A maps to NM_031935.2 L2809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:185892646 C>T maps to NM_031935.2 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:185932924 T>C maps to NM_031935.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:185985291 A>G maps to NM_031935.2 E1704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:185987458 G>A maps to NM_031935.2 K1815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:186120736 G>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:186135358 C>T maps to NM_031935.2 C5121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr15:77770712 C>T maps to NM_018200.2 H256H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:77759490 C>T maps to NM_018200.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:77771627 C>T maps to NM_018200.2 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:77759562 C>T maps to NM_018200.2 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3575587 G>A maps to NM_006339.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3576606 C>T maps to NM_006339.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:34210556 T>C maps to NM_145899.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr13:31037462 T>C maps to NM_002128.4 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:31037342 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:31036812 T>C maps to NM_002128.4 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr4:174253278 C>T maps to NM_002129.3 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:174253969 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:174254124 G>T maps to NM_002129.3 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:174253271 C>A maps to NM_002129.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:174254716 C>T maps to NM_002129.3 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:150156268 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:150154188 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:150154135 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:150154571 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:150155745 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:150156380 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:150154641 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:150156377 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:34329989 C>T maps to NM_145205.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:34329933 A>T maps to NM_145205.4 K48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:24130961 G>A maps to NM_000191.2 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:24140705 C>T maps to NM_000191.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:55360387 G>A maps to NM_019036.2 Y238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:55378891 C>A maps to NM_019036.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr6:55378994 C>G did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr6:55443826 C>T maps to NM_019036.2 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:74655335 G>A maps to NM_000859.2 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr5:74646997 A>G maps to NM_000859.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:43297113 C>T maps to NM_002130.6 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:43292989 G>A maps to NM_002130.6 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:120299897 G>A maps to NM_005518.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:120306999 C>T maps to NM_005518.3 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:120298144 G>A maps to NM_005518.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:120307092 G>T maps to NM_005518.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:40715039 A>G maps to NM_004965.6 *101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr21:40715054 C>A maps to NM_004965.6 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:79911409 C>A maps to NM_004242.2 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:79944268 C>T maps to NM_004242.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:80370452 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:80371809 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:80370323 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:80370592 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:80370240 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:80370391 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:1078016 G>A maps to NM_012292.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:1080496 G>A maps to NM_012292.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:1084253 G>A maps to NM_012292.2 Q991Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:1080777 T>C maps to NM_012292.2 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:162902537 G>A maps to NM_001142556.1 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:162900562 G>T maps to NM_001142556.1 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:162900415 C>T maps to NM_001142556.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:162911238 C>T maps to NM_001142556.1 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:162896762 C>A maps to NM_001142556.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:162900244 C>A maps to NM_001142556.1 Y237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:162891798 G>A maps to NM_001142556.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:162902541 G>T maps to NM_001142556.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:162910313 G>T maps to NM_001142556.1 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:162905752 A>G maps to NM_001142556.1 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr22:35782715 G>A maps to NM_002133.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:35782826 G>A maps to NM_002133.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:35782703 C>T maps to NM_002133.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr22:35782874 T>C maps to NM_002133.2 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr16:4557994 G>A maps to NM_001127205.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr5:173531228 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:61627534 C>T maps to NM_001123366.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:61621712 A>G maps to NM_001123366.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:61627534 C>T maps to NM_001123366.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:1741890 C>T maps to ENST00000382711 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:36099530 C>T maps to NM_000458.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:36099458 G>A maps to NM_000458.2 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr20:43052673 C>T maps to ENST00000338692 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:43036101 C>T maps to ENST00000338692 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr20:43057053 C>T maps to ENST00000338692 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:43034770 C>T maps to ENST00000338692 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:76459820 G>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr8:76472654 T>C maps to NM_004133.4 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:76456169 T>C maps to NM_004133.4 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:76463633 G>T maps to NM_004133.4 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:76465278 C>A maps to NM_004133.4 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:76470900 T>C maps to NM_004133.4 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr8:76456148 C>T maps to NM_004133.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:138762704 C>T maps to NM_006895.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:138738828 G>A maps to NM_001024075.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:138738925 G>T maps to NM_001024075.1 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:138727753 G>T maps to NM_006895.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:138771378 C>T maps to NM_006895.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:54676049 C>A maps to NM_031157.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:53216966 G>T maps to NM_001011725.1 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:26232994 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:26233222 G>A maps to NM_031243.2 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:26232993 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr2:178080755 T>C maps to NM_194247.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:177636357 G>T maps to NM_031266.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:177637232 G>A maps to NM_031266.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:21702316 G>A maps to NM_031314.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:12908007 G>A maps to NM_001013631.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr10:43882342 T>C maps to NM_001098204.1 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr10:43882849 C>T maps to NM_001098204.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:43882867 C>T maps to NM_001098204.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:43883005 G>A maps to NM_001098204.1 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:43883272 C>T maps to NM_001098204.1 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:43882423 G>A maps to NM_001098204.1 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:43882986 G>A maps to NM_001098204.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr5:179042545 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100666986 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100668190 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100667228 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100667726 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100667106 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100667372 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:100668078 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:100667550 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100667199 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100668224 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100667485 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100667549 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100667030 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100667571 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100667945 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100666978 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:70098421 A>G maps to NM_012207.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:70099260 C>T maps to NM_012207.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:86586622 G>A maps to NM_031262.2 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:86585177 C>T maps to NM_031262.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr9:86591915 A>G maps to NM_031262.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr19:39334532 T>A maps to ENST00000221419 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:39334653 G>A maps to ENST00000221419 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:8509929 C>T maps to NM_005968.3 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr1:23640196 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:23637775 C>A maps to ENST00000414299 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:245019365 A>G maps to NM_031844.2 Y669Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:245022652 C>T maps to NM_031844.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:245023759 A>G maps to NM_031844.2 H298H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:245027594 A>G maps to NM_031844.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:245025939 C>A maps to NM_031844.2 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr1:245023702 A>T maps to NM_031844.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:245019774 C>T maps to NM_031844.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:245021576 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:245018830 G>A maps to NM_031844.2 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:41787068 C>T maps to NM_007040.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr19:41800485 G>A maps to NM_007040.3 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:41774191 C>T maps to NM_007040.3 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:41810114 C>A maps to NM_007040.3 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:41778078 C>T maps to NM_007040.3 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62484635 G>A maps to NM_001079559.1 C602C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62489407 G>A maps to NM_001079559.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62491190 C>T maps to NM_001079559.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:62489350 C>A maps to NM_001079559.1 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:62490150 T>C maps to NM_001079559.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:78697766 C>T maps to NM_004272.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:78742961 C>A maps to NM_004272.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:78692719 C>A maps to NM_004272.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr15:83544108 C>T maps to NM_199330.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:19049965 A>G did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:19042847 G>A maps to NM_004838.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:23745809 G>A maps to NM_020834.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:60305990 C>T maps to NM_015888.4 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:60324705 A>G maps to NM_015888.4 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:12882246 G>A maps to NM_013312.2 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:12883471 C>T maps to NM_013312.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:12881973 T>G maps to NM_013312.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:12883471 C>T maps to NM_013312.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:42865470 G>T maps to NM_032410.3 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:42868474 G>T maps to NM_032410.3 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr8:42821744 C>T maps to NM_032410.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:57514963 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:57516882 G>A maps to NM_001145460.1 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:150680762 A>G maps to NM_032132.4 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:150675800 G>T maps to NM_032132.4 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:27224351 G>A maps to NM_005523.5 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:27237954 C>T maps to NM_000522.4 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:27237977 C>A maps to NM_000522.4 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:27238059 G>A maps to NM_000522.4 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:27237870 C>T maps to NM_000522.4 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:27140994 C>A maps to NM_006735.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:27141084 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:27140742 C>A maps to NM_006735.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr7:27141876 G>A maps to NM_006735.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr7:27148283 C>T maps to NM_153631.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:27147899 C>T maps to NM_153631.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:27147923 C>T maps to NM_153631.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:27168962 G>A maps to NM_002141.4 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:27169062 G>A maps to NM_002141.4 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:27183129 G>A maps to NM_019102.2 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:27187200 A>G maps to NM_024014.2 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:27187134 A>G maps to NM_024014.2 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:27196137 C>T maps to NM_006896.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:27195918 G>T maps to NM_006896.3 C82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:27195885 G>A maps to NM_006896.3 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:27209183 C>A maps to ENST00000354032 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:46607945 G>A maps to NM_002144.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:46608206 G>A maps to NM_002144.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:46608098 C>T maps to NM_002144.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:46620630 C>T maps to NM_002145.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr17:46628472 G>A maps to NM_002146.4 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:46629584 C>A maps to NM_002146.4 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:46627788 G>A maps to NM_002146.4 C401C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:46691745 G>A maps to NM_024016.3 Y107Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:54383142 C>T maps to NM_017409.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:54379402 G>A maps to NM_017409.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:54379552 C>T maps to NM_017409.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:54367375 C>T maps to NM_014212.3 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:54448940 C>T maps to NM_153633.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:54428123 G>T maps to NM_018953.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:54427046 C>A maps to NM_018953.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:54422487 C>T maps to NM_004503.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:177054707 C>A maps to ENST00000331462 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:176982172 C>T maps to NM_002148.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr2:176982022 G>A maps to NM_002148.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:176972184 C>T maps to NM_021192.2 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:176973680 C>T maps to NM_021192.2 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:176965304 G>A maps to NM_021193.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:176958190 C>A maps to NM_000523.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:176959293 G>T maps to NM_000523.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:177036311 C>T maps to NM_006898.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:177033955 G>A maps to NM_006898.4 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:177036974 G>A maps to NM_006898.4 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:177036966 C>T maps to NM_006898.4 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr2:177036848 G>A maps to NM_006898.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:177036434 C>T maps to NM_006898.4 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:177016573 G>A maps to NM_014621.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:176988887 C>T maps to NM_014213.3 C348C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:176988683 C>T maps to NM_014213.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:72094269 G>A maps to NM_005143.3 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:72090131 G>A maps to NM_005143.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:72094539 G>A maps to NM_005143.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr1:21091966 G>A maps to NM_016287.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:21074116 G>A maps to NM_016287.3 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:33354831 C>T maps to NM_002143.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:40148354 G>A maps to NM_016257.2 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:122294531 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:45793687 C>T maps to NM_032756.2 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:95229876 C>A maps to NM_014485.2 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:35550786 C>A maps to NM_182983.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:35556500 C>T maps to NM_182983.2 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr19:35557169 C>T maps to NM_182983.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:35556497 C>A maps to NM_182983.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:35551284 C>T maps to NM_182983.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:72110691 G>A maps to ENST00000228226 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:72110691 G>A maps to ENST00000228226 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr16:72109050 C>A maps to ENST00000228226 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr16:72110564 C>G maps to ENST00000228226 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:133609335 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:133627594 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:133627614 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:100185426 G>A maps to NM_000195.2 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:100202988 G>A maps to NM_000195.2 C3C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:100184122 C>T maps to NM_000195.2 W448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:148858899 T>G maps to NM_032383.3 L270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:148857971 G>A maps to NM_032383.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:148875297 C>T maps to NM_032383.3 H557H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:148881675 C>T maps to NM_032383.3 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr22:26860140 C>T maps to NM_022081.4 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:26853847 G>A maps to NM_022081.4 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:26860010 G>A maps to NM_022081.4 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr22:26864582 G>T maps to NM_022081.4 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr22:26860444 G>C maps to NM_022081.4 S384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:18332395 G>T maps to NM_181507.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:18318407 C>A maps to NM_181507.1 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:103826014 C>T maps to NM_024747.4 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:103826223 A>G maps to NM_024747.4 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:103826898 A>G maps to NM_024747.4 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr4:84231996 C>T maps to NM_006665.5 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:84222230 G>A maps to NM_006665.5 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:84227367 G>A maps to NM_006665.5 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:84227367 G>A maps to NM_006665.5 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:84222213 G>A maps to NM_006665.5 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:100503679 G>A maps to NM_021828.4 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:100995355 C>T maps to NM_021828.4 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:100242489 G>A maps to NM_021828.4 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:100380396 G>A maps to NM_021828.4 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:100481489 G>T maps to NM_021828.4 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:100995553 C>T maps to NM_021828.4 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:100249905 G>T maps to NM_021828.4 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:100249905 G>A maps to NM_021828.4 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:6458324 G>T maps to NM_000613.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr8:21976740 G>A maps to NM_005144.4 A1011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:21976785 C>T maps to NM_005144.4 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:21978604 G>A maps to NM_005144.4 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:21986362 C>T maps to NM_005144.4 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:21984754 G>A maps to NM_005144.4 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:21986134 C>T maps to NM_005144.4 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:21979156 G>A maps to NM_005144.4 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:21981246 G>A maps to NM_005144.4 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr8:21978270 C>T maps to NM_005144.4 R856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:21976492 G>A maps to NM_005144.4 D1061D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:63257802 C>A maps to NM_054108.3 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr19:49657957 C>T maps to NM_002152.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:49657708 G>A maps to NM_002152.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:186386776 G>A maps to NM_000412.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:11302048 G>A maps to NM_001098211.1 K442K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr3:11301157 G>A maps to NM_001098211.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr5:175110631 A>C maps to NM_001131055.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:175110340 C>T maps to NM_001131055.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr20:60793588 G>A maps to ENST00000317393 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr20:60791937 C>A maps to ENST00000317393 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:22040748 A>G maps to NM_021624.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:22048791 C>T maps to NM_021624.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:22056853 A>G maps to NM_021624.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:22056739 C>A maps to NM_021624.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:152191524 G>A maps to NM_001009931.1 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:152191917 G>A maps to NM_001009931.1 H729H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:152193096 G>A maps to NM_001009931.1 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:152195693 G>A maps to NM_001009931.1 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:152192978 G>A maps to NM_001009931.1 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:152187194 G>A maps to NM_001009931.1 R2304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:152193957 G>A maps to NM_001009931.1 N49N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr1:152193324 G>A maps to NM_001009931.1 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:152188422 G>T maps to NM_001009931.1 S1894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:152188566 G>A maps to NM_001009931.1 G1846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:152193102 G>A maps to NM_001009931.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr1:152191917 G>A maps to NM_001009931.1 H729H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:152192751 G>A maps to NM_001009931.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr1:152193216 G>A maps to NM_001009931.1 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr1:152193531 G>T maps to NM_001009931.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:20840940 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:87570304 C>T maps to NM_012262.3 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:87569113 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:11400897 C>T maps to NM_005114.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:11401038 G>A maps to NM_005114.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:11401089 G>A maps to NM_005114.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:22926795 T>A maps to NM_006043.1 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:22926604 C>T maps to NM_006043.1 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:22926600 C>T maps to NM_006043.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:26147094 G>A maps to NM_006040.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr16:26147292 C>T maps to NM_006040.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:25704250 C>T maps to NM_006040.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:114379325 G>A maps to NM_153612.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:114378705 G>A maps to NM_153612.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr6:114378561 G>T maps to NM_153612.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:1962097 C>T maps to ENST00000454677 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:129026164 G>A maps to NM_004807.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr2:129025924 G>A maps to NM_004807.2 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:131763059 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:132091280 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:131762591 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:131803195 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:132091056 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:132092367 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:131762881 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:131762416 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:132091269 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:131842516 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:131762343 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:132090982 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:131762334 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:131762795 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:132090958 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:131803179 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:131763054 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:131763079 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:132091209 C>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:132091134 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:83842952 C>T maps to NM_001537.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:29140688 C>T maps to NM_172002.3 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:209907746 G>T maps to NM_005525.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:209879204 C>T maps to NM_005525.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:209905923 G>T maps to NM_005525.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:209907847 C>T maps to NM_005525.2 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:209878260 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:209878328 C>A maps to NM_005525.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:5687544 C>A maps to NM_198706.1 Y178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:40705827 C>T maps to NM_000413.2 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:40705241 C>T maps to NM_000413.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53458421 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53460823 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53458944 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53460711 T>C did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:53461281 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:53459200 A>G did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:88295925 A>T maps to NM_016245.3 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:43861601 C>T maps to NM_016142.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:88235096 G>A maps to NM_178135.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:82131893 G>A maps to NM_002153.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:82069254 G>T maps to NM_002153.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:99012068 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:99006624 C>A maps to NM_000197.1 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:99003165 C>T maps to NM_000197.1 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:99017150 G>A maps to NM_000197.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:118844940 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:118832236 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:118813187 G>A maps to NM_000414.3 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:57178727 C>T maps to NM_003725.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr12:57180966 T>C maps to NM_003725.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:57167812 G>A maps to NM_003725.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr1:162762577 T>C maps to NM_016371.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:33173469 G>A maps to NM_014234.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:120056673 C>T maps to ENST00000235547 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:120050215 C>T maps to ENST00000235547 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:120056715 C>A maps to ENST00000235547 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:120050107 C>A maps to ENST00000235547 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:119964861 A>G maps to NM_000198.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:119958162 G>T maps to NM_000198.3 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:119964696 G>A maps to NM_000198.3 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:119958095 C>T maps to NM_000198.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:119962158 C>A maps to NM_000198.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:30998291 G>A maps to NM_025193.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:84163650 C>T maps to NM_031463.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:115181192 G>T maps to NM_032303.4 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:122740368 T>C maps to NM_004506.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:122741340 G>T maps to NM_004506.3 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:45077959 G>A maps to NM_007031.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:67201025 C>A maps to NM_001040667.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:67201673 T>C maps to NM_001040667.2 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:67201446 G>T maps to NM_001040667.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:67199706 C>T maps to NM_001040667.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:56557626 T>C maps to NM_001080439.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:56557589 G>A maps to NM_001080439.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:16265282 G>A maps to NM_032855.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:16268544 G>T maps to NM_032855.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:16268027 A>G maps to NM_032855.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:102549568 G>T maps to NM_001017963.2 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:44217840 G>T maps to NM_007355.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr6:44219876 C>G maps to NM_007355.2 S535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:44219832 C>T maps to NM_007355.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr6:44217196 C>T maps to NM_007355.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:104336432 G>A maps to NM_003299.1 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:104326615 G>T maps to NM_003299.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:104336436 C>T maps to NM_003299.1 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:104341166 G>T maps to NM_003299.1 E781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:104337000 C>T maps to NM_003299.1 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:118439234 G>A maps to NM_025015.2 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:15746522 G>A maps to NM_006948.4 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:15753822 G>A maps to NM_006948.4 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr21:15746369 C>A maps to NM_006948.4 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:14890637 C>T maps to NM_016299.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:14896174 G>A maps to NM_016299.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:14894492 G>T maps to NM_016299.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:31778027 A>G maps to NM_005527.3 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:31778006 C>T maps to NM_005527.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:31778428 G>A maps to NM_005527.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:31779728 G>A maps to NM_005527.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr6:31778369 C>T maps to NM_005527.3 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr6:31778312 C>T maps to NM_005527.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr6:31778666 G>A maps to NM_005527.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:65008760 C>T maps to NM_021979.3 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr14:65009264 C>T maps to NM_021979.3 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:65007629 C>T maps to NM_021979.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:132403231 G>T maps to NM_002154.3 G97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:132440001 T>C maps to NM_002154.3 N799N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:132427047 G>A maps to NM_002154.3 Q514Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:132409809 A>T maps to NM_002154.3 K219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:132431912 G>T maps to NM_002154.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:132412420 G>T maps to NM_002154.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr4:128732694 C>T maps to ENST00000438626 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:128753836 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:128748464 C>T maps to ENST00000438626 Y714Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:161495419 G>T maps to NM_002155.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:161495095 T>C maps to NM_002155.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:161495833 A>G maps to NM_002155.3 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:161495312 C>T maps to NM_002155.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:122930228 C>A maps to NM_006597.3 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:122928471 G>T maps to NM_006597.3 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:122930652 G>T maps to NM_006597.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:137892254 G>T maps to NM_004134.6 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:137909755 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:54387425 G>A maps to NM_016126.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr12:119617302 C>T maps to NM_014365.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:119631533 A>T maps to NM_014365.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:122459659 A>G maps to NM_024610.4 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:122496714 C>A maps to NM_024610.4 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:198353094 G>A maps to NM_199440.1 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:198359445 C>A maps to NM_199440.1 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:198358871 T>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:22183649 G>A maps to NM_005529.5 N1811N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:22186164 G>A maps to NM_005529.5 S1729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:22207930 G>A maps to NM_005529.5 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:22169364 C>T maps to NM_005529.5 V2936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:22155930 G>A maps to NM_005529.5 F3979F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:22176913 G>A maps to NM_005529.5 S2412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:22179510 C>T maps to NM_005529.5 A2164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:22176665 C>T maps to NM_005529.5 T2438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:22216635 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:22207900 G>A maps to NM_005529.5 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr1:22161376 G>A maps to NM_005529.5 A3505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:22207010 C>T maps to NM_005529.5 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:31719764 C>A maps to NM_006644.2 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:31725210 G>A maps to NM_006644.2 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:31728825 G>A maps to NM_006644.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:31725283 G>A maps to NM_006644.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:31726971 A>G maps to ENST00000439123 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:31727057 G>A maps to NM_006644.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:31711622 C>T maps to NM_006644.2 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:31717954 C>A maps to NM_006644.2 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:31725210 G>A maps to NM_006644.2 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:31725127 G>A maps to NM_006644.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:20404711 C>A maps to NM_001098520.1 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:135593362 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135579892 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135584991 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135586562 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135593719 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr23:135579892 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135581921 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135586594 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:135591315 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135585079 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135593173 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135592249 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135582329 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135584939 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135582833 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:135593791 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:135581911 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:135593665 C>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr5:63257090 G>A maps to NM_000524.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr5:63256592 G>A maps to NM_000524.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr5:63256355 G>A maps to NM_000524.2 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:78172382 C>T maps to NM_000863.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:78172235 G>A maps to NM_000863.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr6:78173084 C>T maps to NM_000863.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:23520424 G>A maps to NM_000864.4 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:23520604 C>T maps to NM_000864.4 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:87725273 C>T maps to NM_000865.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:88040459 T>C maps to NM_000866.3 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:88040985 C>T maps to NM_000866.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr3:88040174 G>A maps to NM_000866.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr3:88040985 C>T maps to NM_000866.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:88040945 C>A maps to NM_000866.3 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:47409724 G>T maps to NM_000621.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:47409001 G>A maps to NM_000621.3 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:47469873 G>T maps to NM_000621.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:47409283 G>A maps to NM_000621.3 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:47408980 G>A maps to NM_000621.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:231988274 T>C maps to NM_000867.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:231973629 T>C maps to NM_000867.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:231974009 G>A maps to NM_000867.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:114141288 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:114082610 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:114082666 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:114141929 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:113965994 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:114141278 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:114141242 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:114141387 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:114082757 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:114141551 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:114141551 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:114141694 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:114082590 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:114141211 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:114082610 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:114141283 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:114141328 G>A did not map to a codon.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr23:114141850 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:114141922 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr11:113853983 C>T maps to NM_213621.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:113860238 C>T maps to NM_213621.3 S435S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D1-A103-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:113860283 G>A maps to NM_213621.3 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:113802104 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:113802526 G>A maps to NM_006028.3 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:113802149 G>A maps to NM_006028.3 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:113815476 G>T maps to NM_006028.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:183777336 T>C maps to NM_130770.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:183772515 C>T maps to NM_130770.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:183774717 C>T maps to NM_130770.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:183774717 C>T maps to NM_130770.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:183756600 C>T maps to NM_001145143.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:183750728 C>T maps to NM_001163646.1 H37H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:183750659 C>A maps to NM_001163646.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:183823623 C>T maps to NM_182589.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr3:183818357 A>G maps to NM_182589.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:183818399 A>G maps to NM_182589.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:147902896 G>T maps to NM_001040173.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:147928295 C>T maps to NM_001040173.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr5:147902902 G>A maps to NM_001040173.2 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:147928310 C>T maps to NM_001040173.2 V91V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A5-A0GP-01A-11W-A062-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-A5-A0R7-01A-31D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr7:154862971 C>T maps to NM_024012.2 D121D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BG-A0LW-01A-11W-A062-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr7:154862797 G>A maps to NM_024012.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:154863211 C>T maps to NM_024012.2 A201A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A17M-01A-21D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:19992560 C>T maps to NM_000871.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:19992507 C>T maps to NM_000871.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:92509290 C>T maps to NM_019859.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:92509290 C>T maps to NM_019859.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:124273724 C>T maps to NM_002775.4 N431N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:124266906 T>C maps to NM_002775.4 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:124273778 C>T maps to NM_002775.4 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:124271542 G>A maps to NM_002775.4 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:74759767 C>T maps to NM_013247.4 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:8288311 G>A maps to NM_053044.3 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:8288440 C>T maps to NM_053044.3 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:8305970 T>G maps to NM_053044.3 Y387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:38840023 G>A maps to NM_153692.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr4:3234945 C>T maps to NM_002111.6 S2774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:3208604 G>A maps to NM_002111.6 T1990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:3241785 A>T maps to NM_002111.6 *3143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:3174088 C>T maps to NM_002111.6 R1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:3101057 C>T maps to NM_002111.6 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:3180051 C>A maps to NM_002111.6 I1497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:3235074 C>T maps to NM_002111.6 I2817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:3100999 G>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:3230403 C>T maps to NM_002111.6 D2637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:33371178 G>A maps to NM_014586.1 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:33371166 C>T maps to NM_014586.1 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:33297019 C>T maps to NM_014586.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr21:33371223 C>T maps to NM_014586.1 H624H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:33371223 C>T maps to NM_014586.1 H624H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr21:33297019 C>T maps to NM_014586.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:48016009 G>T maps to ENST00000433977 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:48008852 A>G maps to NM_004507.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr6:656845 G>T maps to NM_148959.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53561081 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53565351 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53575021 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53596579 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53602138 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53610720 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53641671 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53651561 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53674384 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53561530 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53565300 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53571676 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53585964 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53595735 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53610698 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53616664 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53652151 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53573706 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53577914 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53591640 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53630407 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:53596772 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:53607837 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53574731 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53576320 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53576405 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53579823 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53581810 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53591680 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53634620 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53681047 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:53644302 C>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:53578034 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:53564535 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:53571545 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:53590731 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:53634631 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:53655836 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:53579312 G>A did not map to a codon.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr23:53585659 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53565804 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53574655 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53585964 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53611181 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53615345 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53615459 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53618075 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53674406 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:53569440 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53561129 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53563538 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53571574 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53576422 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53600892 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53672375 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:53565905 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:53561524 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:53571561 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:53566024 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:53634625 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:53563592 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:53616677 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:53627120 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53562405 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53576063 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53579835 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53588829 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53591583 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53595718 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53596640 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53607796 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53610570 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53627239 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:53573450 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:53620410 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:53629525 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53563515 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53566738 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53575176 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53607795 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53610780 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53613849 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53615365 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53564635 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53576424 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53588798 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53595722 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53610791 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53675181 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr23:53574860 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr23:53620423 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:53560306 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:53569497 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:53644086 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:53595724 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:53574887 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:53563195 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:53654452 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:53674312 C>A did not map to a codon.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr23:53627126 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:111087246 G>A maps to NM_001040107.1 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:111089094 G>A maps to NM_001040107.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr3:50355748 C>T maps to NM_033158.4 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:50331101 G>A maps to NM_003549.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:123509140 G>T maps to NM_012269.2 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:123509121 G>A maps to NM_012269.2 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:123508903 G>T maps to NM_012269.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:123517094 T>C maps to NM_012269.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:123517104 G>T maps to NM_012269.2 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:70863565 G>T maps to NM_032821.2 I4688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:70955003 G>A maps to NM_032821.2 G2424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:70941378 C>T maps to NM_032821.2 Q2803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:71196560 G>A maps to NM_032821.2 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:71209608 C>T maps to NM_032821.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:70852325 G>A maps to NM_032821.2 P4858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:70913256 A>G maps to NM_032821.2 L3499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:71015318 G>A maps to NM_032821.2 C1494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:70863631 G>A maps to NM_032821.2 G4666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:70916793 G>A maps to NM_032821.2 F3327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:70926343 C>A maps to NM_032821.2 E3112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:70989395 G>A maps to NM_032821.2 S2065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:70894673 G>A maps to NM_032821.2 R3969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:70929908 G>A maps to NM_032821.2 I3040I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:70942692 G>A maps to NM_032821.2 F2691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:71019105 T>C maps to NM_032821.2 P1437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:71218817 G>A maps to NM_032821.2 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:70868034 T>C maps to NM_032821.2 T4477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:70897081 G>A maps to NM_032821.2 F3824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr16:70889140 C>T maps to NM_032821.2 K4110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:70841824 G>A maps to NM_032821.2 L5007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:70862323 G>T maps to NM_032821.2 L4706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:70913644 G>A maps to NM_032821.2 I3409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:125769317 C>T maps to NM_001134793.1 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:125769317 C>T maps to NM_001134793.1 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:118925352 T>C maps to NM_001130991.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:118919493 G>A maps to NM_001130991.1 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:118917499 T>C maps to NM_001130991.1 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:118917134 C>A maps to NM_001130991.1 E961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:95022437 G>A maps to ENST00000375660 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:95009820 G>A maps to ENST00000375660 R879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:95036764 G>A maps to ENST00000375660 N313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:95022464 G>A maps to ENST00000375660 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:220269470 C>A maps to NM_018060.3 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:220284257 G>A maps to NM_018060.3 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:88731792 G>A maps to NM_004967.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:88731867 G>A maps to NM_004967.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:88732920 C>T maps to NM_004967.3 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:88732593 C>T maps to NM_004967.3 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr4:88733022 C>T maps to NM_004967.3 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:82883145 G>A maps to NM_015525.2 T1245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:82906074 A>G maps to NM_015525.2 G1038G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:82949933 C>T maps to NM_015525.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:82904193 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:82937013 C>T maps to NM_015525.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:82924319 C>A maps to NM_015525.2 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:82933830 C>T maps to NM_015525.2 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:82900916 C>A maps to NM_015525.2 G1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:82924422 G>A maps to NM_015525.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:82943941 C>A maps to NM_015525.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZP-01A-21D-A10M-09 chr6:82950065 A>G maps to NM_015525.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:82906115 G>A maps to NM_015525.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:82924472 C>A maps to NM_015525.2 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:8153570 G>A maps to ENST00000422063 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:8260989 G>A maps to ENST00000422063 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:8268264 C>T maps to ENST00000422063 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:203682143 G>A maps to NM_138468.4 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:10394937 G>A maps to NM_000201.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:62082728 C>T maps to NM_001099789.1 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:62082589 G>A maps to NM_001099789.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:62081148 C>T maps to NM_001099789.1 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:10449541 G>A maps to NM_002162.3 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr19:10403522 C>T maps to NM_003259.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:52871164 G>A maps to NM_016513.4 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:52871164 G>A maps to NM_016513.4 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:52876591 A>C maps to NM_016513.4 Y489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:52878498 C>T maps to NM_016513.4 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr1:6285298 G>A maps to NM_012405.3 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:6285298 G>A maps to NM_012405.3 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:204801595 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr21:45656978 C>G maps to ENST00000400379 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr21:45649972 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:73017087 C>T maps to NM_001545.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:73017019 G>T maps to NM_001545.1 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:30193444 G>A maps to NM_002165.2 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:94223527 G>T maps to NM_004969.3 Y907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:94247009 C>T maps to NM_004969.3 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:94223527 G>A maps to NM_004969.3 Y907Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:209106814 G>A maps to NM_005896.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:209116254 G>A maps to NM_005896.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr2:209113296 G>A maps to NM_005896.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:90628079 C>T maps to NM_002168.2 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:90628112 G>A maps to NM_002168.2 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:78454688 G>A maps to NM_005530.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:78458532 G>A maps to NM_005530.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr20:2644816 T>C maps to NM_006899.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153051701 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:153052954 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:153052992 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153052537 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153053581 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:153053544 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:153051849 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:153051332 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153051810 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153056249 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:153055274 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:153051377 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:1065489 C>A maps to NM_033261.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:39782840 C>A maps to NM_002164.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:39782750 C>T maps to NM_002164.4 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:39785572 C>T maps to NM_002164.4 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:39775464 C>T maps to NM_002164.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:39782261 T>C maps to NM_002164.4 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:39785538 C>T maps to NM_002164.4 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr8:39781001 A>G maps to NM_002164.4 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:39871182 G>A maps to NM_194294.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr8:39873099 A>G maps to NM_194294.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:39840262 G>A maps to NM_194294.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:39862891 C>A maps to NM_194294.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:39847256 G>A maps to NM_194294.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:39840262 G>A maps to NM_194294.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:39871152 C>A maps to NM_194294.2 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr23:148586604 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:148564675 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:148571917 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:148585784 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:148571915 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:148586604 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:148585689 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:148564715 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:148579792 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:148584953 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:148564404 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:148579712 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:148568512 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:995271 G>A maps to NM_000203.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:996008 C>T maps to ENST00000453894 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:30711943 C>T maps to NM_003897.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:6657976 C>A maps to NM_001193457.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:6658969 G>A maps to NM_001193457.1 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:6664574 C>T maps to NM_001193457.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:158984676 C>T maps to ENST00000295809 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:159002360 G>A maps to ENST00000295809 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:94582184 G>A maps to ENST00000448882 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:18286485 C>T maps to NM_006332.3 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:41165617 C>T maps to NM_005533.4 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:41158985 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:79125146 C>T maps to NM_006417.4 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:79125146 C>T maps to NM_006417.4 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:79095506 G>A maps to NM_006820.2 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:79095452 A>C maps to NM_006820.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr1:79095581 C>T maps to NM_006820.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:79093950 G>A maps to NM_006820.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:79093888 G>T maps to NM_006820.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr1:79107235 G>A maps to NM_006820.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:163123733 G>A maps to NM_022168.2 C1018C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:163137870 C>T maps to NM_022168.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:91143945 G>A maps to NM_001010987.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:91066409 G>T maps to NM_001547.4 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:91099365 G>A maps to NM_001549.4 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:91099365 G>A maps to NM_001549.4 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:91178164 C>A maps to NM_012420.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:91177705 C>T maps to NM_012420.2 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:25699348 G>T maps to NM_001145728.1 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:25671819 A>G maps to NM_001145728.1 C366C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:25699312 G>A maps to NM_001145728.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:25679864 A>C maps to NM_001145728.1 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:21440916 G>A maps to NM_024013.1 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:21367942 G>A maps to NM_006900.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr9:21239376 C>T maps to NM_002172.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:21228152 A>C maps to NM_021268.2 L7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:21227959 G>A maps to NM_021268.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:21385070 G>T maps to NM_000605.3 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:21385295 G>A maps to NM_000605.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:21385307 T>C maps to NM_000605.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:21166380 G>T maps to NM_002175.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:21187353 G>A maps to NM_021068.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:21187347 G>A maps to NM_021068.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr9:21305114 G>A maps to NM_002169.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:21201627 T>C maps to NM_021057.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:21409743 G>T maps to NM_002170.3 *190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr9:21409402 C>A maps to NM_002170.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:34632959 C>A maps to NM_207585.1 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr21:34632953 A>G maps to NM_207585.1 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr21:34635804 A>G maps to NM_207585.1 *516W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:34635804 A>G maps to NM_207585.1 *516W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:21077805 G>T maps to NM_002176.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:21481666 A>C maps to NM_176891.4 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:68551972 C>A maps to NM_000619.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:68553344 A>G maps to NM_000619.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:68551692 C>T maps to NM_000619.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:137540443 T>C maps to NM_000416.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:137524735 A>G maps to NM_000416.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr21:34793828 G>A maps to ENST00000381995 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr21:34793915 T>G maps to ENST00000381995 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:34804515 A>G maps to ENST00000381995 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:34804626 C>T maps to ENST00000381995 Y254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:34804626 C>T maps to ENST00000381995 Y254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:27524856 G>T maps to NM_020124.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:27524879 C>T maps to NM_020124.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:27524633 A>G maps to NM_020124.2 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:21141308 G>T maps to NM_002177.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:21141284 G>T maps to NM_002177.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:112096971 G>A maps to NM_001007245.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr7:112112379 C>G maps to NM_001007245.2 S383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:112096079 G>T maps to NM_001007245.2 G75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:112096971 G>A maps to NM_001007245.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:112096971 G>A maps to NM_001007245.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:50326061 G>A maps to ENST00000336089 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:50325911 G>T maps to ENST00000336089 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:129200407 C>T maps to NM_052985.2 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:129236312 C>T maps to NM_052985.2 D1140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:129180094 C>A maps to NM_052985.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr16:1657231 C>T maps to NM_014714.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:1630770 G>A maps to NM_014714.3 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:1639742 G>A maps to NM_014714.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:1636256 G>A maps to NM_014714.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr16:1608120 G>A maps to NM_014714.3 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:27672397 C>A maps to NM_015662.1 E1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:37154435 G>A maps to ENST00000453009 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr11:118425752 G>A maps to NM_020153.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:118422966 T>C maps to NM_020153.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:118416177 C>T maps to NM_020153.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:118425221 C>T maps to NM_020153.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:42249519 G>A maps to NM_016004.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:107910481 G>A maps to ENST00000457963 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:107938331 A>T maps to ENST00000457963 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:107932785 C>A maps to ENST00000457963 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:27048144 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:26980602 T>G maps to NM_025103.2 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:27048261 T>C maps to NM_025103.2 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:27062664 T>C maps to NM_025103.2 N578N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr9:27048228 T>C maps to NM_025103.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:160099506 C>A maps to ENST00000326448 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:160073853 C>A maps to ENST00000483754 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:160037565 C>T maps to ENST00000483754 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:160000392 G>T maps to ENST00000483754 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr3:160073848 T>C maps to ENST00000483754 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:110584775 G>T maps to NM_014055.3 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:110618249 T>C maps to NM_014055.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:110570416 A>G maps to NM_014055.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:110630486 A>G maps to NM_014055.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr12:110643253 A>T maps to NM_014055.3 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr13:21215489 C>T maps to NM_175605.3 H554H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:21219085 T>G maps to NM_175605.3 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:21237728 G>T maps to NM_175605.3 E730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:21165122 A>C maps to NM_175605.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:69354374 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:69368657 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69370136 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69385710 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69354502 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69354499 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:69368673 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:69354514 A>C did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:69366574 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:69385723 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr15:65623541 C>T maps to NM_004884.3 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:65621805 C>T maps to NM_004884.3 E709E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:65682635 G>A maps to NM_020962.1 H755H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:65684565 G>A maps to NM_020962.1 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:65681637 G>A maps to NM_020962.1 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:99250953 G>A maps to NM_000875.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:99486165 C>T maps to NM_000875.3 R1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:99456485 C>A maps to NM_000875.3 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr15:99454553 C>T maps to NM_000875.3 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr15:99500562 G>T maps to NM_000875.3 G1332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:99454652 C>T maps to NM_000875.3 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:99456413 C>T maps to NM_000875.3 Y577Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:99460066 C>A maps to NM_000875.3 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:99442814 C>T maps to NM_000875.3 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:99486275 C>T maps to NM_000875.3 D1194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr15:99467106 G>T maps to NM_000875.3 G830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:99465634 C>T maps to NM_000875.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:99478203 C>T maps to NM_000875.3 N1036N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr11:2161481 G>A maps to NM_001127598.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:47121354 G>A maps to NM_006546.3 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:47075274 T>G maps to NM_006546.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:47121441 C>T maps to NM_006546.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:47123689 C>T maps to NM_006546.3 N532N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:47122408 G>A maps to NM_006546.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:185407234 C>T maps to NM_006548.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr7:23385593 A>G maps to NM_006547.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:160490921 C>T maps to NM_000876.2 A1425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr6:160479062 T>C maps to NM_000876.2 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:160454140 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:160455486 A>T maps to NM_000876.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:160468921 G>A maps to NM_000876.2 E776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:160501266 G>A maps to NM_000876.2 A1931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr6:160492997 G>A maps to NM_000876.2 W1500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:160489364 G>A maps to NM_000876.2 P1400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:160453725 A>C maps to NM_000876.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:160465615 C>T maps to NM_000876.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:160496916 A>G maps to NM_000876.2 P1735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr6:160500778 G>A maps to NM_000876.2 A1882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:160499381 G>A maps to NM_000876.2 T1822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:160468289 T>C maps to NM_000876.2 N717N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:160501308 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:160468921 G>A maps to NM_000876.2 E776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:160445698 G>A maps to NM_000876.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:160467665 G>A maps to NM_000876.2 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr6:160500625 G>A maps to NM_000876.2 S1831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:1841563 C>T maps to NM_001146006.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:45930177 G>A maps to NM_000596.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:45931559 C>T maps to NM_000596.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:217525358 C>T maps to NM_000597.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr2:217526639 G>A maps to NM_000597.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr7:45956826 C>T maps to NM_001013398.1 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:45956250 C>A maps to NM_001013398.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:45956179 G>A maps to NM_001013398.1 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38610178 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:38612717 T>C maps to NM_001552.2 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:38610199 C>T maps to NM_001552.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:217541494 G>A maps to NM_000599.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:53494637 G>A maps to NM_002178.2 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:38414135 G>T maps to NM_001007563.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:38414162 G>A maps to NM_001007563.1 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:46733386 C>A maps to NM_198541.1 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:46664105 C>T maps to NM_001002915.2 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:46543155 G>T maps to NM_001002923.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:201186556 C>A maps to NM_001164586.1 T3246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:201182345 C>T maps to NM_001164586.1 L2775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:201169469 C>T maps to NM_001164586.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:201195193 C>T maps to NM_001164586.1 L3577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr11:68704309 C>T maps to NM_002180.2 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:68696696 C>T maps to NM_002180.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:68675700 G>A maps to NM_002180.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:68703747 T>C maps to NM_002180.2 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:68707090 C>T maps to NM_002180.2 N958N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:68685275 G>T maps to NM_002180.2 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:130408126 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:130412498 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:130408140 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:130408832 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:130411912 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:130407782 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:130412501 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:130416509 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:130419944 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:130408127 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:130413261 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:130416440 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:130416449 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:130417101 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:130408758 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:130415775 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:130416549 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:130415766 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:130411007 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:130411832 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:130408126 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:130409130 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:130415766 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:130417062 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr23:130415642 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:130410117 C>T did not map to a codon.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr23:130411976 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:130408140 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:130408695 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:130412664 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:130408572 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:130409670 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:130413266 T>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:130408073 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:151154875 T>C maps to NM_178822.4 L2491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:151155400 T>C maps to NM_178822.4 R2316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:151171202 C>T maps to NM_178822.4 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:151166049 G>A maps to NM_178822.4 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:151164231 C>T maps to NM_178822.4 S1179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:151171534 G>T maps to NM_178822.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr3:151164291 G>A maps to NM_178822.4 N1159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:151164890 C>A maps to NM_178822.4 E960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr3:151166049 G>A maps to NM_178822.4 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr3:151171412 C>T maps to NM_178822.4 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:151164717 G>A maps to NM_178822.4 G1017G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:151164890 C>A maps to NM_178822.4 E960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:118644957 T>C maps to NM_152538.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr3:118647389 G>A maps to NM_152538.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:18618427 A>G maps to NM_032880.4 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr11:18735878 G>A maps to NM_173588.3 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:18727556 G>A maps to NM_173588.3 N1239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:18739553 G>A maps to NM_173588.3 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:18735672 T>C maps to NM_173588.3 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:18732262 A>G maps to NM_173588.3 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:18740215 G>A maps to NM_173588.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:18732322 G>A maps to NM_173588.3 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:18739490 C>T maps to NM_173588.3 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr11:18733913 G>A maps to NM_173588.3 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:117131529 A>G maps to NM_001542.2 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:117122061 G>A maps to NM_001542.2 L1116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr1:117131532 G>A maps to NM_001542.2 Y761Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr21:41151131 G>A maps to NM_001080444.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:160063800 G>T maps to NM_052868.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:159901255 G>A maps to NM_001135050.1 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:159901684 C>A maps to NM_001135050.1 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:159901640 G>A maps to NM_001135050.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:159898705 G>A maps to NM_001135050.1 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:159901258 C>A maps to NM_001135050.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:159900172 G>A maps to NM_001135050.1 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:159901335 G>A maps to NM_001135050.1 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:133799612 G>T maps to NM_014987.1 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:133792070 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:133799588 G>A maps to NM_014987.1 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr11:133807731 C>T maps to NM_014987.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:133795708 G>A maps to NM_014987.1 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:133805614 C>T maps to NM_014987.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:133806051 G>T maps to NM_014987.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:133801023 C>T maps to NM_014987.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:133790148 C>T maps to NM_014987.1 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:133790489 C>A maps to NM_014987.1 E1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:133807761 C>T maps to NM_014987.1 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr11:133790178 C>T maps to NM_014987.1 L1147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr5:140038907 C>T maps to NM_006083.3 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:99019779 G>T maps to NM_153687.2 Y354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:99007656 G>A maps to NM_201612.1 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr9:111640294 G>A maps to NM_003640.3 Q1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:111655307 G>A maps to NM_003640.3 N972N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:111641820 G>A maps to NM_003640.3 H1159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:42162711 G>A maps to NM_001556.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:42171926 C>T maps to NM_001556.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:42176811 C>T maps to NM_001556.2 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:42162727 G>T maps to NM_001556.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:42178257 C>T maps to NM_001556.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr8:42179635 C>T maps to NM_001556.2 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:42179459 C>T maps to NM_001556.2 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr8:42147733 G>A maps to NM_001556.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:42179576 C>T maps to NM_001556.2 R582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:42179984 G>A maps to NM_001556.2 E653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:42166538 C>T maps to NM_001556.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:42179653 G>T maps to NM_001556.2 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:206650091 C>A maps to NM_014002.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:206665013 G>A maps to NM_014002.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:206667273 G>A maps to NM_014002.3 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:206650073 C>T maps to NM_014002.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:206650050 C>T maps to NM_014002.3 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:206649638 C>T maps to NM_014002.3 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:206666691 C>T maps to NM_014002.3 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153770626 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153780302 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:153780300 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153780394 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153780391 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:50468243 C>T maps to NM_006060.3 N493N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:50444330 C>A maps to NM_006060.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:50367273 C>T maps to NM_006060.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:50444450 C>T maps to NM_006060.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:50444432 C>A maps to NM_006060.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:50367252 A>G maps to NM_006060.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:50468295 C>T maps to NM_006060.3 R511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:213921698 G>A maps to ENST00000342002 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr2:213921725 G>A maps to ENST00000342002 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:37922198 G>A maps to NM_012481.3 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:37949075 C>A maps to NM_012481.3 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:37948937 G>A maps to NM_012481.3 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr17:37922735 G>A maps to NM_012481.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:124753883 A>G maps to NM_022466.5 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:124754152 C>A maps to NM_022466.5 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:206943235 G>A maps to NM_000572.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:206945708 G>T maps to NM_000572.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:206943173 C>T maps to NM_000572.2 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:206944302 C>A maps to NM_000572.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:117870208 C>T maps to NM_001558.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr11:117870359 G>C did not map to a codon.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr11:117870446 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr11:117869600 C>T maps to NM_001558.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:117869686 G>A maps to NM_001558.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:117870142 C>A maps to NM_001558.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:34660442 C>A maps to NM_000628.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:34655473 C>T maps to ENST00000433395 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr9:34657552 A>G maps to NM_001142784.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:34655614 G>A maps to NM_001142784.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:34657071 C>T maps to NM_001142784.1 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr9:34657107 G>A maps to NM_001142784.1 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:158749490 G>A maps to NM_002187.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:158753766 G>T maps to NM_002187.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:158753730 G>A maps to NM_002187.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr19:18174728 C>T maps to NM_005535.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:18174742 G>A maps to NM_005535.1 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:18188465 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:67796419 C>A maps to NM_001559.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:67838134 C>T maps to NM_001559.2 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:67816653 C>T maps to NM_001559.2 H380H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:117900824 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:117900519 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:117900850 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:117925738 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:117892033 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:117925738 C>T did not map to a codon.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr23:117925739 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117895240 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:117875095 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:117895150 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:117895176 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:117925801 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117904555 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:117895130 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:117895258 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:114239851 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:114242604 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:114248404 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:114251803 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:114249051 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:114242566 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:114250257 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:6008165 G>A maps to NM_002189.3 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:81598383 C>T maps to NM_172217.3 R1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:81589279 G>A maps to NM_172217.3 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:81575052 C>T maps to NM_172217.3 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr15:81561923 C>T maps to NM_172217.3 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr15:81517982 G>A maps to NM_172217.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:81575013 C>T maps to NM_172217.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr6:52054068 G>A maps to NM_002190.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:148754105 A>G maps to NM_014443.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:17583193 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr22:17589914 C>T maps to NM_014339.5 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:53892774 C>T maps to NM_018725.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:9960202 C>T maps to NM_153461.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:9962251 C>T maps to NM_153461.2 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr3:9971764 C>T maps to NM_153461.2 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:57139995 C>T maps to NM_017563.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:57132008 G>T maps to NM_017563.3 Y574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:57139956 G>A maps to NM_017563.3 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr3:57132317 C>T maps to NM_017563.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:57139901 G>A maps to NM_017563.3 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:57132050 G>A maps to NM_017563.3 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:57148807 C>A maps to NM_017563.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr3:9953124 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:50436631 G>A maps to NM_001001694.2 C236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr22:50435487 C>T maps to NM_001001694.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:71712522 C>T maps to NM_001145057.1 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:102984393 G>A maps to NM_003855.2 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:103012989 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:103040774 A>G maps to NM_003853.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:103040385 C>T maps to NM_003853.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr2:103063590 T>C maps to NM_003853.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:207010133 G>T maps to NM_153758.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:113590269 G>A maps to NM_000576.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:113588107 G>A maps to NM_000576.2 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:113588107 G>A maps to NM_000576.2 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:113832799 A>G maps to NM_032556.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:102791953 C>A maps to NM_000877.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:102793014 G>A maps to NM_000877.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:102782725 G>T maps to NM_000877.2 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:102792130 A>G maps to ENST00000424272 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:190373676 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:190374359 G>A maps to NM_001167931.1 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:29686617 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:29959908 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:29972788 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:29301088 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:29301120 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:29959860 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:29959904 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:29973498 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:28807487 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:29301233 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:29938180 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:29973826 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:28807471 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:29417400 A>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:29972770 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:29973721 C>T did not map to a codon.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr23:29414418 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:29301119 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:29938064 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:29301120 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:29938173 T>G did not map to a codon.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr23:29973819 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:29973819 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:29301069 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:29973722 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:29973334 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:29973329 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:105011510 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:104999322 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105011594 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:104440221 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:104984675 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:105011617 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:105011229 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:104512092 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:105011354 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:105011601 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105011225 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105011243 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:104440222 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:104984615 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:104440352 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:104984660 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:102968092 G>A maps to NM_016232.4 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:102849438 C>T maps to NM_003854.2 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:102842361 G>A maps to NM_003854.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:102851708 G>A maps to NM_003854.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:102818140 G>A maps to NM_003854.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:102805707 G>A maps to NM_003854.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:123372933 A>G maps to NM_000586.3 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:207039323 C>T maps to NM_018724.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:207041889 G>A maps to NM_018724.3 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:137322748 G>T maps to NM_014432.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:137330411 G>T maps to ENST00000367746 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr6:137330453 C>T maps to NM_014432.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:137323264 C>T maps to NM_014432.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:136701097 G>A maps to NM_144717.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:136699422 C>T maps to NM_144717.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:27454355 C>T maps to NM_181079.4 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:27460099 C>T maps to NM_181079.4 Y393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:27445680 C>T maps to NM_181079.4 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr12:68646603 G>A maps to NM_020525.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:24447552 T>C maps to NM_021258.2 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:24447507 G>A maps to NM_021258.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:24448176 G>A maps to NM_021258.2 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:24448149 G>A maps to NM_021258.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:56733287 G>T maps to NM_016584.2 G81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:67635097 C>A maps to NM_144701.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:67724465 C>A maps to NM_144701.2 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:207073695 C>T maps to NM_001185156.1 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr1:207076379 G>A maps to NM_001185156.1 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:207075401 G>A maps to NM_001185156.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:68595838 C>A maps to NM_018402.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:68619371 C>T maps to NM_018402.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:28511052 G>A maps to NM_145659.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:28515321 C>T maps to NM_145659.3 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:14162975 G>A maps to NM_004843.2 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:14153272 G>A maps to NM_004843.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr19:14162733 G>A maps to NM_004843.2 W555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:24484171 G>A maps to NM_170743.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:24483700 G>A maps to NM_170743.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:39787084 G>A maps to NM_172140.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:6067922 C>A maps to NM_000417.2 G44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:6063597 G>A maps to NM_000417.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:37533662 G>A maps to ENST00000406505 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr22:37528468 C>T maps to ENST00000406505 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:70327659 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:70330098 T>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70329220 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70327597 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:70327597 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70328127 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70329107 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70330491 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70330934 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70329213 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70330088 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr23:70328193 G>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:70329191 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:70330937 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70331380 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:70328507 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:70330375 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:122657059 C>A maps to NM_001014336.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:55185835 C>T maps to NM_139017.4 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:55185890 C>T maps to NM_139017.4 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:55212883 C>A maps to NM_139017.4 S744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr5:55185890 C>T maps to NM_139017.4 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:3117466 G>A maps to ENST00000416912 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:6251253 C>A maps to NM_033439.3 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:70688525 G>A maps to NM_152456.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:1460690 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:1464312 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:1464254 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:1475187 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:1477754 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:1471267 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:1464267 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:1471354 T>C did not map to a codon.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr23:1467395 G>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:1471284 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:1471335 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:1471068 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:1464293 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:132009798 C>T maps to NM_000589.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:132018272 G>A maps to NM_000589.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:50397656 C>T maps to NM_172374.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:50398407 G>A maps to NM_172374.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:50399260 G>T maps to NM_172374.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:27357804 G>T maps to NM_000418.2 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr16:27375003 G>A maps to NM_000418.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:27367144 C>T maps to NM_000418.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr16:27353544 C>T maps to NM_000418.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:131879049 G>A maps to NM_000879.2 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:3116537 C>T maps to NM_000564.3 W368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:3139721 C>A maps to NM_000564.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr3:3144357 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:3146653 C>T maps to NM_000564.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:22767142 G>T maps to NM_000600.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:154406992 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr1:154427025 G>T maps to NM_000565.2 G377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:55247295 C>T maps to NM_002184.3 K612K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:55265399 A>T maps to NM_002184.3 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:55237254 G>A maps to NM_002184.3 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr5:55237110 A>G maps to NM_002184.3 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:55247318 C>A maps to NM_002184.3 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr8:79650846 A>G maps to NM_000880.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:35857129 C>T maps to NM_002185.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:35867467 C>T maps to NM_002185.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:35867626 G>A maps to ENST00000511982 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:35876395 T>C maps to NM_002185.2 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:35873649 G>A maps to NM_002185.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:35876449 G>A maps to NM_002185.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:35867470 G>A maps to NM_002185.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:35874623 C>T maps to NM_002185.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:74607284 G>T maps to NM_000584.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:155227415 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:155233395 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:155231144 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:155232663 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:155230993 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:155239483 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:155233374 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:155227374 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:155227383 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:155235058 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr3:121725877 C>T maps to ENST00000344209 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr3:121725955 C>T maps to ENST00000344209 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:121712605 G>T maps to ENST00000344209 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:121720677 C>T maps to ENST00000344209 W138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:121720275 G>T maps to ENST00000344209 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:153640117 G>A maps to NM_004515.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:10794043 C>T maps to NM_017620.2 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:10794617 C>T maps to NM_017620.2 Y681Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:10798322 G>A maps to NM_017620.2 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:6629278 C>T maps to NM_001014795.1 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:6631057 C>G maps to NM_001014795.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:6629700 C>T maps to NM_001014795.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:239090727 G>A maps to NM_030768.2 Q272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:239096821 G>A maps to NM_030768.2 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:239098613 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:239082245 G>A maps to NM_030768.2 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15226419 C>T maps to NM_006844.3 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr19:15234360 G>A maps to NM_006844.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr19:15226212 C>T maps to NM_006844.3 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:15226686 C>A maps to NM_006844.3 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:31455020 G>A maps to NM_144981.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:110603622 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr7:110303687 C>T maps to NM_032549.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:110603593 G>T maps to NM_032549.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:86400835 C>A maps to NM_006839.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:86406606 G>A maps to NM_006839.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:86378536 C>T maps to NM_006839.2 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:75931981 C>T maps to NM_018285.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:82598198 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:11999050 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:12030426 G>A maps to NM_014214.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:22028089 G>A maps to NM_018439.3 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr18:22008855 A>T maps to NM_018439.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:57878870 G>A maps to NM_017813.3 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:128036693 G>A maps to NM_000883.3 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:49065746 G>A maps to NM_000884.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:49066720 C>T maps to NM_000884.2 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:49062586 C>T maps to NM_000884.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:49062643 C>A maps to NM_000884.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr3:49061926 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:49065165 C>A maps to NM_000884.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr3:49065917 C>A maps to NM_000884.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:76640701 G>A maps to NM_001563.2 C737C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:76660407 G>T maps to NM_001563.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:76657049 G>A maps to NM_001563.2 Y675Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr6:76744411 G>A maps to NM_001563.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr6:76633350 C>T maps to NM_001563.2 K772K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:100949960 G>A maps to NM_016247.2 R1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:101038553 C>A maps to NM_016247.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:100976370 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:100963521 A>G maps to NM_016247.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:101023016 A>T maps to NM_016247.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:100961705 C>A maps to NM_016247.2 E950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr10:105037957 C>T maps to NM_032727.3 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:105048339 G>T maps to NM_032727.3 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:62330145 G>A maps to NM_176877.2 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:62367130 G>A maps to NM_176877.2 E1127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:62582248 C>T maps to NM_176877.2 A1567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:62545129 C>T maps to NM_176877.2 S1378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:62330182 G>T maps to NM_176877.2 E905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:62582809 C>T maps to NM_176877.2 Q1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:62237150 G>A maps to NM_176877.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:62330160 C>A maps to NM_176877.2 A897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:62327231 G>T maps to NM_176877.2 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:62299454 C>T maps to NM_176877.2 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:61919402 C>T maps to NM_001040694.1 G904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:61897922 C>T maps to NM_001040694.1 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:105174846 C>T maps to ENST00000252520 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:105179614 G>A maps to ENST00000252520 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:105179821 C>T maps to ENST00000252520 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105175986 C>T maps to ENST00000252520 R695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:105172393 C>T maps to ENST00000252520 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:105179821 C>T maps to ENST00000252520 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:111371783 G>A maps to NM_005537.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:111372143 G>A maps to NM_005537.3 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:111372063 G>T maps to NM_005537.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr13:111372116 C>T maps to NM_005537.3 C369C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr13:111372126 G>T maps to NM_005537.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr13:111365323 G>T maps to NM_198217.1 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:184431586 G>T maps to NM_001564.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:120609221 C>A maps to NM_019071.2 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:220439617 G>A maps to NM_002191.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:220439554 G>A maps to NM_002191.3 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:41730061 C>T maps to NM_002192.2 W156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:41729874 C>T maps to NM_002192.2 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr7:41739849 G>A maps to NM_002192.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:41739801 G>A maps to NM_002192.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:30793365 G>A maps to NM_006774.4 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:41348849 G>A maps to NM_017553.1 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:41364121 C>T maps to NM_017553.1 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:41339649 A>G maps to NM_017553.1 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr15:41319795 G>A maps to NM_017553.1 R1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:41387831 G>A maps to NM_017553.1 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr2:74683308 G>A maps to ENST00000452361 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:33059309 G>T maps to NM_001098817.1 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:206927769 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:206869529 G>A maps to NM_017759.4 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:30012330 C>A maps to NM_173618.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:191224854 C>T maps to NM_002194.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:191236071 G>T maps to NM_002194.3 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:99152614 G>A maps to NM_001134224.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:99136598 C>T maps to NM_001134224.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:99137181 G>T maps to NM_001134224.1 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:99198036 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:99137181 G>T maps to NM_001134224.1 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:99149900 T>C maps to NM_001134224.1 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr2:99182573 C>T maps to NM_001134224.1 R793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:143324147 A>G maps to NM_003866.2 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:143226666 A>G maps to NM_003866.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:143159139 A>C maps to NM_003866.2 L238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:143067024 G>T maps to NM_003866.2 S563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:143130162 C>A maps to NM_003866.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:143159104 G>A maps to NM_003866.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JS-01A-11D-A10B-09 chr4:143130126 G>A maps to NM_003866.2 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:143130162 C>A maps to NM_003866.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:143003275 C>T maps to NM_003866.2 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:143326388 C>T maps to NM_003866.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:143029297 G>A maps to NM_003866.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr4:143129593 G>A maps to NM_003866.2 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:134540402 C>T maps to NM_005539.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:134463949 G>T maps to NM_005539.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:38331552 G>A maps to ENST00000373026 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr1:38331537 G>C maps to ENST00000373026 A883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:38355259 C>A maps to ENST00000373026 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:38343868 A>G maps to ENST00000373026 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:233925236 G>T maps to ENST00000359570 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:234056166 C>T maps to ENST00000359570 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:234102602 C>T maps to ENST00000359570 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:234091071 C>A maps to ENST00000359570 I696I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:234107007 G>A maps to ENST00000359570 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr2:234112924 G>A maps to ENST00000359570 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr9:139324227 C>A maps to NM_019892.3 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:121569694 C>T maps to NM_014937.2 N551N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr10:121587115 C>T maps to NM_014937.2 R1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:121565907 G>A maps to NM_014937.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:121587395 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:121564922 G>A maps to NM_014937.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr10:121551600 C>A did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr10:121510591 T>C maps to NM_014937.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:31529642 C>A maps to ENST00000331075 I819I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:31529184 C>T maps to ENST00000331075 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:31529642 C>T maps to ENST00000331075 I819I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:1401328 C>T maps to NM_016532.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:1413054 G>A maps to NM_016532.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:1410317 C>T maps to NM_016532.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:71948266 G>A maps to NM_001567.3 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:71943738 C>T maps to NM_001567.3 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:71942193 C>T maps to NM_001567.3 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:71948242 C>A maps to NM_001567.3 A985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:71939396 G>A maps to NM_001567.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:71942079 G>A maps to NM_001567.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:71948374 C>T maps to NM_001567.3 H1029H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:71946493 C>T maps to NM_001567.3 Y886Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:71941404 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr11:71944185 G>A maps to NM_001567.3 W673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr11:71940255 C>A maps to NM_001567.3 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr11:2181138 C>T maps to NM_001185098.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:15197352 C>T maps to NM_001031853.3 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:15247256 C>T maps to NM_001031853.3 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:15247202 C>T maps to NM_001031853.3 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:15222371 G>A maps to NM_001031853.3 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:15197604 C>T maps to NM_001031853.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:15262047 C>T maps to NM_001031853.3 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:15262014 C>A maps to NM_001031853.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:15247226 C>A maps to NM_001031853.3 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:155100007 A>G maps to ENST00000344756 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:155093390 C>T maps to ENST00000344756 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:118864360 C>T maps to NM_016133.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:118865877 G>T maps to NM_016133.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:5231604 C>T maps to NM_002195.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:67263854 C>T maps to NM_005478.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:67263854 C>T maps to NM_005478.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:5164143 G>T maps to NM_007179.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:5185362 G>A maps to NM_007179.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:5185503 G>A maps to NM_007179.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:5185437 G>A maps to NM_007179.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:7120728 C>T maps to NM_000208.2 T1187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7122718 G>A maps to NM_000208.2 D1145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:7117279 G>A maps to NM_000208.2 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:7132247 G>A maps to NM_000208.2 Y921Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:7166225 C>T maps to NM_000208.2 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:7174602 G>A maps to NM_000208.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:7125479 G>A maps to NM_000208.2 T1024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:7168034 C>T maps to NM_000208.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr19:7119482 T>C maps to NM_000208.2 Q1257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr19:7166276 G>C maps to NM_000208.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156810697 G>A maps to NM_014215.2 D1287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156811199 G>T maps to NM_014215.2 G1216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156819236 G>A maps to NM_014215.2 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:156812300 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156819155 G>A maps to NM_014215.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:156823730 G>A maps to NM_014215.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:156821912 G>A maps to NM_014215.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:156821942 G>A maps to NM_014215.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:156813216 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:156821209 C>T maps to NM_014215.2 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:156819068 G>T maps to NM_014215.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:156810787 G>T maps to NM_014215.2 L1257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:156814385 G>A maps to NM_014215.2 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:156823661 G>A maps to NM_014215.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr1:156823973 G>A maps to NM_014215.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:156812264 T>C maps to NM_014215.2 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr7:1542642 G>T maps to ENST00000389470 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:1522286 G>A maps to ENST00000389470 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr7:1510581 G>A maps to ENST00000389470 A2333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr7:1538142 A>G maps to ENST00000389470 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:1529227 G>A maps to ENST00000389470 I880I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:1524820 A>C maps to ENST00000389470 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:1517489 G>T maps to ENST00000389470 A1786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr7:1510260 C>T maps to ENST00000389470 A2389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:1523450 G>A maps to ENST00000389470 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr7:1511260 C>G maps to ENST00000389470 L2281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:19703276 G>T maps to NM_018142.2 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:19681451 C>T maps to NM_018142.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:19682312 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:19684058 G>T maps to NM_018142.2 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr8:19687975 A>G maps to NM_018142.2 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:106614539 A>C maps to NM_020395.3 L138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:106613189 C>T maps to NM_020395.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:60003725 C>A maps to NM_020748.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:59949799 A>G maps to NM_020748.2 I876I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:59944757 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:59949654 C>A maps to NM_020748.2 E925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr17:59944941 T>A maps to NM_020748.2 I1197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:59999169 C>A maps to NM_020748.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:59984899 T>G maps to NM_020748.2 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:153736658 C>T maps to ENST00000428986 H630H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:153713124 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:153736331 C>A maps to ENST00000428986 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:153745424 G>A maps to ENST00000428986 A974A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:153737174 G>A maps to ENST00000428986 E646E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:153744346 G>A maps to ENST00000428986 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:153719801 C>T maps to ENST00000428986 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:153745127 G>A maps to ENST00000428986 T946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:77605370 A>G maps to NM_033547.3 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr11:77594923 C>T maps to NM_033547.3 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:77614591 C>T maps to NM_033547.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:62415820 G>A maps to NM_030628.1 N577N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr11:62417428 G>A maps to NM_030628.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr13:51941945 T>C maps to NM_012141.2 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:52025297 C>A maps to NM_012141.2 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:51939970 G>A maps to NM_012141.2 R861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:51969504 C>A maps to NM_012141.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:212193549 C>T maps to NM_015434.3 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:212184728 C>A maps to NM_015434.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:212156023 C>A maps to NM_015434.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:212180004 A>G maps to NM_015434.3 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:212141298 G>A maps to NM_015434.3 R679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:95850846 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:95853793 G>T maps to NM_017864.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:95885605 G>A maps to NM_017864.2 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:95888710 A>G maps to NM_017864.2 Q955Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:28625703 G>A maps to NM_018250.3 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:28628594 G>A maps to NM_018250.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:28627423 G>A maps to NM_018250.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr8:28638444 G>A maps to NM_018250.3 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:128577839 C>T maps to NM_015693.3 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:128590285 C>T maps to NM_015693.3 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:128627784 A>G maps to NM_015693.3 E644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:128609009 A>G maps to NM_015693.3 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:103054845 G>A maps to NM_014425.2 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr9:103055197 C>T maps to NM_014425.2 Q887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:103035244 C>T maps to NM_014425.2 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:103055257 C>T maps to NM_014425.2 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:103002491 C>T maps to NM_014425.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:103002389 C>T maps to NM_014425.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:49775853 G>A maps to NM_153273.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:48725888 G>T maps to ENST00000395509 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:48725765 G>T maps to ENST00000395509 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:33694610 G>A maps to NM_054111.4 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:33690742 G>T maps to NM_054111.4 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:33693310 G>A maps to NM_054111.4 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:154533945 C>T maps to NM_001130700.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:154481127 C>T maps to NM_001130700.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:154520982 C>T maps to NM_001130700.1 V243V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BG-A0MQ-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:154520991 C>T maps to NM_001130700.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr6:154533924 G>A maps to NM_001130700.1 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr10:60027272 C>T maps to NM_152230.4 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:59955856 G>A maps to NM_152230.4 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:59986888 A>C maps to NM_152230.4 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:61778971 A>G maps to NM_001134779.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr5:61826565 T>C maps to NM_001134779.1 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:61822042 G>A maps to NM_001134779.1 Q697Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:61832565 C>A maps to NM_001134779.1 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:44426860 G>A maps to NM_014652.3 E757E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:44432394 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:44422102 C>T maps to NM_014652.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:44433314 C>T maps to NM_014652.3 C951C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:44423120 T>C maps to NM_014652.3 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:44421994 C>T maps to NM_014652.3 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:44433132 T>C maps to NM_014652.3 P920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24655967 C>T maps to ENST00000458132 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24656956 A>G maps to ENST00000458132 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZP-01A-21D-A10M-09 chr14:24653952 G>C maps to ENST00000458132 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:24649725 G>A maps to ENST00000458132 T1058T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr13:98668013 C>T maps to NM_002271.4 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:98654811 C>T maps to NM_002271.4 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr13:98669038 C>T maps to NM_002271.4 F868F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:98645414 C>T maps to NM_002271.4 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:98654763 C>T maps to NM_002271.4 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:98655173 C>T maps to NM_002271.4 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:98637733 C>A maps to NM_002271.4 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:98668013 C>T maps to NM_002271.4 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:9457906 T>C maps to NM_006391.2 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:9455266 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:30805924 G>A maps to NM_006390.3 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:30818243 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:30805936 C>A maps to NM_006390.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:30819185 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:201832706 C>T maps to NM_018085.4 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:201843996 A>G maps to NM_018085.4 E957E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:201840305 C>T maps to NM_018085.4 F809F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:201832706 C>T maps to NM_018085.4 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:201826319 C>T maps to NM_018085.4 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr1:201843465 C>A maps to NM_018085.4 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:46193312 G>A maps to NM_005897.2 Y346Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:46206617 G>A maps to NM_005897.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:46206707 C>A maps to NM_005897.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:237233330 T>G maps to ENST00000457693 *831Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:237289279 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:237253211 G>A maps to ENST00000457693 N656N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:237396719 C>A maps to ENST00000457693 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:121491422 G>T maps to NM_001023570.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121489232 C>A maps to NM_001023570.2 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:32673224 C>T maps to NM_001160042.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr12:113633448 G>A maps to ENST00000416617 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:113645692 C>T maps to ENST00000416617 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:113645794 C>T maps to ENST00000416617 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr7:2632712 C>T maps to NM_152558.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:2611850 A>G maps to NM_152558.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:2625967 C>T maps to NM_152558.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr7:2629608 C>T maps to NM_152558.3 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:2622272 C>T maps to NM_152558.3 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:2617925 G>T maps to NM_152558.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:51937030 A>G maps to NM_152397.2 H26H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:51928929 A>G maps to NM_152397.2 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:51895691 C>T maps to NM_203424.1 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:51895691 C>T maps to NM_203424.1 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:51897000 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:51895691 C>T maps to NM_203424.1 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:197670735 C>T maps to NM_001134435.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:197659061 G>A maps to NM_001134435.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:197665621 C>T maps to NM_001134435.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:197618314 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:197619578 C>A maps to NM_001134435.1 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr15:67692529 C>A maps to NM_001031715.2 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:67629323 G>A maps to NM_001031715.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:67713869 G>A maps to NM_001031715.2 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:19746685 G>T maps to NM_153208.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:19775390 G>T maps to NM_153208.1 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:19867827 C>T maps to NM_153208.1 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:19746685 G>T maps to NM_153208.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:90991919 C>T maps to NM_003870.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:91009237 C>T maps to NM_003870.3 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:91025224 G>A maps to NM_003870.3 A1121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:91034717 G>T maps to NM_003870.3 E1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr15:91030270 C>T maps to NM_003870.3 D1370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:91030267 C>T maps to NM_003870.3 F1369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:91030267 C>T maps to NM_003870.3 F1369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr15:90999516 G>A maps to NM_003870.3 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:75885465 G>T maps to NM_006633.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:75970447 C>T maps to NM_006633.2 H1147H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:75964619 G>T maps to NM_006633.2 E932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr5:75871582 T>C maps to NM_006633.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:75993817 C>A maps to NM_006633.2 R1405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:75907008 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:75886363 G>T maps to NM_006633.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:75993844 C>T maps to NM_006633.2 R1414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr5:75885533 G>A maps to NM_006633.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:75991442 C>T maps to NM_006633.2 H1386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr5:75970369 C>A maps to NM_006633.2 I1121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:75888750 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156517978 G>A maps to NM_178229.4 N730N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156521850 A>G maps to NM_178229.4 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:156521764 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:156518181 G>C maps to NM_178229.4 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr1:156503613 A>G maps to NM_178229.4 H1309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:156534456 G>T maps to NM_178229.4 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:156498817 C>T maps to NM_178229.4 L1487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:156539205 A>G maps to NM_178229.4 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:12966082 G>A maps to ENST00000429247 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:12963729 G>A maps to ENST00000429247 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:12977153 A>G maps to ENST00000429247 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:12963666 A>G maps to ENST00000429247 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:12983223 G>A maps to ENST00000429247 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:12954972 G>A maps to ENST00000429247 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53268427 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53267431 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:53279931 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53264029 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53279764 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53267429 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:53280283 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr23:53270997 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53272618 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr23:53284061 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53272623 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:53264970 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:53264276 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53267392 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:53279552 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:53265010 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53263915 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53265630 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:248094 C>T maps to NM_001170738.1 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:274961 C>T maps to NM_001170738.1 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:266193 C>T maps to NM_001170738.1 C719C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:271212 C>A maps to NM_001170738.1 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:284039 C>T maps to NM_001170738.1 G1130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:247455 C>T maps to NM_001170738.1 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:266193 C>T maps to NM_001170738.1 C719C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:123152118 C>T maps to NM_178827.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:123149982 T>G maps to NM_178827.4 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:123143343 G>T maps to NM_178827.4 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:123152262 C>T maps to NM_178827.4 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:123092979 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:123105060 T>C maps to NM_178827.4 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:123143415 T>A maps to NM_178827.4 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:123152024 C>A maps to NM_178827.4 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153279716 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:153278086 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153278593 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153283516 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr23:153281961 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:10268099 C>T maps to NM_001570.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:66641569 C>T maps to NM_007199.2 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:66605325 A>G maps to NM_007199.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:66641945 G>T maps to NM_007199.2 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:66638337 C>T maps to NM_007199.2 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:44171543 C>A maps to NM_016123.3 C276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:44167809 C>T maps to NM_016123.3 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:78770657 C>T maps to NM_004136.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:78768615 A>G maps to NM_004136.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:78781053 C>T maps to NM_004136.2 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:78786284 C>T maps to NM_004136.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr5:131822681 G>T maps to NM_002198.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:185320224 G>A maps to NM_002199.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:185340701 G>A maps to NM_002199.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JS-01A-11D-A10B-09 chr4:185320123 C>T maps to NM_002199.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:185339722 G>A maps to NM_002199.3 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:46388372 C>T maps to NM_015649.1 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:46388051 C>T maps to NM_015649.1 W327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr19:46388269 G>A maps to NM_015649.1 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:46388581 G>A maps to NM_015649.1 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:397187 G>A maps to NM_002460.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:397163 G>A maps to NM_002460.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:393187 C>T maps to NM_002460.3 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:394838 G>T maps to NM_002460.3 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr7:128586056 C>T maps to NM_001098629.1 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:128582195 C>T maps to NM_001098629.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr7:128587311 A>G maps to NM_001098629.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:209969891 C>T maps to NM_006147.2 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:612680 G>A maps to NM_004031.2 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr16:85946828 G>A maps to NM_002163.2 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:85948085 G>A maps to NM_002163.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:24632350 C>T maps to NM_006084.4 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr19:44222988 G>A maps to NM_019612.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44223000 G>A maps to NM_019612.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:44222859 G>A maps to NM_019612.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44096975 A>G maps to NM_001007561.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:44097206 G>A maps to NM_001007561.2 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:44097443 C>T maps to NM_001007561.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:227662284 G>A maps to NM_005544.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:227662101 G>A maps to NM_005544.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:227660184 T>G maps to NM_005544.2 A1090A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:107977928 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:107976485 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr23:107977986 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107976062 T>C did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:107977086 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:107977758 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107975896 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107977578 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107976280 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107976871 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107978710 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:107976183 T>C did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:107975872 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr23:107976834 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:107975805 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:107977545 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107976896 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107977380 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:107975810 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:107976971 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:107978704 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr23:107975875 G>A did not map to a codon.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr23:107978446 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107977065 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107978763 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107979043 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107978667 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:107978586 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:107978632 A>T did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr23:107977582 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:107976743 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:107979286 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:107977280 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr5:3599445 C>T maps to NM_024337.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:3599685 C>T maps to NM_024337.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:3600750 G>A maps to NM_024337.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr5:3599604 G>A maps to NM_024337.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:3600334 G>T maps to NM_024337.3 G425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:2749802 C>T maps to NM_033267.4 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:2749748 G>A maps to NM_033267.4 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:2749655 G>A maps to NM_033267.4 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr5:2749778 G>A maps to NM_033267.4 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr5:2747695 G>A maps to NM_033267.4 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:2749568 G>A maps to NM_033267.4 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:2749790 G>A maps to NM_033267.4 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:1879663 G>A maps to NM_016358.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:1879927 G>A maps to NM_016358.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:1879774 G>A maps to NM_016358.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:1878853 G>A maps to NM_016358.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:54967586 C>T maps to NM_005853.5 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:54966804 C>T maps to NM_005853.5 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:54966720 C>T maps to NM_005853.5 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:55360345 C>T maps to NM_024335.2 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr16:55363170 C>T maps to NM_024335.2 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:55361503 C>T maps to NM_024335.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr9:88881106 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:949414 C>T maps to NM_005101.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:89182825 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:156697180 T>C maps to NM_030980.1 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:156697156 A>T maps to NM_030980.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:156697243 G>A maps to NM_030980.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr5:50685747 G>A maps to NM_002202.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:50685597 C>T maps to NM_002202.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:74467744 C>T maps to NM_201526.1 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr15:74467243 G>A maps to NM_201526.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:74467594 C>T maps to NM_201526.1 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:74425418 C>T maps to NM_001130137.1 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:74425184 C>T maps to NM_001130137.1 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr15:74425466 G>A maps to NM_001130137.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:74425595 C>T maps to NM_001130137.1 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:74427233 C>T maps to NM_001130137.1 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:13260507 C>A maps to NM_080826.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:13260441 C>T maps to NM_080826.1 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:77942417 G>A maps to NM_199296.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:77945058 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:77950875 C>T maps to NM_199296.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:77942072 C>T maps to NM_199296.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:77948713 C>T maps to NM_199296.2 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr14:77942009 G>A maps to NM_199296.2 N548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr14:77944648 G>A maps to NM_199296.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:77942411 G>A maps to NM_199296.2 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:77948806 T>C maps to NM_199296.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:16445745 C>A maps to NM_001101426.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:16298580 G>T maps to NM_001101426.3 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:128848974 G>A maps to ENST00000418265 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr3:128849473 G>A maps to ENST00000418265 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:18547676 G>T maps to NM_016368.4 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr19:18545800 C>T maps to NM_016368.4 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:18547670 C>T maps to NM_016368.4 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:18546719 G>A maps to NM_016368.4 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:33080314 G>T maps to ENST00000262650 E818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:33037248 G>T maps to ENST00000262650 E433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:47294541 G>A maps to NM_030790.3 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:47192819 G>T maps to NM_030790.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:2927441 C>T maps to NM_018463.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:310058 C>T maps to NM_032039.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:311464 C>T maps to NM_032039.2 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:314831 C>A maps to NM_032039.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:314617 C>T maps to NM_032039.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:304615 C>T maps to NM_032039.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:52183683 G>T maps to NM_181501.1 G271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:52206092 C>T maps to NM_181501.1 C567C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:145539390 T>C maps to NM_003637.3 T1020T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:145533485 C>T maps to NM_003637.3 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:68624345 G>A maps to ENST00000423218 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr15:68624738 G>A maps to ENST00000423218 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:68695354 G>T maps to ENST00000423218 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr15:68643628 G>A maps to ENST00000423218 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:68643054 G>A maps to ENST00000423218 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr15:68641179 C>T maps to ENST00000423218 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:68642967 G>A maps to ENST00000423218 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr15:68620497 G>A maps to ENST00000423218 C668C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:68631910 C>A maps to ENST00000423218 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:68642967 G>T maps to ENST00000423218 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:68595465 G>A maps to ENST00000423218 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:52344600 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:52379186 C>A maps to NM_002203.3 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:52338051 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:52351366 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:52369004 G>T maps to NM_002203.3 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:52367766 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:52370895 T>A maps to NM_002203.3 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:52344307 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:52360786 G>T maps to NM_002203.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:42458282 G>A maps to NM_000419.3 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:42453284 C>T maps to NM_000419.3 Q839Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:42462340 G>A maps to NM_000419.3 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:42453551 C>T maps to NM_000419.3 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:42454432 G>A maps to NM_000419.3 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:42461927 G>A maps to NM_000419.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:42461927 G>A maps to NM_000419.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr17:48154117 C>T maps to ENST00000505306 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:48155423 C>T maps to NM_002204.2 I718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:48149415 C>A maps to NM_002204.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:48153808 C>T maps to NM_002204.2 N598N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:48145640 C>T maps to NM_002204.2 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:182399042 T>C maps to NM_000885.4 F943F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr2:182360659 C>T maps to NM_000885.4 Y512Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:54795424 G>A maps to NM_002205.2 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:54797075 C>T maps to NM_002205.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:54797092 G>A maps to NM_002205.2 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr12:54803019 G>A maps to NM_002205.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:54803304 G>A maps to NM_002205.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:54793512 C>T maps to NM_002205.2 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:54802017 G>A maps to NM_002205.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:173356013 G>A maps to ENST00000264106 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:173354278 G>T maps to ENST00000264106 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:173351791 T>C maps to ENST00000264106 C671C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:173340370 C>A maps to ENST00000264106 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:173354278 G>T maps to ENST00000264106 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr12:56092630 G>A maps to ENST00000347027 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56094910 G>A maps to ENST00000347027 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr12:56090721 C>T maps to ENST00000347027 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:56082675 C>T maps to ENST00000347027 A1014A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr10:15714702 G>C maps to NM_003638.1 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:15649741 G>A maps to NM_003638.1 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:15600155 G>A maps to NM_003638.1 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:15688893 G>A maps to NM_003638.1 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr10:15730037 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:15634240 G>A maps to NM_003638.1 F758F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:15650255 G>A maps to NM_003638.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:37547524 G>A maps to NM_002207.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:37818989 G>A maps to NM_002207.2 K883K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:37565010 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:31405557 C>T maps to ENST00000444228 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:31435469 C>T maps to ENST00000444228 F1085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:31405650 C>T maps to ENST00000444228 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:31426281 C>T maps to ENST00000444228 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:31422819 C>T maps to ENST00000444228 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:31434446 C>A maps to ENST00000444228 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:31435263 C>T maps to ENST00000444228 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:31435263 C>T maps to ENST00000444228 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:3660422 T>C maps to NM_002208.4 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:3659186 C>T maps to NM_002208.4 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:3631412 C>A maps to NM_002208.4 E988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:30531227 C>T maps to NM_002209.2 Y1093Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:30506071 C>T maps to NM_002209.2 D468D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:30532868 G>A maps to NM_002209.2 P1132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:30505635 A>G maps to NM_002209.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:30531242 C>T maps to NM_002209.2 I1098I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:30507444 C>T maps to NM_002209.2 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:30506047 C>T maps to NM_002209.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:30490697 G>A maps to NM_002209.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:31338184 T>C maps to NM_001145808.1 F880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:31341691 G>T maps to NM_001145808.1 E1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:31335828 C>A maps to NM_001145808.1 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:31332854 G>T maps to NM_001145808.1 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:31341691 G>T maps to NM_001145808.1 E1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:31338178 C>T maps to NM_001145808.1 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:31342550 C>T maps to NM_001145808.1 V1115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:31273068 G>T maps to NM_001145808.1 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:31273103 G>A maps to NM_001145808.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:31284812 G>T maps to NM_001145808.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:31286868 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:31277439 G>A maps to NM_001145808.1 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:187514595 C>T maps to NM_002210.3 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:187521026 C>T maps to NM_002210.3 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:187529284 C>T maps to NM_002210.3 Q664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:187506229 G>A maps to NM_002210.3 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:187541574 G>A maps to NM_002210.3 A988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:187540402 T>C maps to NM_002210.3 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr16:31391379 C>T maps to NM_000887.3 P1018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:31391863 G>A maps to NM_000887.3 S1065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:31393225 T>G maps to NM_000887.3 *1164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr16:31384644 C>A maps to NM_000887.3 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr16:31374589 G>A maps to NM_000887.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr16:31384683 G>A maps to NM_000887.3 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:31367984 C>T maps to NM_000887.3 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr16:31384632 C>T maps to NM_000887.3 D810D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:33201015 G>A maps to ENST00000374956 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:33218761 G>A maps to ENST00000374956 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:9552495 G>A maps to NM_004763.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:70523533 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:70525032 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70522401 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70522356 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70524819 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:3939942 G>T maps to NM_170678.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr21:46308617 A>G maps to NM_000211.3 D690D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:46320324 G>A maps to NM_000211.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:46330267 C>T maps to NM_000211.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:46310003 G>A maps to NM_000211.3 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:46306324 G>A maps to NM_000211.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:46308683 C>T maps to NM_000211.3 E668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:46321550 C>T maps to NM_000211.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:46320234 G>A maps to NM_000211.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:45364458 T>C maps to NM_000212.2 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:45384955 G>T maps to NM_000212.2 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:45360793 C>T maps to NM_000212.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:45361815 G>A maps to NM_000212.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:45367135 C>A maps to NM_000212.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:45363781 C>A maps to NM_000212.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:45364440 G>A maps to NM_000212.2 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:45369719 G>A maps to NM_000212.2 W492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:45363781 C>T maps to NM_000212.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr17:45361920 G>A maps to NM_000212.2 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:45351854 C>T maps to NM_000212.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr1:63974240 A>G maps to ENST00000371092 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:63920056 C>A maps to ENST00000371092 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:63920560 C>T maps to ENST00000371092 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:63944459 C>A maps to ENST00000371092 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:73726521 G>A maps to NM_001005619.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:73751881 C>T maps to NM_001005619.1 C1536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:73752899 C>T maps to NM_001005619.1 I1654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:73738747 C>T maps to NM_001005619.1 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:73753533 C>T maps to NM_001005619.1 G1772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:73732133 C>T maps to NM_001005619.1 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:73725486 C>T maps to NM_001005619.1 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:73753141 C>T maps to NM_001005619.1 F1707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr17:73746834 C>T maps to NM_001005619.1 L1183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:73746855 C>T maps to NM_001005619.1 C1190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:73746786 C>T maps to NM_001005619.1 S1167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:124578152 C>T maps to NM_002213.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:124592336 C>A maps to NM_002213.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr3:124485193 T>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr3:124485151 G>A maps to NM_002213.3 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:160958312 A>G maps to NM_000888.3 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:160968662 C>A maps to NM_000888.3 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:20441520 C>T maps to NM_002214.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:102359118 T>C maps to NM_004791.1 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:102220182 C>A maps to NM_004791.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:102345046 T>C maps to NM_004791.1 C376C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:102250623 C>T maps to NM_004791.1 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:52819169 C>A maps to NM_002215.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52818480 C>A maps to NM_002215.2 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:52821098 C>T maps to NM_002215.2 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:52825803 G>A maps to NM_002215.2 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:52815984 C>T maps to NM_002215.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr10:7773960 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:7768993 C>T maps to NM_002216.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:7769070 G>A maps to NM_002216.2 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr10:7791260 C>T maps to NM_002216.2 F935F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:7747142 C>T maps to NM_002216.2 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr10:7780690 G>T maps to NM_002216.2 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr10:7755152 C>T maps to NM_002216.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:7745474 T>G maps to NM_002216.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr10:7791260 C>T maps to NM_002216.2 F935F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:7762889 C>T maps to NM_002216.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:52830582 C>T maps to NM_002217.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:52835098 C>A maps to NM_002217.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:52842603 C>T maps to NM_002217.3 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:52831849 C>T maps to NM_002217.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:52835038 C>T maps to NM_002217.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:52858578 G>T maps to ENST00000485816 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:52848016 A>G maps to ENST00000485816 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr3:52861122 G>A maps to ENST00000485816 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:52863280 G>T maps to ENST00000485816 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:52860583 G>A maps to ENST00000485816 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr3:52852194 C>T maps to ENST00000346281 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr3:52858869 C>T maps to ENST00000485816 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:7697596 C>T maps to ENST00000256861 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:7627888 G>A maps to ENST00000256861 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:7659203 C>A maps to ENST00000256861 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:7618929 G>T maps to ENST00000256861 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:7618674 G>A maps to ENST00000256861 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr10:7621857 G>A maps to ENST00000256861 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:156608059 G>A maps to NM_005546.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:156638375 G>T maps to NM_005546.3 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr5:156671409 G>A maps to NM_005546.3 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:156641221 T>C maps to NM_005546.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:160850376 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:160849190 C>T maps to NM_017625.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:160922439 C>A maps to NM_080878.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:78616600 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:78616846 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:78622662 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:78616661 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:78618552 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:78616843 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:78616852 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:78616949 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:78616669 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:78622681 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:78616936 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:78616958 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:48833070 G>T maps to NM_021999.4 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:48830414 G>T maps to NM_021999.4 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:48830476 T>C maps to NM_021999.4 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:231741675 C>T maps to NM_030926.4 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:93424558 G>A maps to NM_014216.4 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr14:93460300 C>T maps to NM_014216.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:41794638 C>T maps to NM_002220.1 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:226923524 C>T maps to NM_002221.3 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:226834980 G>A maps to NM_002221.3 F711F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:226827286 C>A maps to NM_002221.3 E842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:226923647 C>T maps to NM_002221.3 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:226924076 G>A maps to NM_002221.3 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:226924445 G>A maps to NM_002221.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr19:41245293 C>T maps to NM_025194.2 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:4699914 C>T maps to ENST00000356617 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:4714882 C>A maps to ENST00000356617 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:4741561 C>T maps to ENST00000356617 I1487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:4836839 G>A maps to ENST00000356617 A2298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:4699824 C>T maps to ENST00000356617 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:4767258 C>A maps to ENST00000356617 A1718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:4730240 C>T maps to ENST00000356617 C1251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:4738853 C>T maps to ENST00000356617 F1431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:4726860 C>T maps to ENST00000356617 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:4852969 G>T maps to ENST00000356617 E2430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:4716843 C>T maps to ENST00000356617 D893D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:4842202 G>T maps to ENST00000356617 R2340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:4687138 C>T maps to ENST00000356617 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:4752142 C>T maps to ENST00000356617 G1655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:4767255 C>T maps to ENST00000356617 N1717N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:4699831 C>T maps to ENST00000356617 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:4854914 G>T maps to ENST00000356617 E2518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:4854853 C>T maps to ENST00000356617 F2497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr3:4824379 G>A maps to ENST00000356617 A2153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr3:4878582 G>A maps to ENST00000356617 T2716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr3:4722337 C>T maps to ENST00000356617 S1019S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:4821244 G>A maps to ENST00000356617 S2099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:4732934 C>T maps to ENST00000356617 H1308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr3:4825555 C>T maps to ENST00000356617 D2187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr3:4808356 C>T maps to ENST00000356617 D1892D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:4817093 G>T maps to ENST00000356617 E2046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr3:4735412 C>T maps to ENST00000356617 D1419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:4735355 C>A maps to ENST00000356617 I1400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:26640040 G>A maps to NM_002223.2 D1838D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:26647175 A>G maps to NM_002223.2 D1760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:26755428 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:26640117 G>A maps to NM_002223.2 R1813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:26877665 C>A maps to NM_002223.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:26634108 T>G maps to NM_002223.2 I2026I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:26875422 C>T maps to NM_002223.2 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr12:26709302 T>A maps to NM_002223.2 V1609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr12:26572095 C>T maps to NM_002223.2 T2332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr12:26755311 G>A maps to NM_002223.2 P1223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:26812091 C>A maps to NM_002223.2 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:26781065 C>T maps to NM_002223.2 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:33645384 G>A maps to ENST00000374316 L1209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr6:33660629 G>A maps to ENST00000374316 Q2528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:33654848 C>T maps to ENST00000374316 R2015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:33630714 G>T maps to ENST00000374316 G296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:33661430 G>A maps to ENST00000374316 K2578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:33638955 G>A maps to ENST00000374316 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:33647658 C>T maps to ENST00000374316 L1325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:33641983 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:33634928 G>A maps to ENST00000374316 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:33636933 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:33632852 G>A maps to ENST00000374316 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:33656125 C>T maps to ENST00000374316 D2162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:33634928 G>A maps to ENST00000374316 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr10:106074609 G>A maps to NM_033397.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:106074372 G>A maps to NM_033397.2 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:106075745 G>A maps to NM_033397.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:106075599 C>T maps to NM_033397.2 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr10:106074996 G>A maps to NM_033397.2 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:96993025 C>T maps to ENST00000420728 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:96992668 C>T maps to ENST00000420728 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:96992563 C>T maps to ENST00000420728 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr2:96993610 C>T maps to ENST00000420728 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:19127111 C>T maps to NM_001034841.3 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:35195905 C>T maps to NM_003024.2 G1044G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:35144423 C>T maps to NM_003024.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:35237481 C>T maps to NM_003024.2 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:35237631 C>T maps to NM_003024.2 F1356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:35237481 C>T maps to NM_003024.2 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:35169760 C>T maps to NM_003024.2 H677H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:35202042 G>A maps to NM_003024.2 E1115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:35124113 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:35134257 A>G maps to NM_003024.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr21:35107495 C>T maps to NM_003024.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr21:35199156 A>G maps to NM_003024.2 G1073G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:35190611 T>C maps to NM_003024.2 P923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:24443777 G>T maps to NM_147152.2 I1245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:24426613 G>A maps to NM_006277.2 R1659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:24509130 C>A maps to NM_006277.2 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:24440836 C>A maps to NM_006277.2 E1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:24469746 G>A maps to NM_006277.2 R1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:24475237 G>A maps to NM_006277.2 N1032N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:24494739 G>A maps to NM_006277.2 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:24435521 T>C maps to NM_006277.2 R1362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:24522990 C>T maps to NM_006277.2 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:24469130 G>A maps to NM_006277.2 F1148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:24509154 C>A maps to NM_006277.2 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:40702992 G>A maps to NM_002225.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:40702917 C>A maps to NM_002225.3 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:152882788 G>A maps to NM_005547.2 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:152883037 C>A maps to NM_005547.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:152883758 C>T maps to NM_005547.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:152882506 G>A maps to NM_005547.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:152883127 C>T maps to NM_005547.2 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:185268899 C>T maps to NM_006469.4 W539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:185270587 G>A maps to NM_006469.4 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:185270182 G>A maps to NM_006469.4 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:128263073 A>G maps to NM_017969.2 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:150715303 T>C maps to NM_203395.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:150710530 C>A maps to NM_203395.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:150713565 C>A maps to NM_203395.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:150690235 C>T maps to NM_203395.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:150690235 C>T maps to NM_203395.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:49246711 G>A maps to NM_182575.2 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:49247788 G>T maps to NM_182575.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr19:49245130 C>T maps to NM_182575.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:49246747 G>A maps to NM_182575.2 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:49245181 C>T maps to NM_182575.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr20:10633169 C>A maps to NM_000214.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:10620232 C>T maps to NM_000214.2 P1190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:10621548 C>T maps to NM_000214.2 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:10621521 G>A maps to NM_000214.2 I1036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:10621880 C>T maps to NM_000214.2 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:10622143 G>A maps to NM_000214.2 N960N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr20:10653354 G>A maps to NM_000214.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr20:10639251 G>A maps to NM_000214.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:105612990 G>T maps to NM_002226.3 R850R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:105617713 C>T maps to NM_002226.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr14:105615412 G>A maps to NM_002226.3 C589C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:9934962 T>C maps to NM_032492.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr3:9932417 A>G maps to NM_032492.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:65321198 C>T maps to NM_002227.2 K547K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:65332776 C>T maps to NM_002227.2 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:65335120 G>A maps to NM_002227.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:65332728 G>T maps to NM_002227.2 Y270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:65348958 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:65311308 C>A maps to NM_002227.2 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:65301898 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr1:65307172 G>A maps to NM_002227.2 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr1:65304195 G>A maps to NM_002227.2 N973N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:65303757 G>A maps to NM_002227.2 Y999Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:5054775 A>G maps to NM_004972.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:5069952 G>A maps to NM_004972.3 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:5055757 A>G maps to NM_004972.3 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:5022007 G>A maps to NM_004972.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:5066738 C>T maps to NM_004972.3 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:5081741 G>T maps to NM_004972.3 E818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:5050745 G>T maps to NM_004972.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:5054767 G>T maps to NM_004972.3 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:5090885 G>T maps to NM_004972.3 E1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:5044401 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:5126392 G>T maps to NM_004972.3 E1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr9:5080678 T>C maps to NM_004972.3 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr19:17937659 G>A maps to NM_000215.3 S1089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:17945530 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:17937710 C>T maps to NM_000215.3 E1072E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:17946812 G>A maps to NM_000215.3 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:17945446 G>T maps to NM_000215.3 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr19:17941384 G>C maps to NM_000215.3 S1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:6043909 C>T maps to NM_001099433.1 K691K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:6086577 C>A maps to NM_001099433.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:6114489 G>A maps to NM_001099433.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:6087176 G>A maps to NM_001099433.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr4:6107415 C>T maps to NM_001099433.1 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:147040560 C>A maps to NM_014790.3 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:147040783 G>T maps to NM_014790.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:147040923 C>A maps to NM_014790.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:147051353 G>A maps to NM_014790.3 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:147019274 C>A maps to NM_014790.3 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:147019323 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:147040923 C>A maps to NM_014790.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:146997515 C>T maps to NM_014790.3 Q768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:147040744 T>C maps to NM_014790.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:133955540 C>T maps to NM_001105521.2 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr10:133950771 C>T maps to NM_001105521.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:133978171 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:133980484 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr10:133967267 C>T maps to NM_001105521.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr21:27081747 G>T maps to NM_021219.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:27081747 G>T maps to NM_021219.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:134019072 C>A maps to NM_032801.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:134014867 A>G maps to NM_032801.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:134015899 C>T maps to NM_032801.3 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:134014271 C>T maps to NM_032801.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:134018493 A>G maps to NM_032801.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:134014229 C>T maps to NM_032801.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr6:15511535 T>C maps to NM_004973.2 I952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:15374448 G>A maps to NM_004973.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:15452402 C>T maps to NM_004973.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:15501453 C>T maps to NM_004973.2 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:15507579 T>C maps to NM_004973.2 H888H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:15497012 C>T maps to NM_004973.2 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:15501282 G>A maps to NM_004973.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:15501453 C>T maps to NM_004973.2 F754F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:139801845 G>A maps to NM_030647.1 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr7:139796397 A>G maps to NM_030647.1 H777H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:59967912 C>T maps to ENST00000356057 Y229Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:59961844 C>T maps to ENST00000356057 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:59965468 C>T maps to ENST00000356057 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:59951312 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:64950713 T>C maps to NM_032776.1 L2077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:64957267 A>G maps to NM_032776.1 C1849C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:64974824 G>A maps to NM_032776.1 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:64967055 A>T maps to NM_032776.1 L1458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:64974534 C>T maps to NM_032776.1 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr10:64974657 T>C maps to NM_032776.1 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:64973313 A>G maps to NM_032776.1 H871H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:64974678 G>T maps to NM_032776.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr10:64974234 G>A maps to NM_032776.1 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr10:64957237 G>A maps to NM_032776.1 V1859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:227921360 G>T maps to NM_023007.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:27225021 C>T maps to NM_001145348.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:27230431 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:74714846 G>A maps to NM_001081461.1 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr15:42135903 C>T maps to NM_005090.3 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:42132761 G>A maps to NM_005090.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:42139692 C>T maps to NM_005090.3 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:42131056 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:42131205 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr15:42133285 C>T maps to NM_005090.3 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:42135888 C>T maps to NM_005090.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:42134746 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:42127281 C>T maps to NM_005090.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr15:42127332 G>A maps to NM_005090.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr15:42131175 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:733165 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:78608306 C>T maps to NM_152405.4 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:78586053 T>C maps to NM_152405.4 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr5:78610591 A>G maps to NM_152405.4 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:78596079 C>A maps to NM_152405.4 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:78573809 C>T maps to NM_152405.4 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:78596068 C>T maps to NM_152405.4 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:78611995 G>T maps to NM_152405.4 E945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:39085018 G>A maps to NM_014876.5 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:51013621 G>A maps to NM_138334.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr8:75157399 G>A maps to NM_020647.2 Y423Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:75227355 G>A maps to NM_020647.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:75227556 G>T maps to NM_020647.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:75227153 C>A maps to NM_020647.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr20:42788454 G>A maps to NM_020433.4 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr20:42744388 A>G maps to NM_020433.4 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:87678542 G>A maps to NM_020655.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:87717828 C>A maps to NM_020655.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:87678380 C>T maps to NM_020655.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:87678245 C>A maps to NM_020655.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:87636892 C>T maps to NM_020655.2 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24040211 G>T maps to NM_032452.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:143746976 C>T maps to NM_003724.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:143746001 C>T maps to NM_003724.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:143747020 C>A maps to NM_003724.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:96124635 C>T maps to NM_003772.3 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:96124379 G>A maps to NM_003772.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:2254234 G>A maps to NM_144616.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:153947268 G>A maps to NM_006694.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:39919432 G>A maps to NM_021991.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:39920982 T>G maps to NM_021991.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr17:39923648 G>A maps to NM_021991.2 Y297Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:39913717 G>A maps to NM_021991.2 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:39914742 C>A maps to NM_021991.2 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:8504915 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:8565162 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:8521995 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:8538611 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:8504976 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:8536292 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:8565126 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:8507776 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:8667762 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr23:8502452 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:8565161 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr23:8522044 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:8591708 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:8553318 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:8538693 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:8555891 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:8504958 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:124438022 T>C maps to NM_001024660.3 C2889C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:124129084 C>T maps to ENST00000393499 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:124165104 C>T maps to NM_001024660.3 F1135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:124209703 G>A maps to NM_001024660.3 T1518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:124352734 G>T maps to NM_001024660.3 E1834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:124174167 C>T maps to NM_001024660.3 R1231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:124431973 C>A maps to NM_001024660.3 I2756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:124438116 G>T maps to NM_001024660.3 E2921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:123946903 C>T maps to NM_001024660.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:124053222 C>T maps to NM_001024660.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:124386001 C>A maps to NM_001024660.3 V2224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:124393287 C>A maps to NM_001024660.3 I2340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr3:124103813 C>T maps to NM_001024660.3 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr3:124017732 G>A maps to NM_001024660.3 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:124418770 C>T maps to NM_001024660.3 I2629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr9:732557 G>A maps to NM_015158.2 R1062R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:712028 C>A maps to NM_015158.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:730165 C>T maps to NM_015158.2 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:712001 C>T maps to NM_015158.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:742406 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:745198 G>A maps to NM_015158.2 T1341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr9:738310 C>T maps to NM_015158.2 H1120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:711731 G>A maps to NM_015158.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:712208 T>C maps to NM_015158.2 H481H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr9:740852 C>T maps to NM_015158.2 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr19:11289253 T>C maps to NM_015493.6 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:11289064 G>T maps to NM_015493.6 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:8398987 G>T maps to NM_198471.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:8389341 G>A maps to NM_198471.2 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:62734110 G>A maps to NM_181712.4 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:62737154 G>A maps to NM_181712.4 N669N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:62703950 A>G maps to NM_181712.4 *996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:62734037 G>A maps to NM_181712.4 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:62737148 C>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:62739622 G>A maps to NM_181712.4 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:75665624 G>A maps to NM_001130089.1 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:75662541 C>T maps to NM_001130089.1 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:75670404 G>A maps to NM_001130089.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr17:40269515 C>T maps to NM_021078.2 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:40271682 C>T maps to NM_021078.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr17:40269587 G>A maps to NM_021078.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:40270018 C>T maps to NM_021078.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:40266993 G>A maps to NM_021078.2 Y645Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:20142826 G>T maps to NM_003884.4 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:20167576 G>T maps to NM_003884.4 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:20167606 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:65480973 G>A maps to NM_182710.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:65480931 G>A maps to NM_182710.1 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:149916231 T>C maps to NM_007044.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:149919453 A>G maps to NM_007044.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:149925800 G>A maps to NM_007044.2 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:30815148 A>G maps to NM_032116.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:30804707 C>T maps to NM_032116.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr13:30829607 A>G maps to NM_032116.3 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:44627363 C>T maps to ENST00000356157 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:44593466 G>T maps to ENST00000356157 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:44625656 C>T maps to ENST00000356157 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:44595964 C>T maps to ENST00000356157 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:57775611 G>A maps to NM_005886.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr16:57789113 C>T maps to NM_005886.2 N460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:57789047 G>A maps to NM_005886.2 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:15287358 G>T maps to NM_201628.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:15390099 G>A maps to NM_201628.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:15439012 C>T maps to NM_201628.2 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:15392235 C>T maps to NM_201628.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:15392181 C>T maps to NM_201628.2 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:15430589 C>T maps to NM_201628.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:127642360 A>T maps to NM_207335.2 K153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:127642522 G>T maps to NM_207335.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr7:32919167 A>G maps to NM_015483.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:105924878 A>G maps to NM_198439.2 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:105924349 G>A maps to NM_198439.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:47594832 G>T maps to NM_018095.4 C418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:47594891 G>A maps to NM_018095.4 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:47597249 A>G maps to NM_018095.4 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:47600557 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:42727391 C>T maps to NM_152393.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:42727694 C>T maps to NM_152393.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:42729741 G>T maps to NM_152393.2 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:42729653 G>A maps to NM_152393.2 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:42727736 G>A maps to NM_152393.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:41705200 G>A maps to NM_152903.4 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr13:41704934 G>A maps to NM_152903.4 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:41705200 G>A maps to NM_152903.4 R483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:41767916 G>T maps to NM_032138.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr13:41767895 T>C maps to NM_032138.4 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:41768222 G>A maps to NM_032138.4 Y57Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:41768246 C>T maps to NM_032138.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:67054473 G>A maps to NM_032505.2 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:67054614 A>C maps to NM_032505.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:67049547 G>T maps to NM_032505.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:85273244 C>T maps to NM_020122.4 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:85255046 C>T maps to NM_020122.4 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:85255078 C>T maps to NM_020122.4 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr2:85276555 C>A maps to NM_020122.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:5021266 C>T maps to NM_000217.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:5021062 C>T maps to NM_000217.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:5021623 C>T maps to NM_000217.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr12:5020636 C>T maps to NM_000217.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:5020711 G>A maps to NM_000217.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:5021722 C>T maps to NM_000217.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:111061202 G>A maps to NM_005549.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr1:111060344 C>T maps to NM_005549.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:111147158 G>A maps to NM_004974.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:111216033 G>A maps to NM_002232.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:111216075 T>C maps to NM_002232.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:111216707 G>A maps to NM_002232.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:111215835 G>A maps to NM_002232.3 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:111216879 G>A maps to NM_002232.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:111216984 G>A maps to NM_002232.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:111216507 G>A maps to NM_002232.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:111216984 G>A maps to NM_002232.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:111217086 G>A maps to NM_002232.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr11:30033154 G>T maps to NM_002233.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:5154344 C>T maps to NM_002234.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:5154059 G>A maps to NM_002234.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:5154510 C>T maps to NM_002234.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:5154290 C>T maps to NM_002234.2 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr12:5153591 C>A maps to NM_002234.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:5153715 C>T maps to NM_002234.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:5154074 C>T maps to NM_002234.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr12:5154641 C>T maps to NM_002234.2 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:5154116 C>A maps to NM_002234.2 C268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:4919423 C>T maps to NM_002235.3 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:4920502 T>C maps to NM_002235.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:4919602 G>A maps to NM_002235.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:4919848 C>A maps to NM_002235.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:4920337 G>A maps to NM_002235.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:4919653 G>A maps to NM_002235.3 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:4919545 C>T maps to NM_002235.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:4920394 C>T maps to NM_002235.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:49573955 G>A maps to NM_031886.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:155860999 C>T maps to NM_003471.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:156249235 C>T maps to NM_172159.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:155861159 G>T maps to NM_003471.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:6155644 C>T maps to NM_003636.3 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:6142304 C>T maps to NM_003636.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:6142304 C>T maps to NM_003636.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7829265 C>T maps to NM_004732.2 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7829018 G>A maps to NM_004732.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:7830992 A>G maps to NM_004732.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:47989644 C>A maps to NM_004975.2 E818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:48098665 C>A maps to NM_004975.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:47991394 G>A maps to NM_004975.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:47991436 G>A maps to NM_004975.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:48098750 C>T maps to NM_004975.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:47990587 G>T maps to NM_004975.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr20:47991189 G>A maps to NM_004975.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:47991268 G>T maps to NM_004975.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:47991331 C>T maps to NM_004975.2 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:73848499 C>T maps to NM_004770.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:73480361 C>A maps to NM_004770.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:73848927 C>T maps to NM_004770.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr8:73849032 C>T maps to NM_004770.2 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:73849014 C>T maps to NM_004770.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:73848531 C>T maps to NM_004770.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:73848393 C>A maps to NM_004770.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:17793312 C>T maps to NM_001112741.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:17757836 C>T maps to NM_001112741.1 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:17793306 G>A maps to NM_001112741.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr11:17793414 C>T maps to NM_001112741.1 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:17793786 G>A maps to NM_001112741.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr11:17757887 C>T maps to NM_001112741.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr12:75444551 G>A maps to NM_139137.2 N411N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr12:75444733 T>G maps to NM_139137.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:75436910 G>A maps to NM_139137.2 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:75444935 C>T maps to NM_139137.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:75444533 C>T maps to NM_139137.2 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr12:75442062 C>T maps to NM_139137.2 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:50827027 G>A maps to NM_004977.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr19:50827144 G>A maps to NM_004977.2 C355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:110766211 G>A maps to NM_004978.4 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:110775554 G>A maps to NM_001039574.2 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:110754615 C>T maps to NM_004978.4 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:110766331 C>T maps to NM_004978.4 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:48826585 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48823115 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:48826119 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48823055 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48823364 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48823446 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48823247 C>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48823508 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48826269 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48826499 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:48826087 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48826149 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:48825858 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr23:48826420 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:48823128 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr7:119915273 C>T maps to NM_012281.2 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:119915168 C>A maps to NM_012281.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:119915021 C>A maps to NM_012281.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:119915072 C>T maps to NM_012281.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:119915258 G>A maps to NM_012281.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:120385850 C>T maps to NM_012281.2 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr7:119915012 C>T maps to NM_012281.2 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:119915652 G>T maps to NM_012281.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:119915337 G>T maps to NM_012281.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:120385962 C>T maps to NM_012281.2 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:119915021 C>T maps to NM_012281.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:119915039 A>G maps to NM_012281.2 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:119915652 G>T maps to NM_012281.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:119915633 A>G maps to NM_012281.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr7:119915537 C>T maps to NM_012281.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:112525297 G>A maps to ENST00000315987 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:112524607 C>T maps to ENST00000315987 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:112524652 C>T maps to ENST00000315987 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:112319679 G>A maps to ENST00000315987 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr1:112524889 C>T maps to ENST00000315987 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:11052695 G>C maps to NM_002236.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr2:11053709 C>T maps to NM_002236.4 N386N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:11052827 G>A maps to NM_002236.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:11053301 C>T maps to NM_002236.4 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:49626089 G>A maps to ENST00000396017 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:77659089 C>T maps to NM_012283.1 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:77659107 C>T maps to NM_012283.1 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:42671673 G>A maps to NM_133329.5 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:84256575 G>A maps to NM_172347.2 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:211263967 T>C maps to NM_172362.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:210971024 C>T maps to NM_172362.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:210857437 C>A maps to NM_172362.2 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:211280623 C>A maps to NM_172362.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:211192436 G>T maps to NM_172362.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:210977485 G>A maps to NM_172362.2 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:150648173 C>T maps to NM_000238.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr7:150642532 G>A maps to NM_000238.2 R1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr7:150649876 C>T maps to NM_000238.2 W398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr12:49935491 C>T maps to NM_012284.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr12:49938133 C>T maps to NM_012284.1 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:49937696 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:49938097 C>T maps to NM_012284.1 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:40328102 G>A maps to NM_012285.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:40321494 C>T maps to NM_012285.2 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:40318549 G>A maps to NM_012285.2 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:40327754 C>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:40328111 G>T maps to NM_012285.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr17:40328189 G>A maps to NM_012285.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:63174948 G>A maps to NM_139318.3 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:63473111 G>A maps to NM_139318.3 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:63269214 G>A maps to NM_139318.3 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:63174831 G>A maps to NM_139318.3 N787N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:63316553 A>G maps to NM_139318.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:61613095 C>T maps to NM_030779.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:61619614 C>A maps to NM_030779.2 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:163253365 A>G maps to NM_033272.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:163393433 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:163236427 G>A maps to NM_033272.2 T1022T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A1DQ-01A-11D-A135-09 chr2:163228549 G>C maps to NM_033272.2 S1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:163292017 G>A maps to NM_033272.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:163228386 G>A maps to NM_033272.2 I1181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:163374591 G>A maps to NM_033272.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:163279812 G>A maps to NM_173162.1 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:163361150 G>T maps to NM_033272.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:163374285 G>A maps to NM_033272.2 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr2:163302757 G>A maps to NM_033272.2 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:163241267 C>T maps to NM_033272.2 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:19492777 C>A maps to NM_144633.2 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:19492883 C>T maps to NM_144633.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:19479729 C>T maps to NM_144633.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr3:19436651 G>A maps to NM_144633.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:19295354 G>T maps to NM_144633.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:19295272 G>A maps to NM_144633.2 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr3:19554676 G>A maps to NM_144633.2 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:170148873 C>T maps to NM_001034837.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:170159895 C>T maps to NM_001034837.1 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:103599590 G>A maps to NM_173194.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:103587925 G>A maps to NM_014591.4 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr10:103590856 C>T maps to NM_014591.4 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:96040618 C>T maps to NM_013434.4 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:96048204 G>A maps to NM_013434.4 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:96012841 C>T maps to NM_001034914.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:20751287 G>A maps to ENST00000382152 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:128710041 C>A maps to NM_000220.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:160012314 G>T maps to NM_002241.4 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:17408609 G>T maps to NM_000525.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:17409395 G>A maps to NM_000525.3 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:21319340 C>T maps to NM_021012.4 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:21319601 C>A maps to NM_021012.4 Y316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:233635850 G>T maps to NM_002242.4 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:233635948 G>A maps to NM_002242.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:233635682 G>A maps to NM_002242.4 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:233633359 G>T maps to NM_002242.4 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:233633449 T>C maps to NM_002242.4 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:48967676 G>A maps to NM_170720.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:48967754 C>T maps to NM_170720.1 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:39671656 C>T maps to NM_170736.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:39671434 C>A maps to NM_170736.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:39671935 C>A maps to NM_170736.1 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:68129134 G>T maps to NM_018658.1 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:68128923 G>A maps to NM_018658.1 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:68171551 C>T maps to NM_000891.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:68171386 C>T maps to NM_000891.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:68171716 C>A maps to NM_000891.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:155555727 C>G maps to NM_002239.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:155711663 G>T maps to NM_002239.2 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:155555493 G>A maps to NM_002239.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:155555700 C>T maps to NM_002239.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:155711563 A>G maps to NM_002239.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:155555712 C>A maps to NM_002239.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:155555700 C>T maps to NM_002239.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:155711566 C>A maps to NM_002239.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:38824104 G>A maps to NM_152868.1 H11H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr22:38823366 C>T maps to NM_152868.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:38822880 G>A maps to NM_152868.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr22:38823648 G>A maps to NM_152868.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:128781407 C>A maps to NM_000890.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:128781509 C>T maps to NM_000890.3 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:128781575 C>T maps to NM_000890.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr11:128781630 C>T maps to NM_000890.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr11:128781782 C>T maps to NM_000890.3 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:128781854 C>T maps to NM_000890.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:39087396 G>A maps to NM_002240.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr21:39086685 C>T maps to NM_002240.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:38997520 G>A maps to NM_002240.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:160054305 G>A maps to NM_004983.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:160054398 C>A maps to NM_004983.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:233807170 C>A maps to NM_002245.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:88652223 G>A maps to NM_138318.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:88652166 G>T maps to NM_138318.2 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:88658646 G>A maps to NM_138318.2 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:88729845 G>A maps to NM_138318.2 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:88693811 T>G maps to NM_138318.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:90650887 C>A maps to NM_022054.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:90650743 C>A maps to NM_022054.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:90650503 C>T maps to NM_022054.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:90651041 C>T maps to NM_022054.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:43379100 C>T maps to ENST00000372861 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr6:39284066 G>A maps to NM_001135106.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:39284618 G>A maps to NM_032115.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:39285665 A>G maps to NM_032115.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:39271748 G>A maps to NM_031460.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:39278711 G>A maps to NM_031460.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:39271778 G>A maps to NM_031460.3 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:39271748 G>A maps to NM_031460.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:118969761 T>C maps to NM_181840.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:118957091 G>A maps to NM_181840.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:118969584 C>T maps to NM_181840.1 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:118969584 C>T maps to NM_181840.1 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:118969236 C>T maps to NM_181840.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:118969584 C>T maps to NM_181840.1 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:215259846 G>A maps to NM_001017425.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:215408242 C>T maps to NM_001017425.2 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:215408379 C>T maps to NM_001017425.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:26951018 C>T maps to NM_002246.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:26950544 C>T maps to NM_002246.2 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:26950589 C>T maps to NM_002246.2 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:26950676 C>T maps to NM_002246.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:39196872 G>A maps to NM_003740.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr6:39158716 G>A maps to NM_003740.3 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:39159103 G>A maps to NM_003740.3 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:39159382 C>T maps to NM_003740.3 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:38817922 G>A maps to NM_004823.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:140630578 C>T maps to NM_016601.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr10:78709028 C>A maps to NM_001161352.1 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:78729730 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:78647230 C>T maps to NM_001161352.1 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:78778780 C>A maps to NM_001161352.1 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:78669849 G>A maps to NM_001161352.1 N1007N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:79011011 A>T maps to NM_001161352.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:78832989 C>T maps to NM_001161352.1 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:78651291 C>T maps to NM_001161352.1 A1111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:169812343 C>T maps to NM_004137.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:169805893 C>T maps to NM_004137.2 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:18085917 C>T maps to ENST00000222249 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:18100608 C>A maps to ENST00000222249 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:113740187 G>A maps to NM_021614.2 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:113831611 T>C maps to NM_021614.2 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:113831629 C>T maps to NM_021614.2 N497N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:113831666 C>T maps to NM_021614.2 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:113831701 C>T maps to NM_021614.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:113831647 C>T maps to NM_021614.2 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:113698483 C>T maps to NM_021614.2 C4C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:154680717 C>A maps to NM_002249.4 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:154842242 A>C maps to NM_002249.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:154680717 C>A maps to NM_002249.4 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:44273177 G>A maps to NM_002250.2 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:44284965 C>T maps to NM_002250.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:2604726 C>T maps to NM_000218.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:62073803 C>T maps to NM_172107.2 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr20:62038257 C>T maps to NM_172107.2 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr20:62055537 C>T maps to NM_172107.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr20:62078191 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:62065097 T>G maps to NM_172109.1 *394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:62039858 C>T maps to NM_172107.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:62059788 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr20:62071055 C>T maps to NM_172107.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:62039858 C>T maps to NM_172107.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:133141655 C>T maps to NM_004519.2 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:133182624 C>T maps to NM_004519.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr8:133141840 G>A maps to NM_004519.2 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:41283840 C>T maps to NM_004700.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:41288068 C>A maps to NM_004700.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:41296857 A>G maps to NM_004700.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:41285895 C>T maps to NM_004700.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:41303993 C>T maps to NM_004700.3 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:41300692 C>T maps to NM_004700.3 Y556Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:73830222 C>T maps to NM_001160133.1 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:73904494 T>C maps to NM_001160133.1 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr6:73751663 C>T maps to NM_001160133.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:73879566 C>T maps to NM_001160133.1 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:73332306 C>T maps to NM_001160133.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:73751663 C>T maps to NM_001160133.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:73332312 C>T maps to NM_001160133.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:73834235 G>A maps to ENST00000370392 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:73905001 C>T maps to NM_001160133.1 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr13:50589731 T>C maps to NM_173605.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:99440686 G>A maps to NM_020697.2 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:99440521 C>T maps to NM_020697.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr8:99441253 C>A maps to NM_020697.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:18112794 A>C maps to NM_002252.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr2:18113231 C>T maps to NM_002252.3 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr2:18113420 G>A maps to NM_002252.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:18112709 G>A maps to NM_002252.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:138651596 C>T maps to ENST00000298480 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr9:138651533 C>T maps to ENST00000298480 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:138649175 C>T maps to ENST00000298480 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:138675961 G>A maps to ENST00000298480 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:138656959 C>T maps to ENST00000298480 H373H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:138662930 C>T maps to ENST00000298480 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:138670611 C>T maps to ENST00000298480 A891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:138649175 C>T maps to ENST00000298480 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:138656989 C>T maps to ENST00000298480 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:138676680 C>T maps to ENST00000298480 A1034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:138660715 C>T maps to ENST00000298480 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:138651626 C>T maps to ENST00000298480 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:138662744 G>A maps to ENST00000298480 K604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:138645824 C>T maps to ENST00000298480 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:138656878 C>T maps to ENST00000298480 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:196205126 C>T maps to NM_198503.2 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:196395069 G>A maps to NM_198503.2 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:196451499 G>T maps to NM_198503.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:196309603 G>T maps to NM_198503.2 C550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:196342343 G>A maps to NM_198503.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:196397312 G>A maps to NM_198503.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:196254801 G>A maps to NM_198503.2 D894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:196285065 G>A maps to NM_198503.2 Y813Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:196459011 G>T maps to NM_198503.2 Y77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:196296001 G>T maps to NM_198503.2 Y707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:196577421 G>A maps to NM_198503.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:36641999 A>G maps to NM_001031836.2 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:36691168 C>T maps to NM_001031836.2 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:36768512 C>A maps to NM_001031836.2 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr8:36793299 A>G maps to NM_001031836.2 Q1104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr8:36780143 C>T maps to NM_001031836.2 A911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:36780066 G>T maps to NM_001031836.2 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr8:36793342 C>T maps to NM_001031836.2 Q1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:110984844 G>A maps to NM_014379.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr8:110986320 G>A maps to NM_014379.2 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:2718737 C>T maps to NM_133497.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:24039622 C>T maps to NM_001142730.1 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr18:24039823 T>C maps to NM_001142730.1 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:24126862 G>T maps to NM_001142730.1 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:24039875 A>C maps to NM_001142730.1 L716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:24126859 G>A maps to NM_001142730.1 C547C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:24128044 G>A maps to NM_001142730.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:7256761 C>T maps to NM_001002914.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:77728196 G>A maps to NM_023930.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:77727773 G>A maps to NM_023930.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr11:77727839 C>T maps to NM_023930.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:143586883 G>T maps to NM_020768.3 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:143586895 G>T maps to NM_020768.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:143586925 C>T maps to NM_020768.3 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:37455387 C>T maps to ENST00000403888 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:37456934 C>T maps to ENST00000403888 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:201371696 G>A maps to NM_152387.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:201371658 C>T maps to NM_152387.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:201355188 C>T maps to NM_152387.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr2:201355263 G>A maps to NM_152387.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:67325283 G>T maps to NM_001100915.1 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:67337115 G>A maps to NM_001100915.1 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:67338336 G>A maps to NM_001100915.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:67338375 C>T maps to NM_001100915.1 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:67328577 C>A maps to NM_001100915.1 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:67338353 C>A maps to NM_001100915.1 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr16:67335724 A>G maps to NM_001100915.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:73058279 C>T maps to NM_015353.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:36447384 T>C maps to NM_173562.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:77884838 A>G maps to NM_001029859.1 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:215781386 G>A maps to NM_016121.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:215775446 C>T maps to NM_016121.3 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:215759844 G>T maps to NM_016121.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:215793425 C>T maps to NM_016121.3 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:215793707 T>C maps to NM_016121.3 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr13:45768018 G>A maps to NM_198404.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:45768389 G>A maps to NM_198404.2 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:2747977 C>T maps to NM_018992.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:2746033 C>T maps to NM_018992.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:58486884 G>A maps to NM_153331.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr3:58486806 C>T maps to NM_153331.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:44176839 C>T maps to NM_198353.2 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:25290915 A>C maps to NM_017634.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr8:25293758 G>A maps to NM_017634.3 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:103443657 G>A maps to NM_024089.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:103449346 A>G maps to NM_024089.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:48892842 C>T maps to NM_006801.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:6505873 G>A maps to NM_006854.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:38877407 C>T maps to NM_016657.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:38864310 A>C maps to NM_016657.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:23405540 C>T maps to NM_001009999.2 C642C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:23406095 C>T maps to NM_001009999.2 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:23409680 C>T maps to NM_001009999.2 R819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:23381622 C>T maps to NM_001009999.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:18222177 A>G maps to ENST00000388870 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:18171682 C>T maps to ENST00000388870 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr6:18197352 C>T maps to ENST00000388870 C345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:18197816 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:18166560 C>T maps to ENST00000388870 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:18171677 C>T maps to ENST00000388870 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:66995539 T>C maps to NM_012308.2 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:67017759 C>T maps to NM_012308.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:66995533 C>T maps to NM_012308.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:121970819 G>A maps to ENST00000377071 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr12:121986792 C>T maps to ENST00000377071 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:121878754 G>A maps to ENST00000377071 G1158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:121970761 G>A maps to ENST00000377071 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:122018752 C>A maps to ENST00000377071 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:121986792 C>T maps to ENST00000377071 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:121880603 C>T maps to ENST00000377071 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:86693924 C>T maps to NM_001146688.1 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:86682258 G>T maps to NM_001146688.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr2:86709195 C>A maps to NM_001146688.1 R886R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:86709672 G>A maps to NM_001146688.1 R926R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:86705033 T>C maps to NM_001146688.1 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:86682258 G>T maps to NM_001146688.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:137727621 C>T maps to NM_016604.3 N767N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:137715345 T>C maps to NM_016604.3 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:137727660 G>A maps to NM_016604.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:137763752 C>T maps to NM_016604.3 I1577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:137750858 T>C maps to NM_016604.3 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:137726817 G>A maps to NM_016604.3 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:137762734 C>T maps to NM_016604.3 R1495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:137762734 C>T maps to NM_016604.3 R1495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr5:137727018 A>G maps to NM_016604.3 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:137734037 C>T maps to NM_016604.3 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:137726893 T>C maps to NM_016604.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:137726778 A>G maps to NM_016604.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr5:137722303 G>T maps to NM_016604.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:5032993 C>T maps to NM_015015.2 Y31Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:5039857 G>A maps to NM_015015.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:5039914 G>A maps to NM_015015.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:5143982 C>T maps to NM_015015.2 C852C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:5131294 C>T maps to NM_015015.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:5119672 G>A maps to NM_015015.2 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:5119849 C>T maps to NM_015015.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:5144087 C>T maps to NM_015015.2 G887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr9:7049118 G>A maps to NM_015061.3 A781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:6805633 C>T maps to NM_015061.3 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:6984369 G>T maps to NM_015061.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr9:7174665 C>T maps to NM_015061.3 A1036A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:7049131 C>T maps to NM_015061.3 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:7049187 G>A maps to NM_015061.3 Q804Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:7011779 G>A maps to NM_015061.3 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr9:7128115 G>A maps to NM_015061.3 T887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:7128232 C>T maps to NM_015061.3 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:94731913 C>T maps to NM_018039.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:94730614 G>T maps to NM_018039.2 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:94730902 C>T maps to NM_018039.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:94758771 G>A maps to NM_001161630.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:94760159 T>G maps to NM_001161630.1 L480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:431629 G>T maps to NM_001042603.1 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:464397 G>A maps to NM_001042603.1 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:432866 A>G maps to NM_001042603.1 C683C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:438056 C>A maps to NM_001042603.1 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:430247 C>A maps to NM_001042603.1 R818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:472155 C>T maps to NM_001042603.1 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:463286 A>G maps to NM_001042603.1 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:432893 C>T maps to NM_001042603.1 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:202704715 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:202702816 G>T maps to ENST00000367264 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:202722176 C>T maps to ENST00000367264 W555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:202705465 G>A maps to ENST00000367264 R1083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K0-01A-11W-A062-09 chr1:202709849 G>A maps to ENST00000367264 D1048D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:202698924 G>A maps to ENST00000367264 P1505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:202722095 C>T maps to ENST00000367264 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:202746213 C>T maps to ENST00000367264 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:202702930 C>T maps to ENST00000367264 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr1:202710775 C>A maps to ENST00000367264 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:202710589 C>T maps to ENST00000367264 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:202705346 G>T maps to ENST00000367264 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53224234 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53228263 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53247578 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53222680 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53223812 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53243993 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53223718 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:53222631 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:53223484 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53228017 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53222380 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53223667 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53225141 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53227671 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53245346 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:53243888 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:53247028 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53226042 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:53228292 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:53224554 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53247532 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53254007 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:53239621 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr23:53231130 C>T did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:53241054 C>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:44919284 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:44921947 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:44928918 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:44879912 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:44935943 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:44937722 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:44942755 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:44820602 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:44919317 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:44870209 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:44945215 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:44929556 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:44929188 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:44911009 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:44969345 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:44949993 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:44879904 G>A did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:44894186 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:7748967 G>A maps to NM_001080424.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7750490 C>T maps to NM_001080424.1 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7750757 G>A maps to NM_001080424.1 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7751192 G>A maps to NM_001080424.1 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7756401 C>A maps to NM_001080424.1 G1565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr17:7750988 G>A maps to NM_001080424.1 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:55946205 C>A maps to NM_002253.2 E1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:55973956 C>T maps to NM_002253.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:55968175 C>T maps to NM_002253.2 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:55946113 A>G maps to NM_002253.2 P1355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:55955604 C>A maps to NM_002253.2 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:55976882 C>T maps to NM_002253.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:55955593 C>T maps to NM_002253.2 R1117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr4:55964920 C>T maps to NM_002253.2 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:61002516 T>C maps to NM_002035.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr19:10610217 G>A maps to NM_203500.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:142658917 G>A maps to NM_000420.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr7:142651031 G>A maps to NM_000420.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:142641466 C>T maps to NM_000420.2 E478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:142651386 C>A maps to NM_000420.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:142655450 G>A maps to NM_000420.2 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:91449938 G>A maps to NM_007035.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:91449938 G>A maps to NM_007035.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:91449557 G>A maps to NM_007035.3 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:73933491 C>T maps to ENST00000370385 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:73933485 C>T maps to ENST00000370385 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:32503459 G>A maps to NM_006559.1 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:32508158 G>A maps to NM_006559.1 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr1:32503579 G>A maps to NM_006559.1 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:62757801 G>T maps to NM_152688.2 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:62995778 C>T maps to NM_152688.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr6:62604683 G>A maps to NM_152688.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:62390965 C>A did not map to a codon.
Sequencing variant TCGA-FI-A2D2-01A-11D-A17D-09 chr6:62887217 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:136594317 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:136533531 T>C maps to NM_006558.1 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:27320507 C>T maps to NM_006488.2 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27322611 C>T maps to NM_006488.2 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:27322560 C>T maps to NM_006488.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr2:27320459 C>T maps to NM_006488.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:27322539 C>T maps to NM_006488.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24901558 G>A maps to NM_015299.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:24905651 C>T maps to NM_015299.2 R582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:6416803 G>A maps to NM_003685.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:6420482 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:6416503 G>A maps to NM_003685.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:6417036 G>A maps to NM_003685.2 H381H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:6418556 G>A maps to NM_003685.2 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:6416503 G>A maps to NM_003685.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:6415545 G>A maps to NM_003685.2 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:6419266 G>A maps to NM_003685.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:6418012 A>G maps to NM_003685.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:6422414 C>T maps to NM_003685.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:2807835 G>A maps to NM_014878.4 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:2810353 A>G maps to NM_014878.4 N571N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr9:2833373 G>A maps to NM_014878.4 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:19561641 C>A maps to NM_015047.1 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:19559252 C>T maps to NM_015047.1 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:26942816 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:26944248 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:26962601 A>T maps to NM_014680.2 L668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:26961802 G>A maps to NM_014680.2 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:26970295 A>G maps to NM_014680.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:26948069 A>C maps to NM_014680.2 T1726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr17:26966355 A>G maps to NM_014680.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:141313950 A>C maps to NM_014773.3 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr5:141307804 C>A maps to NM_014773.3 C118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:141307750 G>A maps to NM_014773.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:141305052 C>T maps to NM_014773.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:48508399 T>C maps to NM_001080394.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr8:48612994 C>G maps to NM_001080394.1 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:48308980 G>T maps to NM_001080394.1 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:48511561 G>T maps to NM_001080394.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:85696593 C>A maps to NM_014615.2 Y756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:85697155 C>T maps to NM_014615.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:85697159 G>T maps to NM_014615.2 E862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:73489845 G>A maps to ENST00000375248 K758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:73484181 C>T maps to ENST00000375248 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:73490738 C>T maps to ENST00000375248 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:73487779 A>G maps to ENST00000375248 E471E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:126061295 G>T maps to ENST00000377985 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:126061250 C>T maps to ENST00000377985 T797T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:126091036 G>A maps to ENST00000377985 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr8:126087248 G>A maps to ENST00000377985 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:126059560 G>A maps to ENST00000377985 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:197403773 G>T maps to NM_014687.1 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:197422754 G>A maps to NM_014687.1 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:197408017 C>T maps to NM_014687.1 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:197431521 T>C maps to NM_014687.1 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:6865198 C>T maps to NM_014743.2 V1030V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr4:6826395 C>G maps to NM_014743.2 Y72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:6865324 G>A maps to NM_014743.2 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:6863011 G>A maps to NM_014743.2 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:6863932 A>T maps to NM_014743.2 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:6862904 G>T maps to NM_014743.2 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:6863222 G>T maps to NM_014743.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:6826411 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:6863443 G>T maps to NM_014743.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:6862934 C>T maps to NM_014743.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:6865324 G>A maps to NM_014743.2 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2D2-01A-11D-A17D-09 chr4:6865465 A>T maps to NM_014743.2 G1119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:42832928 C>T maps to NM_015349.1 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:42797388 G>T maps to NM_015349.1 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:70175519 A>G maps to NM_014734.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:70170205 C>A maps to NM_014734.3 Y72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:70177687 G>T maps to NM_014734.3 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105344259 C>T maps to ENST00000453495 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:105352984 T>C maps to ENST00000453495 N804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:105349570 G>A maps to ENST00000453495 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:105356023 G>A maps to ENST00000453495 T1305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:105359981 G>A maps to ENST00000453495 T1423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:75139613 G>A maps to NM_001039479.1 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:75142431 C>T maps to NM_001039479.1 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:75134249 C>T maps to NM_001039479.1 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:75136386 C>A maps to NM_001039479.1 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:75130720 C>T maps to NM_001039479.1 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:75143372 T>C maps to NM_001039479.1 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:75138186 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr6:24596505 G>A maps to NM_014809.3 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:24596682 G>A maps to NM_014809.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:24588884 G>A maps to NM_014809.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr6:24596138 G>A maps to NM_014809.3 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr6:24563702 A>G maps to NM_014809.3 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:35913886 G>A maps to NM_024874.4 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:34818324 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:34838929 C>T maps to NM_014686.3 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:34791596 C>T maps to NM_014686.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:34810969 C>G maps to NM_014686.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:34839995 C>T maps to NM_014686.3 N921N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:34830781 G>T maps to NM_014686.3 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:34843730 C>T maps to NM_014686.3 A1028A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:34832560 C>T maps to NM_014686.3 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:34832350 G>A maps to NM_014686.3 Q504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:114134095 G>A maps to NM_001080398.1 G1692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:114136276 A>G maps to NM_001080398.1 C1562C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:114184212 C>T maps to NM_001080398.1 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:114152380 A>G maps to NM_001080398.1 G1232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:114134816 C>A maps to NM_001080398.1 E1652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:114131405 C>T maps to NM_001080398.1 E1852E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr9:114133912 C>T maps to NM_001080398.1 T1753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:114125891 C>A maps to NM_001080398.1 E1964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:35736001 C>T maps to NM_014672.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:35649976 T>C maps to NM_014672.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr14:35592627 G>A maps to NM_014672.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr14:35596683 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:127771028 C>T maps to NM_014702.4 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:127771308 C>T maps to NM_014702.4 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:127767690 A>G maps to NM_014702.4 C591C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:127768764 T>C maps to NM_014702.4 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:127768436 C>A maps to NM_014702.4 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:127771347 C>T maps to NM_014702.4 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr7:4824678 C>T maps to ENST00000450194 R1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:4830401 C>T maps to ENST00000450194 F1390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:4823928 C>T maps to ENST00000450194 N950N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:4829515 C>T maps to ENST00000450194 S1298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:4823395 C>T maps to ENST00000450194 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr16:15716919 C>T maps to NM_014647.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:15710961 C>T maps to NM_014647.3 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:15709699 C>T maps to NM_014647.3 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:15727698 C>T maps to NM_014647.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:15733002 T>A maps to NM_014647.3 K30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:15711199 A>C maps to NM_014647.3 Y971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:15711319 G>A maps to NM_014647.3 N931N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:15729638 C>T maps to NM_014647.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:15709699 C>T maps to NM_014647.3 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:15706614 C>T maps to NM_014647.3 S1091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:15695931 G>T maps to NM_014647.3 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:15719456 A>G maps to NM_014647.3 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:15727479 A>G maps to NM_014647.3 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:15706614 C>T maps to NM_014647.3 S1091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:15727569 C>T maps to NM_014647.3 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr16:15728788 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:15711235 C>T maps to NM_014647.3 T959T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:47144186 G>A maps to NM_014774.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:47181972 G>A maps to NM_014774.2 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:47144186 G>A maps to NM_014774.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:47152467 G>A maps to NM_014774.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:85112585 G>A maps to NM_014732.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:85120704 T>C maps to NM_014732.2 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:22680653 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:22627728 C>A maps to ENST00000446597 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:22676469 G>A maps to ENST00000446597 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:22646268 C>A maps to ENST00000446597 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr12:22676469 G>A maps to ENST00000446597 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:22643153 T>C did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:22676469 G>A maps to ENST00000446597 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:22635490 C>T maps to ENST00000446597 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:27720129 C>T maps to NM_015202.2 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr16:27788980 C>T maps to NM_015202.2 S1534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:27789940 G>T maps to NM_015202.2 R1616R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:27763187 C>T maps to NM_015202.2 A1165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:27777740 C>T maps to NM_015202.2 I1307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr16:27789931 G>A maps to NM_015202.2 T1613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr16:27585232 C>T maps to NM_015202.2 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:27781294 C>T maps to NM_015202.2 F1363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:27709760 C>T maps to NM_015202.2 N351N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:27692774 C>T maps to NM_015202.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:42404669 C>T maps to NM_015058.1 Q565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:42361603 G>A maps to NM_015058.1 D713D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr13:42293728 C>T maps to NM_015058.1 K1038K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr13:42245201 G>A maps to NM_015058.1 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:42189118 G>A maps to NM_015058.1 G1571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:42293878 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr13:42273251 C>T maps to NM_015058.1 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr13:42306284 G>T maps to NM_015058.1 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:42295658 G>A maps to NM_015058.1 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:42460120 C>A maps to NM_015058.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:42460120 C>A maps to NM_015058.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr13:42249348 A>G did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr13:42164825 G>A maps to NM_015058.1 L1688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:58909422 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr14:58938914 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:58975382 G>T maps to ENST00000354386 E1480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:58917321 G>A maps to ENST00000354386 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr14:58953771 C>T maps to ENST00000354386 C1117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:58923418 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:2603720 G>A maps to NM_015229.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr17:2598368 G>A maps to NM_015229.3 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:2603704 G>T maps to NM_015229.3 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:2595864 G>A maps to NM_015229.3 D1107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr17:2594034 C>T maps to NM_015229.3 A1261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:2601478 G>A maps to NM_015229.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr17:2604745 G>A maps to NM_015229.3 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:55356964 G>A maps to NM_001098815.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:6493228 G>A maps to NM_014804.2 R886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr17:6503711 C>T maps to NM_014804.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:6515253 C>T maps to NM_014804.2 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:39877574 T>A maps to NM_015038.1 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:39876932 T>C maps to NM_015038.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:39879773 G>A maps to NM_015038.1 E1279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:39877676 G>A maps to NM_015038.1 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:39878347 C>A maps to NM_015038.1 S804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:39879410 C>T maps to NM_015038.1 S1158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:36373755 G>A maps to NM_001100425.1 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:36396629 C>A maps to NM_001100425.1 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:36374748 C>T maps to NM_001100425.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:67213970 G>A maps to NM_001040715.1 C181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:67210740 C>T maps to NM_001040715.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:155899532 G>A maps to NM_014949.2 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:155893423 C>T maps to NM_014949.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:155896609 C>A maps to NM_014949.2 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:155884079 C>T maps to NM_014949.2 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:155883965 A>G maps to NM_014949.2 Y597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:75548883 G>A maps to NM_015037.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:75559935 G>A maps to NM_015037.2 L1611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr10:75557208 C>T maps to NM_015037.2 R1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:75548896 C>T maps to NM_015037.2 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:75560078 G>A maps to NM_015037.2 T1625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:75551988 C>T maps to NM_015037.2 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:154512291 C>T maps to NM_001131007.1 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:154523385 G>A maps to NM_001131007.1 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:154523427 C>T maps to NM_001131007.1 F797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:154557562 G>A maps to NM_001131007.1 T1556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:154512321 C>T maps to NM_001131007.1 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:154479456 G>A maps to NM_001131007.1 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr4:154517411 T>A maps to NM_001131007.1 G666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:154502000 C>A maps to NM_001131007.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:154506757 T>C maps to NM_001131007.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:154507476 A>G maps to NM_001131007.1 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr4:154525122 A>T maps to NM_001131007.1 K987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr4:154544191 G>T maps to NM_001131007.1 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:154557616 G>A maps to NM_001131007.1 P1574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr4:154513670 C>T maps to NM_001131007.1 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:5462443 C>T maps to NM_015325.1 G999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:5457826 G>A maps to NM_015325.1 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:5462191 C>A maps to NM_015325.1 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:5465162 G>T maps to NM_015325.1 E1906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:5463448 C>T maps to NM_015325.1 S1334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:5463595 G>A maps to NM_015325.1 E1383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:5457670 T>C maps to NM_015325.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr5:5476114 G>A maps to NM_015325.1 W2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:5463977 C>T maps to NM_015325.1 R1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:84925112 C>T maps to NM_014895.2 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:84836165 G>A maps to NM_014895.2 F1312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:84913770 C>T maps to NM_014895.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:84859376 A>G maps to NM_014895.2 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:84862664 G>A maps to NM_014895.2 F1076F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:84925055 C>T maps to NM_014895.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:84884489 C>A maps to NM_014895.2 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:84885066 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr15:79750300 C>A maps to NM_015206.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:79755407 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:79748611 G>A maps to NM_015206.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr15:79755629 C>T maps to NM_015206.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:79748656 C>T maps to NM_015206.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:105540854 G>A maps to NM_015275.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:105540891 C>T maps to NM_015275.1 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:105534819 A>G maps to NM_015275.1 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:105536270 C>T maps to NM_015275.1 R610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:105540891 C>T maps to NM_015275.1 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr12:105527565 C>T maps to NM_015275.1 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:105546150 C>T maps to NM_015275.1 R894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:105534076 A>C maps to NM_015275.1 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:34971303 G>A maps to NM_015297.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:123267793 G>A maps to NM_015312.3 G4250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:123165057 G>T maps to NM_015312.3 E1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:123113393 G>A maps to NM_015312.3 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:123265666 T>G maps to NM_015312.3 S4228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:123283344 C>T maps to NM_015312.3 L4987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:123283344 C>T maps to NM_015312.3 L4987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:123207749 C>A maps to NM_015312.3 S3031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:123094203 C>A maps to NM_015312.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:123145759 C>T maps to NM_015312.3 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:123091865 G>T maps to NM_015312.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:123178642 C>T maps to NM_015312.3 F2204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:123283344 C>T maps to NM_015312.3 L4987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:123147896 T>G maps to NM_015312.3 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:123271020 C>T maps to NM_015312.3 F4547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:123283284 G>A maps to NM_015312.3 W4967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:123159346 A>G maps to NM_015312.3 R1225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:123167407 T>C maps to NM_015312.3 D1713D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:123176052 T>C maps to NM_015312.3 T2056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:123226033 C>T maps to NM_015312.3 R3190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:123178642 C>T maps to NM_015312.3 F2204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:141362476 G>A maps to NM_001080392.1 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:141366102 G>A maps to NM_001080392.1 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:141366140 G>A maps to NM_001080392.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:34371852 G>A maps to NM_020702.3 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr9:34372728 C>T maps to NM_020702.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:34372473 G>T maps to NM_020702.3 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:175775041 G>T maps to NM_020444.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:81201517 G>A maps to NM_018689.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:81234602 C>T maps to NM_018689.1 D1208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:81241195 C>T maps to NM_018689.1 D1339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:81230233 G>A maps to NM_018689.1 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:81199154 C>T maps to NM_018689.1 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:81172168 C>T maps to NM_018689.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:118230566 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:118243136 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:118284524 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:118223339 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:118230484 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:118284276 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118221771 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118223491 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118227665 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118230484 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:118223600 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:118227972 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:118239045 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:118250587 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:118284276 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:118222925 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:118250483 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:118222954 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118221430 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118222388 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118222607 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118223456 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:118221534 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:118250477 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:118223295 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:118223409 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:118221638 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:118239011 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118222991 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118223102 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118223627 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:118221156 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:118215298 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:118220781 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:118238965 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:57181002 C>A maps to NM_020722.1 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:57181131 G>A maps to NM_020722.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:57180352 C>T maps to NM_020722.1 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:57182118 G>A maps to NM_020722.1 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr4:57180352 C>T maps to NM_020722.1 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:24822123 G>A maps to NM_019590.3 E1124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr10:24802316 A>T maps to NM_019590.3 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr10:24820876 A>G maps to NM_019590.3 S1067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:24832014 C>T maps to NM_019590.3 G1272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:24508598 G>T maps to NM_019590.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr10:24817011 A>C maps to NM_019590.3 R1016R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr10:24832086 C>A maps to NM_019590.3 T1296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr10:24762698 G>A maps to NM_019590.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr10:24762254 G>A maps to NM_019590.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:138656064 G>T maps to NM_020340.4 E2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:138599678 C>T maps to NM_020340.4 C740C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:138607886 C>T maps to NM_020340.4 I873I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:138608226 C>T maps to NM_020340.4 C934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:138655514 C>T maps to NM_020340.4 D1844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:138559659 G>A maps to NM_020340.4 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:138608296 G>T maps to NM_020340.4 E958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:138634996 G>A maps to NM_020340.4 L1422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr6:138644864 C>T maps to NM_020340.4 C1608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr6:138601197 T>C maps to NM_020340.4 I786I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:138656225 C>T maps to NM_020340.4 S2081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:128712141 C>T maps to NM_020741.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:128690232 T>C maps to NM_020741.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:128694620 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:72324139 G>A maps to NM_014431.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:72292375 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:70775845 C>T maps to NM_015634.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:70775337 T>C maps to NM_015634.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:70760279 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:70775485 G>T maps to NM_015634.3 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:109707136 C>T maps to NM_020775.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:109716352 G>A maps to NM_020775.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:109742790 C>A maps to NM_020775.3 I913I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr1:109734080 C>G maps to NM_020775.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:109714583 C>T maps to NM_020775.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:109656915 G>A maps to NM_020775.3 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:86577217 C>A maps to NM_001142749.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:86542448 C>T maps to NM_001142749.2 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:86548542 C>A maps to NM_001142749.2 G495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:86544101 G>T maps to NM_001142749.2 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:86509845 C>A maps to NM_001142749.2 E1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:86577208 C>A maps to NM_001142749.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:34802111 C>A maps to NM_020776.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:34539299 G>T maps to NM_020776.1 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr18:34415333 G>T maps to NM_020776.1 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:101793444 C>T maps to NM_020802.2 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:101863516 G>T maps to NM_020802.2 E1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:101832650 C>T maps to NM_020802.2 C295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:101833415 T>C maps to NM_020802.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:101834511 G>T maps to NM_020802.2 E916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:232943666 G>A maps to NM_019090.2 K966K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:232941105 C>T maps to NM_019090.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:232941930 T>C maps to NM_019090.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:232941413 C>T maps to NM_019090.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr1:232941440 G>A maps to NM_019090.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:113724407 G>A maps to NM_020817.1 H605H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:113753943 C>A maps to NM_020817.1 E216*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A163-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:95538800 G>A maps to NM_015496.3 C557C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:95539124 G>A maps to NM_015496.3 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:95539307 G>T maps to NM_015496.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:95531222 C>A maps to NM_015496.3 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr8:95511667 C>T maps to NM_015496.3 K1388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:95504925 C>A maps to NM_015496.3 G1588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:95522757 C>T maps to NM_015496.3 Q1171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:95523513 C>A maps to NM_015496.3 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:95508602 C>A maps to NM_015496.3 E1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:95501011 G>A maps to NM_015496.3 S1787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:186111450 A>G maps to NM_020827.1 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:186111549 C>T maps to NM_020827.1 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:186111879 G>A maps to NM_020827.1 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:186111663 C>T maps to NM_020827.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:5770091 G>T maps to ENST00000414202 E1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr9:5742981 C>T maps to ENST00000414202 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr9:5763199 C>T maps to ENST00000414202 R725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:5763750 C>T maps to ENST00000414202 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:5753647 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:5772624 C>T maps to ENST00000414202 G1226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr10:30336624 T>C maps to NM_020848.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:30317816 G>A maps to NM_020848.2 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:30315944 T>C maps to NM_020848.2 S1044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:30318296 C>T maps to NM_020848.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:30315907 G>A maps to NM_020848.2 Q1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr12:13220148 C>G maps to NM_020853.1 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:13214605 A>C maps to NM_020853.1 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:13215873 C>T maps to NM_020853.1 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:13219602 C>T maps to NM_020853.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr18:59925764 A>G maps to NM_020854.3 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:59928877 G>A maps to NM_020854.3 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:59878387 C>T maps to NM_020854.3 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:59949536 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:33237914 G>A maps to NM_020888.2 E1045E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:108288346 A>G maps to NM_020890.2 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:108279657 G>A maps to NM_020890.2 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:108288364 G>A maps to NM_020890.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:108279570 T>C maps to NM_020890.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:108288298 T>C maps to NM_020890.2 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:108298490 G>A maps to NM_020890.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:108288439 A>G maps to NM_020890.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr3:108285485 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:1343497 C>T maps to NM_020894.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:138602289 C>T maps to NM_001164665.1 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr7:138591662 A>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:138554494 G>A maps to NM_001164665.1 L1522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:138554474 G>A maps to NM_001164665.1 I1528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:138554377 G>A maps to NM_001164665.1 R1561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:138602433 C>T maps to NM_001164665.1 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:56919213 G>A maps to NM_020931.2 W639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:56919660 G>T maps to NM_020931.2 *788Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:56918937 A>G maps to NM_020931.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:118728220 A>G maps to NM_001127211.1 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:118711511 G>A maps to NM_001127211.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:118674894 C>T maps to NM_001127211.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:84514194 C>T maps to NM_020947.3 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:84514233 C>T maps to NM_020947.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:180885979 C>T maps to NM_020950.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:180905124 G>T maps to NM_020950.1 G694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:180885601 C>T maps to NM_020950.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:44681522 G>A maps to NM_001099294.1 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:18377401 G>A maps to NM_001145304.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:18378169 C>T maps to NM_001145304.1 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:18377623 C>T maps to NM_001145304.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:18376171 G>A maps to NM_001145304.1 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:18367960 C>T maps to ENST00000358422 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:18377002 C>T maps to NM_001145304.1 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:176829295 C>A maps to NM_030650.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:176802236 G>A maps to NM_030650.1 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr2:176829287 G>T maps to NM_030650.1 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr14:77579793 G>A maps to NM_033426.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:77580237 C>T maps to NM_033426.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr14:77576245 G>A maps to NM_033426.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:1887079 G>A maps to NM_001080484.1 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:1897899 G>T maps to ENST00000434971 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:1888082 G>A maps to ENST00000434971 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:1888103 A>C maps to ENST00000434971 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:1918434 G>A maps to ENST00000434971 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:36841893 T>C maps to NM_001029864.1 A1051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:36846674 C>A maps to NM_001029864.1 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:36869616 C>A maps to NM_001029864.1 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr20:36855588 C>A maps to NM_001029864.1 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:20823050 G>A maps to NM_017794.3 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:20874688 G>T maps to NM_017794.3 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:20981484 G>T maps to NM_017794.3 E1480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:20823039 G>T maps to NM_017794.3 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:20978392 C>T maps to NM_017794.3 S1439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:20982429 C>T maps to NM_017794.3 I1571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr9:20946761 T>C maps to NM_017794.3 A1206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:20764955 C>T maps to NM_017794.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr9:20978377 C>A maps to NM_017794.3 T1434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:233498020 C>T maps to NM_032435.2 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:233497896 C>T maps to NM_032435.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:233514818 G>A maps to NM_032435.2 W689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:233482227 T>C maps to NM_032435.2 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:233489678 G>A maps to NM_032435.2 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:233490679 G>T maps to NM_032435.2 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:233514872 G>A maps to NM_032435.2 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:233507865 G>A maps to NM_032435.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:233515136 G>T maps to NM_032435.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:61319610 G>A maps to NM_001129993.1 W367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:111587331 C>T maps to NM_153369.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:111587428 C>T maps to NM_153369.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:115408029 G>A maps to NM_133465.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:115421997 C>T maps to NM_133465.2 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:115337472 G>A maps to NM_133465.2 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:22473682 C>T maps to NM_021174.5 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:22474980 G>T maps to NM_021174.5 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:22475908 T>G maps to NM_021174.5 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:139701255 G>A maps to NM_001039374.4 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:139699010 C>A maps to NM_001039374.4 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:139700970 G>A maps to NM_001039374.4 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr3:113378746 G>C maps to NM_001009899.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:113378167 C>T maps to NM_001009899.2 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:113374186 G>T maps to NM_001009899.2 Y2114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:113377594 G>T maps to NM_001009899.2 I978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:113374507 A>G maps to NM_001009899.2 F2007F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:73961904 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:73961968 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:73964122 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:73960195 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:73959251 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:73959987 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:73961739 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:73961200 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:73961862 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:73963533 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:73960323 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:73960087 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:73963778 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:73964240 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:73965414 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:73960044 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:73960932 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:73961337 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:73963733 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:73960157 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:73963291 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:73959310 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:73962111 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:73963056 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:73963299 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:73960894 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:73963605 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:73962587 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:5923133 C>T maps to NM_001017969.2 K954K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:5968330 C>A maps to NM_001017969.2 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:5968373 G>A maps to NM_001017969.2 Y619Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:6007564 G>A maps to NM_001017969.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:5988523 C>T maps to NM_001017969.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:5954089 T>A maps to NM_001017969.2 K740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:5922776 C>T maps to NM_001017969.2 W1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr9:5921510 C>T maps to NM_001017969.2 A1495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:5922911 T>G maps to NM_001017969.2 T1028T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr9:5923226 C>T maps to NM_001017969.2 P923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:5920973 A>C maps to NM_001017969.2 A1674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:8873636 G>A maps to NM_020738.2 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:8871068 G>A maps to NM_020738.2 F1699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:8890322 G>A maps to NM_020738.2 F1111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:8910837 A>G maps to NM_020738.2 G991G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:8871068 G>A maps to NM_020738.2 F1699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:8940582 C>A maps to NM_020738.2 E283*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BS-A0UJ-01A-12D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:8943199 C>A maps to NM_020738.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:8873636 G>A maps to NM_020738.2 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:94405237 G>T maps to NM_004523.3 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:94405399 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:17764736 G>A maps to NM_022113.4 A1674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:17800205 G>A maps to NM_022113.4 R865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:17781110 G>T maps to NM_022113.4 S1232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:17800212 G>T maps to NM_022113.4 I862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:17780963 T>C maps to NM_022113.4 K1281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:17797026 C>A maps to NM_022113.4 E939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:17817339 G>A maps to NM_022113.4 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:17809139 G>A maps to NM_022113.4 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:17873611 G>A maps to NM_022113.4 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:17780963 T>C maps to NM_022113.4 K1281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:17781503 A>C maps to NM_022113.4 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:17855717 G>T maps to NM_022113.4 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:29006169 G>A maps to NM_015254.3 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:29023176 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:28976450 C>T maps to NM_015254.3 A1198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:28929185 G>A maps to NM_015254.3 A1723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:28950366 C>T maps to NM_015254.3 L1451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:28980908 A>G maps to NM_015254.3 S1151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:29048511 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:200569494 T>C maps to NM_014875.2 A763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:200583444 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:44879888 C>T maps to NM_020242.2 A1098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:44852417 C>A maps to NM_020242.2 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:44826374 G>T maps to NM_020242.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:44856496 G>A maps to NM_020242.2 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:44844407 G>T maps to NM_020242.2 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:44846649 G>T maps to NM_020242.2 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:44846649 G>T maps to NM_020242.2 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:44844407 G>T maps to NM_020242.2 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:44843456 G>A maps to NM_020242.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr20:16360432 A>G maps to NM_024704.4 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:16359970 G>A maps to NM_024704.4 F892F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:16506811 C>T maps to NM_024704.4 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:16486736 C>A maps to NM_024704.4 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:16506741 C>A maps to NM_024704.4 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:16254032 G>A maps to NM_024704.4 S1273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:16362392 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:16488662 C>T maps to NM_024704.4 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:21011474 C>T maps to NM_020816.2 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:21040032 T>A maps to NM_020816.2 K132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:20992705 C>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:21036291 G>A maps to NM_020816.2 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:28080524 A>T maps to NM_031217.3 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:28057834 G>A maps to NM_031217.3 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:28090820 G>A maps to NM_031217.3 N525N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:28119221 T>C maps to NM_031217.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:28080539 G>A maps to NM_031217.3 N627N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:43012650 G>A maps to ENST00000438933 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:43011338 C>T maps to ENST00000438933 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr17:72350994 C>T maps to NM_153209.3 C927C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72350527 C>T maps to NM_153209.3 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:72351435 C>T maps to NM_153209.3 C994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:72339280 C>A maps to NM_153209.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:72339280 C>A maps to NM_153209.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:72342623 C>T maps to NM_153209.3 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr17:72348988 A>G maps to NM_153209.3 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:241712600 G>A maps to ENST00000373308 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:241679549 G>A maps to ENST00000373308 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:241662025 G>A maps to ENST00000373308 T1512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr2:241664737 C>T maps to ENST00000373308 S1410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr2:241697826 G>A maps to ENST00000373308 T844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:241662007 C>T maps to ENST00000373308 P1518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:241697850 G>A maps to ENST00000373308 I836I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A5-A0VP-01A-21D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:10363225 G>A maps to NM_183416.3 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:10363931 G>T maps to NM_183416.3 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:10408753 C>T maps to ENST00000377086 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:10434509 G>T maps to ENST00000377086 E1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:10435310 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:10364083 T>G maps to NM_183416.3 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:10436635 G>A maps to ENST00000377086 S1814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:4927037 C>A maps to NM_006612.5 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr17:4925484 G>A maps to NM_006612.5 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:4905793 A>G maps to NM_006612.5 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:4905838 G>A maps to NM_006612.5 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:4906118 G>A maps to NM_006612.5 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:4926780 G>T maps to NM_006612.5 E883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:4925424 C>A maps to NM_006612.5 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:137517148 C>A maps to NM_005733.2 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:137518142 G>A maps to NM_005733.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:137518142 G>A maps to NM_005733.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr5:137521311 T>C maps to NM_005733.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:91469784 C>T maps to ENST00000416354 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:91520359 G>A maps to ENST00000416354 S1616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:91468995 G>T maps to ENST00000416354 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:91497199 C>T maps to ENST00000416354 R898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:91486187 G>T maps to ENST00000416354 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:91470857 G>T maps to ENST00000416354 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:91488914 G>T maps to ENST00000416354 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:91498251 A>G maps to ENST00000416354 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr10:91469148 T>G maps to ENST00000416354 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:91488914 G>T maps to ENST00000416354 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:39750649 C>A maps to ENST00000395670 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr12:39716650 G>A maps to ENST00000395670 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:39705327 T>C maps to ENST00000395670 S1330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:39760270 C>A maps to ENST00000395670 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:39734804 C>T maps to ENST00000395670 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr12:39756910 G>A maps to ENST00000395670 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:39750649 C>A maps to ENST00000395670 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:200946392 G>A maps to NM_017596.2 G1411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:200977938 G>A maps to NM_017596.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:200978516 G>T maps to NM_017596.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:200973481 C>T maps to NM_017596.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:200956182 G>A maps to NM_017596.2 D1185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:200944719 G>A maps to NM_017596.2 I1494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:200944035 G>A maps to NM_017596.2 I1527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:200967659 G>A maps to NM_017596.2 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:200972743 C>T maps to NM_017596.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:200959403 C>T maps to NM_017596.2 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr1:200978070 G>C maps to NM_017596.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:29815373 C>A maps to NM_007317.1 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr16:29809772 G>A maps to NM_007317.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:29808346 C>T maps to NM_007317.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:69732391 G>A maps to NM_138555.1 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:69737170 C>T maps to NM_138555.1 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:69737220 C>T maps to NM_138555.1 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:34257618 T>C maps to NM_194313.2 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:34257896 G>A maps to NM_194313.2 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:34257584 G>A maps to NM_194313.2 R674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:34255111 G>A maps to NM_194313.2 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:168440762 G>A maps to NM_030615.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:168445516 G>A maps to NM_030615.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:168439343 G>A maps to NM_030615.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:168445510 C>T maps to NM_030615.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:104640631 C>T maps to NM_015656.1 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:104646045 G>A maps to NM_015656.1 A1856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr14:104641857 C>A maps to NM_015656.1 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr14:104641542 C>A maps to NM_015656.1 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:245766054 C>T maps to NM_018012.3 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:245770972 C>T maps to NM_018012.3 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:245530260 G>A maps to NM_018012.3 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:245583045 C>T maps to NM_018012.3 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:245765914 C>T maps to NM_018012.3 R463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:245772616 C>T maps to NM_018012.3 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:245849258 G>T maps to NM_018012.3 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:245850934 G>A maps to NM_018012.3 P1550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:245849896 C>T maps to NM_018012.3 S1204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:245530311 C>T maps to NM_018012.3 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:245530521 A>G maps to NM_018012.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:86502078 C>A maps to NM_017576.1 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:86518060 G>A maps to NM_017576.1 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:86518019 C>T maps to NM_017576.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:86523390 G>A maps to NM_017576.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:86506302 A>G maps to NM_017576.1 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:86518645 C>A maps to NM_017576.1 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:61668357 C>T maps to NM_001098511.1 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:61811219 A>T maps to NM_001134779.1 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr5:61659572 G>A maps to NM_001098511.1 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:51900438 C>T maps to NM_032559.4 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:51901905 G>T maps to NM_032559.4 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:51901581 T>C maps to NM_032559.4 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:45227625 T>C maps to NM_006845.3 Y574Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:45218892 C>T maps to NM_006845.3 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:45221602 C>T maps to NM_006845.3 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:45226367 T>G maps to NM_006845.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:45216192 G>A maps to NM_006845.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:45221765 T>C maps to NM_006845.3 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:132061828 T>C maps to ENST00000403231 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:132051454 C>A maps to ENST00000403231 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:132069978 A>G maps to ENST00000403231 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:132038593 C>A maps to ENST00000403231 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:132037862 G>A maps to ENST00000403231 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:132051451 C>A maps to ENST00000403231 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:132038593 C>A maps to ENST00000403231 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:30898888 G>T maps to NM_004798.3 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:26204552 C>A maps to NM_002254.6 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:26204162 G>A maps to NM_002254.6 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:26203304 C>T maps to NM_002254.6 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:69626741 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69561669 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69594030 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69623868 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69573541 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69607078 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69623780 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69639611 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69550093 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69573510 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69615611 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:69595116 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:69639625 A>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69595063 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69625745 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69550151 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69639576 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69521843 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69607077 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69639540 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:69607079 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:69595063 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:69639594 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:69510559 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:69594012 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:69640059 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:69553509 C>T did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:69510345 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:69561724 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:69607096 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:69607052 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:154396832 C>T maps to NM_001099293.1 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:154395198 C>T maps to NM_001099293.1 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:57960922 C>A maps to NM_004984.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:57976961 A>C maps to NM_004984.2 *1033Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr12:57961358 C>T maps to NM_004984.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:57963938 C>T maps to NM_004984.2 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:57969052 C>T maps to NM_004984.2 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:57971495 A>C maps to NM_004984.2 T767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr12:57975694 C>T maps to NM_004984.2 G984G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:32306175 C>A maps to NM_004521.2 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:32322805 T>C maps to NM_004521.2 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:32324579 G>A maps to NM_004521.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:149866662 C>T maps to NM_004522.1 N855N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:149868142 C>T maps to NM_004522.1 R943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:149818536 G>T maps to NM_004522.1 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:149837885 A>G maps to NM_004522.1 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:149806435 C>A maps to NM_004522.1 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:149840157 G>T maps to NM_004522.1 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:149679725 C>T maps to NM_004522.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:149793865 C>A maps to NM_004522.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:149847534 G>T maps to NM_004522.1 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:149806435 C>A maps to NM_004522.1 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:149818508 C>T maps to NM_004522.1 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:39325123 G>A maps to NM_145027.4 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:39328200 G>A maps to NM_145027.4 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:39507856 G>A maps to NM_145027.4 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:39313528 G>A maps to NM_145027.4 C756C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:39513421 T>C maps to NM_145027.4 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:90190243 C>A maps to NM_198525.2 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:90176161 C>T maps to NM_198525.2 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:90191959 G>A maps to NM_198525.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr15:90190108 C>T maps to NM_198525.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:47307322 C>T maps to NM_182902.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:47288865 G>A maps to NM_182902.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:47307352 G>A maps to NM_182902.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:169985669 G>T maps to NM_014970.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:169951173 G>A maps to NM_014970.2 D579D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:169947280 G>T maps to NM_014970.2 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:169951124 C>A maps to NM_014970.2 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:169951978 G>A maps to NM_014970.2 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:170003536 C>A maps to NM_014970.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr1:170001111 A>G maps to NM_014970.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:170003557 T>G maps to NM_014970.2 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:169947244 G>A maps to NM_014970.2 D626D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:170015871 A>G maps to NM_014970.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:33373359 G>A maps to NM_002263.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr6:33377449 C>T maps to NM_002263.3 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:57792821 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:7801885 C>T maps to NM_012311.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:7798090 T>C maps to NM_012311.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:55255309 C>A maps to NM_015868.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:55255405 C>T maps to NM_015868.2 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:55324688 C>T maps to ENST00000396289 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:55315133 C>T maps to ENST00000396289 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:55329962 A>G maps to ENST00000355608 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:55363597 C>T maps to NM_006737.2 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr19:55365454 C>A maps to NM_006737.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:55247493 T>G maps to NM_153443.3 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr1:158058236 C>G maps to ENST00000368173 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:158057566 C>A maps to ENST00000368173 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:158063422 C>T maps to ENST00000368173 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:158064181 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:158063225 C>T maps to ENST00000368173 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:158056519 C>T maps to ENST00000368173 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:158057936 T>C maps to ENST00000368173 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:158064534 C>T maps to ENST00000368173 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:158064531 C>T maps to ENST00000368173 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:158064789 G>A maps to ENST00000368173 R734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr1:158063492 C>A maps to ENST00000368173 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:158064849 C>T maps to ENST00000368173 Y754Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr19:36353880 C>T maps to NM_199180.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr19:36349433 C>T maps to NM_199180.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:126314949 G>A maps to NM_032531.3 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:126294648 G>T maps to NM_032531.3 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr11:126343308 C>T maps to NM_032531.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:126294582 G>A maps to NM_032531.3 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:126432805 C>T maps to NM_032531.3 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr11:126318982 C>T maps to NM_032531.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:126294582 G>A maps to NM_032531.3 F743F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:126301253 G>A maps to NM_001161707.1 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr11:126870372 G>A maps to NM_032531.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:55599240 T>C maps to NM_000222.2 I789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:55593626 G>T maps to NM_000222.2 G565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr4:55561762 C>T maps to NM_000222.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:55561690 A>G maps to NM_000222.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:55595592 G>T maps to NM_000222.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:55592205 T>C maps to NM_000222.2 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:55592143 G>T maps to NM_000222.2 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:88910237 T>C maps to NM_000899.4 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:33638010 T>C maps to NM_004795.3 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr13:33635226 C>T maps to NM_004795.3 R671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:39409219 C>A maps to NM_175737.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:39448457 T>C maps to NM_175737.3 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr4:39435900 G>A maps to NM_175737.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:39409384 C>T maps to NM_175737.3 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:104136523 G>A maps to ENST00000445352 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:104153527 G>A maps to ENST00000334553 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:66029412 C>T maps to NM_022822.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:66034014 G>A maps to ENST00000394065 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:45848909 G>A maps to NM_177417.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:43033371 C>T maps to NM_201523.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:12997891 C>T maps to NM_006563.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr8:103663815 C>T maps to NM_005655.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:103664538 A>G maps to NM_005655.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:10188450 C>T maps to NM_003597.4 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:74420000 G>A maps to NM_007249.4 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:74420288 G>T maps to NM_007249.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:130418230 C>T maps to NM_138693.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:130418269 G>A maps to NM_138693.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:126062650 G>A maps to NM_014079.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:126071723 C>T maps to NM_014079.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:1854676 C>T maps to NM_031918.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr19:1863073 G>A maps to NM_031918.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:44584588 C>T maps to NM_173484.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:44595827 C>A maps to NM_173484.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:38690412 C>A maps to NM_016531.5 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:38682296 C>T maps to NM_016531.5 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:38698736 C>T maps to NM_016531.5 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr9:110249443 C>A maps to NM_004235.4 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:110249588 C>T maps to NM_004235.4 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:110249588 C>T maps to NM_004235.4 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:110251327 C>T maps to NM_004235.4 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:73649879 C>T maps to NM_001730.3 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:3824208 C>T maps to NM_001300.5 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:207989095 C>T maps to NM_003709.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:207989074 C>T maps to NM_003709.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:207953245 C>A maps to NM_003709.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:207988558 G>A maps to NM_003709.2 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:56291612 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:56296716 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:56295862 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:56310906 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:56276665 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:56295848 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:56310822 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:56291622 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:56291865 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:56292144 T>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:50218489 A>C maps to NM_172193.2 *407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:129764375 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:129767242 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:129769338 C>T maps to NM_014997.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:129769275 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:50244958 C>T maps to NM_014315.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:42985416 C>A maps to NM_057161.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:87748146 C>T maps to NM_017566.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:87742952 G>A maps to NM_017566.3 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:27933943 G>A maps to NM_020782.1 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr12:27934136 T>G did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr12:27950765 C>T maps to NM_020782.1 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:50987953 C>T maps to NM_138433.3 Y453Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:205307699 G>T maps to NM_018203.1 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:205312456 C>T maps to NM_018203.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:205312474 G>A maps to NM_018203.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49212319 C>A maps to NM_173546.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr3:49213141 C>T maps to NM_173546.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:49211825 C>A maps to NM_173546.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:49210369 G>A maps to NM_173546.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:70281858 G>C maps to NM_020866.2 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:70456596 C>A maps to NM_020866.2 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:70413258 C>T maps to NM_020866.2 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:70456524 C>A maps to NM_020866.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:70370968 G>A maps to NM_020866.2 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:70371055 G>A maps to NM_020866.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:70370968 G>A maps to NM_020866.2 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:40001481 A>C maps to NM_152467.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr17:40011488 G>A maps to NM_018143.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:40010738 T>C maps to NM_018143.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:202863725 G>T maps to NM_021633.2 Y429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:202862410 A>G maps to NM_021633.2 Y512Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:117043860 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:117054290 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:117033083 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:117033287 C>A did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:117079441 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr23:117053678 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:117043787 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:117044001 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:117035909 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:117043464 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117044001 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117053613 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:117044001 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:117043590 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:117033092 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:117043344 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117053528 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:117043930 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:117043366 C>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:24024527 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:24006223 T>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:24006899 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:24024379 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:24006938 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:24024676 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:24007102 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:24006123 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:24024328 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:24006954 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:24024639 T>G did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:24024736 T>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:24024640 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:24024179 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:24006659 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:47384289 C>T maps to NM_025010.4 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:47361147 G>A maps to NM_025010.4 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:47385166 C>A maps to NM_025010.4 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:166231873 C>T maps to NM_001161521.1 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr4:166150051 T>C maps to NM_001161521.1 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:173744869 C>A maps to NM_014458.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:173726139 C>T maps to NM_014458.3 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:6653514 C>T maps to NM_014851.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2D2-01A-11D-A17D-09 chr1:6653712 A>G maps to NM_014851.2 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:20819419 G>A maps to NM_032775.3 N279N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:20843315 G>A maps to NM_032775.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:20819166 G>A maps to NM_032775.3 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr22:20812232 G>A maps to NM_032775.3 H389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:170597965 G>T maps to NM_144711.5 G429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:183396926 A>G maps to NM_017644.3 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:183368369 G>T maps to NM_017644.3 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:183382724 C>T maps to NM_017644.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:18778566 C>T maps to NM_018316.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:45414966 G>A maps to ENST00000355081 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:45403501 C>A maps to ENST00000355081 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr14:45415029 G>C maps to ENST00000355081 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:137045538 C>T maps to NM_017415.2 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:136963984 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:137033999 G>A maps to NM_017415.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:136961466 G>A maps to NM_017415.2 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:136993956 C>A maps to NM_017415.2 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:136997680 C>A maps to NM_017415.2 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:239049613 C>T maps to NM_198582.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:239054441 G>T maps to NM_198582.3 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:239049691 G>A maps to NM_198582.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:53519254 A>G maps to NM_001003760.4 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:97561843 C>A maps to NM_052904.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr6:97562269 G>A maps to NM_052904.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:21674882 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:21674197 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:21675205 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:21675212 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:21674363 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:21675200 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:21675703 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:21675714 T>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:21675236 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:84695222 C>T maps to NM_024731.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:84684523 C>T maps to NM_024731.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:84693478 C>T maps to NM_024731.2 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:124664452 G>A maps to NM_001081675.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:124665124 G>A maps to NM_001081675.2 H14H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:124665016 G>A maps to NM_001081675.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr8:124665025 G>A maps to NM_001081675.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:86924366 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:86924384 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:86924370 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:86868964 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:86873098 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:86877312 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:86869012 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:86887398 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:86888854 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:86919894 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr23:86877346 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:86868988 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:86880686 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:86890614 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:86773234 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:86872943 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:86924378 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:86877276 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:86773264 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:86873029 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:86772972 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:86772977 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:86887340 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:86890626 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:86890710 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:86887421 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:39082795 G>T maps to NM_015990.4 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:39088136 G>A maps to NM_015990.4 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:39064157 A>G maps to NM_015990.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr4:39064613 C>T maps to NM_015990.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:183226155 G>A maps to NM_130446.2 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:183209789 C>T maps to NM_130446.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:183273318 G>T maps to NM_130446.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:183210353 A>G maps to NM_130446.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:183209810 G>A maps to NM_130446.2 C590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:23180388 T>C maps to NM_001031710.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:23205430 C>T maps to NM_001031710.2 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:23213805 C>T maps to NM_001031710.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:23213673 C>T maps to NM_001031710.2 N506N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:88085166 C>T maps to NM_020803.3 W534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:88091266 C>A maps to NM_020803.3 G501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:88084714 G>A maps to NM_020803.3 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:88091293 C>A maps to NM_020803.3 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:88091293 C>A maps to NM_020803.3 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr4:88099655 G>A maps to NM_020803.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr4:88104460 A>G maps to NM_020803.3 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr4:88084714 G>A maps to NM_020803.3 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:88091293 C>A maps to NM_020803.3 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:21334719 C>A maps to NM_018847.2 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:21334599 C>A maps to NM_018847.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:21334099 G>A maps to NM_018847.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:21334590 A>G maps to NM_018847.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:21333754 T>A maps to NM_018847.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr9:21333733 C>T maps to NM_018847.2 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:51323184 T>G maps to NM_002257.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:51518157 G>T maps to NM_001077500.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:687022 G>A maps to NM_214710.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:51563799 G>A maps to NM_015596.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:51329966 C>T maps to NM_017509.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:51359541 C>T maps to NM_001648.2 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:51362790 C>A maps to NM_001030047.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:51361296 C>T maps to NM_001648.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:51413933 C>A maps to NM_004917.3 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:51452124 C>T maps to NM_012427.4 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:51452352 G>A maps to NM_012427.4 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr19:51471318 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:51462488 C>T maps to NM_001012964.1 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr19:51485077 C>A maps to NM_005046.2 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:51501099 G>T maps to NM_144505.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:51503455 C>A maps to NM_144505.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:51506383 C>A maps to NM_012315.1 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:187175829 G>T maps to ENST00000511608 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:187178432 G>T maps to ENST00000511608 E594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr4:187130328 C>T maps to ENST00000511608 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:9751120 G>A maps to NM_002258.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:9747910 C>A maps to NM_002258.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:10599149 C>A maps to NM_213658.2 *234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:10562068 G>A maps to NM_013431.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:10560374 G>A maps to NM_013431.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr12:9985920 A>G maps to NM_016523.1 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:9147868 G>A maps to NM_005810.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:139138359 G>T maps to NM_198508.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:241752098 G>A maps to NM_003679.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:241695751 C>A maps to NM_003679.3 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:241752098 G>A maps to NM_003679.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:47014939 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:135020651 G>A maps to ENST00000368572 A1199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr10:135038273 C>T maps to ENST00000368572 S1712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:135026362 G>A maps to ENST00000368572 G1462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:134981791 C>T maps to ENST00000368572 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:134981809 C>A maps to ENST00000368572 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:135020750 C>A maps to ENST00000368572 S1232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:135038168 C>T maps to ENST00000368572 I1677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:134981756 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:135026383 C>T maps to ENST00000368572 Y1469Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr10:135027553 A>G maps to ENST00000368572 L1537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:135015104 C>T maps to ENST00000368572 F1032F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:135025184 C>T maps to ENST00000368572 I1355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:134981791 C>T maps to ENST00000368572 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr10:135013932 G>A maps to ENST00000368572 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:186459802 G>T maps to NM_001102416.2 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:186445072 G>A maps to NM_001102416.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:186443045 A>G maps to NM_001102416.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:186445125 G>A maps to NM_001102416.2 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:123060103 C>T maps to NM_014708.4 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:123061461 C>G maps to NM_014708.4 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:123034377 T>C maps to NM_014708.4 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr12:123089425 C>T maps to NM_014708.4 D1726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:123057705 A>C maps to NM_014708.4 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:123107037 C>A maps to NM_014708.4 I2133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr12:123082349 C>T maps to NM_014708.4 G1476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:122215397 T>C maps to NM_002264.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:122145777 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:122145713 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:122182860 C>A maps to NM_002264.3 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:50299558 C>T maps to NM_002267.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:160239643 G>A maps to NM_002268.3 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:160243797 T>C maps to NM_002268.3 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:32625023 G>A maps to NM_012316.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:32632804 C>T maps to NM_012316.4 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:45730221 C>T maps to NM_002265.4 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:45755419 C>T maps to NM_002265.4 N704N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:45753823 G>A maps to NM_002265.4 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:45755409 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr17:45754459 C>T maps to NM_002265.4 D690D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:152732099 G>A maps to NM_001025231.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:152733044 C>T maps to NM_001025231.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:152732849 G>A maps to NM_001025231.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:152732924 C>A maps to NM_001025231.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:152732459 C>T maps to NM_001025231.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr19:47983623 G>T maps to NM_007059.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:47978758 G>A maps to NM_007059.2 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr12:25398279 G>A maps to NM_033360.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr12:25398249 T>C maps to NM_033360.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:149416749 G>A maps to NM_032534.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:8272904 C>T maps to NM_213597.2 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:8272949 G>A maps to NM_213597.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:8273632 C>A maps to NM_213597.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:8274702 C>T maps to NM_213597.2 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:88327755 G>A maps to NM_016618.1 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr22:29533327 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:29534699 C>T maps to NM_032045.4 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr16:3018002 G>A maps to NM_172229.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr16:3016719 C>T maps to NM_172229.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:10671738 G>A maps to NM_023008.3 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:10664752 C>T maps to NM_023008.3 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr19:10670339 C>T maps to NM_023008.3 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:10670064 G>A maps to NM_023008.3 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:10670506 G>A maps to NM_023008.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:91870394 A>G maps to NM_194456.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:91852279 G>A maps to NM_194456.1 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:91852279 G>A maps to NM_194456.1 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:91863866 G>A maps to NM_194456.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:91864910 G>A maps to NM_194456.1 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr12:53070922 T>A maps to NM_006121.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:53070090 G>T maps to NM_006121.3 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:38975877 G>A maps to NM_000421.3 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:38976299 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:38976360 A>G maps to NM_000421.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:39021102 C>T maps to NM_000223.3 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:39023059 C>A maps to NM_000223.3 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:39022999 C>A maps to NM_000223.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:39661661 G>A maps to NM_153490.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:39659908 G>A maps to NM_153490.2 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:39658840 C>T maps to NM_153490.2 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:39670903 C>A maps to NM_002275.3 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:39673143 C>T maps to NM_002275.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:39673405 G>T maps to NM_002275.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:39670292 G>A maps to NM_002275.3 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:39670282 C>A maps to NM_002275.3 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:39768883 G>A maps to NM_005557.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr17:39777997 G>A maps to NM_000422.2 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:53345576 G>A maps to NM_000224.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:53343374 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:39680668 G>A maps to NM_002276.4 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:53039138 G>T maps to NM_000423.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:53040561 G>A maps to NM_000423.2 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:53043706 C>T maps to NM_000423.2 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:39041173 C>T maps to NM_019010.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:38813644 C>T maps to NM_152349.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:39086302 G>A maps to NM_015515.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:39084856 T>C maps to NM_015515.3 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:39092800 C>A maps to NM_015515.3 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr17:39079246 G>A maps to NM_015515.3 H421H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:39081738 C>A maps to NM_015515.3 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr17:39081643 G>T maps to NM_015515.3 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr17:39080730 G>A maps to NM_015515.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38856527 G>A maps to NM_019016.2 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr17:38911130 G>A maps to NM_181534.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:38910717 G>T maps to NM_181534.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:38910198 A>G maps to NM_181534.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:38907295 G>A maps to NM_181534.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:38928284 G>T maps to NM_181539.4 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:38925239 G>A maps to NM_181539.4 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:38927476 C>T maps to NM_181539.4 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:38953497 G>A maps to NM_181535.3 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:38950165 G>A maps to NM_181535.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:38953470 C>T maps to NM_181535.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:38956031 G>A maps to NM_181535.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:53184619 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:53184086 G>C maps to ENST00000309505 Y543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:53185492 G>A maps to ENST00000309505 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:39550387 C>T maps to ENST00000393998 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:39553713 G>A maps to ENST00000393998 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:39551122 G>A maps to ENST00000393998 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:39506869 G>T maps to NM_004138.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:39521058 G>T maps to ENST00000394004 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:39577665 C>T maps to NM_003770.4 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:39596906 A>G maps to NM_006771.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr17:39596846 C>T maps to NM_006771.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:39116741 T>C maps to NM_213656.3 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:39118724 C>A maps to NM_213656.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:39122765 G>A maps to NM_213656.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:39122652 C>T maps to NM_213656.3 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr17:39118418 G>A maps to NM_213656.3 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53207692 T>C maps to NM_002272.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:53207817 G>A maps to NM_002272.2 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr12:53204566 G>A maps to NM_002272.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:39138557 C>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:39135093 G>A maps to NM_182497.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr17:39138605 C>A maps to NM_182497.3 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:52911522 G>A maps to NM_000424.3 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:52909582 G>T maps to NM_000424.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr12:52910980 G>A maps to NM_000424.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:52881704 G>A maps to NM_005554.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52884490 G>T maps to NM_005554.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52885361 G>A maps to NM_005554.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:52882329 G>A maps to NM_005554.3 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:52883813 G>A maps to NM_005554.3 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:52881560 A>G maps to NM_005554.3 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:52881704 G>A maps to NM_005554.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:52884490 G>T maps to NM_005554.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:52882215 G>A maps to NM_005554.3 D440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:52845619 G>A maps to NM_005555.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:52843378 G>A maps to NM_005555.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:52842643 G>A maps to NM_005555.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:52842643 G>A maps to NM_005555.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:52841347 G>A maps to NM_005555.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:52867236 G>A maps to NM_173086.4 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:52864990 G>A maps to NM_173086.4 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:52867364 C>A maps to NM_173086.4 G53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr12:52639248 G>A maps to NM_005556.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:52635420 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:52940197 G>A maps to NM_033448.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:52946438 G>A maps to NM_033448.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:52940107 G>A maps to NM_033448.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:52981452 G>A maps to NM_080747.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:52992746 C>T maps to NM_080747.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:53005047 G>T maps to NM_175068.2 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:53004520 C>T maps to NM_175068.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:52967251 A>G maps to NM_175053.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52964593 G>A maps to NM_175053.3 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:52818411 G>A maps to ENST00000252245 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52822461 G>T maps to ENST00000252245 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52824399 G>A maps to ENST00000252245 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52825846 G>A maps to ENST00000252245 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52827608 G>A maps to ENST00000252245 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:52827027 G>A maps to ENST00000252245 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:52827608 G>A maps to ENST00000252245 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:52822524 G>A maps to ENST00000252245 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:52825419 G>A maps to ENST00000252245 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:52825416 T>C maps to ENST00000252245 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:52822461 G>T maps to ENST00000252245 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:53170649 A>G maps to NM_015848.4 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:53169368 C>T maps to NM_015848.4 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:53096798 G>T maps to NM_175078.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr12:53085089 G>T maps to NM_175078.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:53237960 C>T maps to NM_173352.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53217786 G>A maps to NM_175834.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:53227732 C>T maps to NM_175834.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr12:53291256 A>G maps to NM_002273.3 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:53293666 G>A maps to NM_002273.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53298584 C>A maps to NM_002273.3 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:53293803 G>A maps to NM_002273.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr12:53291334 A>G maps to NM_002273.3 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:53291403 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52565229 G>A maps to NM_182507.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr12:52565196 C>T maps to NM_182507.2 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:52566019 G>A maps to NM_182507.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52682171 G>A maps to NM_002281.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr12:52680143 G>A maps to NM_002281.3 C471C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:52680257 G>A maps to NM_002281.3 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05D-01A-11W-A027-09 chr12:52708438 G>A maps to NM_002282.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:52711515 G>A maps to NM_002282.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52709096 G>T maps to NM_002282.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:52713085 G>A maps to NM_002282.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:52760898 G>A maps to NM_002283.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:52758819 G>A maps to NM_002283.3 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:52758912 C>T maps to NM_002283.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr12:52760985 T>C maps to NM_002283.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52760787 G>A maps to NM_002283.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:52756053 G>A maps to NM_002283.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:52756742 C>T maps to NM_002283.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:52756210 A>G maps to NM_002283.3 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:52756072 G>A maps to NM_002283.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:52761036 G>A maps to NM_002283.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr12:52757080 G>A maps to NM_002283.3 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:39723974 G>A maps to NM_000226.3 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:39190715 G>A maps to NM_030966.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:45959457 G>T maps to NM_198691.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:45959706 G>T maps to NM_198691.2 C109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:45959439 G>T maps to NM_198691.2 C198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:46066566 C>T maps to NM_198692.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:46067268 C>A maps to NM_198692.2 C298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:46117415 C>T maps to NM_198699.1 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:46117217 G>A maps to NM_198699.1 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:45993931 C>T maps to NM_198687.1 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:46012161 G>A maps to NM_198688.2 C68C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:46021021 G>A maps to ENST00000380102 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:46032529 C>T maps to NM_198695.2 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr21:32253405 C>A maps to NM_175858.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:32253450 G>A maps to NM_175858.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:32253794 C>A maps to NM_175858.2 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:46074501 G>A maps to NM_198698.1 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:31744459 G>A maps to NM_181621.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:31720613 C>A maps to ENST00000448917 G89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:31797912 G>A maps to NM_181622.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:31802661 C>T maps to NM_181600.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:31812776 C>T maps to NM_181623.1 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr21:31812921 A>C maps to NM_181623.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr21:31812701 G>A maps to NM_181623.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:31812749 C>A maps to NM_181623.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr21:31852450 G>A maps to NM_181607.1 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:31864263 G>A maps to NM_181609.3 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:31874294 G>A maps to NM_181611.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:31874354 G>A maps to NM_181611.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:31874258 G>A maps to NM_181611.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:31914086 G>A maps to ENST00000437381 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:31933554 G>A maps to ENST00000437381 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:31988914 G>T maps to ENST00000399871 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr21:32007683 C>T maps to NM_181616.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:32127678 G>A maps to NM_181619.1 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr21:31973468 C>A maps to NM_181620.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:31655079 G>T maps to NM_001085455.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:31691803 T>G maps to NM_203405.1 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr21:31709533 G>A maps to NM_001077711.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr21:31709533 G>A maps to NM_001077711.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:31709533 G>A maps to NM_001077711.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr21:31709533 G>A maps to NM_001077711.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:39165305 G>A maps to NM_031958.1 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:39155946 T>C maps to NM_031959.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:39340716 G>T maps to ENST00000458321 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:39341100 A>G maps to ENST00000398472 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:39274225 G>T maps to NM_033059.3 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:39279857 G>T maps to NM_031854.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:39316880 G>A maps to NM_032524.1 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:39316646 G>T maps to NM_032524.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:39305851 G>A maps to NM_033188.3 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:39254159 G>A maps to NM_031960.2 C59C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:39262371 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:39261975 G>A maps to NM_001146041.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:1605999 A>G maps to NM_001005922.1 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:1605951 G>T maps to NM_001005922.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr11:1605789 G>A maps to NM_001005922.1 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:71276851 C>T maps to ENST00000422553 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:71293427 G>T maps to ENST00000376535 C152*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:1628991 G>T maps to ENST00000359229 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:1629153 G>A maps to NM_001012708.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:1629150 G>A maps to NM_001012708.2 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:1629027 C>T maps to ENST00000359229 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:1629093 G>A maps to ENST00000359229 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:1643053 G>T maps to ENST00000359229 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:1651402 C>T maps to NM_001001480.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:71238459 C>T maps to NM_001012503.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr21:31986106 G>A maps to NM_181602.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:31971142 G>A maps to NM_181604.1 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:39383020 C>T maps to NM_031961.2 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:39406433 C>T maps to NM_033191.2 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:39394440 C>T maps to NM_031963.2 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr17:39412140 C>T maps to ENST00000431129 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27665952 C>T maps to NM_001168364.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27666335 C>A maps to NM_001168364.1 C184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:25936277 C>T maps to ENST00000268763 N661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:25936227 G>T maps to ENST00000268763 G645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr17:25928931 C>T maps to ENST00000268763 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr12:117968783 C>T maps to ENST00000339824 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:117909046 G>A maps to ENST00000339824 G887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:117962913 G>T maps to ENST00000339824 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:117968753 C>T maps to ENST00000339824 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:117922297 G>A maps to ENST00000339824 N791N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:118199084 C>T maps to ENST00000339824 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:118199258 G>A maps to ENST00000339824 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:52498797 T>C maps to NM_138417.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:56119645 G>A maps to NM_001079521.1 G894G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:56078856 G>T maps to NM_001079521.1 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:56079159 G>T maps to NM_001079521.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:56079017 T>C maps to NM_001079521.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:56139397 C>T maps to NM_001079521.1 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:56078856 G>T maps to NM_001079521.1 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:56134016 T>G maps to NM_001079521.1 L1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:56078895 G>T maps to NM_001079521.1 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:134338003 G>A maps to NM_178554.4 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:134366277 G>A maps to NM_178554.4 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:134369751 G>A maps to NM_178554.4 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr3:134329041 G>T maps to NM_178554.4 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:134323080 G>A maps to NM_178554.4 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:143798010 G>A maps to NM_003937.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:143799613 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr23:153131221 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:153132121 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153128131 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153130061 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153128960 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153130106 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153130076 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr23:153135085 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153133893 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:153133821 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:153129906 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153133527 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:153129847 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153132185 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153133874 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:153135529 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:153130605 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr23:153128231 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr23:153135016 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:153134981 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153128960 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153131249 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153138105 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:153132959 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153132568 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153134335 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153135570 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153130375 A>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153135895 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:153141286 A>G did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:153131168 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:153133558 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:153132201 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:62675690 G>A maps to NM_019079.4 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:62675732 C>A maps to NM_019079.4 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:62676789 G>T maps to NM_019079.4 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:62676426 G>T maps to NM_019079.4 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:62675967 G>T maps to NM_019079.4 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:62675645 C>A maps to NM_019079.4 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:62676978 G>T maps to NM_019079.4 E845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:62672876 G>T maps to NM_019079.4 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:41625568 G>A maps to NM_031488.4 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:41623253 C>T maps to NM_031488.4 C583C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:41615451 G>T maps to NM_031488.4 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:41620973 C>T maps to NM_031488.4 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:41621937 G>A maps to NM_031488.4 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:130454720 C>T maps to NM_032438.2 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr6:130374064 C>A maps to NM_032438.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:130381236 C>T maps to NM_032438.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:130392203 G>A maps to NM_032438.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:130387502 T>C maps to NM_032438.2 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:6263972 G>A maps to NM_173464.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:6241448 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:6263986 C>A maps to NM_173464.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:6239871 C>A did not map to a codon.
Alternatively spliced codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:108645029 C>A maps to ENST00000437715 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:55026145 G>A maps to NM_033277.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr15:63433622 G>T maps to NM_032857.3 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:63419745 G>A maps to NM_032857.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr8:71573966 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr8:71553219 G>A maps to NM_016027.2 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:201352291 G>A maps to NM_005558.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:201355837 C>T maps to NM_005558.3 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:201352332 C>A maps to NM_005558.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:6883842 C>A maps to NM_002286.5 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153706364 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:54870167 C>T maps to ENST00000444687 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:55020243 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:55019340 C>A maps to NM_002288.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr18:6976067 G>A maps to NM_005559.2 A2119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr18:6986213 G>A maps to NM_005559.2 L1767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:6973064 T>C maps to NM_005559.2 G2255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:6950780 C>T maps to NM_005559.2 T2799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:7040193 C>A maps to NM_005559.2 G435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr18:7034620 G>A maps to NM_005559.2 N636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr18:6964760 C>A maps to NM_005559.2 E2413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:6992719 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:6995429 C>A maps to NM_005559.2 E1608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:7050932 G>T maps to NM_005559.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:7016514 G>A maps to NM_005559.2 Y988Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:7032151 G>A maps to NM_005559.2 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr18:6986143 C>A maps to NM_005559.2 E1791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:129371199 C>T maps to NM_000426.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:129573285 G>T maps to NM_000426.3 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:129588355 G>T maps to NM_000426.3 E772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:129635891 C>T maps to NM_000426.3 C1168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:129813195 C>T maps to NM_000426.3 C2683C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:129777578 G>A maps to NM_000426.3 T2269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:129618930 G>A maps to NM_000426.3 W986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:129670460 C>T maps to NM_000426.3 V1485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:129813048 C>T maps to NM_000426.3 I2634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:129573319 C>A maps to NM_000426.3 S659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:129581957 C>A maps to NM_000426.3 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:129687394 C>T maps to NM_000426.3 L1583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:129775317 G>T maps to NM_000426.3 E2198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:129513952 G>A maps to NM_000426.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:129513872 C>T maps to NM_000426.3 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:129573285 G>T maps to NM_000426.3 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:129663486 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:129802566 C>T maps to NM_000426.3 R2578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:129511406 G>T maps to NM_000426.3 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr6:129687451 G>A maps to NM_000426.3 L1602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:129371127 G>T maps to NM_000426.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:129723623 C>A maps to NM_000426.3 V1906V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr6:129636999 C>T maps to NM_000426.3 R1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr6:129748967 C>T maps to NM_000426.3 N1979N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:129371192 G>A maps to NM_000426.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr18:21451570 A>G maps to ENST00000416669 A1650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:21532975 G>A maps to ENST00000416669 L3255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:21523901 C>T maps to ENST00000416669 S3061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr18:21437852 C>T maps to ENST00000416669 S1396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:21413847 C>T maps to ENST00000416669 V962V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:21483938 G>T maps to ENST00000416669 E2123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:21395183 G>T maps to ENST00000416669 G643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:21413943 C>T maps to ENST00000416669 C994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:21413847 C>A maps to ENST00000416669 V962V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:21422438 G>A maps to ENST00000416669 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr18:21534476 G>A maps to ENST00000416669 T3291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:21329414 G>T maps to ENST00000416669 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:21338419 G>A maps to ENST00000416669 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:21496563 C>T maps to ENST00000416669 R2612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr6:112435279 T>C maps to NM_001105206.1 P1775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:112437131 G>A maps to NM_001105206.1 S1682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:112462662 G>A maps to NM_001105206.1 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:112508672 G>A maps to NM_001105206.1 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:112435893 G>A maps to NM_001105206.1 L1726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:112460365 G>A maps to NM_001105206.1 R1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:112460447 G>A maps to NM_001105206.1 F1052F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:112460447 G>A maps to NM_001105206.1 F1052F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:112438972 G>T maps to NM_001105206.1 Y1650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:112493968 A>G maps to NM_001105206.1 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:112430687 T>A maps to NM_001105206.1 A1808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:112471734 C>T maps to NM_001105206.1 K717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr6:112575085 G>A maps to NM_001105209.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:60900479 G>A maps to NM_005560.3 F1807F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:60886293 G>A maps to NM_005560.3 R3338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:60887318 C>T maps to NM_005560.3 S3138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:60887689 C>T maps to NM_005560.3 P3075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr20:60893989 G>A maps to NM_005560.3 A2317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:60886363 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr20:60904035 T>C maps to NM_005560.3 P1437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:60892828 C>T maps to NM_005560.3 R2415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:107575960 G>A maps to NM_002291.2 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:107621119 G>T maps to NM_002291.2 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:107580774 C>T maps to NM_002291.2 E1140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:107626772 C>T maps to NM_002291.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:107635405 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:107600268 G>A maps to NM_002291.2 C775C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:107601683 G>A maps to NM_002291.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr7:107576084 A>T maps to NM_002291.2 I1321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr7:107602115 G>A maps to NM_002291.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:107596053 G>A maps to NM_002291.2 G904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:107570032 T>G maps to NM_002291.2 A1523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49159692 G>A maps to NM_002292.3 R1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49166174 C>T maps to NM_002292.3 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:49161024 G>A maps to NM_002292.3 L1279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:49163582 G>A maps to NM_002292.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:49167057 T>C maps to NM_002292.3 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:49168863 A>G maps to NM_002292.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr3:49161027 C>T maps to NM_002292.3 Q1278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr3:49167371 G>A maps to NM_002292.3 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr3:49169823 G>A maps to NM_002292.3 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:49160169 C>A maps to NM_002292.3 E1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:49159212 C>T maps to NM_002292.3 E1668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:49159122 A>G maps to NM_002292.3 A1698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:209807968 G>A maps to NM_000228.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:209803220 C>T maps to NM_000228.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:209796010 C>T maps to NM_000228.2 E857E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:209797248 A>G maps to NM_000228.2 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:209811972 C>T maps to NM_000228.2 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:209791834 C>T maps to NM_000228.2 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:209799270 C>T maps to NM_000228.2 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:209796999 C>T maps to NM_000228.2 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:209811990 C>T maps to NM_000228.2 W62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:209803265 G>A maps to NM_000228.2 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr7:107708604 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:107684260 G>A maps to NM_007356.2 N1469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:107669499 T>G maps to NM_007356.2 R1712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:107684323 T>C maps to NM_007356.2 E1448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:107717448 G>T maps to NM_007356.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:107743555 G>A maps to NM_007356.2 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:183084655 C>A maps to NM_002293.3 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:183111823 C>T maps to NM_002293.3 R1577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:183111750 C>T maps to NM_002293.3 S1552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:183079640 C>T maps to NM_002293.3 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:183079781 A>G maps to NM_002293.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:183101666 T>C maps to NM_002293.3 N1233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:183111750 C>T maps to NM_002293.3 S1552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:183099620 A>T maps to NM_002293.3 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:183083771 C>T maps to NM_002293.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:183099638 C>T maps to NM_002293.3 I1147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:183093841 C>T maps to NM_002293.3 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:183184585 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:183190056 G>T maps to NM_005562.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:183177130 C>T maps to NM_005562.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:183203500 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:183201844 C>T maps to NM_005562.2 Y691Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr1:183197591 C>T maps to NM_005562.2 Q518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr1:183209467 C>T maps to NM_005562.2 N1090N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:133951326 G>T maps to ENST00000355048 E1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:133942449 C>T maps to ENST00000355048 D817D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:133952639 G>A maps to ENST00000355048 A1232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:133901954 C>T maps to ENST00000355048 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr9:133952630 G>A maps to ENST00000355048 L1229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr9:133952657 C>T maps to ENST00000355048 T1238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:113973964 C>T maps to NM_005561.3 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:113974778 C>T maps to NM_005561.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:119580248 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:119565293 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:119582915 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119562438 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119590620 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr23:119573031 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:119573052 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:119581875 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:119589308 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:119575684 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119565200 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:119573111 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr23:119581761 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:119602961 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:182853646 C>T maps to NM_014398.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:182871802 A>C maps to NM_014398.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:182872168 G>A maps to NM_014398.3 H20H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:55466116 C>T maps to NM_018697.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:55493089 G>A maps to NM_018697.3 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:55499000 G>A maps to NM_018697.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr7:55467754 A>G maps to NM_018697.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:37534987 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:37518856 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:37526655 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:17600149 G>A maps to NM_015907.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:17581473 G>T maps to NM_015907.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:17609064 C>T maps to NM_015907.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:17581473 G>T maps to NM_015907.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:17609064 C>T maps to NM_015907.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:33733631 G>A maps to NM_133642.3 N429N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:34046350 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:33679279 G>A maps to NM_133642.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:34022241 G>A maps to NM_133642.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:34157361 G>A maps to NM_133642.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:33673201 G>A maps to NM_133642.3 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:33670547 G>A maps to NM_133642.3 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr22:33780288 C>T maps to NM_133642.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr22:33673045 C>T maps to NM_133642.3 Q691Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:154170209 T>C maps to ENST00000377643 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:154179433 G>A maps to ENST00000377643 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:154179439 A>G maps to ENST00000377643 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:154181730 T>C maps to ENST00000377643 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:154174735 G>T maps to ENST00000377643 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:154193631 G>A maps to ENST00000377643 S1089S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:154188091 A>G maps to ENST00000377643 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:154169882 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:154173212 G>A maps to ENST00000377643 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:129120620 C>T maps to NM_018078.2 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:129120746 C>T maps to NM_018078.2 C719C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr4:129131183 G>A maps to NM_018078.2 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr4:129019449 C>T maps to NM_018078.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:129043088 C>T maps to NM_018078.2 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:129099655 G>A maps to NM_018078.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:129127661 C>T maps to NM_018078.2 Q797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:50867862 T>C maps to ENST00000429001 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:50869509 C>A maps to ENST00000429001 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr12:50869556 G>A maps to ENST00000429001 Q701Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:859146 G>A maps to NM_015155.1 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:860917 G>A maps to NM_015155.1 Y596Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:875432 C>T maps to NM_015155.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:860669 C>T maps to ENST00000263154 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:71124945 G>A maps to NM_018357.2 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:71144019 C>T maps to NM_197958.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:71124471 G>A maps to NM_018357.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:71125077 G>A maps to NM_018357.2 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:113568386 C>T maps to ENST00000509061 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:113570693 C>T maps to ENST00000509061 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:113574349 G>T maps to ENST00000509061 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:145547761 C>A maps to NM_020117.9 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:145508567 C>T maps to NM_020117.9 K914K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:145522643 C>T maps to NM_020117.9 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr5:145522643 C>T maps to NM_020117.9 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:145557138 G>T maps to NM_020117.9 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:45541931 A>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:45533226 T>G maps to NM_015340.3 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:45530259 G>T maps to NM_015340.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:64744104 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:64749609 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:64749108 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:64749712 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:64751306 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:64753513 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:64737867 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:64749524 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:64751258 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:64749687 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:64744125 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:64738071 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:64738299 C>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:64738004 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:64734848 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:64749619 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:73638054 T>C maps to NM_032464.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:73634559 T>C maps to NM_032464.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr6:150005069 G>A maps to NM_004690.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:150001373 G>A maps to NM_004690.2 R744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:150001394 G>A maps to NM_004690.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:150022964 C>A maps to NM_004690.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:150023018 G>A maps to NM_004690.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:150023018 G>A maps to NM_004690.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:21555629 G>A maps to NM_014572.2 I880I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:21565498 G>A maps to NM_014572.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:21549230 G>A maps to NM_014572.2 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:21549353 G>A maps to NM_014572.2 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:21549115 G>A maps to NM_014572.2 R1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:203740522 C>T maps to NM_017773.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:203743394 T>A maps to NM_017773.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:203743061 C>T maps to NM_017773.3 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:30480453 C>T maps to NM_030915.3 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr2:30480480 G>A maps to NM_030915.3 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:36993327 C>A maps to NM_004139.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:36997772 C>T maps to NM_004139.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:36993348 G>A maps to NM_004139.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:36992638 G>A maps to NM_004139.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:225609787 C>T maps to NM_194442.1 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:102988470 C>T maps to NM_006562.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:80202351 C>A maps to NM_181714.3 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:80197568 C>A maps to NM_181714.3 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:80197370 G>A maps to NM_181714.3 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr21:40778349 C>A maps to NM_152505.3 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:40778044 T>C maps to NM_152505.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:40778019 C>A maps to NM_152505.3 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:40781998 G>A maps to NM_152505.3 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:40783685 G>A maps to NM_152505.3 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:40795314 G>A maps to NM_152505.3 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:40800106 G>A maps to NM_152505.3 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:40781964 C>A maps to NM_152505.3 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr16:67974001 G>A maps to NM_000229.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:67974156 G>A maps to NM_000229.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:67977092 C>T maps to NM_000229.1 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:152800214 C>T maps to NM_178348.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:152800067 C>A maps to NM_178348.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:152800214 C>T maps to NM_178348.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:152785239 T>C maps to NM_178349.1 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:152760047 G>A maps to ENST00000417924 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:152759927 C>T maps to ENST00000417924 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:152659378 T>C maps to NM_014357.4 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GE-01A-11W-A062-09 chr1:152648757 C>T maps to NM_178429.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:152636863 G>T maps to NM_178430.2 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:152586438 C>T maps to NM_178433.1 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:152586478 C>T maps to NM_178433.1 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:152552228 G>A maps to NM_032563.1 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:152538507 G>A maps to NM_178435.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:32740585 C>A maps to ENST00000373564 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:32740927 C>T maps to ENST00000373562 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:32745263 G>A maps to ENST00000373562 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:30785078 C>T maps to NM_182551.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:30756044 G>T maps to NM_182551.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:43620638 A>G maps to NM_014793.4 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:43621840 C>A maps to NM_014793.4 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:43621811 G>A maps to NM_014793.4 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:43621257 A>T maps to NM_014793.4 L477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:138415759 G>A maps to NM_002297.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:138415780 C>A maps to NM_002297.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:139635701 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:139635348 G>A maps to NM_001001712.2 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:139658350 G>A maps to NM_203347.1 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr9:139658341 G>A maps to NM_203347.1 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:139641982 G>T maps to NM_198946.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:139642881 G>A maps to NM_198946.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:139651524 G>A maps to ENST00000371689 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:138555205 C>T maps to ENST00000277526 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:98708915 G>A maps to NM_001170765.1 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:98715672 C>T maps to NM_001170765.1 N432N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:17974508 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:17886185 A>C maps to NM_001166139.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:17910715 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:17885651 A>G maps to NM_001166139.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:17847523 G>A maps to NM_153686.7 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:46716539 C>T maps to NM_002298.4 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:46718605 A>G maps to NM_002298.4 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:169714975 C>T maps to NM_005565.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:169689733 C>T maps to NM_005565.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:169720343 C>T maps to NM_005565.3 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:169720346 C>A maps to NM_005565.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:136567389 C>A maps to NM_002299.2 E843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr2:136547197 G>T maps to NM_002299.2 R1836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:136594349 G>T maps to NM_002299.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:136548387 C>T maps to NM_002299.2 T1725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr2:136562372 G>A maps to NM_002299.2 L1476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:136567237 G>A maps to NM_002299.2 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:136570166 G>A maps to NM_002299.2 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:136567081 G>A maps to NM_002299.2 D945D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:136570024 G>A maps to NM_002299.2 Q737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:136570244 G>A maps to NM_002299.2 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:136575258 G>A maps to NM_002299.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:136566157 C>T maps to NM_002299.2 T1253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:136567501 G>A maps to NM_002299.2 F805F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr15:66850162 G>A maps to NM_207338.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:66844107 T>G maps to NM_207338.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:66857621 C>A maps to NM_207338.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:66853341 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:103868773 C>T maps to ENST00000419270 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:103870824 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:103867900 C>T maps to NM_001113407.1 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:103867890 C>A maps to NM_001113407.1 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:16760786 G>A maps to NM_001290.3 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:88492708 G>A maps to NM_001171610.1 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:88477867 G>A maps to NM_001171610.1 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:88439173 C>T maps to NM_001171610.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr10:88441287 G>A maps to NM_001171610.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:88477763 G>T maps to NM_001171610.1 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:88478488 A>G maps to NM_001171610.1 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:18424560 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:18418409 G>A maps to NM_001165414.1 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:18425414 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:18478262 C>T maps to NM_144972.4 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:18485578 A>G maps to NM_144972.4 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr15:59499420 T>C maps to NM_033195.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr15:59499240 G>A maps to NM_033195.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:59499540 C>T maps to NM_033195.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:18434389 G>A maps to NM_017448.3 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:75146774 G>A maps to NM_153486.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:75148128 G>A maps to NM_153486.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr16:75147501 C>T maps to NM_153486.3 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:11240347 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:11230775 A>C maps to NM_000527.4 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr19:11213430 C>T maps to NM_000527.4 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr19:11238759 C>T maps to NM_000527.4 I796I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:54476072 G>A maps to NM_001010978.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:54477840 G>A maps to NM_001010978.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:22140930 C>T maps to NM_001013693.2 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:36248881 C>T maps to NM_174902.2 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:36057773 C>T maps to NM_174902.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:25891689 G>A maps to NM_015627.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:25893449 C>T maps to NM_015627.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr23:140271161 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:140271140 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:140270794 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:140270991 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:140271019 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:140271115 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr23:140271104 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:140270999 C>T did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:140271050 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140270950 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:132209673 G>A maps to NM_052971.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:53277861 G>A maps to NM_007015.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:53313763 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:53298152 T>C maps to NM_007015.2 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:53298235 C>A maps to NM_007015.2 G122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:135282904 A>G maps to ENST00000512872 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:109002823 G>A maps to NM_016269.4 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:109087429 C>A maps to NM_001166119.1 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:109088812 G>T maps to NM_016269.4 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:226076615 G>A maps to NM_020997.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:156729231 C>T maps to NM_001004316.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:156745951 G>T maps to NM_001004316.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:153177461 C>A maps to NM_001010857.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:153177239 C>T maps to NM_001010857.1 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:153177323 C>T maps to NM_001010857.1 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:205350931 C>A maps to ENST00000367153 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:205350914 C>T maps to ENST00000367153 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:33747938 G>T maps to NM_181336.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:65612347 C>T maps to NM_014319.4 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:65633988 A>G maps to NM_014319.4 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:65612339 G>T maps to NM_014319.4 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:65639660 T>C maps to NM_014319.4 C838C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:54662109 G>A maps to NM_024316.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:54659655 G>A maps to NM_024316.1 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:54660700 C>T maps to NM_024316.1 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:54967521 C>T maps to ENST00000431846 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:54963831 C>T maps to ENST00000431846 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:54973722 G>A maps to NM_198988.1 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:54973908 G>A maps to NM_198988.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:54973605 C>T maps to NM_198988.1 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:52258701 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr15:52258621 A>G maps to NM_138792.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:52242059 G>A maps to NM_138792.2 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:52245324 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:127894590 C>T maps to NM_000230.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:127894783 C>T maps to NM_000230.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:66075637 G>A maps to NM_002303.5 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:66036294 G>A maps to NM_002303.5 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:66088646 G>T maps to NM_002303.5 G886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:66081869 A>G maps to NM_002303.5 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:66088598 C>T maps to NM_002303.5 L870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:43218240 G>A maps to NM_022356.3 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:43213441 G>A maps to NM_022356.3 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:43212929 G>A maps to ENST00000236040 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:189689791 C>T maps to NM_018192.3 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:189688658 A>G maps to NM_018192.3 D613D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:189711930 C>A maps to NM_018192.3 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:189713219 G>A maps to NM_018192.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:189675750 C>A maps to NM_018192.3 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:189705444 C>A maps to NM_018192.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:6939162 G>A maps to NM_014262.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr12:6939548 G>A maps to NM_014262.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr1:65895637 C>T maps to NM_017526.4 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:1817405 G>A maps to NM_012318.2 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:1838248 G>A maps to NM_012318.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:1838248 G>A maps to NM_012318.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:38250200 C>T maps to ENST00000379957 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:38264491 T>G maps to ENST00000379957 L416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:38250179 C>A maps to ENST00000379957 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:2564326 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:63276444 C>T maps to NM_001142535.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:40199910 C>A maps to NM_203471.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:40199883 G>A maps to NM_203471.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr22:37966632 G>A maps to NM_006498.2 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:55603929 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:55604620 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:55604108 G>T maps to NM_002306.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:76968041 G>A maps to NM_005567.3 Y458Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:76967756 C>T maps to NM_005567.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:76967840 G>T maps to NM_005567.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:76968554 G>A maps to NM_005567.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:39292532 G>A maps to NM_006149.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:39303129 G>A maps to NM_006149.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:236706246 C>T maps to NM_201545.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:236711413 C>T maps to NM_201545.1 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:236706119 A>G maps to ENST00000416919 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:236711335 G>T maps to NM_201545.1 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:236702361 G>A maps to NM_201545.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:25958266 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:20354922 G>A maps to ENST00000324290 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:20355193 C>T maps to ENST00000324290 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:18390983 C>T maps to NM_001040078.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:18396151 C>T maps to NM_001040078.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:18390983 C>T maps to NM_001040078.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:95557173 G>T maps to NM_005097.2 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:25005227 C>A maps to NM_018176.3 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:25005431 G>A maps to NM_018176.3 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:25005708 G>A maps to NM_018176.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr4:25005431 G>A maps to NM_018176.3 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:25005843 G>T maps to NM_018176.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr4:25020786 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:22006230 G>A maps to NM_139278.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:22012933 C>T maps to NM_139278.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr8:22009000 C>T did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr8:22009121 C>A maps to NM_139278.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:35625473 G>A maps to NM_139284.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:93179216 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:93179216 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:27393926 A>G maps to NM_018490.2 Y466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:27393234 A>G maps to NM_018490.2 D502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:71974108 G>A maps to NM_003667.2 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:71972592 G>A maps to NM_003667.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:202287857 G>A maps to NM_001017403.1 K809K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:202279403 G>T maps to NM_001017403.1 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:202287842 G>A maps to NM_001017403.1 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:202274868 G>A maps to NM_001017403.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:202245466 G>A maps to NM_001017403.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:206772394 G>A maps to NM_006893.2 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:206769140 G>A maps to NM_006893.2 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:206767136 G>A maps to NM_006893.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:206782804 C>T maps to NM_006893.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr19:49519456 G>T maps to NM_000894.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:48915210 G>T maps to NM_000233.3 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:48915045 G>A maps to NM_000233.3 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:48952827 G>A maps to NM_000233.3 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:48950761 G>A maps to NM_000233.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:48950828 G>T maps to NM_000233.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:48915275 G>A maps to NM_000233.3 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:48941138 C>T maps to NM_000233.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:40175254 G>A maps to NM_005780.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:111874660 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:111914389 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:111914375 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:111903917 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:111914422 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:111903897 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr5:77784761 C>T maps to NM_005779.2 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:9594189 G>T maps to NM_198560.2 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:9594357 C>A maps to NM_198560.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:35773809 C>A maps to NM_182548.3 C121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:35782404 G>A maps to NM_182548.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:35773617 G>A maps to NM_182548.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:126301862 G>A maps to NM_022126.3 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr9:126783390 C>T maps to NM_004789.3 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:126794937 C>T maps to NM_004789.3 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:139092438 G>A maps to NM_014564.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:180241031 C>T maps to NM_033343.3 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:180243365 C>T maps to NM_033343.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:180243593 G>A maps to NM_033343.3 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:113901318 G>A maps to NM_022363.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:113906000 C>T maps to NM_022363.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:124971913 C>T maps to NM_014368.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr9:124979491 G>A maps to NM_014368.3 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:124988737 G>A maps to NM_014368.3 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:75609016 G>T maps to NM_001001933.1 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:75622729 G>A maps to NM_001001933.1 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:75622729 G>A maps to NM_001001933.1 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr1:75614348 G>A maps to NM_001001933.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:197887042 C>T maps to NM_020204.2 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:197889148 C>T maps to NM_020204.2 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:197890484 G>A maps to NM_020204.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr1:197890499 C>T maps to NM_020204.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:197889271 C>T maps to NM_020204.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:39474769 A>G maps to NM_006859.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:39472859 T>C maps to NM_006859.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:38485951 C>T maps to NM_002310.5 E822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:38493807 G>A maps to NM_002310.5 C655C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:38506683 C>A maps to NM_002310.5 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:38527268 C>A maps to NM_002310.5 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:38511952 G>A maps to NM_002310.5 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:38493713 C>A maps to NM_002310.5 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:38510733 C>A maps to NM_002310.5 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:38489297 C>T maps to NM_002310.5 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:38506683 C>A maps to NM_002310.5 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:38490297 C>A maps to NM_002310.5 E721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:38502882 C>A maps to NM_002310.5 G486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:38489297 C>T maps to NM_002310.5 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:48653360 C>T maps to NM_000234.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr19:48638980 C>T maps to NM_000234.1 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:48624459 G>A maps to NM_000234.1 D784D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr19:48640285 G>C maps to NM_000234.1 S437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr17:33328350 C>T maps to NM_013975.3 R803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:33324835 C>T maps to NM_013975.3 R635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:33310368 C>T maps to NM_013975.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:33324835 C>T maps to NM_013975.3 R635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:33319548 C>T maps to NM_013975.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr17:33325654 G>A maps to NM_013975.3 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:33316591 C>T maps to NM_013975.3 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr17:33328948 G>T maps to NM_013975.3 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr13:108862644 T>C maps to NM_001098268.1 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:108862200 A>G maps to NM_001098268.1 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:108863094 A>C maps to NM_001098268.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:108862000 A>C maps to NM_001098268.1 L539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:108861525 C>T maps to NM_001098268.1 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:55106613 C>T maps to NM_006863.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:55105720 C>T maps to NM_006863.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:55106565 A>G maps to NM_006863.1 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:55086444 G>A maps to NM_001130917.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:55085365 C>T maps to ENST00000396321 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:55086387 C>T maps to NM_001130917.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr19:55086930 C>A maps to NM_001130917.1 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:54804146 G>T maps to ENST00000251375 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:54804200 T>C maps to ENST00000391745 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:54849826 G>A maps to NM_012276.3 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:54844845 G>T maps to NM_012276.3 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:54822801 C>T maps to NM_021250.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:54823386 C>T maps to NM_021250.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:54744414 C>T maps to ENST00000419410 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:55144677 C>T maps to ENST00000427581 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:55143458 G>A maps to ENST00000427581 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:54782712 G>T maps to ENST00000391747 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:54782724 T>C maps to ENST00000391747 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr19:54783329 C>T maps to ENST00000391747 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr19:54782388 G>T maps to ENST00000391747 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr19:54725730 G>A maps to NM_001081450.1 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:55175697 C>T maps to ENST00000391733 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:55179162 C>A maps to ENST00000391733 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:54759152 G>A maps to NM_001081442.1 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:54758900 C>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr19:54754939 T>C maps to ENST00000450632 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr19:54761023 G>A maps to NM_001081442.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:54760074 G>A maps to NM_001081442.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:50571458 C>T maps to NM_001113546.1 W557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr12:50571458 C>T maps to NM_001113546.1 W557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr12:50594601 G>A maps to NM_001113546.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:50571713 G>A maps to NM_001113546.1 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:50642470 C>A maps to NM_001113546.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:50571755 C>T maps to NM_001113546.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:41601004 G>A maps to NM_014988.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:41699183 G>A maps to NM_014988.2 G1078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:41621301 G>A maps to NM_014988.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:41684453 T>C maps to NM_014988.2 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:45636514 C>T maps to NM_014240.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr3:45714231 C>T maps to NM_014240.2 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:45714213 C>T maps to NM_014240.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr3:45718490 C>T maps to NM_014240.2 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:73511477 C>T maps to NM_002314.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:73520259 C>A maps to NM_002314.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:31673086 C>A maps to NM_001031801.1 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:31644656 A>G maps to ENST00000438187 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr22:31658714 C>T maps to NM_001031801.1 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:31663017 C>T maps to NM_001031801.1 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:31663017 C>T maps to NM_001031801.1 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:31663017 C>T maps to NM_001031801.1 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:109297178 C>T maps to NM_001193484.1 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:109276171 C>T maps to NM_001193484.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:128400616 C>T maps to NM_017980.4 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr2:128396941 G>A maps to NM_017980.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:26752892 C>T maps to NM_024674.4 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:105526632 C>G maps to NM_001004317.2 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:83857201 G>A maps to NM_194282.2 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:83849322 G>A maps to NM_194282.2 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:83857171 G>A maps to NM_194282.2 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:81205381 G>A maps to NM_004664.2 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:81242056 G>A maps to NM_004664.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:81205449 C>A maps to NM_004664.2 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:49621170 G>A maps to NM_022165.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:27520300 T>C maps to NM_018362.3 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:27520275 G>A maps to NM_018362.3 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:27520992 G>T maps to NM_018362.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:226465560 T>C maps to ENST00000366807 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:77906538 G>A maps to NM_032808.5 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:77906463 G>A maps to NM_032808.5 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:77906804 G>A maps to NM_032808.5 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr15:77907930 G>A maps to NM_032808.5 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:27950530 G>A maps to NM_152570.1 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:27949160 G>A maps to NM_152570.1 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:27950649 G>T maps to NM_152570.1 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:27950433 G>T maps to NM_152570.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:27950530 G>A maps to NM_152570.1 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr9:27949013 G>A maps to NM_152570.1 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:27950433 G>T maps to NM_152570.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:151774543 C>A maps to NM_001004432.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:151773919 G>A maps to NM_001004432.2 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:151774895 C>T maps to NM_001004432.2 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:151774171 G>A maps to NM_001004432.2 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:91005431 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:90983548 C>T maps to NM_000235.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:90983568 C>A maps to NM_000235.2 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr10:90974761 G>A maps to NM_000235.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:91007372 A>G maps to NM_000235.2 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr15:58840772 T>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:58724278 C>T maps to NM_000236.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:58840679 C>A maps to NM_000236.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:58834791 C>T maps to NM_000236.2 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr15:58837950 C>T maps to NM_000236.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:42910520 G>T maps to NM_005357.2 I719I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr19:42911467 G>T maps to NM_005357.2 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:42911500 G>A maps to NM_005357.2 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:90438296 C>T maps to NM_001198829.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:90428501 C>T maps to NM_001198829.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:47109973 C>T maps to NM_006033.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:185232256 C>T maps to NM_139248.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:185232220 G>A maps to NM_139248.2 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:185252651 A>G maps to NM_139248.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:185251431 G>A maps to NM_139248.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:185229438 T>G maps to NM_139248.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:15554118 C>A maps to NM_198996.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:15579229 A>G maps to NM_198996.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:90354534 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:90356596 C>T maps to NM_001010939.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:90356596 C>T maps to NM_001010939.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:90366636 C>A maps to NM_001010939.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:90486553 C>T maps to NM_001080518.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:90492004 C>T maps to NM_001080518.1 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:99778520 T>A maps to NM_015929.3 L34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:99778905 C>A maps to NM_015929.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:99778980 G>A maps to NM_015929.3 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:11650544 G>T maps to NM_001136472.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:11643567 G>A maps to NM_001136472.1 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:11643478 C>T maps to ENST00000381810 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:96443063 G>A maps to NM_153234.4 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:18145003 G>A maps to NM_004140.3 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:18145006 C>T maps to NM_004140.3 C915C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:73567857 G>T maps to NM_001031803.1 E763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:73567104 C>T maps to NM_001031803.1 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:73570745 G>T maps to NM_001031803.1 G1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:66517675 T>G maps to NM_032338.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:57006089 G>A maps to NM_005570.3 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:75105218 T>C maps to NM_021819.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:176764471 G>A maps to NM_006816.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr5:176765528 G>A maps to NM_006816.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:176761348 G>A maps to NM_006816.2 P282P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BS-A0UF-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr7:156619407 C>T maps to ENST00000354505 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:49491510 G>A maps to NM_018113.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:70451711 C>A maps to NM_018368.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:70410688 G>A maps to NM_018368.3 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:36104191 G>A maps to NM_001007527.1 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:36136566 A>C maps to NM_001007527.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:36111271 C>A maps to NM_001007527.1 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:36105248 C>A maps to NM_001007527.1 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:8590415 G>T maps to NM_014583.2 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:1004388 G>T maps to ENST00000262301 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:961005 C>T maps to ENST00000262301 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:929671 G>A maps to ENST00000262301 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:984250 G>A maps to ENST00000262301 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr16:919903 C>G maps to ENST00000262301 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:50944589 G>A maps to NM_033200.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50942055 G>A maps to NM_033200.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50942260 C>T maps to NM_033200.2 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50944526 G>A maps to NM_033200.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:50944589 G>A maps to NM_033200.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:197710883 C>T maps to NM_001136049.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:197702919 G>A maps to NM_001136049.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:197702919 G>A maps to NM_001136049.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:197765444 T>C maps to NM_001136049.2 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:197702961 G>A maps to NM_001136049.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:197762717 T>C maps to NM_001136049.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:197717490 C>T maps to NM_001136049.2 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:197765603 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr3:197751625 G>A maps to NM_001136049.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:126145879 C>T maps to NM_005573.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:126145903 G>A maps to NM_005573.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:2431801 G>A maps to NM_032737.2 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:8246186 G>A maps to ENST00000428101 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:8251932 G>A maps to ENST00000428101 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:8248628 C>T maps to ENST00000428101 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:16753788 G>A maps to ENST00000441439 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:16753659 A>G maps to ENST00000441439 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr1:87805260 G>A maps to NM_006769.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:87797928 C>T maps to NM_006769.3 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:76423416 G>A maps to ENST00000357063 G1381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:76378495 C>T maps to ENST00000357063 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:76370830 T>C maps to ENST00000357063 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:76397786 G>A maps to ENST00000357063 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:76393552 C>T maps to ENST00000357063 R627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:76382123 G>T maps to ENST00000357063 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:76382314 G>A maps to ENST00000357063 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:123303142 G>A maps to NM_207163.1 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:123302464 C>T maps to NM_207163.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:123296064 C>T maps to NM_207163.1 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:123302776 C>A maps to NM_207163.1 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:123296106 G>A maps to NM_207163.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:69168122 G>T maps to NM_198271.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:69169186 C>A maps to NM_198271.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:69168077 C>A maps to NM_198271.3 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:69169180 C>A maps to NM_198271.3 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr7:97823412 C>T maps to NM_014916.3 G1212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr7:97822473 T>C maps to NM_014916.3 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:97784092 G>A maps to NM_014916.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:97816245 G>T maps to NM_014916.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:97823640 C>T maps to NM_014916.3 D1288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:97822251 G>A maps to NM_014916.3 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:97822546 G>T maps to NM_014916.3 E924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:97823421 C>T maps to NM_014916.3 F1215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr7:97822971 C>T maps to NM_014916.3 S1065S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:97820924 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:49001862 C>T maps to NM_001080434.1 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr19:49001748 C>T maps to NM_001080434.1 T888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:49012770 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:165173196 C>A maps to NM_177398.3 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr1:165177315 G>T maps to NM_177398.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:165182973 G>A maps to NM_177398.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr1:165173245 G>A maps to NM_177398.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:129376790 C>T maps to NM_001174147.1 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:129458714 C>A maps to NM_001174147.1 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:129453255 C>T maps to NM_001174147.1 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:129453168 C>T maps to NM_001174147.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr9:129455843 C>T maps to NM_001174147.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:129455574 C>T maps to NM_001174147.1 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:129458720 C>T maps to NM_001174147.1 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:100170794 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:100170634 C>T maps to ENST00000489752 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:100170628 G>T maps to ENST00000489752 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:100170729 T>C maps to ENST00000489752 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:96315349 C>A maps to NM_005575.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:96315394 G>A maps to NM_005575.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:96362354 C>T maps to NM_005575.2 R920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:96315296 A>T maps to NM_005575.2 K159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:54373482 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:54364893 G>A maps to NM_001126328.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:54374222 G>A maps to NM_001126328.1 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:54342948 T>C maps to NM_001126328.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:54347958 G>T maps to NM_001126328.1 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:54374351 C>T maps to NM_001126328.1 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:54344840 G>A maps to NM_001126328.1 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:28136816 G>A maps to NM_153371.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:28143280 A>T maps to NM_153371.3 C180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr13:28136704 G>A maps to NM_153371.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:132121125 G>T maps to NM_001077637.1 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:132120744 T>C maps to NM_001077637.1 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:40172706 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:40172657 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:40172694 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:40172106 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:10049177 C>T maps to NM_001008737.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:28319205 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:28319075 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:28319212 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:28319065 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:13183443 C>T maps to NM_001136561.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr19:11350950 C>T maps to ENST00000252453 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:209605547 G>T did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:209605600 G>A maps to NM_001104548.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:209602683 C>T maps to NM_001104548.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49215383 C>T maps to NM_001080528.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:49215142 G>A maps to NM_001080528.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:43903161 G>T maps to NM_001101330.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:43902717 G>A maps to NM_001101330.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:105005761 G>A maps to NM_001143909.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:105006250 G>A maps to NM_001143909.1 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:20833150 C>T maps to NM_030941.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:20838519 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:5713161 G>A maps to NM_004793.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:5693661 G>A maps to NM_004793.2 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:5707706 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:5711823 C>T maps to NM_004793.2 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:5700907 C>T maps to NM_004793.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:48381503 T>C maps to NM_031490.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:48385566 G>T maps to NM_031490.2 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:48368208 G>A maps to NM_031490.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr16:48296765 G>A maps to NM_031490.2 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:48304096 G>T maps to NM_031490.2 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:48381551 C>T maps to NM_031490.2 D691D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr8:12586680 A>G did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:12592792 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:12594229 G>A maps to NM_152271.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr8:12580660 G>T maps to NM_152271.3 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:100903381 C>T maps to NM_198461.3 E688E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:100916233 C>T maps to NM_198461.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:100900773 C>A maps to NM_198461.3 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:118145892 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:118112307 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:118116814 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:118147052 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:118148282 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118123507 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118145870 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118151558 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:118151555 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:118145841 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr23:118143157 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:118123613 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:118145876 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:118148307 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:118116844 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:118124487 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118151515 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118151585 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:118145884 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:121409719 A>G maps to NM_002317.5 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:74239515 C>A maps to NM_005576.2 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:23186054 G>A maps to NM_002318.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:23167215 G>A maps to NM_002318.2 N615N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:23177457 G>A maps to NM_002318.2 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr8:23156439 G>A maps to NM_002318.2 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:23156382 G>A maps to NM_002318.2 D737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr8:23198554 G>A maps to NM_002318.2 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:23156439 G>A maps to NM_002318.2 F718F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:74779706 G>A maps to NM_032603.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:74762732 G>A maps to NM_032603.2 Y466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:74779577 G>A maps to NM_032603.2 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr2:74761839 C>T maps to NM_032603.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr10:100012176 G>A maps to NM_032211.6 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:161026189 C>A maps to NM_005577.2 G945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:161022042 G>A maps to NM_005577.2 Y1011Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:161026150 C>A maps to NM_005577.2 G958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:160952892 G>A maps to NM_005577.2 F1997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:161032625 C>T maps to NM_005577.2 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:161021991 C>T maps to NM_005577.2 P1028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr6:161087330 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:160978487 C>A maps to NM_005577.2 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr6:160977175 A>G maps to NM_005577.2 H1618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:113703893 G>T maps to NM_057159.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:19737964 G>A maps to NM_004720.5 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19737445 C>T maps to NM_004720.5 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19737856 G>T maps to NM_004720.5 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:85331608 G>A maps to NM_012152.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:85331578 G>T maps to NM_012152.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:85331530 G>A maps to NM_012152.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:85279657 G>A maps to NM_012152.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:85279804 G>A maps to NM_012152.2 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:78010456 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:78010835 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:78011072 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:78011179 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr23:78011375 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:78011218 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:78011104 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:78010479 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:78011059 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr12:6730192 C>A maps to ENST00000435659 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:6729439 C>T maps to ENST00000435659 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:6730177 G>A maps to ENST00000435659 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:6729294 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:6729586 G>A maps to ENST00000435659 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:6729478 G>A maps to ENST00000435659 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:1474751 C>T maps to NM_024830.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:1479738 G>A maps to NM_024830.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:1489944 G>A maps to NM_024830.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:1494890 G>A maps to NM_024830.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr5:1466972 G>A maps to NM_024830.3 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:1501679 G>T maps to NM_024830.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr5:1494911 G>A maps to NM_024830.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:1463837 G>A maps to NM_024830.3 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:55565851 T>C maps to NM_017839.4 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:34655894 C>T maps to NM_153613.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:212002499 G>A maps to NM_014873.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:14288548 G>A maps to NM_001008701.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:14266215 G>A maps to NM_001008701.2 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:14274003 G>A maps to NM_001008701.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:14273874 G>A maps to NM_001008701.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr19:14263121 T>C maps to NM_001008701.2 P1221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:14273439 G>A maps to NM_001008701.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:14270974 C>A maps to NM_001008701.2 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:82372775 C>T maps to ENST00000370717 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:82408794 C>T maps to ENST00000370717 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:82402421 C>T maps to ENST00000370717 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:82409143 C>T maps to ENST00000370717 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:82408870 C>A maps to ENST00000370717 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:82409308 G>T maps to ENST00000370717 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:82432214 C>A maps to ENST00000370717 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr4:62453098 T>C maps to ENST00000506720 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:62542645 C>T maps to ENST00000506720 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:62910215 G>T maps to ENST00000506720 E1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:62935917 C>T maps to ENST00000506720 G1345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:62801728 G>A maps to ENST00000506720 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr4:62758461 C>T maps to ENST00000506720 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:62813969 A>G maps to ENST00000506720 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:62903521 C>A maps to ENST00000506720 S1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:62849099 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr4:62845456 C>G maps to ENST00000506720 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:62849267 C>G maps to ENST00000506720 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:11905771 C>A maps to ENST00000396099 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:11911613 G>A maps to ENST00000396099 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:11960599 G>T maps to ENST00000396099 G867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:11944577 C>T maps to ENST00000396099 N687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:11911550 G>A maps to ENST00000396099 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:2960645 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:2925344 C>T maps to NM_014646.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:2920828 G>A maps to NM_014646.2 T831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:2923855 C>T maps to NM_014646.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:39980720 A>G maps to NM_022896.1 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:39978972 G>A maps to NM_022896.1 W346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr20:39974538 C>T maps to NM_022896.1 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:19809285 G>T maps to NM_000237.2 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:19805712 C>T maps to NM_000237.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:19818441 C>A maps to NM_000237.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:56327918 C>T maps to NM_006151.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:56332251 G>T maps to NM_006151.2 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:56329745 C>T maps to NM_006151.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:56327948 C>A maps to NM_006151.2 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:188478013 C>T maps to NM_005578.3 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:188584082 C>T maps to NM_005578.3 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:188242460 C>T maps to NM_005578.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:188327154 G>A maps to NM_005578.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:188590442 G>T maps to NM_005578.3 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:104048496 C>T maps to NM_017753.2 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:104048496 C>T maps to NM_017753.2 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:104032316 C>A maps to NM_017753.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:104048422 C>A maps to NM_017753.2 S97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:11468408 C>T maps to NM_001170635.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:815722 C>T maps to NM_024888.1 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:99771600 C>T maps to NM_014839.4 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:58322354 A>G maps to NM_004811.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:58294998 C>T maps to NM_004811.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:58317334 C>T maps to NM_004811.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:58317558 C>A maps to NM_004811.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:58295052 C>T maps to NM_004811.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr4:155665690 C>T maps to NM_004744.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:155665753 C>A maps to NM_004744.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:151821206 C>A maps to NM_006726.3 G640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:151223906 G>A maps to NM_006726.3 V2640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:151388830 C>T maps to NM_006726.3 L2269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:151271168 G>T maps to NM_006726.3 S2457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:151773327 T>G maps to NM_006726.3 G1178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr4:151511892 C>T maps to NM_006726.3 V2066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:151821201 T>C maps to NM_006726.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:151203670 G>A maps to NM_006726.3 N2760N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:151773770 C>A maps to NM_006726.3 E1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:151356749 A>C maps to NM_006726.3 S2355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:151223852 G>T maps to NM_006726.3 L2658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:151749773 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:151935595 C>A maps to NM_006726.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:47243165 C>T maps to NM_001164211.1 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:47269154 A>G maps to ENST00000258643 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:47315784 C>T maps to NM_001164211.1 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:47324715 C>A maps to NM_001164213.1 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:114468284 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:114361448 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:114419068 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:114361426 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:114422819 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:114419016 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:114468375 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:114357667 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:114357668 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:114414286 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:114357668 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr23:114468286 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:114400483 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:114357647 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:114400880 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:114468441 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr23:114398299 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:114400024 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:114400179 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:114404894 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:114400019 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:114404977 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:114347853 A>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:114357736 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:114357647 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:114468484 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:114400442 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:197598254 C>T maps to ENST00000425562 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:197598257 T>C maps to ENST00000425562 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:197559118 G>T maps to ENST00000425562 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr3:197562677 G>A maps to ENST00000425562 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:100179705 G>T maps to NM_002319.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr6:40399937 C>T maps to NM_020737.1 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr6:40360308 G>A maps to NM_020737.1 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr6:40400348 G>A maps to NM_020737.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:66625781 C>T maps to NM_024036.4 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:66627248 C>T maps to NM_024036.4 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:42356691 C>A maps to NM_152447.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:42361142 T>G maps to NM_152447.3 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:42356665 G>T maps to NM_152447.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr14:42360557 C>T maps to NM_152447.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:133863331 C>T maps to NM_144648.1 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:133948607 C>T maps to NM_144648.1 Q787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:133812293 C>A maps to NM_144648.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:133876469 C>A maps to NM_144648.1 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:133859355 C>T maps to NM_144648.1 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:133943069 G>T maps to NM_144648.1 E754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:66436417 C>T maps to NM_015541.2 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:66436590 C>A maps to NM_015541.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:66433733 C>T maps to NM_015541.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:66436564 C>T maps to NM_015541.2 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr3:66434448 A>G maps to NM_015541.2 G679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr3:66463323 G>A maps to NM_015541.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:66431202 A>G maps to NM_015541.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:113638975 T>C maps to NM_014813.1 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:113636069 A>G maps to NM_014813.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:113636066 C>A maps to NM_014813.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:113659056 C>T maps to NM_014813.1 D893D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:113636186 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:59282632 T>C maps to NM_153377.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:59266380 A>G maps to NM_153377.3 N1111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:59282692 G>A maps to NM_153377.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:59268112 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:59267936 A>G maps to NM_153377.3 N1005N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:59268110 A>G maps to NM_153377.3 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:59284508 G>A maps to NM_153377.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr10:85992165 G>A maps to NM_015613.2 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:85992453 G>A maps to NM_015613.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:85997336 G>A maps to NM_015613.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:85992219 G>T maps to NM_015613.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:85992258 C>T maps to NM_015613.2 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr10:86001153 C>T maps to NM_015613.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:85993928 G>A maps to NM_015613.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:85997012 A>G maps to NM_015613.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:85984097 C>A maps to NM_001017924.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:85984758 A>G maps to NM_001017924.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:110772981 G>T maps to NM_198506.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:110790808 G>T maps to NM_198506.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:110791602 C>T maps to NM_198506.2 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:110773022 A>G maps to NM_198506.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:25242995 A>G maps to ENST00000354454 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:25254201 G>T maps to ENST00000354454 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:25259875 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr12:57588867 C>T maps to NM_002332.2 D2764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:57549992 C>T maps to NM_002332.2 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:57570836 C>T maps to NM_002332.2 F1335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:57539154 C>T maps to NM_002332.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:57606284 C>T maps to NM_002332.2 R4528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A1DQ-01A-11D-A135-09 chr12:57605983 C>T maps to NM_002332.2 G4478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:57548048 C>T maps to NM_002332.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:57573307 C>T maps to NM_002332.2 N1645N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:57554768 C>A maps to NM_002332.2 I691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:57573649 C>A maps to NM_002332.2 I1684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:57567662 G>A maps to NM_002332.2 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:57591139 C>T maps to NM_002332.2 D3045D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:57599191 C>T maps to NM_002332.2 C3798C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr12:57548390 C>T maps to NM_002332.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:57587772 C>T maps to NM_002332.2 D2632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:57567077 T>C maps to NM_002332.2 C1097C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:57594274 C>T maps to NM_002332.2 T3355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:57605735 C>T maps to NM_002332.2 L4429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr12:57566957 G>A maps to NM_002332.2 R1057R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:57598211 C>T maps to NM_002332.2 D3657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:57598988 C>T maps to NM_002332.2 F3764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr12:57554870 G>A maps to NM_002332.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:23345401 G>A maps to NM_014045.3 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:105507358 A>G maps to NM_013437.4 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:105502996 G>A maps to NM_013437.4 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr8:105521273 T>C maps to NM_013437.4 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:105509324 G>A maps to NM_013437.4 C485C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:105507434 G>T maps to NM_013437.4 S528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:105509843 A>G maps to NM_013437.4 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr2:141143522 G>A maps to NM_018557.2 P3490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:142012121 G>A maps to NM_018557.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:141259432 G>A maps to NM_018557.2 C2891C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:141771269 C>T maps to NM_018557.2 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:141806734 C>A maps to NM_018557.2 G537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:141200148 C>T maps to NM_018557.2 T3446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:141641456 G>A maps to NM_018557.2 G1366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:141707849 G>A maps to NM_018557.2 D1030D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:141816551 G>A maps to NM_018557.2 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:141135778 T>C maps to NM_018557.2 G3536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:141751606 G>A maps to NM_018557.2 D867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:141055422 A>C maps to NM_018557.2 P4307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:141609263 G>T maps to NM_018557.2 C1556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:141816551 G>A maps to NM_018557.2 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:141526903 G>T maps to NM_018557.2 S1879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr2:141081612 G>A maps to NM_018557.2 I4121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:141116420 G>A maps to NM_018557.2 C3742C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:141135855 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:141571367 C>T maps to NM_018557.2 S1739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:141625666 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:141806572 C>A maps to NM_018557.2 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:142238076 G>A maps to NM_018557.2 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:141083334 T>C maps to NM_018557.2 K4112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:141260529 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:141458113 A>G maps to NM_018557.2 C2168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr2:140992399 C>T maps to NM_018557.2 P4538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:141242988 G>T maps to NM_018557.2 L3116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:141245265 C>A maps to NM_018557.2 E3055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:141709477 G>A maps to NM_018557.2 F973F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:142012121 G>A maps to NM_018557.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:141253233 A>G maps to NM_018557.2 C2978C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:141259443 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:141571367 C>T maps to NM_018557.2 S1739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:141607770 G>A maps to NM_018557.2 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:141609353 T>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:141298571 G>A maps to NM_018557.2 R2495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:141299428 C>A maps to NM_018557.2 G2436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:141609281 C>T maps to NM_018557.2 R1550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:141812766 A>G maps to NM_018557.2 C490C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:141004709 G>A maps to NM_018557.2 G4423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:141072501 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:170062573 G>A maps to NM_004525.2 R2505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:170011077 G>A maps to NM_004525.2 R4063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:170112622 G>T maps to NM_004525.2 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:170026248 G>A maps to NM_004525.2 S3820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:170038804 G>A maps to NM_004525.2 R3290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:170136003 G>T maps to NM_004525.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:170044765 C>T maps to NM_004525.2 R3014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:170147507 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:170030639 G>A maps to NM_004525.2 C3601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:170115721 C>A maps to NM_004525.2 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:170136003 G>T maps to NM_004525.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:170136019 C>T maps to NM_004525.2 W476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:170139419 G>T maps to NM_004525.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:170026257 G>A maps to NM_004525.2 C3817C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:170013914 G>A maps to NM_004525.2 F3995F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:170033018 G>A maps to NM_004525.2 C3491C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:170059305 G>A maps to NM_004525.2 N2723N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr2:170038732 G>T maps to NM_004525.2 A3314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr2:170044630 G>A maps to NM_004525.2 D3059D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:170025121 A>G maps to NM_004525.2 C3854C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:170018980 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:170129435 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:170014000 C>A maps to NM_004525.2 E3967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:169999223 G>T maps to NM_004525.2 G4356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:170097654 G>A maps to NM_004525.2 C1296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:170062107 G>A maps to NM_004525.2 I2532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:170072888 G>A maps to NM_004525.2 I1900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:186294140 C>T maps to ENST00000362004 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:186299232 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:186299361 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:186294106 C>A maps to ENST00000362004 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:33693775 G>A maps to NM_002333.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:33697584 C>T maps to NM_002333.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:46918426 C>T maps to ENST00000256991 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:46896418 G>T maps to ENST00000256991 V1432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:46894757 G>A maps to ENST00000256991 H1537H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:46903372 G>T maps to ENST00000256991 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:68213989 G>A maps to NM_002335.2 A1525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:68201118 C>T maps to NM_002335.2 I1271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:68204420 C>T maps to NM_002335.2 C1355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:68216348 C>T maps to NM_002335.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:68205995 C>T maps to NM_002335.2 F1398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:68125315 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:68213917 G>A maps to NM_002335.2 P1501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:25755984 C>T maps to NM_001135772.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr22:25750680 G>A maps to NM_001135772.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:12397550 G>A maps to NM_002336.2 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:12315299 G>A maps to NM_002336.2 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:12311985 C>T maps to NM_002336.2 E856E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:12334364 C>A maps to NM_002336.2 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:12397409 C>A maps to NM_002336.2 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11M-01A-11D-A122-09 chr12:12284808 G>A maps to NM_002336.2 R1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr12:12274227 A>G maps to NM_002336.2 S1558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:12284875 G>T maps to NM_002336.2 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:12339860 T>A maps to NM_002336.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr12:12291315 G>A maps to NM_002336.2 R1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:53732179 G>T maps to NM_004631.3 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:53726247 G>A maps to NM_004631.3 N648N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:53741372 G>T maps to NM_004631.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:53732281 G>A maps to NM_004631.3 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:53729953 A>G maps to NM_004631.3 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:3516625 G>A maps to NM_002337.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:3516637 G>A maps to NM_002337.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:44128598 G>T maps to NM_133259.3 T1143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:44201429 T>C maps to NM_133259.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:44173294 G>A maps to NM_133259.3 R723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:44175657 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:44209439 G>A maps to NM_133259.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:44209566 T>G maps to NM_133259.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:44209550 G>A maps to NM_133259.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:44204164 A>C maps to NM_133259.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:53707018 C>T maps to NM_018214.4 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:53764613 G>T maps to NM_018214.4 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:53778653 C>T maps to NM_018214.4 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr6:53761632 T>A maps to NM_018214.4 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:53785513 G>A maps to NM_018214.4 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:70004477 G>A maps to NM_201550.2 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:70004062 G>A maps to NM_201550.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr5:195287 C>T maps to NM_001080478.1 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:194080098 G>A maps to NM_001135057.2 C564C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:194080533 C>T maps to NM_001135057.2 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:194081244 C>T maps to NM_001135057.2 T182T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:25600665 C>T maps to NM_017640.5 R1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:25556970 G>T maps to NM_017640.5 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:25515973 A>C maps to NM_017640.5 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr6:25551202 C>T maps to NM_017640.5 H798H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:24529253 C>A maps to NM_138360.3 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:24523003 C>T maps to NM_138360.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr14:24529363 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24525591 C>T maps to NM_138360.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:24524015 C>T maps to NM_138360.3 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:24527944 A>G maps to NM_138360.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr14:24529964 G>A maps to NM_138360.3 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:24528582 C>T maps to NM_138360.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr14:24523618 G>A maps to NM_138360.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:102584867 G>A maps to NM_001031692.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr7:102574434 T>C maps to NM_001031692.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:102574545 G>A maps to NM_001031692.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:102574506 A>G maps to NM_001031692.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr10:50121576 C>T maps to NM_001006939.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:50121504 C>T maps to NM_001006939.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:26996330 C>T maps to NM_022901.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:26999610 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:26996330 C>T maps to NM_022901.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:46574378 C>A maps to NM_024512.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:46586568 C>T maps to NM_024512.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:72136223 G>A maps to NM_207119.1 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr12:7022148 C>T maps to NM_201650.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:7015782 T>C maps to NM_201650.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr19:18507464 C>T maps to NM_145256.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:18502931 A>G maps to NM_145256.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:134150893 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr10:134178969 C>T maps to NM_030626.2 H444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:134188616 C>A maps to NM_030626.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:99796185 G>A maps to NM_144598.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:99892664 C>A maps to NM_144598.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr21:45876937 C>T maps to NM_030891.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:45876781 G>A maps to NM_030891.3 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:7231780 C>T maps to NM_001105581.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:7231660 C>T maps to NM_001105581.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:7231720 G>A maps to NM_001105581.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr18:7231738 C>T maps to NM_001105581.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:169572613 G>A maps to NM_024727.2 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:169557828 C>A maps to NM_024727.2 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:76370730 G>A maps to NM_001128922.1 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr3:196386687 C>T maps to NM_198565.1 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:196387044 C>T maps to NM_198565.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:196387779 C>T maps to NM_198565.1 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:196386810 C>T maps to NM_198565.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:196387101 C>T maps to NM_198565.1 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:196388262 G>A maps to NM_198565.1 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:196387101 C>T maps to NM_198565.1 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:169521849 G>A maps to NM_001172779.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:67381428 A>G maps to NM_018296.5 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr16:67399259 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:67401081 C>A maps to NM_018296.5 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:44626545 G>A maps to NM_001006607.2 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:44618187 G>A maps to NM_001006607.2 T998T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:44626101 C>T maps to NM_001006607.2 N1199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:44626699 G>T maps to NM_001006607.2 E1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:62893153 C>T maps to NM_199340.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:62892244 C>T maps to NM_199340.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:62854991 C>A maps to NM_199340.2 E1572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:62856435 G>A maps to NM_199340.2 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:62857071 C>T maps to NM_199340.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:30354828 C>A maps to ENST00000327564 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:30348821 A>G maps to ENST00000327564 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:30361940 C>T maps to ENST00000327564 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:30349428 G>T maps to ENST00000327564 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:100620647 C>T maps to NM_144620.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:100620721 C>A maps to NM_144620.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:100621828 G>A maps to NM_144620.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:26751177 C>T maps to NM_052953.2 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:26751198 C>A maps to NM_052953.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr3:26751940 T>C maps to NM_052953.2 *260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr7:127669747 G>A maps to NM_022143.4 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr7:127669970 C>T maps to NM_022143.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr7:127670300 G>A maps to NM_022143.4 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:70650520 C>A maps to NM_017768.4 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:70639321 G>A maps to NM_017768.4 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:70650529 G>A maps to NM_017768.4 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:70618138 C>T maps to NM_017768.4 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:70618192 G>A maps to NM_017768.4 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:70639321 G>A maps to NM_017768.4 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:46745900 G>A maps to ENST00000254454 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:46744468 G>A maps to ENST00000254454 Q813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:46751280 G>A maps to ENST00000254454 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:46751280 G>A maps to ENST00000254454 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr1:46746142 G>A maps to ENST00000254454 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:122677293 C>T maps to NM_001098519.1 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:122676047 C>T maps to NM_001098519.1 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:45913079 C>T maps to NM_033413.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr17:45914405 C>T maps to NM_033413.3 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:3698150 A>T maps to NM_020710.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:3712529 C>A maps to NM_020710.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:3701713 G>T maps to NM_020710.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:3703547 G>T maps to NM_020710.2 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:3712463 C>A maps to NM_020710.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:17887220 C>T maps to NM_031294.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:17907720 G>A maps to NM_031294.3 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr17:17897632 G>A maps to NM_031294.3 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:71185951 A>G maps to NM_017691.3 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:71272450 G>A maps to NM_017691.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:71276465 C>T maps to NM_017691.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:51022594 G>A maps to NM_001080457.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:51022263 G>A maps to NM_001080457.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:51022594 G>A maps to NM_001080457.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr19:51022291 C>T maps to NM_001080457.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:51021652 C>T maps to NM_001080457.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:40137470 C>T maps to NM_020929.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:40136150 C>T maps to NM_020929.1 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:40137620 G>T maps to NM_020929.1 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:40137422 C>T maps to NM_020929.1 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr11:40136522 G>A maps to NM_020929.1 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:165513623 C>T maps to NM_001005214.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:165513862 C>T maps to NM_001005214.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:165532832 G>A maps to NM_001005214.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:165532949 C>T maps to NM_001005214.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:56954755 C>T maps to NM_001005210.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr11:56949970 C>T maps to NM_001005210.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:56954952 G>A maps to NM_001005210.2 *342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:550079 C>T maps to NM_198075.3 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:540861 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:540758 G>A maps to NM_198075.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:42839520 G>A maps to NM_153260.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:42837297 G>A maps to NM_153260.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:42837297 G>A maps to NM_153260.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:48462479 C>T maps to NM_018509.3 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:133645193 C>A maps to ENST00000250173 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:52861243 C>T maps to NM_001024611.1 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr4:52861564 A>G maps to NM_001024611.1 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:52862197 C>T maps to NM_001024611.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:52861615 C>T maps to NM_001024611.1 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:52883431 G>A maps to NM_001024611.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr4:52883572 G>A maps to NM_001024611.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:52860795 T>G maps to NM_001024611.1 R798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr4:52862251 G>A maps to NM_001024611.1 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:70504470 C>T maps to NM_020794.2 I950I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:70257821 G>T maps to NM_020794.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:70484448 G>A maps to NM_020794.2 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:70504344 C>A maps to NM_020794.2 V908V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:70541779 G>A maps to NM_020794.2 T1379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:70397243 C>T maps to NM_020794.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:70486790 C>T maps to NM_020794.2 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:70257821 G>T maps to NM_020794.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:70451978 G>T maps to NM_020794.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:70573493 T>C maps to NM_020794.2 G1497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:70493871 C>T maps to NM_020794.2 R567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:70300474 C>T maps to NM_020794.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:70226018 C>T maps to NM_020794.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:70225910 C>T maps to NM_020794.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:131670315 C>T maps to NM_001127244.1 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:131669934 C>T maps to NM_001127244.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:131669934 C>T maps to NM_001127244.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:90058349 G>T maps to NM_015350.2 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:90049897 G>A maps to NM_015350.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:90180018 C>T maps to NM_032270.4 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:90180018 C>T maps to NM_032270.4 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:90152056 C>T maps to NM_032270.4 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:90179103 C>T maps to NM_032270.4 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:90180366 G>A maps to NM_032270.4 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:90178738 G>T maps to NM_032270.4 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:90400108 G>A maps to NM_001134479.1 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:90399925 T>C maps to NM_001134479.1 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:90398817 C>A maps to NM_001134479.1 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:90400489 C>T maps to NM_001134479.1 D621D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:90400676 C>T maps to NM_001134479.1 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr19:7965386 C>T maps to NM_025061.3 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:7963686 T>C maps to NM_025061.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:7963574 C>T maps to NM_025061.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:7960527 C>T maps to NM_025061.3 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:7963811 C>T maps to NM_025061.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:86019586 C>T maps to NM_033402.4 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:86042231 C>T maps to NM_033402.4 R569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:86021898 C>T maps to NM_033402.4 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:86041454 C>T maps to NM_033402.4 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:86044055 G>T maps to NM_033402.4 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:86021898 C>T maps to NM_033402.4 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:86044097 G>T maps to NM_033402.4 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:238601157 G>A maps to NM_001137552.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:238629455 A>G maps to NM_001137552.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:238632192 G>A maps to ENST00000391999 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:238671279 C>T maps to NM_001137552.1 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:238671279 C>A maps to NM_001137552.1 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:238647879 G>A maps to ENST00000391999 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:238672065 G>A maps to NM_001137552.1 K570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:238667389 G>T maps to ENST00000391999 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:238659842 G>T maps to NM_001137552.1 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:238672227 C>T maps to NM_001137552.1 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr2:238626418 G>C maps to ENST00000391999 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:37107797 C>A maps to NM_006309.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:37107797 C>A maps to NM_006309.2 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:37114351 T>A maps to NM_006309.2 K465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:37116607 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr3:37107759 G>A maps to NM_006309.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr12:85449932 G>A maps to NM_001079910.1 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr12:85449563 G>A maps to NM_001079910.1 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:85518170 T>G maps to NM_001079910.1 L1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:85449800 A>G maps to NM_001079910.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:85492268 C>T maps to NM_001079910.1 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:85449945 G>T maps to NM_001079910.1 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:85492208 T>C maps to NM_001079910.1 C988C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:85450242 G>T maps to NM_001079910.1 G558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:85623376 T>A maps to NM_001079910.1 L1635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:85441176 G>T maps to NM_001079910.1 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:85518259 C>T maps to NM_001079910.1 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:85434285 G>T maps to NM_001079910.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:85449555 C>T maps to NM_001079910.1 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:85449785 T>C maps to NM_001079910.1 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:85515613 G>T maps to NM_001079910.1 E1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:85450148 A>G maps to NM_001079910.1 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:74492526 G>A maps to NM_001105659.1 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:74492497 C>A maps to NM_001105659.1 *625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:74540474 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:74492645 C>A maps to NM_001105659.1 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:169555389 G>T maps to NM_001080460.1 G552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr3:169540099 A>T maps to NM_001080460.1 K131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr3:169540296 C>T maps to NM_001080460.1 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr15:101549157 C>T maps to NM_024652.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:101605654 A>T maps to NM_024652.3 S1671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:101565168 C>T maps to NM_024652.3 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:101606266 C>T maps to NM_024652.3 C1875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:101595157 C>T maps to NM_024652.3 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:101550768 C>T maps to NM_024652.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:101606266 C>T maps to NM_024652.3 C1875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:101550768 C>T maps to NM_024652.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:101565168 C>T maps to NM_024652.3 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr15:101566276 A>G maps to NM_024652.3 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr15:101567916 G>A maps to NM_024652.3 V867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:101605789 C>T maps to NM_024652.3 I1716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr15:101606111 C>T maps to NM_024652.3 L1824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:40688679 C>T maps to NM_198578.3 R948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:40745391 T>C maps to NM_198578.3 L2145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:40758659 G>T maps to NM_198578.3 E2400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:40687399 G>T maps to NM_198578.3 E915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:40714928 A>G maps to NM_198578.3 G1703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:40671814 A>G maps to NM_198578.3 Q689Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:40757320 A>G maps to NM_198578.3 K2382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:40637379 C>T maps to NM_198578.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:40697828 G>T maps to NM_198578.3 E1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr12:40671964 A>C maps to NM_198578.3 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:40742221 G>T maps to NM_198578.3 E2098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:40631799 G>T maps to NM_198578.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:40677789 G>A maps to NM_198578.3 Q785Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:40716968 C>A maps to NM_198578.3 L1839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:40637446 G>T maps to NM_198578.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr12:40692187 G>A maps to NM_198578.3 V1080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr3:3886562 C>T maps to NM_020873.5 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:3887914 C>T maps to NM_020873.5 Y530Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:3888262 G>A maps to NM_020873.5 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:3887557 G>A maps to NM_020873.5 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:3887914 C>T maps to NM_020873.5 Y530Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:204588280 G>A maps to NM_201630.1 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:204588397 G>A maps to NM_201630.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:204587950 G>A maps to NM_201630.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:110763329 C>T maps to NM_018334.4 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:110764618 C>T maps to NM_018334.4 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:110763329 C>T maps to NM_018334.4 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:110763788 A>T maps to NM_018334.4 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:6021784 G>A maps to NM_152611.3 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:80530158 G>A maps to NM_178839.4 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:80530116 G>A maps to NM_178839.4 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:80530140 G>A maps to NM_178839.4 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:138208725 C>T maps to NM_015564.2 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:138209550 C>T maps to NM_015564.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr5:138208800 C>A maps to NM_015564.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr5:138208848 G>C maps to NM_015564.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:138209445 G>A maps to NM_015564.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:68687036 C>A maps to NM_178011.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:68687273 C>A maps to NM_178011.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:68687849 A>G maps to NM_178011.3 K392K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:68687468 C>T maps to NM_178011.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:68857439 C>A maps to NM_178011.3 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:68687468 C>T maps to NM_178011.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:68687196 C>T maps to NM_178011.3 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:77745827 G>T maps to NM_001134745.1 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:130217326 C>A maps to NM_001005374.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:130236143 C>T maps to NM_001005374.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:130224571 C>T maps to NM_001005374.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:54958793 C>T maps to NM_020678.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:54952686 C>T maps to NM_020678.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:71807682 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:71807923 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr11:71817086 G>A maps to NM_001145309.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:116163740 C>A maps to NM_002338.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:115805183 G>T maps to NM_002338.3 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:194362880 G>A maps to NM_018385.2 N631N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BS-A0TJ-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:157182233 C>T maps to NM_173491.2 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:157178401 C>T maps to NM_173491.2 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:34663591 C>A maps to NM_001114093.1 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:34685432 C>T maps to NM_001114093.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:34712436 G>T maps to NM_001114093.1 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:60701385 G>A maps to NM_144703.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:60708445 C>T maps to NM_144703.2 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr20:60705593 C>T maps to NM_144703.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:60705676 C>T maps to NM_144703.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr20:60701478 C>T maps to NM_144703.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:60705676 C>T maps to NM_144703.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:14223155 C>T maps to NM_014463.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:18420490 G>A maps to NM_012321.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:18423461 G>A maps to NM_012321.3 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:147108496 C>T maps to NM_007080.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:2324172 G>A maps to NM_016199.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr11:1874397 G>A maps to NM_002339.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:35749872 G>A maps to NM_205834.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr21:47633707 G>A maps to NM_002340.5 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:47616168 C>T maps to NM_002340.5 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:47641852 C>T maps to NM_002340.5 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr21:47611101 C>A maps to NM_002340.5 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr21:47627344 A>G maps to NM_002340.5 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr21:47630622 G>A maps to NM_002340.5 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:21168706 C>T maps to ENST00000381541 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:21201766 C>T maps to ENST00000381541 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:21220307 C>T maps to ENST00000381541 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:21201730 T>C maps to ENST00000381541 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:21205159 G>T maps to ENST00000381541 G462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:21207444 G>A maps to ENST00000381541 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr6:31541367 G>A maps to NM_000595.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:96421322 C>A maps to NM_000895.1 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:24785006 C>A maps to NM_181657.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24780694 C>A maps to ENST00000336557 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:24779966 C>T maps to ENST00000336557 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:24780793 C>T maps to ENST00000336557 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr2:33614374 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:33412121 C>T maps to ENST00000354476 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:33622305 C>A maps to ENST00000354476 C1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:33411977 T>C maps to ENST00000354476 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:33590410 G>T maps to ENST00000354476 E1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:33622299 C>T maps to ENST00000354476 C1646C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:33468747 A>G maps to ENST00000354476 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:33526655 T>C maps to ENST00000354476 F1143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:33498721 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:33246090 G>A maps to ENST00000354476 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr2:33526604 G>A maps to ENST00000354476 Q1126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:33335647 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr14:74976052 A>G maps to NM_000428.2 C1097C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:74970734 G>A maps to NM_000428.2 F1492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:75019631 G>A maps to NM_000428.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr14:74969605 G>A maps to NM_000428.2 R1640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:74976907 C>A maps to NM_000428.2 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:74995781 C>T maps to NM_000428.2 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr11:65320665 G>A maps to NM_001130144.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65309113 G>A maps to NM_001130144.2 C894C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr11:65321624 G>A maps to NM_001130144.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:41133105 C>T maps to ENST00000308370 F1470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:41123098 C>T maps to ENST00000308370 Y1079Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:41117095 C>T maps to ENST00000308370 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:41125349 G>T maps to ENST00000308370 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:41132886 C>T maps to ENST00000308370 F1397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:41133685 C>T maps to ENST00000308370 C1547C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:41118969 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:41128309 G>A maps to ENST00000308370 T1140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:41133069 C>T maps to ENST00000308370 F1458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:41132886 C>T maps to ENST00000308370 F1397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:6495233 G>T maps to NM_002342.1 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:6495304 C>T maps to NM_002342.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:46484954 G>T maps to NM_002343.3 Y544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:46480852 C>T maps to NM_002343.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:46482910 A>G maps to NM_002343.3 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:46501163 C>T maps to NM_002343.3 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:46479587 C>T maps to NM_002343.3 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:46491356 C>T maps to NM_002343.3 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:144184234 C>T maps to NM_032860.3 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:144181561 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:144178564 G>T maps to NM_032860.3 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr6:144165624 T>G maps to NM_032860.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:144184234 C>T maps to NM_032860.3 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:144178921 A>G maps to NM_032860.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:144184234 C>T maps to NM_032860.3 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:249117 G>A maps to NM_201412.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:139094313 C>T maps to NM_016019.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:139102311 C>T maps to NM_016019.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:139106918 G>T maps to NM_016019.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:48821072 G>T maps to ENST00000393227 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:91502198 G>A maps to NM_002345.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:23419383 G>A maps to NM_001142546.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:23418351 A>G maps to NM_001142546.1 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:23418969 C>T maps to NM_001142546.1 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:23417870 C>A maps to NM_001142546.1 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:23419110 G>A maps to NM_001142546.1 N548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:23418888 T>C maps to NM_001142546.1 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:23418834 C>T maps to NM_001142546.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:23420202 T>C maps to NM_001142546.1 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:23419074 A>G maps to NM_001142546.1 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:23419869 A>G maps to NM_001142546.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr1:23420408 G>A maps to NM_001142546.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:24750753 C>A maps to NM_001009909.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:25004763 A>G maps to NM_001009909.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:24753683 G>A maps to NM_001009909.2 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:24927593 G>T maps to NM_001009909.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr23:114541133 G>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:114540794 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:114541202 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:114524337 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:114540913 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:114536566 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:114540771 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:114540932 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:114541002 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:114541266 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:114540853 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:114540953 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:114540908 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:114536676 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:114540908 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:158386886 G>A maps to NM_020169.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:143866840 C>T maps to NM_003695.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:31686977 G>T maps to NM_025261.1 C91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:31675499 C>T maps to ENST00000375834 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:160735802 G>A maps to NM_001198759.1 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:160741775 G>A maps to NM_001198759.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:160661610 G>A maps to NM_002349.3 R1705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:160661722 G>A maps to NM_002349.3 Y1667Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:160737751 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:160769684 C>T maps to ENST00000263285 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:160771613 C>T maps to NM_001033667.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:160769723 C>T maps to ENST00000263285 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:160784423 C>A maps to ENST00000263285 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:160766003 T>C maps to ENST00000263285 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:160788071 G>A maps to ENST00000263285 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:160769744 C>A maps to ENST00000263285 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:160769603 C>T maps to ENST00000263285 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:74922306 G>T maps to NM_015364.4 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:4275355 C>T maps to NM_017816.2 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr4:4276124 G>A maps to NM_017816.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:4281194 G>A maps to NM_017816.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:56860207 C>A maps to NM_002350.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:56863238 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:56922614 C>T maps to NM_002350.2 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:56860183 G>A maps to NM_002350.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:56910957 G>A maps to NM_002350.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:143856698 G>A maps to NM_177457.3 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:143857092 G>A maps to NM_023946.2 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:143831823 G>A maps to NM_205545.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr8:143833839 C>T maps to NM_205545.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:43965981 A>G maps to NM_014400.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:42341228 G>T maps to NM_173506.4 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:24121189 G>T maps to NM_007260.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:219366580 A>C maps to NM_138794.3 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:20927015 C>T maps to NM_020424.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:25357132 G>T maps to NM_001001660.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:151137685 G>A maps to NM_212551.4 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:89814745 C>A maps to NM_198273.1 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:89815069 C>A maps to NM_198273.1 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:89814995 C>T maps to NM_198273.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr15:100269519 A>G maps to NM_152449.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:100269824 C>A maps to NM_152449.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:100269633 G>A maps to NM_152449.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:100269336 C>T maps to NM_152449.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:235894437 C>T maps to NM_000081.2 W2947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:235944235 C>A maps to NM_000081.2 E1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:235972194 A>G maps to NM_000081.2 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:235973535 C>T maps to NM_000081.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:235955092 A>G maps to NM_000081.2 C1483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:235969377 C>A maps to NM_000081.2 E1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:235972814 C>A maps to NM_000081.2 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:235907457 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:235971813 G>A maps to NM_000081.2 C768C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:235892949 G>A maps to NM_000081.2 R3018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:235909821 G>A maps to NM_000081.2 R2596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:235922750 A>G maps to NM_000081.2 N2134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:235827793 G>A maps to NM_000081.2 I3722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:235969066 C>T maps to NM_000081.2 K1123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:235969711 G>A maps to NM_000081.2 C908C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr1:235956907 G>A maps to NM_000081.2 C1337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:235955080 A>G maps to NM_000081.2 A1487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:235907457 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:235826245 G>A maps to NM_000081.2 A3800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:235875428 C>A maps to NM_000081.2 E3285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:235929421 G>A maps to NM_000081.2 Y2026Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:235918788 G>A maps to NM_000081.2 G2406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:30915091 G>A maps to NM_183058.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr10:30915086 C>T maps to NM_183058.2 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:30915091 G>A maps to NM_183058.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:42445553 C>A maps to NM_144634.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr17:34263831 G>A maps to NM_020426.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:34264833 G>A maps to NM_020426.1 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:9995548 C>T did not map to a codon.
Alternatively spliced codon TCGA-A5-A0RA-01A-21D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:21346042 G>A maps to NM_006767.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:21341852 G>A maps to NM_006767.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr22:21346096 C>T maps to NM_006767.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr22:21343947 C>T maps to NM_006767.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:20112431 G>A maps to NM_021020.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:20112629 C>T maps to NM_021020.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:20110673 G>T maps to NM_021020.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:20107307 G>A maps to NM_021020.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr8:20112431 G>A maps to NM_021020.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:102762411 C>T maps to NM_032429.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:9098822 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:36049738 G>T maps to NM_005584.4 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:36049450 C>T maps to NM_005584.4 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:36049216 C>T maps to NM_005584.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:36049405 G>A maps to NM_005584.4 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:36050038 A>G maps to NM_005584.4 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:36049309 C>T maps to NM_005584.4 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:151504444 C>T maps to NM_006439.4 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:151504636 C>T maps to NM_006439.4 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:151504882 C>T maps to NM_006439.4 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:151504636 C>T maps to NM_006439.4 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:151504831 G>A maps to NM_006439.4 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr4:151505012 C>T maps to NM_006439.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:151504357 C>T maps to NM_006439.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:151504522 C>T maps to NM_006439.4 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:20199212 C>T maps to NM_182762.3 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:20197898 A>G maps to NM_182762.3 Y695Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:20198623 C>A maps to NM_182762.3 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:39776605 T>G maps to ENST00000361689 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:39907952 C>T maps to ENST00000361689 H4244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:39854194 A>G maps to ENST00000361689 L3165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:39906688 G>A maps to ENST00000361689 E4095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:39750067 G>T maps to ENST00000361689 G372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:39757631 G>A maps to ENST00000361689 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:39790349 A>G maps to ENST00000361689 E1479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:39835719 T>C maps to ENST00000361689 S2257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:39844152 G>T maps to ENST00000361689 G2350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:39785403 C>A maps to ENST00000361689 Y1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:39896505 C>T maps to ENST00000361689 Q3693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:39924809 T>C maps to ENST00000361689 S5024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:39818719 C>T maps to ENST00000361689 I1685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:39853301 C>T maps to ENST00000361689 R2868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:39776599 T>C maps to ENST00000361689 I1071I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:39781298 G>T maps to ENST00000361689 E1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:39788285 G>T maps to ENST00000361689 E1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:39799006 C>T maps to ENST00000289893 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:39749188 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:39909115 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:39827168 C>T maps to ENST00000361689 F2135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr1:39784127 A>G maps to ENST00000361689 Q1267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr1:39826511 C>T maps to ENST00000361689 R2036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:39799306 C>A maps to ENST00000289893 V789V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:39800846 G>T maps to ENST00000289893 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:39823058 G>T maps to ENST00000361689 E1751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:39888403 C>T maps to ENST00000361689 V3265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:39898740 C>T maps to ENST00000361689 R3765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:39765916 C>T maps to ENST00000361689 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:39801530 C>T maps to ENST00000289893 R1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:39914354 C>T maps to ENST00000361689 P4667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:39812756 C>T maps to ENST00000289893 R2004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:39898787 C>A maps to ENST00000361689 I3780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:39908226 C>T maps to ENST00000361689 L4305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:39800836 A>C maps to ENST00000289893 S1299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:39827292 C>T maps to ENST00000361689 L2177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:39818803 G>A maps to ENST00000361689 S1713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:15866407 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:15210604 G>A maps to ENST00000310348 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:15967781 G>T maps to ENST00000310348 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:15866407 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:1938024 C>T maps to NM_003550.2 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr7:1997344 G>A maps to NM_003550.2 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:120986965 G>A maps to NM_002358.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:120986913 G>A maps to NM_002358.3 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:120982089 G>A maps to NM_002358.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:498580 C>T maps to NM_130760.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:47311498 G>A maps to NM_003682.3 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:47305746 T>C maps to NM_003682.3 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:47330218 C>T maps to NM_003682.3 S1279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:47350242 C>T maps to NM_003682.3 Y1609Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:47304521 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:47336778 C>T maps to NM_003682.3 R1426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:47330218 C>T maps to NM_003682.3 S1279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:47345319 G>A maps to NM_003682.3 T1492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr11:47317527 C>T maps to NM_003682.3 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr11:47303964 C>T maps to NM_003682.3 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr11:47296641 G>A maps to NM_003682.3 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:47306580 G>A maps to NM_003682.3 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:47336865 C>A maps to NM_003682.3 I1455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:47348330 C>T maps to NM_003682.3 R1589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:47303241 G>A maps to NM_003682.3 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:1326589 C>T maps to ENST00000505177 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr4:1305834 C>T maps to ENST00000505177 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:166990947 C>T maps to NM_032858.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:166959018 G>T maps to NM_032858.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:166973531 C>A maps to NM_032858.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:166974587 C>T maps to NM_032858.1 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:166985474 G>T maps to NM_032858.1 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:166959015 C>T maps to NM_032858.1 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:166959015 C>T maps to NM_032858.1 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:166974628 C>T maps to NM_032858.1 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:166958630 C>T maps to NM_032858.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:79632689 C>T maps to NM_005360.4 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:145160853 C>T maps to NM_032272.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:145161331 C>T maps to NM_032272.4 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:39317283 C>T maps to NM_005461.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:79880678 G>A maps to NM_002359.2 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:1579605 G>A maps to NM_002360.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:1579905 C>A maps to NM_002360.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:35801471 C>T maps to NM_002361.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:35801543 G>A maps to NM_002361.3 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr19:35786681 G>A maps to NM_002361.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:152482344 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152482581 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:152482796 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152482131 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152482738 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:152482515 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:151303419 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:151303055 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:151303121 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:151303342 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:151303782 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:151303927 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:151303591 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:151303644 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:151304046 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:151303232 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:151303312 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:151303630 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr23:151303894 T>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:148797884 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:148798433 T>G did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:148794846 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:148797848 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:148798157 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:148797733 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:148797857 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:148797685 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:148798092 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr23:148797814 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr23:148794853 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:148797492 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr23:148797769 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:151900161 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:151900773 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:151900097 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:151900572 G>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:151900075 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:151900362 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:151935710 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:151935503 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:151935664 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:151935749 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr23:151935793 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:151935538 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:151092444 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:151092621 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:151092532 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:151092298 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:151092415 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:151093031 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:151092410 A>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:151092751 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:151092938 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:151283764 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr23:151283932 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:151869695 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:151870227 G>A did not map to a codon.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr23:151870060 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:151869727 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:149013421 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:149013492 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:149013918 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:149013739 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:149013294 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:149013070 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:30269194 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:30268790 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:30269433 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:30269599 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:30268652 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:30269040 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:30268715 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:30268841 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:27840125 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:27839921 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:27840253 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:27839519 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:27839717 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:27839737 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:27840185 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:27839726 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:27839810 G>T did not map to a codon.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr23:27840073 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27839675 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27839757 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:27840280 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:27839468 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:27840251 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:27840331 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:27839533 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:27839797 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:27839703 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:35820593 A>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:35820752 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:35820971 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:35821008 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:35820657 G>T did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:35820801 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:26158105 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:26157752 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:26157747 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:26157354 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:26157654 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:26157840 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:30237264 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:30236748 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:30237365 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:30237086 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:30237494 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:30236742 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:30237384 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:30237457 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:30255029 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:30254266 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:30254400 G>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:30254803 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:30254666 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:30255005 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:30254162 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:30254510 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:30260290 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:30260409 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:30261225 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:30260278 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:30261223 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:30260721 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:30260593 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:30260500 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:30261093 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:30261071 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:30260348 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:30260943 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:30260589 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:30260998 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:26212132 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:26212107 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:26212153 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:26212351 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:26212934 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr23:26213092 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:26213127 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:26212570 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:26213142 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:26212235 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:26212947 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:26212722 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:26212947 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:26213145 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:26212349 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:26212646 G>C did not map to a codon.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr23:26213017 C>T did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:26212149 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr23:140996433 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:140995709 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:140996047 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:140995487 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:140995944 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:140995272 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:140994184 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:140995030 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:140995132 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:140994245 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:140994163 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:140994793 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:140996288 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:140995709 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:140993717 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:140996603 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:140993797 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:140993697 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:140993417 C>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:140993945 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:140995127 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:140995850 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:140996063 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:140995519 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:140992753 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140993311 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140994058 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140994382 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140995445 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140995512 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140996033 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140996288 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr23:140993430 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:140994740 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:140994514 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:140993460 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:140996465 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr23:141291698 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:141291305 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:141291751 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:141291040 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:141291723 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:141291247 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:141291730 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:141291754 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr23:141291032 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:141291528 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:140953311 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:140953352 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:140969478 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:140969299 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:140983077 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:140969521 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:140983134 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:140985509 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:140983219 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:140985559 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:140967124 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:140926143 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:140969521 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:140985115 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:140985269 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:140985543 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:140984462 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:140984702 C>G did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr23:140983338 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:140969308 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:140984749 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:140985178 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140953279 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:140985225 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:140953338 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:140983094 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:140985098 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:140969294 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:140984966 G>T did not map to a codon.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr23:140953317 T>G did not map to a codon.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr23:140966993 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:51641400 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:51641395 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:51637809 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:51643294 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:51639774 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:51640955 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:51638233 A>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:51638591 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:51638370 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:51638375 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:51640889 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:51641228 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:51640706 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:51640955 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:51644760 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:51641228 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:51639540 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:51640665 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:51638384 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:51638466 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:51637765 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:51639857 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:51640085 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:51639643 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54836182 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54837535 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54838029 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:54837553 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:54837721 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:54839571 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:54837338 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:54836276 G>T did not map to a codon.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr23:54837459 T>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:75649759 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:75650268 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:75648524 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:75649148 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:75650084 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:75650881 G>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:75649699 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:75650128 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:75650772 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:75649420 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:75649145 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:75649285 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:75650687 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:75649107 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:75649814 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr23:75648565 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:75649357 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr23:75649040 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:75004796 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:75003704 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:75003493 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:75004124 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:75004485 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:75003636 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:75004057 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:75003797 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:75004746 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:75004571 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:75003799 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:75003440 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:75003856 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:75004606 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:75003490 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:75003814 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:75004185 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:75004276 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:55478971 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:55479058 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:55479388 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:55478865 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:55479280 G>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:55479211 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:55479303 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:55479121 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:55479289 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:55478989 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:55479357 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:55479356 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:23889355 T>G maps to NM_019066.4 A1178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:23890411 G>T maps to NM_019066.4 A826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:23890243 G>A maps to NM_019066.4 S882S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:23890780 C>T maps to NM_019066.4 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:23889184 G>A maps to NM_019066.4 T1235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:65367588 G>A maps to NM_001033057.1 H888H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:65367699 G>A maps to NM_001033057.1 D851D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:65350538 G>A maps to NM_001033057.1 T1093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr3:65346922 G>A maps to NM_001033057.1 R1195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:65349222 G>A maps to NM_001033057.1 R1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:65415324 G>A maps to NM_001033057.1 G679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:65365098 G>A maps to NM_001033057.1 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr3:65342358 G>A maps to NM_001033057.1 R1361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:65367611 G>A maps to NM_001033057.1 Q881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:65433694 A>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:65415720 G>A maps to NM_001033057.1 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:77764482 A>G maps to NM_012301.3 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:77789393 G>A maps to NM_012301.3 F931F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:77764506 G>A maps to NM_012301.3 I954I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:77824257 G>T maps to NM_012301.3 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:77998504 G>A maps to NM_012301.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:78256492 C>A maps to NM_012301.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:77708378 G>T maps to NM_012301.3 I1197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:77756686 G>A maps to NM_012301.3 R1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:77789375 G>A maps to NM_012301.3 S937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr7:79082495 C>T maps to NM_012301.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:77885377 G>A maps to NM_012301.3 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:77756686 G>A maps to NM_012301.3 R1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:114225876 T>C maps to NM_001142782.1 S1229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:114225948 T>C maps to NM_001142782.1 D1253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:114225543 G>A maps to NM_001142782.1 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:114191890 C>T maps to NM_001142782.1 R730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:114193754 C>A maps to NM_001142782.1 V789V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:114226480 G>T maps to NM_001142782.1 E1431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:114201835 C>T maps to NM_001142782.1 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:114123197 A>G maps to NM_001142782.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:114165483 C>T maps to NM_001142782.1 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:49021529 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49022512 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:49021199 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49021410 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr23:49019237 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:49022528 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:49021098 A>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:53699324 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:53694614 G>A maps to NM_002370.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:77096799 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:77126381 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:77112894 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:77112295 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:77150821 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:77150840 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:77130971 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:33346657 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:33354772 C>T maps to NM_032509.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:33346628 C>T maps to NM_032509.3 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:56400686 C>T maps to NM_006785.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr9:72741135 C>T maps to NM_153267.4 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:72758651 G>T maps to NM_153267.4 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:72741210 C>A maps to NM_153267.4 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:72723295 T>C maps to NM_153267.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:72741173 C>A maps to NM_153267.4 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr9:139750060 G>A maps to ENST00000392881 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr9:139748475 C>T maps to ENST00000392881 H206H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:179192382 C>T maps to NM_014757.4 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:179192803 G>T maps to NM_014757.4 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:95712720 G>A maps to NM_032427.1 N954N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:95825379 C>T maps to NM_032427.1 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:95825682 G>A maps to NM_032427.1 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:140811419 C>T maps to ENST00000509479 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:140812084 G>A maps to ENST00000509479 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:140812012 G>A maps to ENST00000509479 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr4:140812061 C>T maps to ENST00000509479 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr4:140640758 T>A maps to ENST00000509479 P1045P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:140651728 G>A maps to ENST00000509479 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:149639739 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:149638176 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:149642013 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:149638112 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:149639580 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:149639108 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:149678273 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:149638874 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:149638406 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:149638880 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:149639659 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:149639362 C>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:149638420 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:49218962 C>T maps to NM_001130915.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:49222282 G>A maps to NM_001130915.1 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:119510928 G>A maps to NM_005907.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:119501046 G>A maps to NM_005907.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:117944904 C>T maps to NM_006699.3 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:118003120 C>T maps to NM_006699.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr1:26110183 C>T maps to NM_020379.2 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:109049312 C>T maps to NM_002372.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:109181687 G>T maps to NM_002372.2 G941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:109106194 C>A maps to NM_002372.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:109178113 T>G maps to NM_002372.2 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:109183455 C>T maps to NM_002372.2 R981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr5:109103383 G>A maps to NM_002372.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr5:109117132 C>T maps to NM_002372.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:109152985 C>T maps to NM_002372.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:109181639 C>A maps to NM_002372.2 I925I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:109103260 T>C maps to NM_002372.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:91456174 G>A maps to NM_006122.2 A846A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:91452691 G>A maps to NM_006122.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:91454462 G>A maps to NM_006122.2 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:91456602 G>A maps to NM_006122.2 Q895Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:91455310 C>T maps to NM_006122.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr15:91455836 C>A maps to NM_006122.2 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:12760964 T>C maps to NM_000528.3 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:12758068 C>T maps to NM_000528.3 R967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:12763240 G>A maps to NM_000528.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:12774640 G>A maps to NM_000528.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:6588777 C>T maps to NM_015274.1 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:6580181 C>T maps to NM_015274.1 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr4:6621700 G>A maps to NM_015274.1 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:6612844 C>T maps to NM_015274.1 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr4:6594920 C>T maps to NM_015274.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr15:75650840 G>A maps to NM_006715.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr15:75652020 G>A maps to NM_006715.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:75648662 G>A maps to NM_006715.2 V955V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:103578883 A>G maps to NM_005908.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:35944748 G>A maps to NM_022077.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr6:96034638 C>T maps to NM_024641.2 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:96053887 C>T maps to NM_024641.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:96034600 C>T maps to NM_024641.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:38265665 C>T maps to NM_001113482.1 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:38265838 G>A maps to NM_001113482.1 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:12483125 G>A maps to NM_018050.2 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:12496239 G>A maps to NM_018050.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr12:12483035 G>A maps to NM_018050.2 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:43542834 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:43571136 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:43591971 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:43603734 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:43590497 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:43601288 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:43542758 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:43587480 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:43571955 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:43603382 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:43599939 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:43603369 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr23:43515637 G>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:43587531 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:43603403 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr23:43655001 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:43627945 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:43652823 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:43741524 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:43655002 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:43655066 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:43656485 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:43662651 C>G did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:43628655 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:43698146 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:43640731 C>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:43656378 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:43628559 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:43814660 C>T maps to ENST00000382031 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:43820901 C>T maps to ENST00000382031 Q2649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:43814324 G>A maps to ENST00000382031 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:43814847 C>T maps to ENST00000382031 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr15:43814381 T>C maps to ENST00000382031 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr15:43814042 G>A maps to ENST00000382031 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:43820258 C>T maps to ENST00000382031 F2434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:43813865 C>T maps to ENST00000382031 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:71490798 T>C maps to NM_005909.3 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:71495598 C>A maps to NM_005909.3 G2139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:71491086 G>A maps to NM_005909.3 E635E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:71493589 G>T maps to NM_005909.3 E1470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:71495574 G>A maps to NM_005909.3 P2131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:71495814 G>A maps to NM_005909.3 S2211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:71496126 G>A maps to NM_005909.3 E2315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:71493807 G>A maps to NM_005909.3 T1542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:71493330 C>T maps to NM_005909.3 P1383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:71491141 G>T maps to NM_005909.3 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:71491645 G>T maps to NM_005909.3 E822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:71492419 G>T maps to NM_005909.3 E1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:71493045 C>T maps to NM_005909.3 V1288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:71492658 C>T maps to NM_005909.3 F1159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr5:71492952 G>A maps to NM_005909.3 P1257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:71491716 T>G maps to NM_005909.3 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:71411571 G>T maps to NM_005909.3 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:71493724 G>T maps to NM_005909.3 E1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:71494320 A>G maps to NM_005909.3 Q1713Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:71491248 G>A maps to NM_005909.3 K689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:71493724 G>T maps to NM_005909.3 E1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:87432440 C>T maps to NM_022818.4 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:87436621 T>C maps to NM_022818.4 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:242159596 G>T maps to NM_001004343.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:242162092 G>A maps to NM_001004343.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:17835910 G>A maps to NM_018174.4 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr19:17836982 C>T maps to NM_018174.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr19:17838511 G>A maps to NM_018174.4 R773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:17831763 C>T maps to NM_018174.4 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:17837744 G>T maps to NM_018174.4 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:17836708 C>T maps to NM_018174.4 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:17836864 C>T maps to NM_018174.4 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:17838757 A>G maps to NM_018174.4 Q855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:210559863 C>T maps to NM_002374.3 F990F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:210518032 G>T maps to NM_002374.3 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:210559606 C>T maps to NM_002374.3 R905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:210558210 A>G maps to NM_002374.3 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:210558576 A>C maps to NM_002374.3 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:210565058 C>T maps to NM_002374.3 V1527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:210558459 C>T maps to NM_002374.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:210574836 C>T maps to NM_002374.3 V1644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:210559515 G>A maps to NM_002374.3 K874K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:210559863 C>T maps to NM_002374.3 F990F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:210517947 G>A maps to NM_002374.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:66729163 G>A maps to NM_002755.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:66777516 A>C maps to NM_002755.3 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr15:66729190 C>T maps to NM_002755.3 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:4099274 C>G maps to NM_030662.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:4097336 G>A maps to NM_030662.3 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:4101082 G>A maps to NM_030662.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:21207807 C>T maps to NM_145109.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:11984690 C>T maps to ENST00000415385 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr17:12044468 T>C maps to ENST00000415385 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:12028609 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:11984781 C>T maps to ENST00000415385 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:12032541 G>A maps to ENST00000415385 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:68065068 G>A maps to NM_145160.1 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:67938600 G>A maps to NM_145160.1 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr15:67984844 C>T maps to NM_145160.1 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:67855619 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:67893069 C>T maps to NM_145160.1 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:7976442 C>T maps to ENST00000425613 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7976406 G>A maps to ENST00000425613 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:56177718 G>T maps to NM_005921.1 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:56167794 G>T maps to NM_005921.1 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:56179373 A>G maps to NM_005921.1 G1229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:56152445 G>T maps to NM_005921.1 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:56168493 G>T maps to NM_005921.1 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:56177541 G>T maps to NM_005921.1 E839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:56177933 C>A maps to NM_005921.1 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:56181802 G>T maps to NM_005921.1 E1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:40698396 G>A maps to NM_002446.3 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:40698468 C>A maps to NM_002446.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:40710394 C>T maps to NM_002446.3 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:40698267 C>T maps to NM_002446.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:65375135 G>A maps to NM_002419.3 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:65380716 G>A maps to NM_002419.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:53881027 G>A maps to NM_001193511.1 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:53880859 G>A maps to NM_001193511.1 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:185155361 T>C maps to NM_004721.3 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:185198022 C>A maps to NM_004721.3 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:185181352 G>T maps to NM_004721.3 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:185184656 C>T maps to NM_004721.3 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:185191356 C>A maps to NM_004721.3 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:185181415 G>T maps to NM_004721.3 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:185146803 T>C maps to NM_004721.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:185190871 C>T maps to NM_004721.3 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:185191450 G>T maps to NM_004721.3 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:43364300 G>A maps to ENST00000344686 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:43350918 G>A maps to ENST00000344686 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr17:43364208 G>A maps to ENST00000344686 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:43362316 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:19433333 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:19410498 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:19428089 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:19444455 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:19475044 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19379622 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19391813 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19410541 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19410573 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19433337 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:19380891 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:19392700 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:19410217 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:19390876 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:19392700 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:19398267 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:19410583 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:19443761 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:19444456 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:19390899 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr23:19444397 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr23:19428043 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:19482521 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:19507061 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:19389134 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:19387211 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:19425369 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:19410118 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:19410129 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:19416386 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:19387273 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:19431502 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:19433337 G>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:19389181 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:19391795 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:19431479 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:19533069 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:128075797 C>A maps to NM_006609.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:128065304 G>T maps to NM_006609.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:128075797 C>A maps to NM_006609.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:61766241 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:61769600 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:161528979 G>T maps to NM_005922.2 G1366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:161470618 G>T maps to NM_005922.2 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:136944050 G>A maps to NM_005923.3 Y695Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:136904817 C>A maps to NM_005923.3 E1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:136904863 C>T maps to NM_005923.3 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:136977483 G>A maps to NM_005923.3 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:137112938 C>T maps to NM_005923.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr6:136972139 G>A maps to NM_005923.3 H590H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr6:136913358 C>T maps to NM_005923.3 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:136944050 G>A maps to NM_005923.3 Y695Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr6:136972136 C>T maps to NM_005923.3 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr6:136958467 G>A maps to NM_005923.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:27685357 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:27683214 C>T maps to NM_004672.3 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:27685057 C>T maps to NM_004672.3 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:27685261 C>A maps to NM_004672.3 E841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:91263237 A>G maps to NM_145331.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr10:30728034 C>T maps to NM_005204.2 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:30728028 T>C maps to NM_005204.2 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:30748326 G>A maps to NM_005204.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:71197582 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:71205029 T>C maps to NM_033141.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:71206810 G>T maps to NM_033141.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:71215623 C>T maps to NM_033141.2 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:71197423 A>G maps to NM_033141.2 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:71199706 T>C maps to NM_033141.2 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr14:71199562 G>A maps to NM_033141.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr3:47908734 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:48040232 C>A maps to ENST00000426837 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr3:47951629 A>G maps to ENST00000426837 N1444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:47957624 C>T maps to ENST00000426837 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:47957821 C>A maps to ENST00000426837 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:47951017 T>C maps to ENST00000426837 Q1648Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:47958044 A>G maps to ENST00000426837 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:39108526 G>A maps to NM_001042600.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:39090564 C>A maps to NM_001042600.1 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:39087673 C>T maps to NM_001042600.1 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:64567682 C>T maps to NM_004579.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:64557390 C>A maps to NM_004579.2 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:64570126 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:64570096 T>C maps to NM_004579.2 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:39477793 A>G maps to NM_003618.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:39487797 G>A maps to NM_003618.2 R753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:39481628 T>A maps to NM_003618.2 K835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:39487797 G>A maps to NM_003618.2 R753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr2:39505604 G>A maps to NM_003618.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:102481498 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:102472449 A>G maps to NM_145686.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr14:50895428 A>G maps to NM_198794.1 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:50971533 G>T maps to NM_198794.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:50904245 G>A maps to NM_198794.1 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:50904245 G>A maps to NM_198794.1 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:75298156 G>A maps to NM_033063.1 R797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:36636646 C>A maps to NM_018067.3 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:36639005 G>A maps to NM_018067.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:36636620 C>T maps to NM_018067.3 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:20034377 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:20033416 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:20043895 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:20043996 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:20071039 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:20028970 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:20029054 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:20030501 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:20028937 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:20060676 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:20081542 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:20082868 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:20043078 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:20028926 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:20030575 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:20034396 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:20060709 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:20043148 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:20028970 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:20033394 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:20033382 C>G did not map to a codon.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr23:20071070 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:20074838 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:20034377 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:20060722 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:20043938 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:20033441 C>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:20043905 T>C did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:20068978 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:20029057 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:20043154 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:135313106 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135310844 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135313779 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135326843 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135328443 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135314032 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135323417 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135326886 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:135314005 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:135304593 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135302931 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135308093 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135313872 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135322579 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:135303100 G>A did not map to a codon.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr23:135313851 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr23:135313916 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135312623 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135313718 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135314246 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:135326866 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr23:135301808 G>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:135312581 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:135318440 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr23:135310848 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:156278656 A>G maps to NM_001039580.1 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:156296098 A>G maps to NM_001039580.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr4:156269030 A>G maps to NM_001039580.1 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:156274071 A>G maps to NM_001039580.1 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:156269056 C>A maps to NM_001039580.1 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:22123542 C>A maps to NM_138957.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr4:86938452 G>T maps to NM_138982.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:87024346 G>A maps to NM_138982.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:86950427 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50704972 G>A maps to NM_002751.5 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50703849 G>A maps to NM_002751.5 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr22:50695215 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr22:50693653 G>A maps to NM_002969.3 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:36104431 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:36020553 G>A maps to NM_139012.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:36070397 G>A maps to NM_139012.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:144800247 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:55529949 G>A maps to NM_144578.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:30128009 G>A maps to NM_002746.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:48241531 C>T maps to NM_002747.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:48256196 C>T maps to NM_002747.3 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:48190384 C>T maps to NM_002747.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr18:48190375 C>T maps to NM_002747.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:48190558 C>T maps to NM_002747.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:48190846 G>A maps to NM_002747.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:48190558 C>T maps to NM_002747.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:52338953 G>A maps to NM_002748.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:52356957 G>T maps to NM_002748.3 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr15:52353494 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:19283194 C>T maps to NM_139034.2 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:19284086 T>C maps to NM_139034.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:49612894 C>T maps to NM_139049.1 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr10:49635121 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:49639234 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:49612988 G>T maps to NM_139049.1 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:45924220 G>A maps to NM_005456.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:51044079 C>A maps to ENST00000329492 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:51048401 G>A maps to ENST00000008876 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:1816242 C>T maps to NM_015133.3 N883N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr16:1812349 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:1797220 C>T maps to NM_015133.3 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:1818559 C>T maps to NM_015133.3 V1274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:1812896 G>A maps to NM_015133.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:1798617 C>T maps to NM_015133.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:1817299 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:1817614 G>A maps to NM_015133.3 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:1818559 C>A maps to NM_015133.3 V1274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr16:1814327 G>A maps to NM_015133.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:179669621 G>T maps to NM_002752.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:179663506 G>A maps to NM_002752.4 N384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr5:179665377 A>G maps to NM_002752.4 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:128434763 A>C maps to NM_001006617.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr15:42104214 C>T maps to NM_001128608.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:42113807 T>G maps to NM_001128608.1 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:42107554 G>A maps to NM_001128608.1 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr15:42107464 C>T maps to NM_001128608.1 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:42105266 C>T maps to NM_001128608.1 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:42107835 C>A maps to NM_001128608.1 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr15:42104787 C>G maps to NM_001128608.1 Y191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:31413783 A>G maps to NM_012325.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr18:32706966 A>G maps to NM_014268.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:32712069 C>T maps to NM_014268.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:32720379 C>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr17:44073954 C>T maps to NM_001123066.3 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr17:44087689 T>C maps to NM_001123066.3 N614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:44060841 C>T maps to NM_001123066.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:164506905 G>T maps to ENST00000514618 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr4:164775226 C>T maps to ENST00000514618 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:164466832 G>A maps to ENST00000514618 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:60813929 G>A maps to NM_152598.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:60779069 G>A maps to NM_152598.2 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:60799911 G>A maps to NM_152598.2 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:60813386 A>G maps to NM_152598.2 D614D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:60814633 C>A maps to NM_152598.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:16067798 G>A maps to NM_001102562.1 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:16067798 G>A maps to NM_001102562.1 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:16067732 C>T maps to NM_001102562.1 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:217234572 A>G maps to NM_020814.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:217142542 T>C maps to NM_020814.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:94109125 T>A maps to NM_017824.4 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:94109495 C>T maps to NM_017824.4 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:10382055 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:10410325 A>T maps to NM_005885.2 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:10402235 A>G maps to NM_005885.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:160585682 T>G maps to NM_022826.2 Y50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:45953941 G>A maps to NM_145021.4 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:58152015 G>A maps to NM_138396.4 W213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:58152075 C>A maps to NM_138396.4 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:119750793 C>T maps to NM_006770.3 D449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:119750011 T>C maps to NM_006770.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:119750727 C>T maps to NM_006770.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:220826577 C>T maps to NM_018650.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:220805633 T>C maps to NM_018650.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:220825471 C>T maps to NM_018650.3 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:220835409 C>T maps to NM_018650.3 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:220804391 C>T maps to NM_018650.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:220791761 C>A maps to NM_018650.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:220809307 C>T maps to NM_018650.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:220752805 G>A maps to NM_018650.3 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:220804391 C>T maps to NM_018650.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:63666537 G>A maps to NM_001039469.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:63663106 T>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:103958326 C>T maps to ENST00000335102 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:103946819 G>T maps to ENST00000335102 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:103958315 C>T maps to ENST00000335102 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:103958315 C>T maps to ENST00000335102 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:103969221 C>T maps to ENST00000335102 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:103918264 C>T maps to ENST00000335102 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr14:103871417 G>C maps to ENST00000335102 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:103941403 G>T maps to ENST00000335102 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:45774875 C>T maps to NM_031417.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr19:45766387 C>T maps to NM_031417.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:57910041 G>A maps to NM_004990.2 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:57910282 G>A maps to NM_004990.2 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:57884412 C>G maps to NM_004990.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr12:57908505 T>C maps to NM_004990.2 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:57910041 G>T maps to NM_004990.2 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:198571611 C>T maps to NM_138395.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:198571805 A>G maps to NM_138395.3 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:198571778 G>A maps to NM_138395.3 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:68715619 C>A maps to NM_001038603.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:68728460 A>G maps to NM_001038603.2 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:71674368 C>T maps to NM_001017967.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:71674488 G>A maps to NM_001017967.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:160328625 G>A maps to NM_002377.2 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr6:160328586 G>A maps to NM_002377.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:29454671 C>T maps to NM_052967.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr6:29454572 G>T maps to NM_052967.1 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:29455511 C>T maps to NM_052967.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:29455511 C>T maps to NM_052967.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:186971010 G>A maps to NM_139125.3 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:186978565 G>A maps to NM_139125.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:186947584 G>A maps to NM_001879.5 H468H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:186954002 G>A maps to NM_139125.3 H552H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:186953582 G>A maps to NM_139125.3 C692C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:186965162 G>A maps to NM_001031849.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:11087088 C>G maps to NM_006610.2 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:11097839 T>G maps to NM_006610.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:11106968 G>T maps to NM_006610.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:11087646 T>C maps to NM_006610.2 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:12963196 C>T maps to NM_014975.2 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:12984423 C>T maps to NM_014975.2 G1151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:12963206 G>T maps to NM_014975.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr19:12984585 G>A maps to NM_014975.2 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:12954345 G>A maps to NM_014975.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr19:12976254 C>T maps to NM_014975.2 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:12963196 C>T maps to NM_014975.2 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:12969353 C>T maps to NM_014975.2 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:46487716 C>T maps to NM_015112.2 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:46290202 T>C maps to NM_015112.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:46494444 C>T maps to NM_015112.2 C686C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:46476460 C>T maps to NM_015112.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:46488981 C>T maps to NM_015112.2 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:46496748 C>T maps to NM_015112.2 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:46496690 G>A maps to NM_015112.2 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:46348056 A>C maps to NM_015112.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:46496398 C>T maps to NM_015112.2 R892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:18245424 G>A maps to NM_015016.1 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:18255894 G>A maps to NM_015016.1 P936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:18258321 C>T maps to NM_015016.1 S1094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr19:18242812 C>T maps to NM_015016.1 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:18254743 C>T maps to NM_015016.1 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr19:18254803 C>A maps to NM_015016.1 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:66462737 C>T maps to NM_001164664.1 N2577N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:66460007 C>A maps to NM_001164664.1 S1667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:66084564 C>T maps to NM_001164664.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:66426062 G>T maps to NM_001164664.1 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:66459108 C>T maps to NM_001164664.1 R1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:66460559 C>T maps to NM_001164664.1 N1851N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr5:66459209 A>G maps to NM_001164664.1 G1401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr5:66448519 G>A maps to NM_001164664.1 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:66460508 C>T maps to NM_001164664.1 D1834D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:66460439 C>T maps to NM_001164664.1 S1811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:66462005 C>T maps to NM_001164664.1 H2333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr5:66459509 C>T maps to NM_001164664.1 R1501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:27454095 A>G maps to NM_001172303.1 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:27458958 G>A maps to NM_001172303.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr10:27459300 C>T maps to NM_001172303.1 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:27448624 G>T maps to NM_001172303.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:27470464 G>T maps to NM_001172303.1 E813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:27459915 T>C maps to NM_001172303.1 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:27469942 C>T maps to NM_001172303.1 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr10:82043687 G>A maps to NM_000429.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:82040036 C>T maps to NM_000429.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr10:82043702 G>A maps to NM_000429.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr10:82034907 G>A maps to NM_000429.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:82036142 C>A maps to NM_000429.2 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr10:82034886 A>G maps to NM_000429.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:82040060 G>A maps to NM_000429.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:162945312 G>T maps to NM_013283.3 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:162943749 A>G maps to ENST00000421814 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:3785118 G>T maps to NM_139355.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:3778560 A>G maps to NM_002378.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:3778593 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:31188061 C>T maps to NM_002379.3 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:99039800 C>A maps to ENST00000254898 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:20192872 T>C maps to NM_002381.4 *487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:20201811 C>A maps to NM_002381.4 G316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:138658443 C>T maps to ENST00000394800 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:138643731 G>T maps to ENST00000394800 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:3842923 G>A maps to NM_020746.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr20:3846536 G>T maps to NM_020746.3 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:65543382 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:47806308 G>A maps to ENST00000424334 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:47802219 G>A maps to ENST00000424334 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:47796109 C>T maps to NM_015845.3 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:51692511 C>A maps to NM_003927.3 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:51692487 C>A maps to NM_003927.3 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:129155412 G>A maps to NM_003925.1 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:129156755 C>A maps to NM_003925.1 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:129156118 G>T maps to NM_003925.1 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:149226987 A>G maps to ENST00000404807 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:149243368 G>A maps to ENST00000404807 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:149247397 G>A maps to ENST00000404807 L1399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:149248066 C>A maps to ENST00000404807 V1622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:149243473 C>T maps to ENST00000404807 C1236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:149240763 C>T maps to ENST00000404807 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:149241078 C>A maps to ENST00000404807 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:149227407 C>T maps to ENST00000404807 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:149247559 C>T maps to ENST00000404807 G1453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:149220181 C>T maps to ENST00000404807 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr12:57920712 T>C maps to NM_052897.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:57920358 C>A maps to NM_052897.3 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:57920419 G>T maps to NM_052897.3 G498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr12:57919198 C>T maps to NM_052897.3 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:36783804 G>A maps to NM_016586.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:89756989 C>T maps to NM_203406.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:89757174 C>A maps to NM_203406.1 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:152018101 G>A maps to NM_021038.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:152177109 G>A maps to NM_021038.3 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:98009737 C>A maps to ENST00000376673 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:98043600 C>T maps to ENST00000376673 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr13:98009869 C>T maps to ENST00000376673 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:131540406 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:131524952 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:131515409 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:131540343 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:131524944 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:131516288 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:131520693 G>A did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:131540407 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:131526330 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:131525092 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:131520812 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:20109845 C>T maps to NM_001080480.1 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr6:20124708 C>T maps to NM_001080480.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr6:20113106 C>T maps to NM_001080480.1 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:20124774 C>T maps to NM_001080480.1 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr6:20152859 G>A maps to NM_001080480.1 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:20124768 C>T maps to NM_001080480.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:20128942 G>A maps to NM_001080480.1 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:9017114 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr19:54691156 G>T maps to NM_024298.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:54687419 G>A maps to NM_024298.3 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:54691081 C>T maps to NM_024298.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:54677941 G>A maps to NM_024298.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:54687461 G>A maps to NM_024298.3 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:54691191 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr18:74729150 C>A maps to NM_001025101.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr18:74696817 G>A maps to NM_001025101.1 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:49272617 G>A maps to ENST00000389496 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr17:49270230 A>G maps to ENST00000389496 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:84108261 C>T maps to NM_003791.2 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:84097033 C>T maps to NM_003791.2 K816K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:84129288 C>T maps to NM_003791.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr16:84088248 C>T maps to NM_003791.2 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:84125348 C>T maps to NM_003791.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:84129261 C>T maps to NM_003791.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr16:84100136 G>A maps to NM_003791.2 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr16:84132697 C>T maps to NM_003791.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:21900746 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:21900746 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:21863411 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:21869645 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:21886607 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:21871535 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:21900708 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:21871503 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:21896623 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:21887759 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:21896200 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:21887784 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr16:89986142 G>A maps to ENST00000304984 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr16:89986226 C>T maps to ENST00000304984 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:89986079 C>T maps to ENST00000304984 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:13885385 G>A maps to NM_000529.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:13884764 G>A maps to NM_000529.2 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:54823913 C>A maps to ENST00000371389 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:54824255 C>T maps to ENST00000371389 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:54824795 C>T maps to ENST00000371389 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:54824012 C>A maps to ENST00000371389 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:54824207 C>T maps to ENST00000371389 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr18:58038892 G>A maps to NM_005912.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:58038775 G>T maps to NM_005912.2 I269I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AX-A05Z-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:119185256 G>T maps to NM_006500.2 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr11:119182785 G>A maps to NM_006500.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:37888315 G>A maps to NM_033412.3 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:37888016 C>T maps to NM_033412.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:37878549 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr9:37878123 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:37888315 G>A maps to NM_033412.3 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:37879094 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:103349181 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:103349150 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:103349492 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:103349720 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:103349916 G>A did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:103349475 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:43529111 G>A maps to NM_173467.4 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:43537189 G>A maps to NM_173467.4 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr5:112363112 C>T maps to NM_001085377.1 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:112384780 C>T maps to ENST00000514701 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:112439957 G>A maps to NM_001085377.1 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:112364656 G>A maps to NM_001085377.1 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:112364679 G>A maps to NM_001085377.1 R944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:112364656 G>A maps to NM_001085377.1 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:112420988 G>A maps to NM_001085377.1 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:182737953 G>A maps to NM_020166.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:182751848 A>G maps to NM_020166.3 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:70898443 C>T maps to NM_022132.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:70888802 G>A maps to NM_022132.4 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:138679689 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:138699863 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:138678813 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:138687891 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:138668596 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:138664609 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:138686868 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:138701778 T>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:138678814 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:138697184 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:138664651 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:138697170 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:138667232 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:138667241 C>G did not map to a codon.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr23:138727726 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr23:138672081 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:138711972 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr23:138713562 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:138672030 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:138680646 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:138697207 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:138678781 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:138698529 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:138678724 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:138698523 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:138699761 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:138708878 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:138711990 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:113748870 C>T maps to NM_001112732.1 D1056D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:113740520 C>T maps to NM_001112732.1 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:113634064 G>A maps to NM_024979.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr3:183017867 G>A maps to NM_015078.2 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:183014772 G>A maps to NM_015078.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:182923938 G>A maps to NM_015078.2 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:182925517 G>A maps to NM_015078.2 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr3:182897275 G>T maps to NM_015078.2 T1079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:183107516 C>A maps to NM_015078.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:182941974 C>A maps to NM_015078.2 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr3:183041106 G>A maps to NM_015078.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:182923729 C>A maps to NM_015078.2 E940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:182933831 T>C maps to NM_015078.2 Q807Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:183056596 C>T maps to NM_015078.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr2:47135062 C>T maps to NM_001171506.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:47135053 C>T maps to NM_001171506.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:47136208 G>T maps to NM_001171506.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:41077325 G>T maps to NM_005297.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr22:41075454 A>G maps to NM_005297.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:41077595 C>A maps to NM_005297.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr6:100368977 A>G maps to NM_032503.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:100368962 G>T maps to NM_032503.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:100368968 G>T maps to NM_032503.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:150551565 G>A maps to NM_021960.4 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:13214436 A>G maps to NM_182751.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:13243518 C>T maps to NM_182751.2 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:13228177 C>T maps to NM_182751.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr10:13231044 C>T maps to NM_182751.2 Y461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:127336821 C>T maps to NM_004526.2 Y637Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:127318294 A>G maps to NM_004526.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:127325069 G>A maps to NM_004526.2 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:127339934 C>A maps to NM_004526.2 S823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr3:127325476 C>T maps to NM_004526.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:127339992 G>A maps to NM_004526.2 E842E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:52138632 G>A maps to ENST00000419835 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr6:52131451 G>A maps to ENST00000419835 Y750Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr21:47697504 A>G maps to NM_003906.3 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr21:47704792 G>A maps to NM_003906.3 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:47676827 G>A maps to NM_003906.3 C1269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr21:47704177 C>A maps to NM_003906.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr21:47704815 G>A maps to NM_003906.3 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:47695123 G>A maps to NM_003906.3 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:47663376 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:47663439 G>A maps to NM_003906.3 I1745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr21:47705106 G>A maps to NM_003906.3 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr21:47664964 G>A maps to NM_003906.3 G1598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr21:47705020 C>T maps to NM_003906.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:47695123 G>A maps to NM_003906.3 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:47705050 C>T maps to NM_003906.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr21:47692707 C>T maps to NM_003906.3 T744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:48882424 C>A maps to NM_182746.1 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:48882365 C>T maps to NM_182746.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:48883363 C>T maps to NM_182746.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:48882478 T>C maps to NM_182746.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:48875322 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:35808620 C>T maps to NM_006739.3 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr22:35809930 A>T maps to NM_006739.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr22:35796454 C>T maps to NM_006739.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:136624274 A>T maps to NM_005915.4 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:136620178 G>A maps to NM_005915.4 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr2:136624160 C>T maps to NM_005915.4 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:99693412 G>A maps to NM_005916.3 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:99693650 G>A maps to NM_005916.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:99695871 C>T maps to NM_005916.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:5966606 C>T maps to NM_032485.4 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:119238765 G>A maps to ENST00000316316 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:119238765 G>A maps to ENST00000316316 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:7593141 C>T maps to NM_020533.2 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:7592590 C>T maps to ENST00000394321 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7593143 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7593846 C>T maps to NM_020533.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:7591449 G>A maps to NM_020533.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:7593141 C>T maps to NM_020533.2 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:85417961 G>A maps to NM_153259.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:85412740 A>G maps to NM_153259.2 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:85412773 G>T maps to NM_153259.2 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:85499895 A>C maps to NM_018298.9 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:85506860 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:85506704 G>A maps to NM_018298.9 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:6302851 G>T maps to NM_024596.3 G537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:6299627 C>T maps to NM_024596.3 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:6301993 T>C maps to NM_024596.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:49959428 G>A maps to NM_001012300.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr12:49953510 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:49952464 G>A maps to NM_001012300.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr12:49959911 G>A maps to NM_001012300.1 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:94259727 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:94206651 G>A maps to NM_024717.4 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:94248612 G>A maps to NM_024717.4 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:94207063 G>A maps to NM_024717.4 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:94206162 C>A maps to NM_024717.4 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:94245011 G>T maps to NM_024717.4 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:94204091 G>A maps to NM_024717.4 Y794Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:94043259 C>A maps to NM_024717.4 E981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr5:94114834 C>A maps to NM_024717.4 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:94204079 G>A maps to NM_024717.4 C798C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:94207063 G>A maps to NM_024717.4 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr15:94927302 G>A maps to NM_018349.3 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:94942188 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:94911014 C>T maps to NM_018349.3 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:95022206 G>T maps to NM_018349.3 E861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:94943205 C>T maps to NM_018349.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:95001397 C>A maps to NM_018349.3 I761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:94841797 G>T maps to NM_018349.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:94913374 A>G maps to NM_018349.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:94858792 C>T maps to NM_018349.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:95022226 C>T maps to NM_018349.3 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:94983436 A>G maps to NM_018349.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr15:94841637 C>T maps to NM_018349.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:119742127 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119742211 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:119738718 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:119739327 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:119742117 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:30673548 G>A maps to NM_014641.2 V1137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:30672363 G>A maps to NM_014641.2 P1532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:30673008 G>T maps to NM_014641.2 S1317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr6:41613888 G>A maps to NM_005586.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:114655850 C>T maps to NM_199072.4 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:114582420 G>A maps to NM_199072.4 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:37622576 C>T maps to ENST00000297153 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:37623535 G>A maps to ENST00000297153 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr6:37606348 C>T maps to ENST00000297153 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:37622254 C>T maps to ENST00000297153 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr6:37611597 G>A maps to ENST00000297153 Y844Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:37626168 G>A maps to ENST00000297153 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:37626099 C>T maps to ENST00000297153 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:37611585 G>A maps to ENST00000297153 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr14:47389345 C>A maps to NM_001113498.2 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:47600938 C>T maps to NM_001113498.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:47566316 G>T maps to NM_001113498.2 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:47389307 G>A maps to NM_001113498.2 N715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:47530476 G>A maps to NM_001113498.2 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:47342740 G>A maps to NM_001113498.2 R883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr14:47770652 A>G maps to NM_001113498.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:47530476 G>A maps to NM_001113498.2 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:63824539 C>T maps to NM_005917.3 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:63822606 C>T maps to NM_005917.3 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:63821629 A>G maps to NM_005917.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:63832496 C>T maps to NM_005917.3 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:63824539 C>T maps to NM_005917.3 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:207619865 G>T maps to NM_001039845.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:207604377 C>T maps to NM_001039845.1 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:207625717 A>G maps to NM_001039845.1 Y14Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:75694216 C>T maps to NM_005918.2 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:75695640 T>G maps to NM_005918.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:68709979 C>T maps to NM_017440.4 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:68707474 C>A maps to NM_017440.4 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:68696630 G>A maps to NM_017440.4 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:69222704 G>A maps to NM_002392.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:69229688 T>C maps to NM_002392.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:69222704 G>A maps to NM_002392.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:69233595 A>G maps to NM_002392.3 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:69233328 A>G maps to NM_002392.3 E398E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:69222704 G>A maps to NM_002392.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:204511936 C>T maps to NM_002393.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:204518365 G>A maps to NM_002393.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:204507383 C>T maps to NM_002393.3 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:204518767 C>T maps to NM_002393.3 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:204494631 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr6:90428608 C>T maps to NM_014611.1 G2066G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:90422343 G>T maps to NM_014611.1 I2460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:90354745 A>G maps to NM_014611.1 N5530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:90385235 G>A maps to NM_014611.1 L4236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:90393042 G>T maps to NM_014611.1 L3970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:90409351 G>A maps to NM_014611.1 R2989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr6:90397135 G>A maps to NM_014611.1 R3793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:90374242 A>G maps to NM_014611.1 F4733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:90428120 G>A maps to NM_014611.1 R2183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:90448051 A>G maps to NM_014611.1 D1572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr6:90353885 C>T maps to NM_014611.1 P5543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:90418264 T>C maps to NM_014611.1 Q2616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:90466101 C>A maps to NM_014611.1 E904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:90468640 G>T maps to NM_014611.1 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:90466005 C>A maps to NM_014611.1 G936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:90382358 G>A maps to NM_014611.1 R4513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:90425448 G>A maps to NM_014611.1 P2261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:90491103 G>A maps to ENST00000421327 Q553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr6:90387362 C>T maps to NM_014611.1 E4155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr6:90426501 G>A maps to NM_014611.1 R2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:90422328 G>T maps to NM_014611.1 L2465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24683256 G>A maps to NM_138476.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:84108192 G>T maps to NM_002395.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:84117530 A>G maps to NM_002395.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:84117620 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:48422201 G>A maps to NM_002396.4 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:48446852 C>T maps to NM_002396.4 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:86270832 C>T maps to NM_001014811.1 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:86198419 G>A maps to NM_001014811.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:86176190 G>T maps to NM_001014811.1 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:86161398 G>A maps to NM_001014811.1 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:86158142 G>T maps to NM_001014811.1 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:37967577 C>T maps to NM_022756.4 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:168818725 C>T maps to NM_004991.3 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr3:168812893 G>A maps to NM_004991.3 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:168838907 C>T maps to NM_004991.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr3:169099102 G>A maps to NM_004991.3 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:168833244 G>A maps to NM_004991.3 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153296264 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153297984 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153296851 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153295847 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153296408 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr23:153297784 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:153297781 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:153296523 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:37565089 A>G maps to NM_004774.3 S1128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:37566108 C>A maps to NM_004774.3 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr23:70348504 C>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:70349667 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr23:70352741 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr23:70338668 C>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:70357463 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:70360643 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70347830 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70347915 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70357763 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70346836 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70347845 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70339976 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70344917 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70349660 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70357178 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:70347823 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70342420 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70340857 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70342186 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70345926 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70346973 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70348203 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70349036 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70349537 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70351408 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70357481 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:70346842 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr23:70338670 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr23:70343020 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:70360550 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr23:70343019 C>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:70348504 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:70341622 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:70345249 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70338655 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70339567 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70344017 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70350001 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70356384 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70339567 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70339676 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70344690 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:70343075 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr23:70346289 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:70349540 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:70354596 G>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:70344971 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:70348197 C>T did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:70354253 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:70343020 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:70343013 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:70344690 C>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:70361120 A>G did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:70361204 C>A did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:70351963 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:151090520 C>T maps to NM_053002.4 Y1242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:150874065 A>G maps to NM_053002.4 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:150883217 G>A maps to NM_053002.4 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:151105725 G>A maps to NM_053002.4 E1704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:151105608 C>A maps to NM_053002.4 V1665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:151131059 C>T maps to NM_053002.4 R2057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:151129262 G>A maps to NM_053002.4 S2001S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:151134182 C>A maps to NM_053002.4 L2092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:151067899 C>T maps to NM_053002.4 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:151085986 C>A maps to NM_053002.4 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:150877701 C>T maps to NM_053002.4 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:151097957 A>G maps to NM_053002.4 G1477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:150874029 C>T maps to NM_053002.4 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:60042539 C>T maps to NM_005121.2 S1557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:60112893 T>C maps to NM_005121.2 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:60038241 G>A maps to NM_005121.2 I1822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:60050217 A>C maps to NM_005121.2 L1279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:60050216 G>A maps to NM_005121.2 R1280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:60072518 T>C maps to NM_005121.2 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr17:60038435 G>A maps to NM_005121.2 R1758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:60111235 G>T maps to NM_005121.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:60060272 G>A maps to NM_005121.2 Q1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:116429042 G>T maps to NM_015335.4 S1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr12:116408545 G>A maps to NM_015335.4 R1974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr12:116399193 C>T maps to NM_015335.4 L2170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr12:116446899 G>A maps to NM_015335.4 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:116403922 A>T maps to NM_015335.4 C2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:116434447 A>G maps to NM_015335.4 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:116399187 C>T maps to NM_015335.4 Q2172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:116457217 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:116422042 C>T maps to NM_015335.4 E1491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:116460321 T>C maps to NM_015335.4 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:116549267 C>T maps to NM_015335.4 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr12:116446264 G>A maps to NM_015335.4 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:40514261 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:40556322 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:40552056 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:40571530 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:40573901 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:40511097 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:40541159 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:40531193 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:40586068 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:40522195 C>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:40513705 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:40523563 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:40547715 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:40568615 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:40568692 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:40570549 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:40534559 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:40551964 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr23:40522213 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:40518691 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:40518846 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:40569375 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:40551442 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:40526048 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:40568697 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:40511080 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:40522195 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:40556308 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:40573154 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr23:40513706 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:40518691 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:40540142 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:40551442 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr22:20939480 C>T maps to NM_001003891.1 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr22:20939197 G>A maps to NM_001003891.1 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:20921088 A>G maps to NM_001003891.1 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:868891 G>A maps to NM_005481.2 C790C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:93523798 C>A maps to NM_004268.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:93545170 C>T maps to NM_004268.4 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr1:28661168 C>T maps to NM_017638.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:57472675 C>T maps to ENST00000431606 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:27181244 G>T maps to NM_004264.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:136211068 C>T maps to NM_133640.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:136212098 G>A maps to NM_133640.3 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr9:136213508 C>T maps to NM_133640.3 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:136213478 C>T maps to NM_133640.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:131926555 A>G maps to ENST00000403834 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:131911566 T>G maps to ENST00000403834 V1240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:131929075 C>A maps to ENST00000403834 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr6:131948558 G>A maps to ENST00000403834 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr6:131931364 G>A maps to ENST00000403834 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:131931322 G>A maps to ENST00000403834 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:131943112 G>A maps to ENST00000403834 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr17:38179413 G>A maps to NM_014815.3 G740G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:38183242 G>A maps to NM_014815.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38178658 G>A maps to NM_014815.3 R837R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:38178265 C>T maps to NM_014815.3 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:38178255 G>A maps to NM_014815.3 R859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:38178255 G>A maps to NM_014815.3 R859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr17:38178658 G>A maps to NM_014815.3 R837R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:38178255 G>A maps to NM_014815.3 R859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:38185181 G>A maps to NM_014815.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:38184192 A>G maps to NM_014815.3 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr17:38186101 G>A maps to NM_014815.3 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:38178229 A>G maps to NM_014815.3 D867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:38179521 C>T maps to NM_014815.3 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50338307 G>A maps to NM_030973.3 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50340137 G>A maps to NM_030973.3 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:16687311 C>T maps to NM_004831.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:16688022 G>T maps to NM_004831.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:16688319 G>A maps to NM_004831.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:134738460 G>A maps to NM_004269.2 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:118533267 C>A maps to NM_080651.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:6553751 A>G maps to NM_016060.2 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:48655849 C>A maps to NM_014166.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:48651339 C>A maps to NM_014166.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:156565791 C>T maps to NM_004270.4 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:156566250 G>A maps to NM_004270.4 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:43853257 G>A maps to NM_052877.3 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:43853171 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:100211574 C>T maps to ENST00000338042 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr15:100211862 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:19257941 C>T maps to ENST00000410050 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:88018518 C>A maps to NM_002397.4 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:88027589 G>A maps to NM_002397.4 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:88018657 A>G maps to NM_002397.4 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:156452285 G>A maps to NM_005920.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:156449103 G>A maps to NM_005920.2 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr1:156438045 G>A maps to NM_005920.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:156449094 G>A maps to NM_005920.2 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr16:3293383 C>T maps to NM_000243.2 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:3304287 G>T maps to NM_000243.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:3304251 G>A maps to NM_000243.2 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:3299712 G>T maps to NM_000243.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:3297084 G>A maps to NM_000243.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:126781359 C>T maps to NM_032446.2 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:126770442 C>T maps to NM_032446.2 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:126746239 C>A maps to NM_032446.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:126774146 C>T maps to NM_032446.2 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:126758396 C>T maps to NM_032446.2 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr5:126755817 C>T maps to NM_032446.2 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr5:126771170 C>T maps to NM_032446.2 D698D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:126732326 C>T maps to NM_032446.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:126770451 C>T maps to NM_032446.2 C638C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr15:66249926 G>A maps to NM_032445.2 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:66411505 C>T maps to NM_032445.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:3407116 C>T maps to ENST00000452816 P1610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:3427356 G>A maps to ENST00000452816 C483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:3407476 T>G maps to ENST00000452816 S1596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:3428132 T>C maps to ENST00000452816 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:3416452 G>A maps to ENST00000452816 Q990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:42879870 C>T maps to ENST00000251268 D2494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:42855829 C>T maps to ENST00000251268 C1006C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:42857078 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:42874366 G>A maps to ENST00000251268 P2287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:42880347 C>T maps to ENST00000251268 S2653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:42853850 C>T maps to ENST00000251268 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:42858852 C>T maps to ENST00000251268 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:42867311 C>T maps to ENST00000251268 C2057C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:42872633 C>T maps to ENST00000251268 R2101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:42860266 C>T maps to ENST00000251268 F1475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr19:42855480 C>T maps to ENST00000251268 C950C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:123374716 G>T maps to ENST00000426959 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:42191506 G>A maps to NM_152513.3 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:42180643 C>T maps to NM_152513.3 R1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:42189900 G>A maps to NM_152513.3 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:42099402 G>A maps to NM_152513.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr22:42141898 G>T maps to NM_152513.3 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr22:42166877 C>A maps to NM_152513.3 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:15008517 G>A maps to NM_001080836.2 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:37390283 C>T maps to NM_170675.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:37388588 G>A maps to NM_170675.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:37388588 G>A maps to NM_170675.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr15:37390259 G>A maps to NM_170675.2 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:47912804 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:47912788 G>A maps to NM_020160.1 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:36665507 T>G maps to NM_014791.2 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:36651774 T>C maps to NM_014791.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:36581736 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:36671151 A>C maps to NM_014791.2 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:32117133 G>A maps to NM_015955.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:32117148 T>C maps to NM_015955.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:32117133 G>A maps to NM_015955.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:64572649 G>A maps to NM_130804.2 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:64577224 C>T maps to NM_130804.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:41738728 C>T maps to NM_004527.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:41720947 G>A maps to NM_004527.3 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:41738737 C>T maps to NM_004527.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:15725509 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:15666459 C>A maps to NM_005924.4 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr6:46806776 C>T maps to NM_005588.2 H715H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr6:46801255 G>A maps to NM_005588.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:29782854 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:29775401 G>A maps to NM_005925.2 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:29797904 C>T maps to NM_005925.2 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100028960 G>A maps to NM_019606.5 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:88766991 G>A maps to ENST00000395102 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:88766559 C>T maps to ENST00000395102 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:112751979 C>T maps to NM_006343.2 H483H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:112779109 C>T maps to NM_006343.2 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:130144806 G>A maps to NM_002402.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr7:130144785 G>A maps to NM_002402.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:130138026 G>A maps to NM_002402.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:116339803 G>A maps to NM_001127500.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:116417488 C>T maps to NM_001127500.1 G1120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:116414969 C>T maps to NM_001127500.1 R1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:116398559 C>A maps to NM_001127500.1 S717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:116411994 G>T maps to NM_001127500.1 E1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:116339776 G>A maps to NM_001127500.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:116339776 G>A maps to NM_001127500.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:116436063 C>T maps to NM_001127500.1 N1371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:116339803 G>A maps to NM_001127500.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:99962264 C>T maps to NM_015143.2 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:99962202 G>T maps to NM_015143.2 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:99969980 A>C maps to NM_015143.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:95905695 A>G maps to NM_006838.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:95868077 G>A maps to NM_006838.3 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:767305 C>A maps to NM_024042.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:81052134 C>T maps to NM_001004431.1 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:58163159 G>A maps to ENST00000408972 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:126453988 C>T maps to NM_212554.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:126463243 C>T maps to NM_212554.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:126463269 C>A maps to NM_212554.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:132395012 C>T maps to NM_014064.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:132394987 G>A maps to NM_014064.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:119626969 C>T maps to NM_020961.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:60525999 A>G maps to NM_181725.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr7:128128474 A>G maps to ENST00000419443 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:128119314 G>A maps to NM_018396.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:128119263 C>T maps to NM_018396.2 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:21971600 G>T maps to NM_019852.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:21967458 G>A maps to NM_019852.3 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:21967926 C>A maps to NM_019852.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:2539054 C>A maps to NM_022840.3 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:170681092 C>T maps to NM_014168.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:170677647 G>A maps to NM_014168.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:15466515 C>T maps to NM_152396.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:56077751 C>T maps to NM_152637.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:172216952 G>A maps to NM_024770.3 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr2:172182369 T>C maps to NM_024770.3 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr2:172248707 C>G did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr16:21666671 A>G maps to NM_016025.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:82336904 G>T maps to NM_032246.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:82336337 C>T maps to NM_032246.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:82336601 C>T maps to NM_032246.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:82336226 C>T maps to NM_032246.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr18:48702834 T>C maps to NM_016626.4 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:48702882 G>A maps to NM_016626.4 H606H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:44106702 G>A maps to NM_005926.2 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr15:44106855 G>A maps to NM_005926.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr5:153429188 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:153429139 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:153429119 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:170913335 G>A maps to NM_021647.6 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr4:170913365 G>A maps to NM_021647.6 Y131Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:170927021 G>A maps to NM_021647.6 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:170912543 G>A maps to NM_021647.6 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:170913056 G>A maps to NM_021647.6 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:8800773 A>G maps to NM_003480.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:8803125 G>A maps to NM_003480.2 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:8808409 C>T maps to NM_003480.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:228205010 C>T maps to NM_020194.4 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:228221780 C>A maps to NM_020194.4 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:228207511 A>T maps to NM_020194.4 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:89453044 G>A maps to NM_005928.2 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:89442928 C>T maps to NM_005928.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:89442928 C>T maps to NM_005928.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:89453023 C>T maps to NM_005928.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:89449889 G>A maps to NM_005928.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr15:89453092 C>T maps to NM_005928.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:8749617 G>A maps to NM_004225.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:8748255 C>T maps to NM_004225.2 A771A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:8748672 C>T maps to NM_004225.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:8748536 G>A maps to NM_004225.2 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:196735777 G>T maps to NM_005929.5 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:196743976 G>A maps to NM_005929.5 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:196736573 G>A maps to NM_005929.5 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr3:196735828 G>A maps to NM_005929.5 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr3:196735690 G>A maps to NM_005929.5 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:179093117 T>C maps to NM_033540.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:179093042 C>T maps to NM_033540.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:179069713 C>T maps to NM_033540.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:179096176 C>T maps to NM_033540.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:12064139 C>T maps to NM_014874.3 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:37876340 G>A maps to ENST00000424765 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:119215036 G>A maps to NM_031433.2 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:119216801 G>A maps to NM_031433.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:119217039 G>T maps to NM_031433.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:119215628 C>A maps to NM_031433.2 G243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:119213351 G>A maps to NM_031433.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:119213383 G>A maps to NM_031433.2 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:158541308 T>A maps to NM_022736.2 Y439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:158523261 C>T maps to NM_022736.2 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:158531786 C>T maps to NM_022736.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:158539859 C>T maps to NM_022736.2 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:2932776 C>T maps to ENST00000514800 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr4:2934095 C>T maps to NM_001146069.1 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:74738062 C>T maps to NM_024311.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:74765943 G>T maps to NM_024311.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr1:40431005 G>C maps to NM_001136493.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr1:40432828 C>A maps to NM_001136493.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:24246467 C>T maps to ENST00000338315 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr8:145735791 C>T maps to NM_138431.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:205554118 G>A maps to NM_181644.4 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:205561344 C>T maps to NM_181644.4 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr1:205548877 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205553090 G>A maps to NM_181644.4 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:205568356 G>A maps to NM_181644.4 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:205538343 G>A maps to NM_181644.4 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53646864 C>A maps to NM_001170790.1 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:191301948 C>T maps to NM_017694.3 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:191301981 G>A maps to NM_017694.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:191301768 G>A maps to NM_017694.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:191301375 T>C maps to NM_017694.3 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:191301981 G>A maps to NM_017694.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:191301649 G>T maps to NM_017694.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:8700938 G>A maps to NM_152599.3 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:8702264 G>A maps to NM_152599.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:8701865 A>G maps to NM_152599.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:680359 C>T maps to ENST00000404286 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr4:678561 G>C maps to ENST00000404286 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:678564 C>T maps to ENST00000404286 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:128861054 G>A maps to NM_152778.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:128842717 G>T maps to NM_152778.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:41999947 G>T maps to ENST00000219905 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:42003058 C>T maps to ENST00000219905 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr15:42052640 G>T maps to ENST00000219905 E2487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:42046765 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:42034888 C>T maps to ENST00000219905 V1626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:42042398 C>T maps to ENST00000219905 D2247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:42042414 G>T maps to ENST00000219905 E2253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr15:42005420 C>T maps to ENST00000219905 R1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr15:42052627 G>A maps to ENST00000219905 R2482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:42041073 C>T maps to ENST00000219905 R1867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:42028599 C>T maps to ENST00000219905 R1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:42053984 G>T maps to ENST00000219905 G2532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:41991099 G>T maps to ENST00000219905 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:42003030 G>A maps to ENST00000219905 Q856Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:42041534 A>G maps to ENST00000219905 Q1959Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:42058208 C>T maps to ENST00000219905 D2692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:41988690 C>T maps to ENST00000219905 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:42021427 C>T maps to ENST00000219905 R1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr15:41962042 A>G maps to ENST00000219905 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr15:42003483 A>G maps to ENST00000219905 K1007K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr15:42053938 C>A maps to ENST00000219905 A2516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:42042456 G>T maps to ENST00000219905 E2267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:42019409 C>T maps to ENST00000219905 R1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:41988690 C>T maps to ENST00000219905 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:41988479 G>A maps to ENST00000219905 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:42042213 G>T maps to ENST00000219905 E2186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:141727523 C>T maps to ENST00000475668 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:141736693 C>T maps to ENST00000475668 R716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:141708420 T>G maps to ENST00000475668 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:141708460 G>T maps to ENST00000475668 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:141786118 C>A maps to ENST00000475668 V2247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:141727468 C>T maps to ENST00000475668 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:141747585 C>T maps to ENST00000475668 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:141755384 C>A maps to ENST00000475668 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:141756675 G>T maps to ENST00000475668 G1209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:141781919 C>A maps to ENST00000475668 L2028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr7:141763354 C>T maps to ENST00000475668 D1438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:141727516 C>T maps to ENST00000475668 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:141762503 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:141781862 C>T maps to ENST00000475668 G2009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:141805624 C>T maps to ENST00000475668 I2733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr7:141755852 C>T maps to ENST00000475668 D1179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:141752762 G>A maps to ENST00000475668 K1046K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:141754552 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:141791804 A>C maps to ENST00000475668 P2302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr7:141764253 C>T maps to ENST00000475668 D1472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:141708372 T>G maps to ENST00000475668 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:141765549 T>C maps to ENST00000475668 A1563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:141803175 T>C maps to ENST00000475668 S2708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr7:141759682 C>T maps to ENST00000475668 Q1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:141727468 C>T maps to ENST00000475668 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:141734095 C>A maps to ENST00000475668 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:180218663 C>T maps to NM_001114617.1 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:180218999 G>A maps to NM_001114617.1 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:50088477 C>T maps to NM_002408.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr14:50088756 C>T maps to NM_002408.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:39884800 G>A maps to NM_001098270.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:39884800 G>A maps to NM_001098270.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr22:39884785 C>T maps to NM_001098270.1 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr22:39883585 G>A maps to NM_001098270.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr22:39884263 G>A maps to NM_001098270.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:99260418 G>A maps to NM_012214.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:179225551 G>A maps to NM_054013.3 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:179225277 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:179225524 C>T maps to NM_054013.3 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:86383186 G>A maps to ENST00000393205 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:86383240 G>A maps to ENST00000393205 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:135102551 C>T maps to NM_002410.3 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:135206231 C>A maps to NM_002410.3 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr2:135012072 C>T maps to NM_002410.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:103558651 G>A maps to NM_012215.3 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:103550781 G>A maps to NM_012215.3 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:103558651 G>A maps to NM_012215.3 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:103559086 C>A maps to NM_012215.3 G441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr3:127429496 C>T maps to NM_007283.5 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:4736258 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:4732877 C>T maps to NM_015246.2 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:4738830 C>T maps to NM_015246.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:16516747 G>T maps to NM_145764.1 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:165624647 C>T maps to ENST00000367886 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:39716612 G>T maps to NM_054024.3 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:39722404 A>C maps to NM_054024.3 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr14:39722147 T>C maps to NM_054024.3 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:39716255 C>T maps to NM_054024.3 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:222825625 C>T maps to NM_198551.2 C1346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:222803357 A>G maps to NM_198551.2 E932E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:222818993 G>A maps to NM_198551.2 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:222803504 T>G maps to NM_198551.2 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:222828135 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:222825567 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:222838873 A>G maps to NM_198551.2 L1879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:222800981 T>C maps to NM_198551.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:222827810 T>C maps to NM_198551.2 C1486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:222835661 C>T maps to NM_198551.2 L1750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:222801140 C>T maps to NM_198551.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:19437118 G>A maps to NM_020774.2 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:19438603 G>A maps to NM_020774.2 E959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr1:1563169 G>A maps to NM_080875.2 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr1:1563439 G>A maps to NM_080875.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:1563679 G>A maps to NM_080875.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:1563490 C>T maps to NM_080875.2 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:31380114 G>A maps to NM_000247.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:31380195 T>C maps to NM_000247.1 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr6:31379862 G>A maps to NM_000247.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:109767901 A>G maps to NM_022765.3 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:109770559 T>C maps to ENST00000368957 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr6:109774937 G>A maps to NM_022765.3 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:109771544 G>A maps to NM_022765.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr6:109774990 G>A maps to NM_022765.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:109773592 G>A maps to NM_022765.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:12183866 C>A maps to NM_014632.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:12241935 C>T maps to NM_014632.2 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:12247820 G>T maps to NM_014632.2 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:12244955 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:12229645 C>T maps to NM_014632.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:12241935 C>T maps to NM_014632.2 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:12245008 C>T maps to NM_014632.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:12263952 C>T maps to NM_014632.2 Q844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr11:12237866 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr22:18305805 G>A maps to NM_015241.2 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:18379531 T>G maps to NM_015241.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:18371973 G>A maps to NM_015241.2 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:18347629 A>G maps to NM_001136004.1 R1004R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:12313762 G>A maps to NM_032867.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:12315535 G>A maps to NM_032867.2 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:12379957 G>T maps to NM_032867.2 E674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:12315872 G>T maps to NM_032867.2 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:38329084 C>T maps to NM_033386.2 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:31477679 C>T maps to NM_005931.3 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:31474085 C>T maps to NM_005931.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:10535157 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:10535511 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:10535282 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:10417510 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:10417742 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:10427814 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:10450528 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:10491157 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:10450554 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:10534973 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:10535359 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:10417524 G>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:10535108 C>G did not map to a codon.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr23:10417723 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:38664237 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:38664652 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107159234 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107169519 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107169954 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:107084162 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:107160966 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:107167641 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:107169459 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:107169423 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:107169396 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:107084061 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:107084384 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107083937 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107170004 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:107148758 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:107084108 A>C did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:107167710 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107160756 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107160907 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107170264 G>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:107084521 T>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:107084466 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:107084208 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:107084191 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:107084340 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:107169330 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:1255463 G>A maps to NM_177401.4 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:1254476 G>A maps to NM_177401.4 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr19:1255011 G>T maps to NM_177401.4 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:67423746 C>T maps to NM_001077700.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:67390728 A>G maps to NM_001077700.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:326548 G>A maps to NM_017550.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:311868 G>A maps to NM_017550.1 N320N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:307462 C>T maps to NM_017550.1 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:56231270 G>A maps to ENST00000381226 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:73262835 G>A maps to NM_020679.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:12091393 C>T maps to NM_021933.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr3:97669668 G>A maps to NM_153182.2 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:97686376 G>A maps to NM_153182.2 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:97664029 A>G maps to NM_153182.2 *466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:97686296 C>T maps to NM_153182.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:97664731 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:97686035 C>T maps to NM_153182.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:4799328 C>T maps to NM_153827.4 I1132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:4791000 C>T maps to NM_153827.4 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:4794896 G>A maps to NM_153827.4 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr17:4787716 C>A maps to NM_153827.4 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:4798500 C>T maps to NM_153827.4 R1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:89264869 T>C maps to NM_004897.4 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr7:7612369 A>G maps to NM_019005.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:7629049 C>T maps to NM_019005.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50928212 G>A maps to NM_017584.5 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:56847524 C>T maps to NM_012064.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:56847476 G>A maps to NM_012064.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:56848271 C>A maps to NM_012064.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr12:56847527 C>T maps to NM_012064.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr13:24453489 C>T maps to NM_005932.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:24460498 C>T maps to NM_005932.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:37739654 G>T maps to NM_001195296.1 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:5392281 G>T maps to NM_024039.1 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:5392782 C>T maps to NM_024039.1 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:99786038 C>A maps to NM_138798.1 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:99787078 C>A maps to NM_138798.1 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:69928296 G>A maps to ENST00000448226 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:69928452 C>T maps to ENST00000448226 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:70005627 C>T maps to ENST00000448226 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:70014332 C>T maps to ENST00000448226 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:69928356 A>G maps to ENST00000448226 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:70014375 G>T maps to ENST00000448226 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:226413317 G>A maps to NM_031944.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr10:129900902 G>A maps to NM_002417.4 S3067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GN-01A-11W-A062-09 chr10:129903107 C>A maps to NM_002417.4 T2332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:129904111 G>A maps to NM_002417.4 R1998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:129913771 G>A maps to NM_002417.4 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:129905846 G>A maps to NM_002417.4 H1419H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:129903142 C>A maps to NM_002417.4 E2321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:129913861 G>A maps to NM_002417.4 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:129902272 C>A maps to NM_002417.4 E2611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:129903566 C>T maps to NM_002417.4 R2179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:129907285 C>A maps to NM_002417.4 E940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr10:129910412 C>T maps to NM_002417.4 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:129901984 C>A maps to NM_002417.4 E2707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:129913669 G>A maps to NM_002417.4 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:129901013 C>T maps to NM_002417.4 K3030K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:129906133 C>A maps to NM_002417.4 E1324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:129904804 C>A maps to NM_002417.4 E1767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:129907046 T>G maps to NM_002417.4 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:129913908 C>A maps to NM_002417.4 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:129903331 G>A maps to NM_002417.4 R2258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:129899689 C>T maps to NM_002417.4 A3179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:129900878 C>T maps to NM_002417.4 E3075E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:129905539 C>A maps to NM_002417.4 E1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:129906752 T>C maps to NM_002417.4 E1117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:129913401 C>A maps to NM_002417.4 G424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:129913861 G>A maps to NM_002417.4 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr10:129906122 G>A maps to NM_002417.4 T1327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr10:129902978 T>C maps to NM_002417.4 A2375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:129901853 C>T maps to NM_002417.4 T2750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:129899689 C>T maps to NM_002417.4 A3179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:129900917 C>T maps to NM_002417.4 A3062A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:129907280 G>A maps to NM_002417.4 N941N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:129913276 C>T maps to NM_002417.4 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:122493248 G>T maps to NM_032390.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:122485319 G>A maps to NM_032390.4 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:122488591 T>C maps to NM_032390.4 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:40807615 C>T maps to NM_020831.3 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:40816570 G>A maps to NM_020831.3 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:40816855 C>T maps to NM_020831.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr22:40815124 A>G maps to NM_020831.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:14328067 C>T maps to NM_014048.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr16:14312791 G>A maps to NM_014048.3 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:14306211 T>G maps to NM_014048.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:14340433 C>T maps to NM_014048.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:14354881 C>T maps to NM_014048.3 Q911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr16:14340821 G>T maps to NM_014048.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:14311131 G>T maps to NM_014048.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:14342790 A>G maps to NM_014048.3 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:14352004 C>A maps to NM_014048.3 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:14340859 C>A maps to NM_014048.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:131128389 C>T maps to NM_013255.4 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:131155700 G>T maps to NM_013255.4 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:131128289 T>A maps to NM_013255.4 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:131155688 G>T maps to NM_013255.4 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:131071895 C>T maps to NM_013255.4 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:47042320 G>A maps to NM_003684.4 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:47059837 A>C did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr7:140159710 G>A maps to NM_013446.3 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:12610445 G>A maps to NM_014160.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:12613700 C>T maps to NM_014160.3 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:23811081 G>A maps to NM_005664.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:23811282 G>A maps to NM_005664.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:23811981 A>G maps to NM_005664.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:23812276 C>T maps to NM_005664.3 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:56294035 G>T maps to NM_017777.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:56296011 G>A maps to NM_017777.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:56291172 A>G maps to NM_017777.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:56291741 G>A maps to NM_017777.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr10:28023577 G>T maps to NM_173576.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:5897629 C>T maps to NM_005511.1 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:50523211 C>T maps to NM_015166.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:158310253 C>T maps to NM_001195432.1 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:158310340 G>T maps to NM_001195432.1 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:185618875 A>C maps to NM_024629.3 Y356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:185616485 G>A maps to NM_024629.3 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr4:185652121 G>A maps to NM_024629.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:185650070 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:37090093 C>A maps to NM_000249.3 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:37090468 G>A maps to NM_000249.3 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr3:37055973 T>C maps to NM_000249.3 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr3:37090504 G>A maps to NM_000249.3 Q700Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:37055923 G>T maps to NM_000249.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:37035137 G>T maps to NM_000249.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:75514327 C>T maps to NM_001040108.1 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:75509148 G>A maps to NM_001040108.1 S1104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:75514602 C>A maps to NM_001040108.1 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:75515685 C>A maps to NM_001040108.1 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:75515685 C>A maps to NM_001040108.1 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:75508376 C>A maps to NM_001040108.1 E1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:75515073 C>A maps to NM_001040108.1 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:74719438 C>T maps to NM_152649.2 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:74719432 G>A maps to NM_152649.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:74726278 C>A maps to NM_152649.2 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:118350937 C>T maps to NM_001197104.1 Q1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:118347552 C>T maps to NM_001197104.1 R1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:118348797 C>T maps to NM_001197104.1 R1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:118362639 G>A maps to NM_001197104.1 R1667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:118373689 G>A maps to NM_001197104.1 S2361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:118373750 C>T maps to NM_001197104.1 R2382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:118374994 A>G maps to NM_001197104.1 G2796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:118343055 G>A maps to NM_001197104.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:118363797 C>T maps to NM_001197104.1 P1677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:118373177 C>T maps to NM_001197104.1 R2191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:118392632 C>T maps to NM_001197104.1 R3889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V7-01A-21D-A122-09 chr11:118378312 G>A maps to NM_001197104.1 G3608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:118343092 C>T maps to NM_001197104.1 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:118342584 T>C maps to NM_001197104.1 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr12:49421000 C>T maps to NM_003482.3 P4916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:49420067 G>T maps to NM_003482.3 C5227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:49438016 C>T maps to NM_003482.3 A1718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:49448122 A>G maps to NM_003482.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:49416531 G>A maps to NM_003482.3 T5393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:49447332 G>A maps to NM_003482.3 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr12:49435228 C>T maps to NM_003482.3 P2108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:49427549 C>T maps to NM_003482.3 G3646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:49427368 G>A maps to NM_003482.3 R3707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:49416076 G>A maps to NM_003482.3 T5466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:49427311 G>A maps to NM_003482.3 Q3726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:49438623 G>A maps to NM_003482.3 G1622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr12:49433505 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:49445443 C>T maps to NM_003482.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:49438066 G>A maps to NM_003482.3 R1702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr12:49433788 G>A maps to NM_003482.3 H2588H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:151842290 A>G maps to ENST00000355193 G4764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:151879228 G>A maps to ENST00000355193 R1906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:151836854 G>A maps to ENST00000355193 R4846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:151877957 T>G maps to ENST00000355193 G2329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:151904507 C>A maps to ENST00000355193 E1240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:151859206 C>A maps to ENST00000355193 G3819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:151860293 G>A maps to ENST00000355193 S3456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:151859924 T>C maps to ENST00000355193 G3579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:151891160 C>T maps to ENST00000355193 A1531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr7:151921109 G>A maps to ENST00000355193 Q1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:151848637 A>G maps to ENST00000355193 H4242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:151854872 C>T maps to ENST00000355193 S3938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:151860425 C>T maps to ENST00000355193 R3412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:151876995 A>C maps to ENST00000355193 Y2455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:152009029 C>A maps to ENST00000355193 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr7:151878862 G>A maps to ENST00000355193 R2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:151879154 T>C maps to ENST00000355193 S1930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:151836803 G>A maps to ENST00000355193 R4863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:151843689 C>T maps to ENST00000355193 A4732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:151873822 T>C maps to ENST00000355193 V2905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:151880124 C>T maps to ENST00000355193 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:151945685 C>A maps to ENST00000355193 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:151843731 C>T maps to ENST00000355193 E4718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr7:151851511 A>G maps to ENST00000355193 G4050G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:151841930 G>T maps to ENST00000355193 S4794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:151921188 G>A maps to ENST00000355193 C1078C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:151859762 C>T maps to ENST00000355193 P3633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr19:36228644 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:36222960 C>T maps to NM_014727.1 R1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:36217156 C>T maps to NM_014727.1 R1302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:36221278 C>T maps to NM_014727.1 R1705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36212060 A>G maps to NM_014727.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36216637 C>T maps to NM_014727.1 C1268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36229205 C>T maps to NM_014727.1 R2632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:36211365 G>T maps to NM_014727.1 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:36211574 A>G maps to NM_014727.1 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:36220136 C>T maps to NM_014727.1 F1619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:36228978 C>T maps to NM_014727.1 R2587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:36229455 T>C maps to NM_014727.1 *2716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr19:36216170 C>T maps to NM_014727.1 L1193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr19:36219001 C>T maps to NM_014727.1 L1501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:36222960 C>T maps to NM_014727.1 R1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:36221481 G>A maps to NM_014727.1 S1747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:36224406 C>T maps to NM_014727.1 G2319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:36227816 G>A maps to NM_014727.1 A2434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr19:36224758 G>A maps to NM_014727.1 W2382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:36229235 G>A maps to NM_014727.1 T2642T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:104747617 T>A maps to NM_182931.2 I951I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:104748329 C>T maps to NM_182931.2 I1142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:104717561 A>G maps to NM_182931.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:104747883 G>T maps to NM_182931.2 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:104741943 G>T maps to NM_182931.2 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:104748201 C>T maps to NM_182931.2 R1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr7:104747056 T>A maps to NM_182931.2 Y895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:104752567 G>A maps to NM_182931.2 T1455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:104753134 G>A maps to NM_182931.2 P1644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:104746104 G>T maps to NM_182931.2 E806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:104747984 C>T maps to NM_182931.2 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:6270617 C>T maps to NM_005934.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:6213121 G>A maps to NM_005934.3 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:22016783 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:22022448 C>A maps to NM_004641.3 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:21884329 A>G maps to NM_004641.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:20414131 C>A maps to NM_004529.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:20414131 C>A maps to NM_004529.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:20413790 C>T maps to NM_004529.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:20413784 C>T maps to NM_004529.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:168312027 G>A maps to ENST00000400822 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:168363249 T>G maps to ENST00000344191 V1662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:168343834 C>A maps to ENST00000400822 I1034I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:168265426 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:168317818 T>C maps to ENST00000400822 N864N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr6:168299117 G>C maps to ENST00000400822 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:168363234 C>T maps to ENST00000400822 D1655D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:168271105 A>G maps to ENST00000400822 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:168343845 C>A maps to ENST00000400822 S1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:168352650 C>T maps to ENST00000400822 I1531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr6:168352413 G>A maps to ENST00000400822 P1452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:168271064 G>T maps to ENST00000400825 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:168276056 G>A maps to ENST00000400822 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:36876023 C>A maps to NM_005937.3 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:36876981 G>A maps to NM_005937.3 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:36865493 C>T maps to NM_005937.3 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:36872947 T>C maps to NM_005937.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:49796386 C>T maps to NM_001507.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:49796401 G>A maps to NM_001507.1 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr13:49796254 G>A maps to NM_001507.1 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr13:49796242 C>T maps to NM_001507.1 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:2258335 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:122615475 C>T maps to NM_014938.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:122614660 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:122622802 C>T maps to NM_014938.3 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:73010179 G>A maps to NM_032951.2 A726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:83940606 C>T maps to NM_012213.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:83948889 C>T maps to NM_012213.2 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:53478885 C>A maps to NM_012329.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:154886356 C>T maps to NM_007289.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:154802048 C>A maps to NM_007289.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:154802093 C>T maps to NM_007289.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:154834334 T>G maps to NM_007289.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr3:154802022 C>T maps to NM_007289.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr3:154834289 T>A maps to NM_007289.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr3:154802022 C>T maps to NM_007289.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:154889949 T>A maps to NM_007289.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:154802111 C>T maps to NM_007289.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:154886414 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:2537011 G>A maps to NM_033467.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:2537719 G>A maps to NM_033467.3 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:2541133 G>A maps to NM_033467.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:2523036 G>A maps to NM_033467.3 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:2526774 G>A maps to NM_033467.3 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:135053265 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135053239 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:135047190 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:135047285 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:102662128 G>A maps to NM_002421.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:102662185 G>A maps to NM_002421.3 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:102661238 G>A maps to NM_002421.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:102665951 A>G maps to NM_002421.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:102662128 G>A maps to NM_002421.3 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:102647026 G>A maps to NM_002425.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:102646041 G>A maps to NM_002425.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr22:24124434 C>T maps to NM_005940.3 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:102745642 G>A maps to ENST00000326227 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:102742357 G>A maps to ENST00000326227 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:102816438 C>T maps to NM_002427.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:23313909 C>T maps to NM_004995.2 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:23310848 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:23313704 C>T maps to NM_004995.2 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr16:58073997 C>A maps to NM_002428.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:58075752 C>T maps to NM_002428.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:58074472 C>T maps to NM_002428.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:58075770 C>T maps to NM_002428.2 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:89053880 G>A maps to NM_005941.4 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:89081700 G>T maps to ENST00000286611 Y424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:89198753 G>A maps to NM_005941.4 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:89179982 A>G maps to NM_005941.4 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:89081621 C>A maps to ENST00000286611 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:89198805 G>A maps to NM_005941.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:89209502 C>T maps to NM_005941.4 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:89068483 C>T maps to NM_005941.4 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:89198759 G>A maps to NM_005941.4 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:132329674 C>T maps to NM_016155.4 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr12:132329683 C>T maps to NM_016155.4 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:56230954 A>G maps to NM_002429.4 N464N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:56230885 A>T maps to NM_002429.4 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr12:56233466 G>A maps to NM_002429.4 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:55516865 C>T maps to NM_004530.4 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr16:55522488 G>A maps to NM_004530.4 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:55523650 C>T maps to NM_004530.4 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:55518002 C>T maps to NM_004530.4 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:55532270 A>T maps to NM_004530.4 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:102487787 C>T maps to NM_004771.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:102480738 G>A maps to NM_004771.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:102449839 G>A maps to NM_004771.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr11:102479680 G>T maps to NM_004771.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:127464237 G>A maps to NM_147191.1 H51H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:127455502 G>A maps to NM_147191.1 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr10:127460874 C>T maps to NM_147191.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:127455502 G>A maps to NM_147191.1 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr20:33834665 T>C maps to NM_006690.3 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:33834788 C>T maps to NM_006690.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:33842519 C>T maps to NM_006690.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:33834650 A>G maps to NM_006690.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr20:33842486 C>T maps to NM_006690.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:33842451 G>T maps to NM_006690.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:33842429 C>T maps to NM_006690.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:33842429 C>T maps to NM_006690.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:5009522 G>T maps to NM_021801.3 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:102567513 G>T maps to NM_022122.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:102562586 T>C maps to NM_022122.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:34097110 G>A maps to NM_024302.3 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:34094837 G>A maps to NM_024302.3 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:34094810 C>T maps to NM_024302.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:34097215 G>A maps to NM_024302.3 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr17:34093677 G>A maps to NM_024302.3 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:34105997 G>A maps to NM_024302.3 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:34093520 A>G maps to NM_024302.3 *520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:102713509 G>A maps to NM_002422.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr11:102710975 G>T maps to NM_002422.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:102395703 G>A maps to NM_002423.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:102589166 G>A maps to NM_002424.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:102589166 G>A maps to NM_002424.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:102593329 G>A maps to NM_002424.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:102584174 G>T maps to NM_002424.2 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:102584156 A>C maps to NM_002424.2 Y442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:102593329 G>A maps to NM_002424.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:44639848 C>T maps to NM_004994.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:44640920 C>T maps to NM_004994.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:44642391 G>A maps to NM_004994.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr20:44639226 G>A maps to NM_004994.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:44641108 G>T maps to NM_004994.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:90856948 A>G maps to NM_007351.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:90816472 C>A maps to NM_007351.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:90856330 T>C maps to NM_007351.2 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:90849081 C>T maps to NM_007351.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:90856294 A>G maps to NM_007351.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr4:90872814 A>C maps to NM_007351.2 R1060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:90857866 C>T maps to NM_007351.2 N1012N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr4:90857545 G>A maps to NM_007351.2 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:90857911 C>T maps to NM_007351.2 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:99219024 G>A maps to ENST00000422291 A994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:99219418 G>A maps to ENST00000422291 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:99226620 G>A maps to ENST00000422291 C466C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr10:99219220 G>C maps to ENST00000422291 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:28195196 G>A maps to NM_002430.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr22:28193930 G>A maps to NM_002430.2 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr22:28193834 G>A maps to NM_002430.2 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:28193351 C>T maps to NM_002430.2 S1060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:28193903 C>T maps to NM_002430.2 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:28147004 G>A maps to NM_002430.2 D1287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:154318478 G>T maps to NM_032117.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:158815561 C>T maps to NM_002432.1 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:158815561 C>T maps to NM_002432.1 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:158815498 G>A maps to NM_002432.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:158812195 G>T maps to NM_002432.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr1:158815480 C>T maps to NM_002432.1 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:158819026 A>G maps to NM_002432.1 *408W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:56748598 C>A maps to NM_018365.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr15:56735641 T>A maps to NM_018365.2 K333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:56739141 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr17:2290572 G>A maps to NM_020310.2 H457H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:2298205 C>A maps to NM_020310.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:2298308 C>T maps to NM_020310.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:2290509 C>T maps to NM_020310.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr14:93650119 G>C maps to NM_022151.4 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:33780266 G>A maps to NM_017947.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:33795777 G>A maps to NM_017947.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:33840065 T>C maps to NM_017947.2 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:39895155 C>T maps to ENST00000425303 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:39881153 G>A maps to ENST00000425303 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:39880703 G>A maps to ENST00000425303 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr6:39895236 G>A maps to ENST00000425303 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr6:29638161 C>T maps to NM_002433.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:29635427 C>T maps to NM_002433.4 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:223554122 C>A maps to NM_058165.2 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:75428944 C>T maps to NM_025098.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:100839507 G>T maps to NM_178176.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:100843788 G>A maps to NM_178176.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:100839477 G>T maps to NM_178176.2 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr7:100839301 C>T maps to NM_178176.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100841521 G>A maps to NM_178176.2 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:100839423 C>T maps to ENST00000440203 W305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:100839426 C>T maps to ENST00000440203 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr2:74689171 G>A maps to NM_006302.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:74689388 G>A maps to NM_006302.2 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:49946461 C>T maps to NM_032355.3 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:49949094 A>G maps to NM_032355.3 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr16:77228730 G>A maps to NM_014940.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:62929490 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:62949800 C>T maps to ENST00000393630 R1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr12:62959120 G>A maps to ENST00000393630 Q1380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:62943555 C>T maps to ENST00000393630 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr12:62926420 C>A maps to ENST00000393630 S535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:62981909 C>A maps to ENST00000393630 S1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:62926221 G>T maps to ENST00000393630 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr12:62943445 A>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:62902071 G>T maps to ENST00000393630 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:108725917 G>A maps to NM_014429.3 D575D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:108778651 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:108723663 C>T maps to NM_014429.3 Q695Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:108724111 A>G maps to NM_014429.3 H606H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:108677820 C>T maps to NM_014429.3 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:108698372 C>T maps to NM_014429.3 K822K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:108818258 C>T maps to NM_014429.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:108818273 C>T maps to NM_014429.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:108782078 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:108677918 A>G maps to NM_014429.3 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:108682455 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:108751618 C>A maps to NM_014429.3 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:108754190 T>C maps to NM_014429.3 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:108690196 C>A maps to NM_014429.3 E844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:108677945 C>A maps to NM_014429.3 E941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:31334181 C>A maps to ENST00000397641 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:37705951 G>A maps to ENST00000290384 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:37713712 G>T maps to ENST00000290384 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:37741862 G>T maps to ENST00000290384 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:37744697 A>G maps to ENST00000290384 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr21:37713695 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:37741409 G>T maps to ENST00000290384 E583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:106186103 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:106185366 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:106229367 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:106229373 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr23:106219825 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:106229257 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:106184843 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:106186000 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:106198308 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:106228329 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:106236469 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:106186103 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:106186070 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:106228349 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:106185791 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:106198162 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:106201643 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:106198294 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:106228329 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:106184835 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:106185284 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:106185267 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:106198281 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:106200225 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0V7-01A-21D-A122-09 chr23:106198230 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr23:106199720 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:106224707 C>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:106224217 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:174537668 G>T maps to NM_006792.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:79170559 C>T maps to NM_206839.1 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:79186454 T>C maps to NM_206839.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:102931113 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:102931700 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:102931422 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102931324 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102931446 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:102931864 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:102931452 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:102931602 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:102931670 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:2319696 G>A maps to NM_024848.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:122091081 G>A maps to NM_173855.4 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:122097188 G>A maps to NM_173855.4 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:99377005 G>T maps to NM_001098831.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:124936901 C>T maps to NM_198469.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr9:124936901 C>T maps to NM_198469.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:124936829 C>T maps to NM_198469.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:57026184 G>A maps to NM_005372.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:57025875 G>A maps to NM_005372.1 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:57025881 G>A maps to NM_005372.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:57026207 G>A maps to NM_005372.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:57026040 G>A maps to NM_005372.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:134030820 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:134030869 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134033403 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:134033117 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:134031041 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:134033311 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:134030899 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:14921085 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:14932660 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:14936833 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:14910867 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:14929460 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:14932666 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:14930382 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:100210576 C>T maps to NM_023948.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:113217558 C>T maps to NM_020963.3 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:113231748 C>A maps to NM_020963.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50559017 C>A maps to NM_018995.2 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50589273 G>A maps to NM_018995.2 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr22:50553598 C>T maps to NM_018995.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:50599251 C>T maps to NM_018995.2 R1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:50573013 C>T maps to NM_018995.2 N675N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50528924 C>T maps to NM_001164105.1 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50591505 C>T maps to NM_018995.2 H975H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:132649649 G>A maps to NM_015529.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:132713399 C>T maps to ENST00000392401 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:132649727 C>T maps to NM_015529.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:132694009 G>A maps to NM_015529.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:13123226 G>A maps to ENST00000319217 C1626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:13221475 C>T maps to ENST00000319217 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:13109030 T>C maps to ENST00000319217 L1990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:13186352 C>T maps to ENST00000319217 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:13126741 G>A maps to ENST00000319217 S1498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr9:13150533 C>T maps to ENST00000319217 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:13162794 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:13196199 C>A maps to ENST00000319217 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr9:13188938 G>A maps to ENST00000319217 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:13123199 C>T maps to ENST00000319217 G1635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr9:13110021 C>T maps to ENST00000319217 Q1957Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:13217244 C>A maps to ENST00000319217 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr9:13119572 T>C maps to ENST00000319217 G1769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr9:13162787 A>C maps to ENST00000319217 T1087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:58979986 C>A maps to NM_001039396.1 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:58979204 G>A maps to NM_001039396.1 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr11:58978598 G>A maps to NM_001039396.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:129690 C>T maps to NM_002434.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:71360707 T>C did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:71361824 C>A maps to NM_005791.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:82197736 G>T maps to NM_005792.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:20220986 C>T maps to ENST00000414242 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:20224200 T>C maps to ENST00000414242 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:20220648 G>T maps to ENST00000414242 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:20240599 C>T maps to ENST00000414242 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:123702943 A>G maps to NM_022782.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr12:123645771 G>A maps to NM_022782.2 Q946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:123687556 C>T maps to NM_022782.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr12:123679112 A>G maps to NM_022782.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:123649914 C>A maps to NM_022782.2 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr15:75182952 T>C maps to NM_002435.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:75188520 C>A maps to NM_002435.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:75185123 G>A maps to NM_002435.1 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:43805738 C>T maps to NM_005373.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:43818391 C>A maps to NM_005373.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:56350805 G>T maps to ENST00000340482 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:56355383 G>A maps to ENST00000340482 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr17:56349218 C>T maps to ENST00000340482 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:56357782 G>A maps to ENST00000340482 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:56352920 G>A maps to ENST00000340482 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:154007494 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:154009924 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:154009540 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:154011764 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:154020558 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:154018252 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154007510 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:154020089 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:154009907 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:154009531 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:154011736 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:154012322 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:154014660 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:154012302 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:41891442 T>G maps to ENST00000398393 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr17:41903183 G>C maps to ENST00000398393 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:41878963 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:202512532 G>A maps to NM_033066.2 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:67746177 C>T maps to NM_022474.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:67768116 T>G maps to NM_022474.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:67783592 G>T maps to NM_022474.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:67787843 C>T maps to NM_022474.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:67787843 C>T maps to NM_022474.2 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:24681339 T>C maps to ENST00000409253 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:24681472 G>T maps to ENST00000409253 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:24689293 G>T maps to ENST00000409253 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr10:28347422 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:28358699 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:28348652 T>C maps to NM_173496.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:28413984 C>T maps to NM_173496.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr22:43821057 C>T maps to NM_001044370.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr22:43870646 C>T maps to NM_001044370.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr11:30439136 G>A maps to NM_001584.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr17:17083922 C>G maps to NM_201274.2 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:17057705 G>A maps to NM_015134.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:17064564 C>T maps to NM_015134.2 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:17041248 C>T maps to NM_015134.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:17077284 C>T maps to NM_015134.2 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:17069107 C>T maps to ENST00000313485 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:17046880 T>C maps to NM_015134.2 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr22:37420423 C>T maps to NM_021126.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:15501959 G>A maps to NM_001128423.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:18306902 T>C maps to ENST00000445735 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:18305799 C>T maps to NM_032683.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:167741532 C>T maps to NM_003953.5 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:118128023 C>A maps to NM_144765.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:181022715 A>G maps to NM_001531.2 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr1:181019378 A>G maps to NM_001531.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:181021593 C>T maps to NM_001531.2 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:181024395 C>T maps to NM_001531.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr21:33684267 G>A maps to ENST00000445271 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:84772651 C>T maps to NM_138409.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:84765112 G>T maps to NM_138409.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:138091916 C>T maps to NM_001085049.1 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:17865380 G>T maps to NM_002438.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:17922586 C>T maps to NM_002438.2 R924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:60757797 C>T maps to NM_006039.3 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:60766910 G>A maps to NM_006039.3 A1121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:60769592 G>A maps to NM_006039.3 A1407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:60769697 C>T maps to NM_006039.3 I1442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:60768090 C>T maps to NM_006039.3 G1327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:60767289 G>A maps to NM_006039.3 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:60755962 C>T maps to NM_006039.3 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:60744838 G>A maps to NM_006039.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:60767313 C>T maps to NM_006039.3 D1211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:94163103 C>T maps to NM_005591.3 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:94192695 C>A maps to NM_005591.3 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:94163103 C>T maps to NM_005591.3 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:6711020 C>T maps to NM_203462.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr11:68773001 C>T maps to NM_145015.4 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:68772955 G>A maps to NM_145015.4 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:18978440 G>A maps to ENST00000433222 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:18955788 G>A maps to NM_147199.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:18956061 G>T maps to NM_147199.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:18955857 C>T maps to NM_147199.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:19077036 G>A maps to NM_054030.2 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:19077883 A>G maps to NM_054030.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:19077226 A>G maps to NM_054030.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr11:18158871 G>A maps to NM_054031.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:18158856 C>T maps to NM_054031.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:18159291 C>T maps to NM_054031.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr11:18194946 G>T maps to NM_054032.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:18195096 C>T maps to NM_054032.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:18195756 C>T maps to NM_054032.3 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr11:18195144 C>T maps to NM_054032.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:13879743 C>T maps to NM_001031727.2 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:13879810 C>T maps to NM_001031727.2 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr19:13879241 C>G maps to NM_032285.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:34964440 C>A maps to NM_024864.3 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:48335755 C>T maps to NM_031939.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:78804527 C>T maps to NM_020236.3 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:78871006 T>G maps to NM_020236.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:78804459 G>T maps to NM_020236.3 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:45901588 G>A maps to NM_145255.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:79674063 C>T maps to NM_002949.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:44081684 G>A maps to NM_032111.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:55055302 T>C maps to NM_014175.3 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6703507 G>A maps to NM_022061.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr6:160212047 T>C maps to NM_014161.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:75879718 C>T maps to NM_014763.3 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:75879328 G>T maps to NM_014763.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:43024148 G>A maps to NM_015950.3 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr6:43023659 C>A maps to NM_015950.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:43023722 C>T maps to NM_015950.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:1342348 C>A maps to NM_017971.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:1973407 C>T maps to NM_021134.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:1977577 C>T maps to NM_021134.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:418577 G>A maps to NM_006428.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:131220528 A>G maps to ENST00000425847 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:131181683 G>A maps to ENST00000425847 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:131220559 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:99811386 G>A maps to ENST00000409145 *102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:42977148 C>T maps to NM_031903.2 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:86437650 C>T maps to NM_016622.3 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:73895041 G>A maps to NM_032478.3 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:26961194 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:26972137 G>A maps to NM_080794.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:26978929 C>T maps to NM_080794.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr22:19423196 T>C maps to NM_003776.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:224828558 G>A maps to NM_022915.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:224824262 G>A maps to NM_022915.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:224824262 G>A maps to NM_022915.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:36454587 T>A maps to NM_032351.3 C80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:36462517 C>T maps to NM_032351.3 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:179320487 C>A maps to NM_020409.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:179320487 C>A maps to NM_020409.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:179320487 C>A maps to NM_020409.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:228295392 G>A maps to NM_181462.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:151733312 G>A maps to NM_031420.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:42181890 G>A maps to NM_018141.3 H51H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:42179540 C>A maps to NM_018141.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:89021167 C>A maps to NM_022839.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr15:89018469 G>A maps to NM_022839.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:89020249 C>T maps to NM_022839.3 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:36923544 T>C maps to NM_031280.3 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:36921489 T>G maps to NM_031280.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:138395783 C>A maps to NM_016034.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:138395576 C>T maps to NM_016034.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:138393781 C>T maps to NM_016034.3 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:138395465 G>A maps to NM_016034.3 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:150280626 C>T maps to NM_031901.4 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:139065744 G>A maps to NM_020191.2 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:139065786 G>A maps to NM_020191.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:139074616 A>G maps to NM_020191.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:139065786 G>A maps to NM_020191.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:55917272 G>T maps to NM_016070.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:55917164 C>T maps to NM_016070.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:43906354 A>G maps to NM_032014.2 C149C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:15100933 C>T maps to NM_022497.3 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:71516975 C>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:80831265 T>A maps to NM_014018.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:44811232 C>T maps to NM_016640.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:44812046 G>T maps to NM_016640.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:44811232 C>T maps to NM_016640.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:41345245 T>C maps to NM_005830.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr13:41340975 G>A maps to NM_005830.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:41345203 G>A maps to NM_005830.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:140710250 G>T maps to NM_053035.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:27908272 G>T maps to NM_021821.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:27908272 G>T maps to NM_021821.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:95773963 C>T maps to NM_031902.3 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:95780829 T>C maps to NM_031902.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:105687915 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:10622543 C>T maps to NM_001098579.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:10602107 C>A maps to NM_001098579.1 E788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:10651141 G>A maps to NM_001098579.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:60233602 C>A maps to NM_152866.2 Y182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:60235910 C>A maps to NM_152866.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr11:60233392 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:60567342 C>A maps to NM_206893.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:60558481 C>A maps to NM_206893.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:60561443 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:60561563 C>A maps to NM_206893.3 Y160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr11:60561575 G>A maps to NM_206893.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:60264856 A>G maps to NM_017716.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:60292793 C>T maps to NM_001012417.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:60285567 C>A maps to NM_001012417.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:60296836 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:60296926 C>A maps to NM_001012417.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:60164182 C>A maps to NM_032597.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:60184291 G>A maps to NM_032597.3 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:60167888 G>T maps to NM_032597.3 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:60170428 G>A maps to NM_032597.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:60183176 G>T maps to NM_032597.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:60541389 C>T maps to NM_001098835.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:60064692 G>T maps to NM_148975.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:60070111 G>A maps to NM_148975.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr11:60073604 G>T maps to NM_148975.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:60070084 G>T maps to NM_148975.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:60197293 C>A maps to NM_023945.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:59947426 G>T maps to NM_152852.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:60157008 G>A maps to NM_206939.1 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:60470943 G>T maps to NM_031457.1 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:72754928 G>A maps to NM_005098.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:17997997 C>T maps to NM_001105569.1 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:17998321 A>C maps to NM_001105569.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:17998264 G>A maps to NM_001105569.1 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:47693875 A>G maps to NM_000251.1 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:47698122 G>T maps to NM_000251.1 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:47698179 G>T maps to NM_000251.1 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr2:47703671 G>A maps to NM_000251.1 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:47690229 G>T maps to NM_000251.1 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:80024749 G>T maps to NM_002439.3 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:79961017 G>T maps to NM_002439.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:80063901 G>T maps to NM_002439.3 E683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:76262678 G>A maps to NM_002440.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:76342661 C>A maps to NM_002440.2 Y449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:76363708 G>T maps to NM_002440.2 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:76356454 G>A maps to NM_002440.2 T767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:76349313 G>T maps to NM_002440.2 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:76356484 T>C maps to NM_002440.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:76363590 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:76363708 G>T maps to NM_002440.2 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:76378490 A>G maps to NM_002440.2 R910R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:76355042 G>T maps to NM_002440.2 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:76345820 C>A maps to NM_002440.2 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:31727938 G>A maps to ENST00000375742 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:31712013 C>T maps to ENST00000375742 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:31729015 G>T maps to ENST00000375742 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:31727656 C>T maps to ENST00000375742 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:31711941 G>A maps to ENST00000375742 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr6:31711920 A>G maps to ENST00000375742 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:31712013 C>T maps to ENST00000375742 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:31729605 C>A maps to ENST00000375742 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:48030685 G>A maps to NM_000179.2 T1100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:48033395 G>T maps to NM_000179.2 E1234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:48033640 G>A maps to NM_000179.2 T1284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:48033752 G>T maps to NM_000179.2 E1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:48027957 G>T maps to NM_000179.2 E946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:48027042 G>T maps to NM_000179.2 E641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:48030685 G>A maps to NM_000179.2 T1100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:48028262 G>A maps to NM_000179.2 W1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:48032785 G>T maps to NM_000179.2 E1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:48025791 G>T maps to NM_000179.2 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:48026078 G>A maps to NM_000179.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:48027843 G>T maps to NM_000179.2 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:120783432 G>A maps to NM_002442.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:120800928 G>A maps to NM_002442.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:120796838 C>T maps to NM_002442.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:55704602 C>T maps to NM_138962.2 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:55752312 C>T maps to ENST00000416426 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:38289293 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:38285496 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:38282491 C>T maps to ENST00000398532 N275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:38285833 G>A maps to ENST00000398532 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:135870120 A>G maps to NM_018133.3 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:135870273 G>A maps to NM_018133.3 C483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:135870846 C>T maps to NM_018133.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:135870846 C>T maps to NM_018133.3 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:135871458 C>T maps to NM_018133.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:135870723 C>T maps to NM_018133.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:11780337 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:11781113 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:11793133 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:11782014 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:11781097 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:11786781 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr23:11777910 G>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:11793125 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:11778570 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:816098 C>T maps to NM_013404.4 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:815168 C>T maps to NM_013404.4 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr16:823012 C>T maps to NM_001025190.1 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:820110 C>T maps to NM_001025190.1 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:51556767 G>T maps to NM_002443.2 G43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr9:35753673 G>A maps to NM_001044264.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr9:35754029 C>A maps to NM_001044264.1 G33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:64957101 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:64951038 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:64951828 C>T did not map to a codon.
Sequencing variant TCGA-AP-A052-01A-11W-A027-09 chr23:64956746 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:64959669 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:64959737 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:64950980 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:64951767 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:64951736 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:64957090 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:64958438 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:64949442 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:64949522 A>C did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:64959709 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:64947703 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr23:64947696 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:64955177 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:64959668 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:64951039 G>A did not map to a codon.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr23:64959737 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:16012620 G>A maps to ENST00000445506 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:15977936 G>A maps to ENST00000445506 H422H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:16026068 G>A maps to ENST00000445506 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:16035479 G>A maps to ENST00000445506 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:16026302 C>T maps to ENST00000445506 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:15977987 G>T maps to ENST00000445506 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:15978080 G>A maps to ENST00000445506 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:16035393 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr10:23393073 G>A maps to ENST00000277598 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:23408271 G>A maps to ENST00000277598 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:65847598 C>A maps to NM_001031679.2 C128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49721808 C>A maps to NM_020998.3 G652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:49723303 C>A maps to NM_020998.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr3:49928691 G>A maps to NM_002447.2 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:49940853 G>A maps to NM_002447.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:49940853 G>A maps to NM_002447.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:49928837 A>T maps to NM_002447.2 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:49940301 A>G maps to NM_002447.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:131188762 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:131188716 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:131188890 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:131206846 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:131206348 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:131206365 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:131205162 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:131203644 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:131188796 G>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:131202579 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:131207097 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:190922196 C>T maps to NM_005259.2 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:190922042 C>A maps to NM_005259.2 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:190921989 G>A maps to NM_005259.2 C374C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:190925093 T>C maps to NM_005259.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:155582019 C>T maps to NM_018116.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:56660459 C>A maps to ENST00000330439 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:56624812 C>T maps to NM_005954.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:56624851 C>A maps to NM_005954.2 C66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:105929555 C>A maps to NM_004689.3 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr14:105905012 C>T maps to NM_004689.3 Y11Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:105924685 C>T maps to NM_004689.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:62366045 G>T maps to NM_004739.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:62361789 C>T maps to NM_004739.2 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:21837987 G>A maps to NM_002451.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:21854694 C>T maps to NM_002451.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr9:21837984 G>A maps to NM_002451.3 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr9:21854832 G>C maps to NM_002451.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:121473459 A>G maps to NM_022045.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr8:121509637 C>T maps to NM_022045.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:121463475 T>G maps to NM_022045.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:121473427 G>T maps to NM_022045.3 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:47657123 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:154290193 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154290174 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:97251838 A>G maps to NM_015942.3 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:97256206 C>T maps to NM_015942.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:97270774 G>T maps to NM_015942.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:242038981 G>A maps to NM_182501.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:242035460 G>A maps to NM_182501.3 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:107371511 T>C maps to NM_025198.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:107372325 G>T maps to NM_025198.3 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:107371352 T>C maps to NM_025198.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:38300837 G>A maps to NM_005955.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr1:38305668 G>A maps to NM_005955.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:93575838 C>T maps to NM_007358.3 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:93595006 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:93602457 T>C maps to NM_007358.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:93594883 C>T maps to NM_007358.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:93594883 C>T maps to NM_007358.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:65295438 C>T maps to NM_139242.3 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:66617039 G>A maps to NM_014637.3 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr8:66619443 A>G maps to NM_014637.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:66620282 G>T maps to NM_001145839.1 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:135212691 G>T maps to NM_138384.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:135215054 C>T maps to NM_138384.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:64882458 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:64908848 C>T maps to NM_005956.3 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:64892895 C>T maps to NM_005956.3 Y371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:64909119 G>A maps to NM_005956.3 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:74438943 C>T maps to NM_006636.3 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:75040294 A>G maps to NM_001144978.1 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:75040312 A>C maps to NM_001144978.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:75147243 T>G maps to NM_001144978.1 L303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:11851347 C>T maps to ENST00000376585 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:11863019 G>A maps to ENST00000376585 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr1:11853999 C>G maps to ENST00000376585 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:11861220 C>A maps to ENST00000376585 G199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr15:80137599 G>A maps to NM_006441.3 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr15:80137572 G>A maps to NM_006441.3 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:86582141 C>T maps to NM_001159377.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:86575808 G>A maps to NM_001159377.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr16:86585862 C>T maps to NM_001159378.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:55490924 G>A maps to NM_002453.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:68512543 T>C maps to NM_004923.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:68483394 G>T maps to NM_004923.3 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:68506226 G>A maps to NM_004923.3 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:149807439 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:149839963 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:149826442 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:149828137 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:149767060 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:149764967 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:149814291 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:149767148 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:149787585 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:149787531 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:149831986 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:149831927 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:149839985 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:149814234 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:149818304 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:149761102 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:149767148 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:149809877 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:149832077 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:149828908 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:149783118 G>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:149814322 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:149765037 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:149809882 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:149814234 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:149901187 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:149896164 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:149931090 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:149901024 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:149905163 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:149919522 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr23:149901033 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:149896154 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:149924253 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:149924249 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:149931130 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:149898616 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:149867755 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:149905190 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:149924160 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:149899994 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:149896164 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:149901201 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:149905240 G>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:149905203 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:31251127 G>A maps to NM_017762.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr15:31251069 G>A maps to NM_017762.2 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:31253153 C>A maps to NM_017762.2 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:149904174 G>A maps to NM_001145862.1 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:149901143 T>C maps to NM_001145862.1 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:149906097 G>A maps to NM_001145862.1 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:149907228 G>A maps to NM_001145862.1 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:32230299 G>A maps to NM_001040446.1 R610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:32239136 G>A maps to NM_001040446.1 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:32239256 G>A maps to NM_001040446.1 C398C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:32242201 C>A maps to NM_001040446.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:32230093 G>A maps to NM_001040446.1 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:32229973 G>A maps to NM_001040446.1 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:9730664 C>T maps to NM_001077525.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:9730629 C>T maps to NM_001077525.2 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:9726296 C>A maps to NM_001077525.2 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:9729563 G>A maps to NM_001077525.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:9704037 A>G maps to NM_001077525.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr3:9719672 C>T maps to NM_001077525.2 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:95568385 T>G did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:95581054 A>G maps to NM_016156.5 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:95581039 A>G maps to NM_016156.5 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:30416036 C>T maps to NM_021090.3 R797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:30409418 G>A maps to NM_021090.3 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr22:30416036 C>T maps to NM_021090.3 R797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:30418644 C>T maps to NM_021090.3 C1128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:30416317 C>T maps to NM_021090.3 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:30403265 C>T maps to NM_021090.3 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:56572903 C>A maps to NM_004687.4 G867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:56572537 G>A maps to NM_004687.4 Q989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:56581752 G>A maps to NM_004687.4 Q466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:56572620 G>T maps to NM_004687.4 S961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:25831381 C>T maps to NM_004685.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:25848322 G>A maps to NM_004685.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:25841967 C>A maps to NM_004685.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:25831921 C>T maps to NM_004685.3 W307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:17163437 C>A maps to NM_004686.4 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:17230724 G>A maps to NM_004686.4 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:17163466 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:17218732 C>A maps to NM_004686.4 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr8:17157433 A>G maps to NM_004686.4 H640H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:17228549 C>T maps to NM_004686.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:17163437 C>A maps to NM_004686.4 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:17198898 G>A maps to NM_004686.4 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:63576164 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:63576214 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:63488754 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:63488910 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:63565021 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:63579381 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr23:63569875 C>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:63574802 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:63488627 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:63551598 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:63556008 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr23:63488654 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:63488789 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:63551631 C>T did not map to a codon.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr23:63551613 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:63574666 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:63565044 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:11157610 G>A maps to NM_015458.3 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:11180243 C>T maps to NM_015458.3 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:11180243 C>T maps to NM_015458.3 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:11174402 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:11174276 C>T maps to NM_015458.3 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:187455421 G>A maps to NM_005958.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:187455367 C>T maps to NM_005958.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:187455556 G>A maps to NM_005958.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr4:187455685 C>T maps to NM_005958.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:187455703 G>T maps to NM_005958.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:187455364 G>A maps to NM_005958.3 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:187476402 C>T maps to NM_005958.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:92715303 C>T maps to NM_005959.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:92715309 C>A maps to NM_005959.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr11:92715123 C>T maps to NM_005959.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:92714817 C>A maps to NM_005959.3 C143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:74201959 T>G maps to NM_001123226.1 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:74192332 C>T maps to NM_001123226.1 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:74171594 C>T maps to NM_001123226.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:11206810 G>A maps to NM_004958.3 I1536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:11308097 C>T maps to NM_004958.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:11298480 G>A maps to NM_004958.3 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:11206827 C>A maps to NM_004958.3 E1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:11318548 C>T maps to NM_004958.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:11194484 G>T maps to NM_004958.3 T1723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:30602740 G>A maps to ENST00000358107 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:30630456 C>T maps to ENST00000358107 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:30629334 A>G maps to ENST00000358107 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:237023144 G>T maps to NM_000254.2 G656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:237052541 C>T maps to NM_000254.2 D971D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:237057808 C>T maps to NM_000254.2 D1119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:237013714 T>C maps to NM_000254.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:237060868 T>C maps to NM_000254.2 Y1241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:237052484 G>A maps to NM_000254.2 K952K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr1:237016363 T>C maps to NM_000254.2 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr13:41808077 C>T maps to NM_004294.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:41834649 C>A maps to NM_004294.2 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:41800680 C>A maps to NM_004294.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr6:153311074 G>A maps to NM_019041.5 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:7900143 A>G maps to NM_024010.2 K717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:7878242 C>T maps to NM_024010.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:7897234 C>T maps to NM_024010.2 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:125577934 G>A maps to NM_014751.4 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr8:125580657 G>A maps to NM_014751.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:70712235 C>T maps to NM_138383.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:70713779 G>A maps to NM_138383.2 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:100532501 G>A maps to ENST00000511045 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:100534267 G>T maps to ENST00000511045 G757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:100543897 G>T maps to ENST00000511045 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr4:100534203 C>T maps to ENST00000511045 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:17541986 C>T maps to NM_001001924.2 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr8:17507461 G>A maps to NM_001001924.2 Q1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:17512099 G>A maps to NM_001001924.2 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:17554819 G>A maps to NM_020749.4 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:17612041 C>T maps to NM_001001924.2 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr8:17512151 A>G maps to NM_001001924.2 H1044H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:17612056 A>G maps to NM_001001924.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:17612116 C>T maps to NM_001001924.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr8:17611237 A>G maps to NM_001001924.2 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:29599632 A>G maps to NM_001033602.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:29599047 T>C maps to NM_001033602.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:30077217 C>T maps to NM_001033602.2 L1339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr13:29675048 A>T maps to NM_001033602.2 S872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr13:29599206 G>A maps to NM_001033602.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:29600919 C>A maps to NM_001033602.2 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr13:29600847 G>A maps to NM_001033602.2 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr13:29600583 G>A maps to NM_001033602.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:30072622 G>A maps to NM_001033602.2 K1259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr13:30054375 C>T maps to NM_001033602.2 Q1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:29600649 C>A maps to NM_001033602.2 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:29933427 C>T maps to NM_001033602.2 R989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr13:29599665 C>T maps to NM_001033602.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:155178720 C>A maps to NM_002455.3 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:155180409 C>T maps to NM_002455.3 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr2:177193630 A>G maps to NM_006554.4 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:79279512 C>T maps to ENST00000512528 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:155160213 C>T maps to ENST00000425082 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:124627179 C>T maps to NM_033049.3 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:124646447 C>A maps to NM_033049.3 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:124642453 G>T maps to NM_033049.3 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr19:9066388 C>T maps to NM_024690.2 S7019S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:9061015 G>T maps to NM_024690.2 A8810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr19:9047100 G>T maps to NM_024690.2 S11510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:9086054 C>T maps to NM_024690.2 E1920E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:9077865 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:9085139 A>G maps to NM_024690.2 G2225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:9056731 C>T maps to NM_024690.2 T10238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9009658 G>A maps to NM_024690.2 Q13023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9019329 G>T maps to NM_024690.2 T12519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9060847 C>T maps to NM_024690.2 S8866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9071377 C>T maps to NM_024690.2 Q5356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9073036 A>G maps to NM_024690.2 S4803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9075097 G>A maps to NM_024690.2 A4116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:9072739 G>T maps to NM_024690.2 I4902I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:9087023 C>T maps to NM_024690.2 G1597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:9088636 C>A maps to NM_024690.2 G1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:9090008 C>T maps to NM_024690.2 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:9083555 C>T maps to NM_024690.2 A2753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9049419 C>A maps to NM_024690.2 V10737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9058600 G>T maps to NM_024690.2 V9615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9073925 G>T maps to NM_024690.2 S4507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9087578 T>G maps to NM_024690.2 S1412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9087800 G>T maps to NM_024690.2 V1338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:9085145 G>A maps to NM_024690.2 S2223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr19:9049152 C>T maps to NM_024690.2 T10826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:9057355 C>T maps to NM_024690.2 T10030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:9059403 C>A maps to NM_024690.2 E9348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:9068796 C>A maps to NM_024690.2 E6217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:9077596 G>T maps to NM_024690.2 V3283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr19:9048228 C>A maps to NM_024690.2 G11134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:9012884 G>T maps to NM_024690.2 L12853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:9058990 C>T maps to NM_024690.2 E9485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:9071136 G>A maps to NM_024690.2 Q5437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:9075607 A>C maps to NM_024690.2 P3946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:9075898 A>C maps to NM_024690.2 T3849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:9090037 C>A maps to NM_024690.2 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:9056816 G>T maps to NM_024690.2 S10210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:9057301 A>G maps to NM_024690.2 F10048F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr19:9000564 G>A maps to NM_024690.2 T13473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr19:9057121 T>C maps to NM_024690.2 G10108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr19:9068020 T>C maps to NM_024690.2 S6475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr19:9074415 G>A maps to NM_024690.2 Q4344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr19:9088484 G>A maps to NM_024690.2 V1110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:9059464 A>C maps to NM_024690.2 S9327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:9064602 C>A maps to NM_024690.2 E7615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:9072981 C>A maps to NM_024690.2 E4822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:9089249 A>G maps to NM_024690.2 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:9062560 A>G maps to NM_024690.2 P8295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:9072316 A>G maps to NM_024690.2 F5043F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr19:9086933 G>T maps to NM_024690.2 S1627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:9060594 C>A maps to NM_024690.2 E8951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:9076795 G>A maps to NM_024690.2 I3550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:9077445 C>A maps to NM_024690.2 E3334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr19:8993433 C>A maps to NM_024690.2 L13885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:9073255 G>A maps to NM_024690.2 D4730D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9048564 A>G maps to NM_024690.2 S11022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9059364 C>A maps to NM_024690.2 E9361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9060253 C>T maps to NM_024690.2 R9064R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9063256 G>T maps to NM_024690.2 T8063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9064398 C>A maps to NM_024690.2 E7683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9065928 C>A maps to NM_024690.2 E7173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9088465 C>A maps to NM_024690.2 E1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:9090866 C>T maps to NM_024690.2 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:9074386 G>T maps to NM_024690.2 I4353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:9082699 C>A maps to NM_024690.2 E3039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:8987332 G>A maps to NM_024690.2 T13918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:9058857 C>A maps to NM_024690.2 E9530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:9067615 G>T maps to NM_024690.2 V6610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:9084553 C>A maps to NM_024690.2 E2421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:100685022 C>T maps to NM_001040105.1 I3442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:100677106 G>T maps to NM_001040105.1 G804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:100683039 T>C maps to NM_001040105.1 P2781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:100683242 C>A maps to NM_001040105.1 S2849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:100695186 C>A maps to NM_001040105.1 V4349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:100663430 G>T maps to NM_001040105.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:100695123 C>T maps to NM_001040105.1 F4328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:100684767 T>C maps to NM_001040105.1 A3357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:100677286 A>C maps to NM_001040105.1 R864R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:100679004 T>G maps to NM_001040105.1 S1436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:100695204 C>T maps to NM_001040105.1 L4355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100684830 T>C maps to NM_001040105.1 S3378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:100681251 T>G maps to NM_001040105.1 P2185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:100682701 G>T maps to NM_001040105.1 G2669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:100695177 C>T maps to NM_001040105.1 G4346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:100692639 C>T maps to NM_001040105.1 V4233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:1079700 G>A maps to ENST00000441003 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:1085742 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr11:1092569 C>A maps to ENST00000441003 T1463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr11:1103860 G>A maps to ENST00000441003 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:1102460 C>T maps to ENST00000441003 F2615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:1093933 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:1096349 G>A maps to ENST00000441003 P2125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:195451791 C>T maps to ENST00000447234 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:195451791 C>T maps to ENST00000447234 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:30955898 T>C maps to NM_001010909.2 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:30954107 G>T maps to NM_001010909.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:195508187 G>A maps to NM_018406.5 H3421H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:195517634 G>T maps to NM_018406.5 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:195490449 G>A maps to NM_018406.5 L4703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:195516940 C>A maps to NM_018406.5 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr3:195505718 G>A maps to NM_018406.5 S4244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:195514358 A>G maps to NM_018406.5 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:195512219 G>A maps to NM_018406.5 H2077H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr3:195512870 G>A maps to NM_018406.5 T1860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr3:195492261 G>A maps to NM_018406.5 L4559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr3:195509291 G>A maps to NM_018406.5 H3053H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr3:195509354 T>G maps to NM_018406.5 S3032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr3:195516479 G>A maps to NM_018406.5 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:195516935 C>T maps to NM_018406.5 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:195475885 G>T maps to NM_018406.5 G5307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:195512861 G>T maps to NM_018406.5 S1863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:195511049 G>T maps to NM_018406.5 G2467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:195512819 G>A maps to NM_018406.5 D1877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:195508157 G>T maps to NM_018406.5 S3431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:195492173 G>A maps to NM_018406.5 R4589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:195511211 G>A maps to NM_018406.5 H2413H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:195493606 G>A maps to NM_018406.5 F4515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:195475900 G>A maps to NM_018406.5 C5302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:1263422 C>T maps to ENST00000447027 P1774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:1267605 G>T maps to ENST00000447027 E3169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:1262636 G>A maps to ENST00000447027 W1512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:1271141 C>A maps to ENST00000447027 P4347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:1271333 G>A maps to ENST00000447027 T4411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:1267353 G>T maps to ENST00000447027 E3085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:1271342 G>A maps to ENST00000447027 P4414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr11:1269158 C>A maps to ENST00000447027 P3686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:1250475 C>T maps to ENST00000447027 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:1263137 G>A maps to ENST00000447027 T1679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:1263797 G>A maps to ENST00000447027 T1899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:1270847 G>A maps to ENST00000447027 T4249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:1270907 G>A maps to ENST00000447027 T4269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:1264229 C>A maps to ENST00000447027 S2043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:1267409 G>A maps to ENST00000447027 P3103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:1268762 G>A maps to ENST00000447027 S3554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:1270289 G>A maps to ENST00000447027 Q4063Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:1274082 C>T maps to ENST00000447027 C5033C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr11:1267070 A>G maps to ENST00000447027 P2990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:1266353 G>A maps to ENST00000447027 P2751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr11:1272485 G>A maps to ENST00000447027 V4795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr11:1263749 C>T maps to ENST00000447027 D1883D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:1266524 G>A maps to ENST00000447027 S2808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr11:1257719 C>T maps to ENST00000447027 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:1267631 G>A maps to ENST00000447027 T3177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:1272167 G>T maps to ENST00000447027 T4689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:1261038 G>A maps to ENST00000447027 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr11:1271702 C>A maps to ENST00000447027 G4534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr11:1278482 C>T maps to ENST00000447027 P5420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:1268288 G>A maps to ENST00000447027 T3396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr11:1274055 C>T maps to ENST00000447027 T5024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:1264526 G>A maps to ENST00000447027 T2142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:1263857 G>A maps to ENST00000447027 T1919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:1265549 C>A maps to ENST00000447027 S2483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:1272386 G>A maps to ENST00000447027 W4762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:1272614 G>A maps to ENST00000447027 T4838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:1271834 C>T maps to ENST00000447027 T4578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:1031684 G>A maps to NM_005961.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:1028727 G>A maps to NM_005961.2 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:1025029 G>A maps to NM_005961.2 F1013F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:1026029 G>A maps to NM_005961.2 F886F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:1031886 G>T maps to NM_005961.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr11:1031223 G>A maps to NM_005961.2 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:71347159 G>A maps to NM_152291.2 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:71346887 G>T maps to NM_152291.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:55248906 G>A maps to NM_058173.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:55248900 G>A maps to NM_058173.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:55248939 T>G maps to NM_058173.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:57741090 C>T maps to ENST00000431972 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:57755706 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:57741640 T>C maps to ENST00000446279 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:57741090 C>T maps to ENST00000431972 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:57741282 T>C maps to ENST00000431972 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:20827755 C>T maps to NM_024544.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr19:1371013 C>G maps to NM_032853.3 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:1360169 G>T maps to NM_032853.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:1358631 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:1358630 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:1362258 T>G maps to NM_032853.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:105449986 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:105450437 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:105450761 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105450190 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105451312 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:105450197 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:105451078 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:105451181 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:105451272 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:105451329 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105450376 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105450472 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105450675 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:105450492 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:105449723 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:105450066 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:105450887 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:105450668 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:105450109 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:105449763 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:103340658 G>A maps to NM_001018116.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:103340454 T>G maps to NM_001018116.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:65631350 C>T maps to NM_025128.4 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr11:65633513 C>T maps to NM_025128.4 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr9:113431246 T>C maps to ENST00000189978 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr9:113530240 G>A maps to ENST00000189978 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr9:113562661 C>T maps to ENST00000189978 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:113563223 C>T maps to ENST00000189978 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr9:113547893 G>A maps to ENST00000189978 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:113530084 C>T maps to ENST00000189978 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:113562623 G>T maps to ENST00000189978 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr9:113530129 C>T maps to ENST00000189978 C323C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D1-A17A-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr6:49415411 G>A maps to NM_000255.3 R511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:49425412 A>G maps to NM_000255.3 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:8041476 G>A maps to NM_201280.2 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:8062846 G>T maps to ENST00000397456 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:8062774 C>A maps to NM_201280.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:8041461 A>G maps to NM_201280.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:8062774 C>A maps to NM_201280.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:45799120 G>A maps to NM_001128425.1 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:110024569 C>T maps to NM_001114185.1 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr12:110019244 C>T maps to NM_001114185.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:110029056 C>T maps to NM_001114185.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:110019208 G>A maps to NM_001114185.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:29845106 G>A maps to NM_017458.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:29853119 C>T maps to NM_017458.3 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:29853262 G>A maps to NM_017458.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:42823163 C>T maps to NM_001144925.1 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr21:42813697 C>T maps to NM_001144925.1 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:42830544 C>T maps to NM_001144925.1 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr21:42813697 C>T maps to NM_001144925.1 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:42762526 G>A maps to NM_002463.1 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:42771164 G>T maps to NM_002463.1 G439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:42775239 C>T maps to NM_002463.1 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr21:42767547 C>T maps to NM_002463.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:42749777 C>T maps to NM_002463.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:42767677 G>T maps to NM_002463.1 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:42780135 A>G maps to NM_002463.1 Q708Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:70165235 C>T maps to NM_002357.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:176737698 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr10:112044687 T>C maps to NM_130439.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:3239635 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:3248191 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:3235843 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:3235844 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:3240919 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:3248756 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:3239464 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:3241609 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:3242311 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:3229292 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:3235548 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:3239623 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:3242385 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:3242611 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:3261698 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:3242711 T>C did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:3228928 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:3229626 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:3235778 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:3239120 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:3240129 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:3241517 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:3228137 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:3238117 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:3248261 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:3235954 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:3240543 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:3235792 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:3240250 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:3228182 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:3228261 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:3235933 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:3238983 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:3239693 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:3242912 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:3242624 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:3228395 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:3238159 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:3239175 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:3239335 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:3239866 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:3235222 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:3242756 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:3229490 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:3235153 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:3235466 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:3238979 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:3242274 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:3261804 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:3227896 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:3240191 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:3248072 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:3235654 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:3238182 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:3238563 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:3248103 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:74681239 G>A maps to NM_001008528.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:54377400 C>T maps to NM_001020818.1 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:135518457 G>A maps to NM_001130173.1 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:135516132 C>T maps to ENST00000237302 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr6:135518268 G>A maps to NM_001130173.1 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr17:4442892 G>A maps to NM_001105538.1 P1268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:4455261 G>T maps to NM_001105538.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:4457343 G>A maps to NM_001105538.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:67488481 G>A maps to NM_001080416.2 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:67511362 A>G maps to NM_001080416.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:67488481 G>A maps to NM_001080416.2 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:42331263 C>T maps to NM_002466.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr20:42320904 G>A maps to NM_002466.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:102025860 C>T maps to NM_002465.2 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr12:102061573 G>T maps to NM_002465.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:102067365 C>T maps to NM_002465.2 F925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr12:102071161 C>T maps to NM_002465.2 I1033I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr19:50957350 G>A maps to NM_004533.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:50962429 G>A maps to NM_004533.3 V886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50944178 C>T maps to NM_004533.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:50958842 G>T maps to NM_004533.3 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:50945543 C>T maps to NM_004533.3 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:50965289 G>A maps to NM_004533.3 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:47353625 G>A maps to ENST00000399249 R1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:47364234 G>A maps to ENST00000399249 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:47372886 C>T maps to ENST00000399249 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:47372954 G>A maps to ENST00000399249 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr11:47365113 G>C maps to ENST00000399249 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:47357475 C>A maps to ENST00000399249 G897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr11:47362770 G>A maps to ENST00000399249 D605D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr11:47372095 C>T maps to ENST00000399249 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr11:47364403 C>T maps to ENST00000399249 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:109837841 G>T maps to NM_001010985.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:109840146 G>A maps to NM_001010985.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:109839669 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:109840068 G>A maps to NM_001010985.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:39333232 C>T did not map to a codon.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr13:77763182 C>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr13:77764430 A>G maps to NM_015057.4 N1370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:77714204 C>A maps to NM_015057.4 G2499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:77836211 C>T maps to NM_015057.4 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr13:77671901 C>T maps to NM_015057.4 L3129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:77750697 C>T maps to NM_015057.4 T1802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:77754339 G>T maps to NM_015057.4 S1685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:77739482 C>A maps to NM_015057.4 V2128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:77740512 C>T maps to NM_015057.4 K2097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:77619572 T>G maps to NM_015057.4 P4659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:77671897 C>A maps to NM_015057.4 E3131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:77738654 C>A maps to NM_015057.4 E2161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:77807289 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:77754432 C>T maps to NM_015057.4 G1654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:77730337 C>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr13:77779465 G>A maps to NM_015057.4 F1256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:77844652 C>T maps to NM_015057.4 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:77740589 T>G maps to NM_015057.4 R2072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:77651413 G>A maps to NM_015057.4 R3865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:77739405 A>G did not map to a codon.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr13:77672320 G>T maps to NM_015057.4 R2990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:48600974 G>T maps to NM_032133.4 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:48597027 C>T maps to NM_032133.4 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:48599411 C>T maps to NM_032133.4 C452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:40367034 C>T maps to NM_001033082.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:16085654 C>T maps to NM_005378.4 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:153019054 T>C maps to NM_025107.2 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:153042955 T>C maps to NM_025107.2 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:38182704 C>A maps to NM_001172567.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:48444098 T>A maps to NM_016132.3 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:48458135 A>G maps to NM_016132.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:48441449 G>A maps to NM_016132.3 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:48444475 C>A maps to NM_016132.3 G365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr15:48443670 A>G maps to NM_016132.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:69063726 G>A maps to NM_138768.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:69063084 G>A maps to NM_138768.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:69062907 C>A maps to NM_138768.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:69063096 C>T maps to NM_138768.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:241073379 C>A maps to NM_138336.1 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:241073418 C>A maps to NM_138336.1 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:81111051 G>A maps to NM_005593.2 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:81110889 C>T maps to NM_005593.2 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:81110889 C>T maps to NM_005593.2 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:81110958 C>T maps to NM_005593.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:81112814 C>T maps to NM_005593.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:81101836 C>T maps to NM_002469.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:81101668 C>T maps to NM_002469.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:81101836 C>T maps to NM_002469.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:81102373 C>T maps to NM_002469.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:81101836 C>T maps to NM_002469.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:81101836 C>T maps to NM_002469.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:10408616 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:10411989 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10400423 C>A maps to NM_005963.3 E1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10400700 G>A maps to NM_005963.3 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10411893 T>C maps to NM_005963.3 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10415161 G>T maps to NM_005963.3 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:10415203 C>T maps to NM_005963.3 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:10405137 C>A maps to NM_005963.3 E1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:10406060 C>A maps to NM_005963.3 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:10419659 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:10417436 C>A maps to NM_005963.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:10419572 T>C maps to NM_005963.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:10398577 C>T maps to NM_005963.3 Q1742Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A5-A0VP-01A-21D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:8379142 C>T maps to ENST00000360416 T2001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:8397074 C>T maps to ENST00000360416 K1395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:8457294 G>A maps to ENST00000360416 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:8381706 G>T maps to ENST00000360416 I1885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:8439125 G>A maps to ENST00000360416 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:8413227 G>A maps to ENST00000360416 Q998*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BS-A0UF-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:8395664 G>A maps to ENST00000360416 R1541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:8381681 G>A maps to ENST00000360416 R1894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:8416950 C>A maps to ENST00000360416 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:8526264 G>A maps to ENST00000360416 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr16:15847281 G>A maps to NM_001040114.1 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:15814758 G>A maps to NM_001040114.1 F1583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr16:15813108 C>T maps to NM_001040114.1 L1720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:15850311 C>T maps to NM_001040114.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:15878553 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:15814758 G>A maps to NM_001040114.1 F1583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:15826558 C>T maps to NM_001040114.1 K1178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:15814758 G>A maps to NM_001040114.1 F1583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:15814848 C>T maps to NM_001040114.1 T1553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:15835507 G>A maps to NM_001040114.1 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:15854401 C>A maps to NM_001040114.1 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:15872637 G>A maps to NM_001040114.1 T270T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BG-A0LX-01A-11W-A062-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr16:15818053 C>T maps to NM_001143979.1 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr16:15844129 G>A maps to NM_001040114.1 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:15854401 C>A maps to NM_001040114.1 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:15802673 C>T maps to NM_001040113.1 S1944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:15814758 G>A maps to NM_001040114.1 F1583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:15831462 C>A maps to NM_001040114.1 E1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr16:15829236 A>G maps to NM_001040114.1 T1171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr16:15829296 G>A maps to NM_001040114.1 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:10267772 G>A maps to NM_003802.2 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:10204884 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:10213081 G>A maps to NM_003802.2 S1574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:10247366 G>T maps to NM_003802.2 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:10213111 G>A maps to NM_003802.2 R1564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:10212663 G>A maps to NM_003802.2 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:10223759 C>T maps to NM_003802.2 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10263502 G>A maps to NM_003802.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10265585 G>T maps to NM_003802.2 Y118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:10261056 T>A maps to NM_003802.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:10267751 G>A maps to NM_003802.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:10248789 G>T maps to NM_003802.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:10265486 G>A maps to NM_003802.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:10243692 G>A maps to NM_003802.2 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr17:10216653 C>T maps to NM_003802.2 A1334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr17:10247165 C>T maps to NM_003802.2 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr17:10216010 G>A maps to NM_003802.2 C1415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:10223704 C>A maps to NM_003802.2 E1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:10219221 G>A maps to NM_003802.2 Q1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:10223477 C>A maps to NM_003802.2 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:10248557 G>A maps to NM_003802.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:10209947 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:10250058 G>A maps to NM_003802.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:10253951 C>T maps to NM_003802.2 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:50783319 G>A maps to NM_001145809.1 A1353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50726364 C>T maps to NM_001145809.1 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50770175 C>T maps to NM_001145809.1 Q913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:50713889 C>T maps to NM_001145809.1 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:50758525 G>A maps to NM_001145809.1 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr19:50755951 C>T maps to NM_001145809.1 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr19:50753884 C>T maps to NM_001145809.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:50774730 G>A maps to NM_001145809.1 T1033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:50713972 C>T maps to NM_001145809.1 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:108172883 G>A maps to NM_014981.1 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr3:108224617 T>C maps to NM_014981.1 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:108188906 G>A maps to NM_014981.1 C532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:108124194 C>A maps to NM_014981.1 E1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:108156432 G>A maps to NM_014981.1 S1083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:108163623 C>A maps to NM_014981.1 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:108224632 G>A maps to NM_014981.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:108110671 G>A maps to NM_014981.1 L1809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:10443281 C>T maps to NM_017534.5 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:10447241 C>A maps to NM_017534.5 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10433229 A>G maps to NM_017534.5 C953C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10451104 C>A maps to NM_017534.5 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:10434981 C>A maps to NM_017534.5 E889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr17:10428767 G>A maps to NM_017534.5 Q1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:10432486 C>A maps to NM_017534.5 E1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:10446200 C>A maps to NM_017534.5 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr17:10447072 G>C maps to NM_017534.5 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:10547727 C>T maps to NM_002470.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:10543992 G>A maps to NM_002470.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:10553001 G>A maps to NM_002470.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:10543318 T>C maps to NM_002470.2 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10536041 C>A maps to NM_002470.2 V1569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:10541192 C>T maps to NM_002470.2 K1263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:10549320 G>A maps to NM_002470.2 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:10533658 G>A maps to NM_002470.2 A1801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:10551926 G>A maps to NM_002470.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:10537011 C>A maps to NM_002470.2 E1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:10543344 C>A maps to NM_002470.2 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr17:10352297 A>C maps to NM_017533.2 A1416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:10352034 C>T maps to NM_017533.2 E1477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:10368885 G>A maps to NM_017533.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:10351338 G>A maps to NM_017533.2 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:10363558 G>A maps to NM_017533.2 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10366475 G>A maps to NM_017533.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10368789 G>A maps to NM_017533.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:10348291 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:10367893 A>C maps to NM_017533.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:10348120 G>T maps to NM_017533.2 L1854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:10356555 C>T maps to NM_017533.2 Q1008Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:10362606 G>A maps to NM_017533.2 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:10352279 C>T maps to NM_017533.2 K1422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:10363546 G>A maps to NM_017533.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr17:10352031 C>T maps to NM_017533.2 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:10355524 G>A maps to NM_017533.2 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:10367851 G>T maps to NM_017533.2 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:10348367 C>T maps to NM_017533.2 L1797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:23855526 C>T maps to NM_002471.3 L1652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:23874883 G>T maps to NM_002471.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:23876243 G>A maps to NM_002471.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:23869470 G>A maps to NM_002471.3 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:23869929 G>A maps to NM_002471.3 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:23866209 G>A maps to NM_002471.3 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:23869482 G>A maps to NM_002471.3 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:23863306 C>T maps to NM_002471.3 E885E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr14:23866242 G>A maps to NM_002471.3 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:23859508 G>A maps to NM_002471.3 I1163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:23862682 G>A maps to NM_002471.3 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:23863357 G>A maps to NM_002471.3 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:23863429 G>A maps to NM_002471.3 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:23858685 C>T maps to NM_002471.3 A1298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:23870130 C>T maps to NM_002471.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:23851749 G>A maps to NM_002471.3 L1895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:23889131 C>T maps to NM_000257.2 K1216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:23901905 G>A maps to NM_000257.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:23883021 G>A maps to NM_000257.2 I1912I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:23896947 G>T maps to NM_000257.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:23886422 G>A maps to NM_000257.2 N1486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:23889158 G>A maps to NM_000257.2 I1207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:23894612 G>A maps to NM_000257.2 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr14:23884311 C>T maps to NM_000257.2 A1817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:23883050 G>A maps to NM_000257.2 L1903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr14:23888456 G>A maps to NM_000257.2 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr14:23902427 G>A maps to NM_000257.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr14:23886118 C>T maps to NM_000257.2 E1534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr14:23899002 C>T maps to NM_000257.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:23886132 G>A maps to NM_000257.2 R1530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:23902376 G>A maps to NM_000257.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr14:23887567 G>A maps to NM_000257.2 C1340C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr20:33584222 G>A maps to NM_020884.3 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:33570345 G>A maps to NM_020884.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr20:33568514 C>T maps to NM_020884.3 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:33578555 C>T maps to NM_020884.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr20:33584522 T>G maps to NM_020884.3 A1118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:33568433 C>A maps to NM_020884.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:33584192 G>T maps to NM_020884.3 V1038V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:33586108 G>A maps to NM_020884.3 E1295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:33574719 C>T maps to NM_020884.3 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:33581219 G>A maps to NM_020884.3 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:33576004 C>T maps to NM_020884.3 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr20:33577712 C>T maps to NM_020884.3 Y628Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:10304726 G>A maps to NM_002472.2 T991T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:10310212 A>G maps to NM_002472.2 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr17:10307664 C>T maps to NM_002472.2 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:10304271 C>A maps to NM_002472.2 E1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:10304474 G>A maps to NM_002472.2 R1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:10299771 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:10309588 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr17:10312470 C>T maps to NM_002472.2 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:10301855 C>T maps to NM_002472.2 Q1361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:10301909 G>A maps to NM_002472.2 C1343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:10304220 C>A maps to NM_002472.2 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:10303991 G>A maps to NM_002472.2 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:10322055 G>A maps to NM_002472.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:36681201 A>G maps to NM_002473.4 I1816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:36716406 G>A maps to NM_002473.4 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:36716899 C>A maps to NM_002473.4 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr22:36681936 G>A maps to NM_002473.4 D1708D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr22:36691021 G>A maps to NM_002473.4 Q1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:36681954 C>T maps to NM_002473.4 E1702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:36696277 G>A maps to NM_002473.4 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:211158525 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:211167230 G>A maps to NM_079420.2 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr2:211179706 C>A maps to NM_079420.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:101259513 G>A maps to NM_138403.4 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:101267463 C>T maps to NM_138403.4 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:3255762 C>A maps to NM_006471.2 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:111348946 G>A maps to NM_000432.3 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:45297349 C>T maps to NM_002476.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr17:45286871 C>A maps to NM_002476.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:672841 G>A maps to ENST00000513662 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:672538 C>T maps to NM_002477.1 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:56548598 C>T maps to NM_002475.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr12:56551276 G>A maps to NM_002475.4 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:44179032 T>C maps to ENST00000446581 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr20:35176483 G>A maps to NM_006097.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:16145247 A>G maps to NM_013262.3 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:123419104 G>A maps to NM_053025.3 D1070D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:123451944 G>A maps to NM_053025.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr3:123383093 G>A maps to NM_053025.3 S1281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:123426707 G>T maps to NM_053025.3 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:123337603 T>C maps to NM_053025.3 Q1794Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr3:123411621 G>A maps to NM_053025.3 D1175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:123426686 G>A maps to NM_053025.3 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:30421539 C>T maps to NM_033118.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:30414692 C>T maps to NM_033118.3 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr20:30408196 C>T maps to NM_033118.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:2679680 G>A maps to ENST00000268446 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:2685564 G>A maps to NM_001012418.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:2749474 C>T maps to NM_001012418.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:169496756 A>G maps to NM_018657.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:169497146 G>A maps to NM_018657.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:169497264 G>T maps to NM_018657.4 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr3:169501295 G>C maps to NM_018657.4 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr5:16670991 A>C maps to NM_012334.2 Y1842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr5:16673853 C>A maps to NM_012334.2 T1703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:16675127 G>A maps to NM_012334.2 R1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:16701802 G>A maps to NM_012334.2 Q901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:16755014 G>A maps to NM_012334.2 D617D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:16668424 G>A maps to NM_012334.2 I2012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:16673970 C>T maps to NM_012334.2 E1664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:16676254 G>T maps to NM_012334.2 C1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:16769224 C>A maps to NM_012334.2 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:16672834 G>A maps to NM_012334.2 R1758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:16681496 G>A maps to NM_012334.2 N1435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:16701922 C>A maps to NM_012334.2 E861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:16701653 G>T maps to NM_012334.2 I950I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:16670649 C>T maps to NM_012334.2 T1956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:16701874 C>A maps to NM_012334.2 E877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:16694658 G>A maps to NM_012334.2 F1207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:16818216 C>T maps to NM_012334.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:16672856 G>A maps to NM_012334.2 H1750H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr5:16762722 G>T maps to NM_012334.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:18067132 C>A maps to ENST00000205890 I3256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:18059601 G>A maps to ENST00000205890 A2851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:18049346 G>A maps to ENST00000205890 E2145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:18051828 G>A maps to ENST00000205890 P2237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:18055204 G>A maps to ENST00000205890 E2611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr17:18060278 C>T maps to ENST00000205890 Y2871Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:18054220 C>T maps to ENST00000205890 P2489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr17:18045515 C>T maps to ENST00000205890 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:18024993 G>A maps to ENST00000205890 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr17:18045434 C>T maps to ENST00000205890 R1898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:18082108 C>T maps to ENST00000205890 A3506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:18064643 C>T maps to ENST00000205890 R3134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:18025221 G>A maps to ENST00000205890 K1036K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:18034584 C>T maps to ENST00000205890 F1357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:18040944 C>T maps to ENST00000205890 N1609N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:18044099 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:18051501 G>A maps to ENST00000205890 A2223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr17:18035774 C>T maps to ENST00000205890 N1405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:109672231 C>A maps to NM_015011.1 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:109318423 G>A maps to NM_015011.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:109661345 A>G maps to NM_015011.1 E826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr13:109779689 C>T maps to NM_015011.1 A1259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:109831938 G>A maps to NM_015011.1 G1769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:109318318 G>C maps to NM_015011.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:109704684 G>A maps to NM_015011.1 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr13:109793503 C>T maps to NM_015011.1 A1626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:109318318 G>A maps to NM_015011.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:109704684 G>A maps to NM_015011.1 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:27448729 G>A maps to NM_078471.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:27493373 C>T maps to NM_078471.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:27425843 G>A maps to NM_078471.3 D1260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr17:27419898 G>A maps to NM_078471.3 R1683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:27442682 T>A maps to NM_078471.3 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:27425882 G>A maps to NM_078471.3 I1247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:27434172 G>A maps to NM_078471.3 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:27424908 G>A maps to NM_078471.3 Y1333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:26423547 C>T maps to ENST00000407587 D2538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:26400783 C>T maps to ENST00000407587 R2147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:26423187 G>A maps to ENST00000407587 E2418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr22:26228933 C>T maps to ENST00000407587 T1012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr22:26164431 C>T maps to ENST00000407587 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:26423518 C>T maps to ENST00000407587 R2529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:26224835 G>A maps to ENST00000407587 A962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:26273939 G>A maps to ENST00000407587 T1415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:26351275 C>T maps to ENST00000407587 D2036D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:26399264 C>T maps to ENST00000407587 R2110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr22:26351221 G>A maps to ENST00000407587 Q2018Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr22:26222379 C>G maps to ENST00000407587 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:26164251 C>A maps to ENST00000407587 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:26164524 G>A maps to ENST00000407587 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:34862951 G>A maps to NM_001163735.1 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:34861201 C>T maps to NM_001163735.1 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:34869478 G>A maps to NM_001163735.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:34869277 G>T maps to NM_001163735.1 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr17:34869253 C>T maps to NM_001033580.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:34852153 G>A maps to NM_001163735.1 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:34867239 C>A maps to NM_001163735.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:34852166 G>A maps to NM_001163735.1 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:34854313 C>T maps to NM_001163735.1 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:34857025 G>A maps to NM_001163735.1 D710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:57440381 G>A maps to NM_005379.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:57437787 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:57442127 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:57441501 G>A maps to NM_005379.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:57430618 C>T maps to NM_005379.2 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:192252125 C>T maps to NM_001130158.1 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:192141710 C>A maps to NM_001130158.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:192228518 A>G maps to NM_001130158.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:192255134 C>A maps to NM_001130158.1 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:192255111 C>T maps to NM_001130158.1 R626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:192248003 A>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:1370832 C>T maps to NM_001080779.1 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:31087409 G>A maps to NM_015194.1 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:31075975 G>A maps to NM_015194.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:31087348 C>A maps to NM_015194.1 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:31039082 G>A maps to NM_015194.1 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:59466361 G>A maps to NM_004998.2 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:59445849 G>A maps to NM_004998.2 R1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:59502774 T>G maps to NM_004998.2 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:59510098 G>A maps to NM_004998.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:59430409 A>G maps to NM_004998.2 D1079D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr15:59516938 G>A maps to NM_004998.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:59466007 G>A maps to NM_004998.2 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:59501032 G>T maps to NM_004998.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:8615467 G>A maps to NM_012335.3 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:8595421 G>A maps to NM_012335.3 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:8612973 G>A maps to NM_012335.3 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:8613156 G>A maps to NM_012335.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:8612925 G>A maps to NM_012335.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:8615485 G>A maps to NM_012335.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:8618064 G>A maps to NM_012335.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:8595361 G>A maps to NM_012335.3 Y713Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:8595115 G>A maps to NM_012335.3 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:8609297 G>A maps to NM_012335.3 H469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:8613156 G>A maps to NM_012335.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:8595190 G>A maps to NM_012335.3 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:8612994 G>A maps to NM_012335.3 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:8616641 G>A maps to NM_012335.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:8618245 G>A maps to NM_012335.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:45004046 G>A maps to NM_033054.2 F866F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:45006353 G>A maps to NM_033054.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:45004019 G>A maps to NM_033054.2 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:45005291 C>T maps to NM_033054.2 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:45010463 C>T maps to NM_033054.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr7:45005712 G>A maps to NM_033054.2 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr7:45015244 G>A maps to NM_033054.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:45009016 G>A maps to NM_033054.2 D523D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:109839040 C>T maps to NM_001101421.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:109879448 C>T maps to NM_001101421.3 I840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:109882289 C>T maps to NM_001101421.3 V967V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:109870700 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:109845745 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr12:109826582 C>T maps to NM_001101421.3 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:109826588 C>T maps to NM_001101421.3 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:109870710 C>A maps to NM_001101421.3 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:26385499 C>T maps to NM_017433.4 Y555Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:26465694 G>A maps to NM_017433.4 Q1453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:26500837 C>T maps to NM_017433.4 F1599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr10:26436438 C>T maps to NM_017433.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:26315377 T>A maps to NM_017433.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:26377187 C>A maps to NM_017433.4 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:26414327 T>C maps to NM_017433.4 C635C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:26385313 G>T maps to NM_017433.4 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:26463290 G>A maps to NM_017433.4 L1366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:26315345 G>T maps to NM_017433.4 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:26357704 C>A maps to NM_017433.4 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:26465647 G>T maps to NM_017433.4 E1438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:26241068 C>A maps to NM_017433.4 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:26465647 G>T maps to NM_017433.4 E1438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:26286167 A>T maps to NM_017433.4 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:26492001 G>T maps to NM_017433.4 E1566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:171259405 C>T maps to NM_138995.3 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:171092514 G>A maps to NM_138995.3 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:171256756 C>T maps to NM_138995.3 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:171256756 C>T maps to NM_138995.3 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:171056671 G>T maps to NM_138995.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:171256756 C>T maps to NM_138995.3 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr2:171258201 G>A maps to ENST00000317915 W709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:171256756 C>T maps to NM_138995.3 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:171243707 G>A maps to NM_138995.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:171248959 C>T maps to NM_138995.3 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:52672035 C>T maps to ENST00000358212 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:52615556 C>A maps to ENST00000358212 E1599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:52662388 G>A maps to ENST00000358212 R1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr15:52611396 C>T maps to ENST00000358212 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:52605945 C>A maps to ENST00000358212 E1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:52659252 G>A maps to ENST00000358212 I1045I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr15:52641024 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr15:52662538 G>A maps to ENST00000358212 R965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:52643531 G>A maps to ENST00000358212 S1256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:52689483 G>T maps to ENST00000358212 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:52688554 G>A maps to ENST00000358212 C453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:52620131 G>A maps to ENST00000358212 R1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr15:52681433 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:47500802 G>A maps to NM_001080467.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr18:47500856 C>T maps to NM_001080467.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr18:47379827 G>A maps to NM_001080467.2 N1404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:47500877 G>A maps to NM_001080467.2 Y388Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:47421508 G>A maps to NM_001080467.2 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:47566621 G>T maps to NM_001080467.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:47389646 A>G maps to NM_001080467.2 V1298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:47480727 G>A maps to NM_001080467.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:47365601 G>A maps to NM_001080467.2 T1588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:47518777 G>A maps to NM_001080467.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:47404156 A>T maps to NM_001080467.2 T1124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr18:47390600 G>A maps to NM_001080467.2 H1251H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr18:47480806 T>C did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr18:47581651 G>A maps to NM_001080467.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:52517723 G>T maps to NM_018728.3 I1071I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:52543639 C>A maps to NM_018728.3 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:52536688 G>A maps to NM_018728.3 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:52486107 A>G maps to NM_018728.3 N1740N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:52538196 G>A maps to NM_018728.3 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:76558213 A>C maps to ENST00000428345 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:76624711 C>T maps to ENST00000428345 Q1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:76566843 T>C maps to ENST00000428345 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:76558135 G>A maps to ENST00000428345 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:76591411 G>T maps to ENST00000428345 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:76596584 C>T maps to ENST00000428345 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:76901162 G>A maps to NM_000260.3 P1243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:76905481 C>T maps to NM_000260.3 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:76870491 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:76873339 C>A maps to NM_000260.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:76868004 G>A maps to NM_000260.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:76886419 C>T maps to NM_000260.3 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:76917165 G>A maps to NM_000260.3 P1887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:76900499 C>T maps to NM_000260.3 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr11:76893629 G>A maps to NM_000260.3 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:128331543 G>A maps to ENST00000389524 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:128393412 C>T maps to ENST00000389524 V1954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:128335787 C>T maps to ENST00000389524 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:128321786 C>T maps to ENST00000389524 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:128390928 C>T maps to ENST00000389524 D1809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr2:128370145 C>T maps to ENST00000389524 I1096I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:128345976 G>A maps to ENST00000389524 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:128327423 C>T maps to ENST00000389524 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:128334252 C>T maps to ENST00000389524 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:128384849 C>A maps to ENST00000389524 L1449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:128394397 G>A maps to ENST00000389524 K2054K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:128387254 C>T maps to ENST00000389524 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:128331573 C>T maps to ENST00000389524 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:128338330 C>T maps to ENST00000389524 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:128339542 G>T maps to ENST00000389524 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr2:128363481 C>A maps to ENST00000389524 C801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:72146757 C>T maps to ENST00000424560 S2173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:72193585 G>T maps to ENST00000424560 V1032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:72119283 G>A maps to ENST00000424560 V2499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:72154895 G>A maps to ENST00000424560 Y2083Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:72208708 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:72190135 C>A maps to ENST00000424560 E1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:17273841 C>T maps to NM_004145.3 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:17311161 C>T maps to NM_004145.3 G1433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:17291735 C>T maps to NM_004145.3 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:17309108 C>T maps to NM_004145.3 V1410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:17313981 C>T maps to NM_004145.3 F1635F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:17316099 C>T maps to NM_004145.3 C1673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:17283271 G>A maps to NM_004145.3 V640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:17321594 C>T maps to NM_004145.3 G1956G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:17273272 C>T maps to NM_004145.3 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:17273227 G>A maps to NM_004145.3 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:17283259 C>T maps to NM_004145.3 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:17317183 C>T maps to NM_004145.3 V1795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr19:17291837 C>T maps to NM_004145.3 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:171605765 G>A maps to NM_000261.1 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr17:12639553 G>A maps to NM_001146312.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:12655808 C>T maps to NM_001146312.1 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:12647660 G>A maps to NM_001146312.1 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:12639538 C>T maps to NM_001146312.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:12666894 C>T maps to NM_001146312.1 I965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:12656374 A>G maps to NM_001146312.1 Q590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:17741457 C>T maps to NM_002478.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:95069866 G>A maps to NM_013451.3 I2019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:95121311 G>A maps to NM_013451.3 N957N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:95159232 C>T maps to NM_013451.3 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr10:95115442 C>T maps to NM_013451.3 K1115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:95089472 G>A maps to NM_013451.3 R1644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:95134653 G>A maps to NM_013451.3 R723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:95111508 G>A maps to NM_013451.3 F1192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:95111301 G>A maps to NM_013451.3 S1230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:203055008 G>A maps to NM_002479.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:203054720 G>A maps to NM_002479.4 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:3116478 C>T maps to NM_003803.3 R1051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:3134676 G>T maps to NM_003803.3 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:3164278 G>A maps to NM_003803.3 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:3142038 C>T maps to NM_003803.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:3067448 G>A maps to NM_003803.3 F1623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:3094274 C>A maps to NM_003803.3 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:3100369 G>A maps to NM_003803.3 C1210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:3131412 A>T maps to NM_003803.3 Y822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:3164278 G>A maps to NM_003803.3 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:3188780 G>A maps to NM_003803.3 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:3141948 G>T maps to NM_003803.3 Y671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:3189035 C>A maps to NM_003803.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr18:3079333 G>A maps to NM_003803.3 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:3164278 G>A maps to NM_003803.3 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr8:2088762 C>T maps to NM_003970.2 F1306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr8:2071147 C>T maps to NM_003970.2 T1159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:2071480 C>T maps to NM_003970.2 G1207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:2077193 C>T maps to NM_003970.2 D1258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:2044162 G>A maps to NM_003970.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:2088657 C>A maps to NM_003970.2 I1271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:2071142 G>T maps to NM_003970.2 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:2050458 C>A maps to NM_003970.2 V874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:2065710 G>A maps to NM_003970.2 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:2088762 C>T maps to NM_003970.2 F1306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:2065710 G>A maps to NM_003970.2 T1141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:1998972 A>G maps to NM_003970.2 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:2063841 C>T maps to NM_003970.2 Q1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:2092607 G>A maps to NM_003970.2 T1367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:2000350 G>A maps to NM_003970.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr8:2037976 G>T maps to NM_003970.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:24432468 C>T maps to ENST00000330966 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:24413251 G>A maps to ENST00000330966 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:24426188 G>A maps to ENST00000330966 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:24388445 G>T maps to ENST00000330966 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:24433625 G>A maps to ENST00000330966 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:24397701 G>A maps to ENST00000330966 R1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:24400739 C>A maps to ENST00000330966 E961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:24388599 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:24417404 G>A maps to ENST00000330966 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:24417404 G>A maps to ENST00000330966 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:75397603 C>T maps to NM_021245.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:69934350 G>A maps to NM_032578.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:69948678 C>T maps to NM_032578.2 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:69959198 G>A maps to NM_032578.2 K1120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:69881449 C>T maps to NM_032578.2 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:69881861 G>T maps to NM_032578.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:69881405 G>T maps to NM_032578.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr10:69955260 C>A maps to NM_032578.2 R1044R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:69955231 T>A maps to NM_032578.2 L1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:69881326 C>T maps to NM_032578.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:40085744 C>T maps to NM_015460.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:40211446 C>T maps to NM_015460.2 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:40085636 G>A maps to NM_015460.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:40251478 T>C maps to NM_015460.2 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:40204301 G>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:40231458 C>T maps to NM_015460.2 Y390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:59132738 G>A maps to NM_001085487.1 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:59147934 C>A maps to NM_001085487.1 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:59133516 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:59147838 C>A maps to NM_001085487.1 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:62871695 C>T maps to NM_004535.2 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:62854670 G>A maps to NM_004535.2 K829K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:62839374 G>T maps to NM_004535.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr20:62863621 G>A maps to NM_004535.2 G927G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:1842964 G>A maps to ENST00000399161 C1012C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:1926427 C>T maps to ENST00000399161 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:1895991 G>A maps to ENST00000399161 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:1926853 G>T maps to ENST00000399161 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:1946754 G>A maps to ENST00000399161 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:1983497 G>A maps to ENST00000399161 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:1926388 C>T maps to ENST00000399161 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:1805565 C>A maps to ENST00000399161 E1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:1890317 C>A maps to ENST00000399161 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:1926268 G>A maps to ENST00000399161 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:1906993 C>T maps to ENST00000399161 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:1891377 C>A maps to ENST00000399161 E842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:1896006 G>A maps to ENST00000399161 Y695Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:59082702 C>T maps to NM_198055.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:59080674 C>T maps to NM_198055.1 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:48580065 G>A maps to NM_153029.3 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:48595185 T>C maps to NM_153029.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:48585337 G>T maps to NM_153029.3 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:48585328 G>A maps to NM_153029.3 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:48595437 T>C maps to NM_153029.3 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:40133539 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:40103770 C>T maps to NM_018177.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:40124820 G>T maps to NM_018177.3 E1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:40146307 C>A maps to NM_018177.3 I1677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:40146334 G>A maps to NM_018177.3 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:40099125 G>T maps to NM_018177.3 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:40133419 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:40146328 G>A maps to NM_018177.3 S1684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr4:40124795 G>A maps to NM_018177.3 A1416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:40123634 G>T maps to NM_018177.3 E1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:32977189 G>A maps to NM_052818.2 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:32977198 C>T maps to NM_052818.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:32978344 C>A maps to NM_001079691.1 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:33016948 A>C maps to NM_033111.3 Y575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:33092050 G>T maps to NM_033111.3 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:33016681 A>G maps to NM_033111.3 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:177547465 C>T maps to NM_015111.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:177547387 C>T maps to NM_015111.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:30248810 C>A maps to NM_013240.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr21:30252189 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:30248810 C>A maps to NM_013240.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:21306150 C>A maps to NM_174928.1 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:21331635 G>A maps to NM_174928.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:21331604 C>A maps to NM_174928.1 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:21306204 C>A maps to NM_174928.1 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:21331635 G>A maps to NM_174928.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:21303260 G>A maps to NM_174928.1 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:153195636 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr23:153199857 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:140306111 C>A maps to NM_057175.3 S761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:140264093 G>T maps to NM_057175.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:140306064 G>A maps to NM_057175.3 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:140270694 C>T maps to NM_057175.3 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:140306064 G>A maps to NM_057175.3 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:140272759 G>T maps to NM_057175.3 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr4:140263991 C>T maps to NM_057175.3 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:41943310 G>A maps to NM_024561.4 K613K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:41932461 G>A maps to NM_024561.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:41946361 C>A maps to NM_024561.4 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr13:41947887 C>T maps to NM_024561.4 N757N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:41947822 G>T maps to NM_024561.4 E736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:41943242 G>T maps to NM_024561.4 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:41936196 G>T maps to NM_024561.4 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr13:41899892 G>A maps to NM_024561.4 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:20007507 C>T maps to NM_016100.3 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:20013244 G>A maps to NM_016100.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr20:20007524 T>C maps to NM_016100.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:20006395 G>T maps to NM_016100.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:112509854 C>A maps to NM_024953.3 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:112516536 C>T maps to NM_024953.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:112471068 C>A maps to NM_024953.3 E922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:112481548 C>T maps to NM_024953.3 K710K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:112492279 G>A maps to NM_024953.3 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:112499138 C>T maps to NM_024953.3 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:112499020 C>A maps to NM_024953.3 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:112528620 G>T maps to NM_024953.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:112481610 G>A maps to NM_024953.3 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:112518861 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:57857737 G>A maps to NM_001011713.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr14:57876143 T>A maps to NM_001011713.2 Y333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:88633681 G>A maps to NM_024635.3 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr9:88628662 C>G maps to NM_024635.3 T473T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:117831990 G>T maps to NM_016200.4 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr7:117825748 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:63721842 C>T maps to NM_024771.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:113442889 T>G maps to NM_025146.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:76846890 G>A maps to NM_014435.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:76842252 G>A maps to NM_014435.3 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr4:76861236 G>A maps to NM_014435.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:64812877 T>C maps to ENST00000340252 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:64813874 C>A maps to ENST00000427272 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:174814659 C>T maps to NM_207015.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:175181198 C>T maps to NM_207015.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K0-01A-11W-A062-09 chr3:174814722 C>T maps to NM_207015.2 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:175293914 C>T maps to NM_207015.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr3:175184905 A>C maps to NM_207015.2 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:191551946 C>T maps to NM_005966.3 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:57485366 C>T maps to NM_005967.3 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:57485213 C>A maps to NM_005967.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr12:57485291 C>T maps to NM_005967.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:57112748 A>G maps to NM_001113203.1 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:57113582 G>A maps to NM_001113203.1 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:57114323 A>C maps to NM_001113203.1 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:13248997 C>T maps to NM_052876.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr19:13246887 C>T maps to NM_052876.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:1685085 G>T maps to ENST00000344463 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:71191889 C>T maps to NM_018161.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:66839818 C>A maps to ENST00000359087 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr16:66850555 A>G maps to ENST00000359087 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:66857469 C>A maps to ENST00000359087 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:66842481 C>T maps to ENST00000359087 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr4:164069550 C>T maps to NM_138386.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:164048187 G>A maps to NM_001128931.1 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:164050141 T>C maps to NM_138386.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:42463768 G>A maps to NM_000262.2 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:71305598 C>T maps to NM_017567.4 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr2:71297698 C>T maps to NM_017567.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr2:71298829 C>T maps to NM_017567.4 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:71300687 C>T maps to NM_017567.4 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr17:40696160 C>T maps to NM_000263.3 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:40693126 C>A maps to NM_000263.3 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:40695865 C>T maps to NM_000263.3 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K0-01A-11W-A062-09 chr16:5075658 C>T maps to NM_016256.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr13:101717778 G>A maps to NM_052867.2 D1527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:101833634 G>A maps to ENST00000376196 C606C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:101890180 G>A maps to NM_052867.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:101997749 T>C maps to NM_052867.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:101742109 G>T maps to NM_052867.2 I1131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:101736071 C>T maps to NM_052867.2 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:101881902 T>C maps to NM_052867.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:102047614 C>T maps to NM_052867.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:102047641 G>A maps to NM_052867.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:101881807 G>T maps to NM_052867.2 S521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:105915424 G>T maps to NM_005746.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr19:13988361 C>T maps to NM_001098622.1 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr20:25596671 A>G maps to NM_152667.2 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:100840538 C>T maps to NM_018946.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:100845298 G>T maps to NM_018946.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:72433612 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:72433306 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:72433163 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:72433578 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:72434282 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:72434246 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:72433252 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:72433913 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:72434158 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:72433245 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:72434020 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:72433306 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:72433923 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:92927568 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:92928264 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:92928062 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:92928236 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:92927594 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:92927486 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:92927864 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:92926977 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:92928248 C>T did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:92926833 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:2997296 G>A maps to ENST00000399624 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:2976985 A>G maps to ENST00000399624 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr11:2975807 G>T maps to ENST00000399624 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:2975770 C>A maps to ENST00000399624 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:2997258 G>A maps to ENST00000399624 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:2972530 G>A maps to ENST00000399624 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:2997296 G>A maps to ENST00000399624 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:89618473 G>A maps to NM_153757.2 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:47991634 G>A maps to NM_003827.2 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:47996259 C>T maps to NM_003827.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:48003992 C>T maps to NM_003827.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr19:47995334 G>A maps to NM_003827.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:102760025 C>T maps to ENST00000455523 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:102760657 C>A maps to ENST00000455523 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:144657670 G>A maps to ENST00000276844 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr8:144657498 G>A maps to ENST00000276844 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:144659342 G>A maps to ENST00000276844 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr8:144657593 G>A maps to ENST00000276844 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr19:50862270 G>T maps to NM_004851.1 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:50862330 G>A maps to NM_004851.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:80422165 G>T maps to ENST00000374611 G38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:80430506 C>T maps to ENST00000374611 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:782341 G>A maps to NM_022493.1 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:789674 C>A maps to NM_022493.1 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:60748861 G>A maps to NM_024611.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:60745903 G>T maps to NM_024611.4 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:60760322 G>A maps to NM_024611.4 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:60745903 G>T maps to NM_024611.4 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:60747575 G>A maps to NM_024611.4 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:55283185 C>A maps to NM_004539.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:55274765 G>A maps to NM_004539.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:46073248 G>A maps to NM_002482.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:46073566 G>A maps to NM_002482.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:34158211 C>T maps to NM_024662.2 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:34145923 C>T maps to NM_024662.2 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:34154664 T>C maps to NM_024662.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:34129865 C>T maps to NM_024662.2 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr11:34129796 C>T maps to NM_024662.2 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:50334432 G>A maps to NM_012191.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:201755601 C>T maps to ENST00000367296 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:201778598 C>A maps to ENST00000367296 G1445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:201687544 C>T maps to ENST00000367296 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:201759816 C>T maps to ENST00000367296 Q1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:201777083 C>T maps to ENST00000367296 R1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:201750231 C>T maps to ENST00000367296 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:201682024 C>T maps to ENST00000367296 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:201762973 C>T maps to ENST00000367296 R1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:201618224 G>A maps to ENST00000367296 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:20127103 G>A maps to ENST00000396087 E2283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:20113855 G>A maps to ENST00000396087 P1978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:20099591 C>T maps to ENST00000396087 N1763N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:20127100 G>A maps to ENST00000396087 T2282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:20122628 C>A maps to ENST00000396087 R2169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:19914111 A>G maps to ENST00000396087 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:20119197 G>T maps to ENST00000396087 E2089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:19901610 G>A maps to ENST00000396087 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:20057531 C>T maps to ENST00000396087 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:19955427 G>A maps to ENST00000396087 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr11:19970407 C>T maps to ENST00000396087 N832N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:19955751 T>C maps to ENST00000396087 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:19970341 G>A maps to ENST00000396087 Q810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr11:19955322 G>A maps to ENST00000396087 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:78415620 C>T maps to NM_014903.4 Q668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:78513518 A>G maps to NM_014903.4 P1181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:78579469 C>T maps to NM_014903.4 R1906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:78562549 G>T maps to NM_014903.4 E1629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:78574653 G>T maps to NM_014903.4 E1819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:78516052 G>A maps to NM_014903.4 P1361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:78400725 G>T maps to NM_014903.4 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:78513542 G>A maps to NM_014903.4 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:78540154 G>T maps to NM_014903.4 E1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:78452856 C>T maps to NM_014903.4 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:78594319 G>A maps to NM_014903.4 W2239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:78593312 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:78444888 C>T maps to NM_014903.4 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:78392173 C>T maps to NM_014903.4 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:78562558 G>T maps to NM_014903.4 E1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:78334097 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:78360007 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:78593139 G>T maps to NM_014903.4 E2160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:78513503 G>A maps to NM_014903.4 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:15470889 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:15307192 G>A maps to NM_015909.2 R2365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:15679466 C>T maps to NM_015909.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:15514761 C>A maps to NM_015909.2 E1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:15427291 G>A maps to NM_015909.2 S1681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:15555768 C>T maps to NM_015909.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:15326949 C>T maps to NM_015909.2 T2209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:35692378 G>A maps to ENST00000400445 K699K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:35733259 C>T maps to ENST00000400445 I984I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:36124664 C>T maps to ENST00000400445 R2213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:35644112 T>C maps to ENST00000400445 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:36202286 C>T maps to ENST00000400445 R2507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr13:35716411 A>G maps to ENST00000400445 K781K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:35751131 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:36223883 C>A maps to ENST00000400445 T2600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:36125115 C>A maps to ENST00000400445 V2251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr13:35672508 A>G maps to ENST00000400445 K549K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:35733259 C>T maps to ENST00000400445 I984I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr13:35619114 C>A maps to ENST00000400445 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:35733741 C>A maps to ENST00000400445 S1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr13:35734111 C>T maps to ENST00000400445 D1268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:35615081 G>T maps to ENST00000400445 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:35692367 C>T maps to ENST00000400445 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr13:35733685 T>C maps to ENST00000400445 N1126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:35615081 G>T maps to ENST00000400445 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:204000890 G>A maps to NM_001114132.1 S1406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:204000623 C>A maps to NM_001114132.1 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:204002959 C>T maps to NM_001114132.1 N1518N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:204037514 C>T maps to NM_001114132.1 R2059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:203914575 T>C maps to NM_001114132.1 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:203948034 G>T maps to NM_001114132.1 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:203995129 T>C maps to NM_001114132.1 N1136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:204013737 C>T maps to NM_001114132.1 R1748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:204067504 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:203933114 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:204034490 C>T maps to NM_001114132.1 R1978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:203990779 C>A maps to NM_001114132.1 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:204037555 C>T maps to NM_001114132.1 N2072N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:204045183 G>T maps to NM_001114132.1 E2153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:203995184 G>T maps to NM_001114132.1 E1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:203996721 G>A maps to NM_001114132.1 T1168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:204001462 G>T maps to NM_001114132.1 E1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:47041650 G>A maps to NM_015175.1 T1354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:47049304 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:47030238 G>A maps to NM_015175.1 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:47037426 C>T maps to NM_015175.1 C679C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:47039651 A>G maps to NM_015175.1 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:19981561 C>T maps to NM_182744.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:90960059 C>A maps to NM_002485.4 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:90967654 G>T maps to NM_002485.4 S418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:16913692 A>C maps to NM_017940.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:16913704 T>C maps to NM_017940.3 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:16901183 C>T maps to NM_017940.3 E732E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:16913589 C>A maps to NM_017940.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:16890674 G>A maps to NM_017940.3 S1062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:16901177 C>T maps to NM_017940.3 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:16913589 C>A maps to NM_017940.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:148025815 G>A maps to ENST00000310701 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:148025815 G>A maps to ENST00000310701 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:148021592 C>A maps to ENST00000310701 G206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:21771693 G>T maps to NM_032264.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:21804792 C>T maps to NM_032264.2 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:21800013 C>T maps to NM_032264.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:120384161 G>T maps to NM_001047980.1 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:120379944 C>T maps to NM_001047980.1 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:120384183 C>G maps to NM_001047980.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:144828615 G>A maps to NM_001037675.2 P886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:144822043 A>G maps to NM_001037675.2 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:144822052 A>G maps to NM_001037675.2 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:41341819 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:41348510 C>T maps to NM_005899.3 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:41338322 C>T maps to NM_005899.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:113076885 T>C maps to ENST00000316851 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:113126683 C>T maps to ENST00000316851 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:113126680 C>T maps to ENST00000316851 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr11:113078004 G>A maps to ENST00000316851 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:113102479 C>T maps to ENST00000316851 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:113075179 C>T maps to ENST00000316851 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:113085169 C>T maps to ENST00000316851 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:113103489 G>A maps to ENST00000316851 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:22707872 C>T maps to NM_004540.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:22746190 C>T maps to NM_004540.2 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:22696761 G>T maps to NM_004540.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:22746329 G>T maps to NM_004540.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:22804428 C>T maps to NM_004540.2 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:22658623 G>T maps to NM_004540.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:22696761 G>T maps to NM_004540.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:22782690 A>C maps to NM_004540.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:22881352 C>T maps to NM_004540.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:22910221 G>T maps to NM_004540.2 E820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr21:22804569 C>A maps to NM_004540.2 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:22790867 G>T maps to NM_004540.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:22658605 G>T maps to NM_004540.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:22804552 G>T maps to NM_004540.2 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:22790867 G>T maps to NM_004540.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:19356195 G>A maps to NM_004386.2 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:19359639 C>T maps to NM_004386.2 R1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:19344628 T>C maps to NM_004386.2 C1017C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:19335210 C>T maps to NM_004386.2 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19344691 C>T maps to NM_004386.2 F1038F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:19337618 C>A maps to NM_004386.2 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:19351487 C>A maps to NM_004386.2 T1162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:19338348 A>G maps to NM_004386.2 K640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:19327779 C>A maps to NM_004386.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:19356267 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:134073085 C>T maps to NM_015261.2 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:134073951 G>A maps to NM_015261.2 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:134037889 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr11:134051034 C>T maps to NM_015261.2 E832E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:134038878 C>A maps to NM_015261.2 E1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:134028309 G>A maps to NM_015261.2 C1316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:134054819 C>T maps to NM_015261.2 K771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr11:134022867 G>A maps to NM_015261.2 R1490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:134062672 C>T maps to NM_015261.2 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:134072708 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:17824681 G>T maps to NM_022346.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:17836071 G>T maps to NM_022346.3 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:17819655 G>T maps to NM_022346.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:17819699 C>T maps to NM_022346.3 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr4:17816536 T>C maps to NM_022346.3 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr4:17826606 C>G maps to NM_022346.3 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:158468348 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:158482636 G>A maps to NM_017760.5 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:158486102 C>T maps to NM_017760.5 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:158439162 C>T maps to NM_017760.5 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:158468201 C>T maps to NM_017760.5 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr7:158476039 G>A maps to NM_017760.5 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:158437051 C>T maps to NM_017760.5 E1103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:158482642 A>G maps to NM_017760.5 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:158464268 C>T maps to NM_017760.5 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:97031742 G>T maps to NM_015341.3 G610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:97020045 C>T maps to NM_015341.3 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:97024852 G>T maps to NM_015341.3 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50957141 C>T maps to NM_001185011.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:50956231 G>A maps to NM_001185011.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr22:50956003 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:100403100 G>A maps to NM_002486.4 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:100426659 A>G maps to NM_002486.4 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:100405600 G>T maps to NM_002486.4 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:100405548 G>A maps to NM_002486.4 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:100403115 T>C maps to NM_002486.4 N25N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:196664431 G>A maps to NM_007362.3 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:39688693 C>T maps to NM_001001414.1 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:39691012 C>T maps to NM_001001414.1 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:36025979 C>A maps to NM_001014839.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:172351690 G>A maps to NM_001146276.1 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:74197280 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:74197396 C>T maps to NM_000265.4 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:183543657 T>C maps to NM_001127651.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:183536424 C>A maps to NM_001127651.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr22:37271768 C>T maps to NM_013416.3 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:37263464 C>T maps to NM_013416.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:106471674 G>A maps to NM_001004720.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:183866907 C>T maps to NM_205842.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:183859609 A>C maps to NM_205842.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:183832074 G>T maps to NM_205842.1 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:183793627 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:183846022 G>A maps to NM_205842.1 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:54910704 C>T maps to NM_005337.4 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:54912711 A>T maps to NM_005337.4 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:54891609 G>T maps to NM_005337.4 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:54902243 G>C maps to NM_005337.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:54925333 G>A maps to NM_005337.4 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:54932727 C>T maps to NM_005337.4 R1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:54925973 A>G maps to NM_005337.4 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:54901635 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr12:54913005 G>A maps to NM_005337.4 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:54902171 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:54936411 T>C maps to NM_005337.4 P1109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:54911614 T>C maps to NM_005337.4 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:133489550 C>T maps to NM_207363.2 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr2:133543152 G>A maps to NM_207363.2 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:133541679 C>A maps to NM_207363.2 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr2:133554302 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr2:133542211 A>G maps to NM_207363.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:133540642 A>G maps to NM_207363.2 D1247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:50186234 G>A maps to NM_001037806.3 T1262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:50189688 G>A maps to NM_001037806.3 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:50185726 G>A maps to NM_001037806.3 A1300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:50189688 G>A maps to NM_001037806.3 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr12:50187162 G>A maps to NM_001037806.3 A1104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:50190544 C>T maps to NM_001037806.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:48712083 G>A maps to NM_016453.2 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:48717011 C>T maps to NM_016453.2 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:232320271 G>A maps to NM_005381.2 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:232321429 A>G maps to NM_005381.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:232322045 C>T maps to ENST00000356936 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:232324993 C>T maps to NM_005381.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:232321447 G>A maps to NM_005381.2 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3198895 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:24888780 C>T maps to NM_003743.4 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr2:24952428 G>A maps to NM_003743.4 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:24888779 A>G maps to NM_003743.4 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:24952645 C>T maps to NM_003743.4 R1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:24951194 A>G maps to NM_003743.4 Q912Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:71069129 A>G maps to NM_006540.2 H490H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:71071855 G>T maps to NM_006540.2 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr8:71039072 C>T maps to NM_006540.2 Q1297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:71078840 G>A maps to NM_006540.2 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:71039221 G>A maps to NM_006540.2 R1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:71036304 C>T maps to NM_006540.2 Q1369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:71068553 C>T maps to NM_006540.2 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr8:71036974 G>A maps to NM_006540.2 Q1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr20:46279844 G>A maps to NM_181659.2 Q1257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr20:46275920 G>A maps to NM_181659.2 G1119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:46262819 A>G maps to NM_181659.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:51585490 C>A maps to NM_001145260.1 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:33345023 T>C maps to NM_014071.2 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:33328529 C>A maps to NM_014071.2 E1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:33337267 G>A maps to NM_014071.2 N910N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:33328766 C>A maps to NM_014071.2 E1765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:33324530 A>C maps to NM_014071.2 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr20:33345245 G>A maps to NM_014071.2 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:33356353 G>A maps to NM_014071.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr20:33320379 G>T maps to NM_014071.2 A1994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:126210976 C>T maps to NM_181782.4 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr6:126236502 T>C maps to NM_181782.4 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:126206489 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:126210228 G>A maps to NM_181782.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:126210829 G>T maps to NM_181782.4 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:126196038 C>T maps to NM_181782.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:15943782 G>T maps to ENST00000395857 I2250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:15935668 G>A maps to ENST00000395857 R2436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:16004601 G>A maps to ENST00000395857 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:16001707 C>T maps to ENST00000395857 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:15965476 C>A maps to ENST00000395857 G1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:15965582 G>A maps to ENST00000395857 G1756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:15978860 G>A maps to ENST00000395857 I1235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:15989673 C>T maps to ENST00000395857 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr17:15974944 A>G maps to ENST00000395857 D1326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:15974838 C>A maps to ENST00000395857 E1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:16001703 G>A maps to ENST00000395857 R949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:15938172 C>T maps to ENST00000395857 T2361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:124968162 C>T maps to NM_006312.4 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:124824694 G>A maps to NM_006312.4 P1855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:124829467 C>T maps to NM_006312.4 A1470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:124840067 C>T maps to NM_006312.4 P1104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:124856848 C>T maps to NM_006312.4 E842E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:124870323 G>A maps to NM_006312.4 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:124841218 C>T maps to NM_006312.4 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:124835277 C>T maps to NM_006312.4 T1240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:124810004 G>A maps to NM_006312.4 D2503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:124825247 C>T maps to NM_006312.4 P1753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:124817803 C>T maps to NM_006312.4 T2216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:124971111 G>A maps to NM_006312.4 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:55424404 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:55417543 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:55418076 C>T maps to NM_004829.5 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:55417574 C>T maps to NM_004829.5 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr19:55424387 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:41309819 C>T maps to NM_004828.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:160325696 G>A maps to NM_015331.2 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr18:2610794 C>T maps to NM_006101.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:2575029 G>A maps to NM_006101.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:2587860 G>A maps to NM_006101.2 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:15785180 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:8349092 T>C maps to ENST00000402554 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:8349145 T>C maps to ENST00000402554 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:8383848 G>A maps to ENST00000299734 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:141511804 G>T maps to NM_030571.3 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr13:80107521 T>C maps to NM_019080.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:80125171 G>T maps to NM_019080.2 G310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:23932115 C>T maps to NM_002487.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:140108703 G>A maps to NM_001144026.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:140109575 C>T maps to NM_001144026.1 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:140110729 C>T maps to NM_001144026.1 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr9:140110747 C>T maps to NM_001144026.1 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:43817751 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:43817871 G>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:43809220 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:134292491 G>A maps to NM_006096.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:134254284 G>A maps to NM_006096.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr14:21486182 G>A maps to NM_201537.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr14:21490569 G>A maps to NM_201537.1 Y68Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr20:35310918 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:35293466 C>T maps to ENST00000373803 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr20:35317080 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:58538088 C>T maps to NM_001130487.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:58540316 G>A maps to NM_001130487.1 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:149901155 G>T maps to NM_001543.4 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr5:149914444 C>T maps to NM_001543.4 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:149907772 C>A maps to NM_001543.4 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:149927802 A>G maps to NM_001543.4 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:149915383 G>A maps to NM_001543.4 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr5:149907715 G>A maps to NM_001543.4 W288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:149929319 C>A maps to NM_001543.4 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:149907757 G>A maps to NM_001543.4 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr5:149901259 C>T maps to NM_001543.4 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:75564576 G>T maps to NM_003635.3 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:119059285 T>G maps to NM_004784.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:119158199 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:119161688 C>A maps to NM_004784.2 S710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr4:115792021 G>A maps to NM_022569.1 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr4:115997533 C>T maps to NM_022569.1 W220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:115997733 G>T maps to NM_022569.1 Y153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:115997919 G>A maps to NM_022569.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:115997706 G>A maps to NM_022569.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr4:115754766 T>C maps to NM_022569.1 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:115769380 C>A maps to NM_022569.1 G644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr4:115767074 C>T maps to NM_022569.1 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119007338 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr5:140026925 G>A maps to NM_002488.4 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:54609271 C>T maps to NM_004542.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:123197307 A>C maps to ENST00000340034 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr22:42482195 G>A maps to NM_002490.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:4763594 G>T maps to NM_005002.4 G63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:23598621 G>A maps to NM_005003.2 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:41680689 G>A maps to NM_016013.2 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:41689011 G>A maps to NM_016013.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:41688708 A>G maps to NM_016013.2 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:2009723 C>A maps to NM_004548.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47001821 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:47001816 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:47001817 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47001751 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:47002087 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:201950286 A>G maps to NM_002491.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:179341806 G>A maps to NM_002492.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:32573022 C>T maps to NM_002493.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:102286731 C>T maps to NM_005004.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr4:140213764 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:206991489 G>A maps to ENST00000455934 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:207006671 G>A maps to ENST00000455934 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:207012474 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:207007416 C>A maps to ENST00000455934 G390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:207017231 G>A maps to ENST00000455934 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:207012289 G>T maps to ENST00000455934 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr2:207006793 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161176353 T>C maps to NM_004550.4 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:47603689 G>A maps to NM_004551.2 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:39494584 C>T maps to NM_004552.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:39494494 C>T maps to NM_004552.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:67803718 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:67379696 G>A maps to NM_007103.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:67378976 C>T maps to NM_007103.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:9122647 C>T maps to NM_021074.4 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:9126839 A>G maps to NM_021074.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:44323763 G>A maps to NM_021075.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:44323481 T>G maps to NM_021075.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr21:44323718 C>A maps to NM_021075.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:152384041 G>T maps to NM_001164507.1 R7265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:152410410 G>A maps to NM_001164507.1 H6519H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:152473958 G>A maps to NM_001164507.1 D3700D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:152484096 C>T maps to NM_001164507.1 T3361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:152352869 C>A maps to NM_001164507.1 E8136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:152507273 C>T maps to NM_001164507.1 K2347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:152346552 G>A maps to NM_001164507.1 R8446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:152374875 G>A maps to NM_001164507.1 L7586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:152484105 G>A maps to NM_001164507.1 H3358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:152543980 G>A maps to NM_001164507.1 D863D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr2:152432727 G>T maps to NM_001164507.1 Y5615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:152506893 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:152520328 A>G maps to NM_001164507.1 I1832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:152534650 G>A maps to NM_001164507.1 F1102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr2:152510503 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr2:152359955 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:152468834 G>A maps to NM_001164507.1 V3890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:152527650 G>A maps to NM_001164507.1 G1464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:152376269 C>A maps to NM_001164507.1 E7498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:152350677 G>A maps to NM_001164507.1 S8192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:152466589 A>G maps to NM_001164507.1 I4021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:152553745 G>A maps to NM_001164507.1 Y462Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:152347011 G>T maps to NM_001164507.1 R8391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:152357902 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:152381753 C>A maps to NM_001164507.1 G7399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:152411512 A>G maps to NM_001164507.1 L6454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:152520059 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:152417532 C>T maps to NM_001164507.1 K6397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:152553249 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr2:152409910 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:152352789 C>T maps to NM_001164507.1 S8162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:152354219 C>A maps to NM_001164507.1 E8074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:152376269 C>A maps to NM_001164507.1 E7498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:152473982 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:152500983 C>A maps to NM_001164507.1 E2548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:152354866 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:152520139 G>A maps to NM_001164507.1 N1895N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:152388410 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:152424841 C>T maps to NM_001164507.1 R5908R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:21139389 T>C maps to ENST00000430741 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:21108432 C>A maps to ENST00000430741 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:21124548 C>A maps to ENST00000430741 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:21120213 C>A maps to ENST00000430741 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr10:21461310 C>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:21112216 C>A maps to ENST00000430741 E628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:21139418 C>A maps to ENST00000430741 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:21169799 C>A maps to ENST00000430741 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:21115411 G>A maps to ENST00000430741 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:21158734 C>T maps to ENST00000430741 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:21129774 C>A maps to ENST00000430741 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:21074699 C>T maps to ENST00000430741 A1009A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:21139351 G>T maps to ENST00000430741 S363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr10:21158715 G>A maps to ENST00000430741 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:21097514 G>A maps to ENST00000430741 D897D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:91837009 G>T maps to NM_022351.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:91962080 G>T maps to NM_022351.4 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:84012113 G>T maps to NM_019065.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:84034370 C>A maps to NM_019065.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:32258500 C>T maps to NM_031232.3 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:8242582 C>T maps to NM_015509.3 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:16770222 G>A maps to NM_018090.4 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr1:16782331 G>A maps to NM_018090.4 W229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:97345795 C>T maps to NM_001135175.1 R657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:97328800 C>T maps to NM_001135175.1 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:56142855 G>A maps to ENST00000508342 Q830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:56155147 C>A maps to ENST00000508342 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:56208080 C>A maps to ENST00000508342 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:56155160 A>C maps to ENST00000508342 Y627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:56130750 C>A maps to ENST00000508342 E1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:56122765 G>T maps to ENST00000508342 S1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:56208153 G>T maps to ENST00000508342 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:56063431 C>A maps to NM_001144967.1 T953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:55833030 T>C maps to NM_001144967.1 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:24686359 C>G maps to NM_006156.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:11190844 G>A maps to NM_006403.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:29885033 G>T maps to NM_021076.3 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:29884891 G>A maps to NM_021076.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:29885533 G>A maps to NM_021076.3 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:24810435 C>A maps to ENST00000221169 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:24811122 G>A maps to ENST00000221169 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:24813396 C>T maps to ENST00000221169 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr8:24813309 G>A maps to ENST00000221169 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:24811752 C>A maps to ENST00000221169 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:24811705 A>G maps to ENST00000221169 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:24775099 G>T maps to NM_005382.2 E578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:24775107 C>T maps to NM_005382.2 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:24775343 C>A maps to NM_005382.2 S659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:24775395 G>A maps to NM_005382.2 E676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:24773230 C>T maps to NM_005382.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:24775489 G>T maps to NM_005382.2 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:24774858 G>A maps to NM_005382.2 E497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:24773230 C>T maps to NM_005382.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:24771944 G>A maps to NM_005382.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:72400819 C>T maps to NM_173808.2 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:11637330 C>T maps to NM_145043.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:178256850 C>T maps to NM_018248.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr4:178243639 C>T maps to NM_018248.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:170477247 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:170321764 G>A maps to ENST00000507142 C1207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:170384531 C>A maps to ENST00000507142 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:27157453 G>T maps to ENST00000396636 G1149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr3:27204087 C>T maps to ENST00000396636 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:27326399 C>T maps to ENST00000396636 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr3:27215930 G>A maps to ENST00000396636 F925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr3:27257370 A>G maps to NM_199347.2 C697C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:27387665 C>T maps to ENST00000396636 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:130947484 G>T maps to NM_024800.4 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:130887711 G>A maps to NM_024800.4 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:130962296 G>A maps to NM_024800.4 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:130873878 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:211842454 G>A maps to NM_002497.2 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:211842577 G>A maps to NM_002497.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:52728045 A>C maps to NM_002498.2 L98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:52725351 A>C maps to NM_002498.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:52710258 G>A maps to NM_002498.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:52780124 G>T maps to NM_003157.4 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:52802353 C>T maps to NM_003157.4 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:52802571 G>A maps to NM_003157.4 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:52661488 G>A maps to NM_199289.1 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:52646103 C>A maps to NM_199289.1 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:52676335 G>T maps to NM_199289.1 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:52684546 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:127113222 C>A maps to NM_001166171.1 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr9:127055224 C>A maps to NM_001166171.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:198231715 A>G maps to NM_133494.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:198231749 G>T maps to NM_133494.2 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr1:198222178 C>A maps to NM_133494.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:27067574 C>T maps to NM_178170.2 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr17:27065213 G>C maps to NM_178170.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:27062352 C>T maps to NM_178170.2 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr14:75553934 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:140347303 G>A maps to ENST00000371482 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:20948912 T>C maps to NM_006157.3 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:21592381 G>T maps to NM_006157.3 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:20869221 C>T maps to NM_006157.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:20982021 G>T maps to NM_006157.3 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:20948957 T>C maps to NM_006157.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:45173725 C>A maps to NM_001145107.1 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:45097553 G>A maps to NM_001145107.1 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:45105093 G>A maps to NM_001145107.1 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:44917207 A>G maps to NM_001145107.1 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:45170902 A>G maps to NM_001145107.1 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:73551135 C>T maps to NM_002499.3 R708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:73580686 T>G maps to NM_002499.3 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:73575380 C>T maps to NM_002499.3 G1113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:73580791 C>T maps to NM_002499.3 P1183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:73562743 C>T maps to NM_002499.3 R936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:73590696 C>T maps to NM_002499.3 R1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:73562474 G>A maps to NM_002499.3 T873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:156640789 C>A maps to NM_006617.1 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156641537 G>A maps to NM_006617.1 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:156641105 G>A maps to NM_006617.1 D958D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:156641686 G>A maps to NM_006617.1 R765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:156642853 C>A maps to NM_006617.1 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr1:156639575 G>A maps to NM_006617.1 P1468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr1:156639377 A>T maps to NM_006617.1 G1534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:156640192 G>A maps to NM_006617.1 Q1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:5498746 C>A maps to NM_001047160.1 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:5496963 C>T maps to NM_001047160.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr18:70461453 G>A maps to NM_153181.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr18:70461477 C>T maps to NM_153181.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:70417352 G>A maps to NM_153181.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr18:70461399 G>A maps to NM_153181.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr18:70417388 C>T maps to NM_153181.2 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:70461639 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:70526288 C>A maps to NM_153181.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:70526219 G>A maps to NM_153181.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:47156681 C>T maps to NM_018092.3 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:47143459 G>A maps to NM_018092.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:47163218 G>A maps to NM_018092.3 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:47143459 G>A maps to NM_018092.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:47156684 G>A maps to NM_018092.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:233899289 C>T maps to NM_005383.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr2:233899245 C>T maps to NM_005383.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:233897399 C>T maps to NM_005383.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:233899475 G>A maps to NM_005383.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:74717221 G>A maps to NM_006656.5 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:74705602 G>A maps to NM_006656.5 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:74716543 T>C maps to NM_006656.5 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:105331433 C>T maps to NM_004210.4 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr10:105331310 C>T maps to NM_004210.4 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:44517425 C>A maps to NM_080749.2 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:44517456 C>T maps to NM_080749.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7225194 C>A maps to NM_032442.2 E954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7228214 C>T maps to NM_032442.2 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:7221994 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7226347 G>A maps to NM_032442.2 R838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:7224119 G>A maps to NM_032442.2 I1161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:182543446 G>A maps to NM_002500.2 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:55420519 G>A maps to NM_021191.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:55420813 C>A maps to NM_021191.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:55421197 C>G maps to NM_021191.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:31378270 G>T maps to NM_022728.2 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:31378473 G>A maps to NM_022728.2 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:31377934 G>A maps to NM_022728.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:31378021 G>A maps to NM_022728.2 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr7:31377934 G>A maps to NM_022728.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr7:31378674 C>A maps to NM_022728.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:134870741 G>A maps to NM_006161.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:71332478 G>A maps to NM_020999.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:71332648 C>A maps to NM_020999.3 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr10:71332228 G>A maps to NM_020999.3 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr10:71332418 G>A maps to NM_020999.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:71332238 C>T maps to NM_020999.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:78399025 G>A maps to NM_144573.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:78395035 A>G maps to NM_144573.3 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:78408307 G>T maps to NM_144573.3 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:78408165 G>A maps to NM_144573.3 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:78408156 G>A maps to NM_144573.3 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:29559120 A>G maps to NM_001042492.2 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:29587515 G>A maps to NM_001042492.2 Q1520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:29533377 C>T maps to NM_001042492.2 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:29663720 T>C maps to NM_001042492.2 H2072H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:29585393 C>T maps to NM_001042492.2 I1402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:29676186 A>G maps to NM_001042492.2 L2413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:29592268 G>T maps to NM_001042492.2 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:29559727 T>C maps to NM_001042492.2 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:29560096 G>T maps to NM_001042492.2 E1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:29676252 C>T maps to NM_001042492.2 S2435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:29533314 C>T maps to NM_001042492.2 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:29657346 T>G maps to NM_001042492.2 T1881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr17:29657367 C>T maps to NM_001042492.2 I1888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr17:29483097 T>A maps to NM_001042492.2 L53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:29557325 G>A maps to NM_001042492.2 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:29652999 T>C maps to NM_001042492.2 F1666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr17:29654614 A>G maps to NM_001042492.2 E1789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:29533377 C>T maps to NM_001042492.2 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:29576110 C>T maps to NM_001042492.2 R1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:29664428 A>G maps to NM_001042492.2 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:29486039 G>T maps to NM_001042492.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:30061013 C>T maps to NM_181832.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:30077490 C>T maps to NM_181832.2 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:30032796 G>T maps to NM_181832.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr22:30070929 G>A maps to NM_181832.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:204945906 C>A maps to ENST00000367172 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr1:204938039 C>T maps to ENST00000367172 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:204937940 C>T maps to ENST00000367172 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:204953236 C>T maps to ENST00000367172 S851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr1:204948556 C>T maps to ENST00000367172 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:204944397 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:204955129 C>T maps to ENST00000367172 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:204966469 T>C maps to ENST00000367172 A1092A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:204919691 T>A maps to ENST00000367172 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:204919702 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:204985519 G>A maps to ENST00000367172 V1299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:69726136 C>T maps to NM_138713.2 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:69725884 C>T maps to NM_138713.2 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:69689634 G>T maps to NM_138713.2 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:69727273 G>A maps to NM_138713.2 P1182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:69726448 G>A maps to NM_138713.2 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr16:69726421 G>A maps to NM_138713.2 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:77211118 C>T maps to NM_172387.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:77221338 G>A maps to NM_172387.1 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr18:77193713 G>A maps to NM_172387.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr18:77227529 C>T maps to NM_172387.1 N667N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr18:77170556 C>T maps to NM_172387.1 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:50007934 A>G maps to NM_173091.2 *926Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr20:50139978 G>A maps to NM_012340.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:50133421 C>T maps to NM_012340.3 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:50048729 G>A maps to NM_012340.3 Q866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:50139987 C>T maps to NM_012340.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr20:50090622 G>A maps to NM_012340.3 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:68156016 G>A maps to NM_173165.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr16:68200743 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:68191840 C>T maps to NM_173165.2 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr16:68225385 G>A maps to NM_173165.2 P938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24838783 T>C maps to NM_001136022.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24839239 C>A maps to NM_001136022.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:24846073 G>A maps to NM_001136022.1 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:24845665 C>T maps to NM_001136022.1 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:54686358 C>T maps to NM_001136023.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr17:46133896 C>T maps to ENST00000362042 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:178097914 A>C maps to ENST00000423513 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:26224487 T>C maps to NM_004289.6 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:26225318 C>T maps to NM_004289.6 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:26224515 G>T maps to NM_004289.6 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:26224677 G>T maps to NM_004289.6 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:26217743 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:61892168 C>T maps to NM_001145512.1 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:61872301 G>A maps to NM_001145512.1 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:14150217 G>A maps to ENST00000397581 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:14155845 T>G maps to ENST00000397581 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:14120611 G>A maps to ENST00000397581 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:3381846 G>A maps to ENST00000269778 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:3381813 C>T maps to ENST00000269778 H45H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:94171906 G>A maps to NM_005384.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:94172509 C>T maps to NM_005384.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:94171921 G>A maps to NM_005384.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:94171798 T>C maps to NM_005384.2 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:94171921 G>A maps to NM_005384.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:13201122 G>A maps to ENST00000397661 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:13184759 G>A maps to ENST00000397661 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:13184242 A>G maps to ENST00000397661 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:13201122 G>A maps to ENST00000397661 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr19:13192666 C>T maps to ENST00000397661 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:13184741 G>A maps to ENST00000397661 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:103514669 C>T maps to NM_003998.3 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:103533675 T>C maps to NM_003998.3 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:103517331 T>C maps to NM_003998.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:103533625 C>T maps to NM_003998.3 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:104159893 T>C maps to NM_001077494.1 Y509Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:104160066 G>A maps to NM_001077494.1 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr10:104156227 C>T maps to NM_001077494.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:104157318 G>T maps to NM_001077494.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:104160051 G>A maps to NM_001077494.1 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:35871788 A>G maps to NM_020529.2 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:39395888 G>A maps to NM_002503.3 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:39395909 C>T maps to NM_002503.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr19:39397876 C>T maps to NM_002503.3 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36381485 C>T maps to ENST00000340950 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:36381356 G>A maps to ENST00000352614 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:36381326 C>T maps to ENST00000352614 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:44229416 C>A maps to NM_004556.2 E352*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:101572629 G>A maps to NM_031419.3 W420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:129744219 A>G maps to NM_006165.3 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:129754721 C>T maps to NM_006165.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:129755504 C>A did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr11:129742892 A>G maps to NM_006165.3 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr11:129743891 T>C maps to NM_006165.3 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:129744048 G>A maps to NM_006165.3 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:129739724 G>A maps to NM_006165.3 G1090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:34285710 C>T maps to NM_021100.4 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:33364780 C>T maps to NM_147133.2 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr9:33344085 C>T maps to NM_002504.4 C748C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:33294586 C>A maps to NM_002504.4 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:33344157 C>T maps to NM_002504.4 C772C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:47905268 C>T maps to NM_152995.4 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:47912919 A>G maps to NM_152995.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:47907318 C>A maps to NM_152995.4 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:47916106 C>T maps to NM_152995.4 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:41065137 C>A maps to NM_002505.4 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:41048548 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:41060779 C>T maps to NM_002505.4 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:41236497 T>A maps to ENST00000308733 *459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:41235025 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr1:41218845 T>C maps to ENST00000308733 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:23945536 C>T maps to NM_001042635.1 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:23944462 A>C maps to NM_001042635.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:233834930 C>A maps to NM_019850.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:233748692 T>G maps to NM_019850.2 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:233791859 G>A maps to NM_019850.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:115828831 C>T maps to NM_002506.2 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:115829406 A>G maps to NM_002506.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:102632725 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:102632524 C>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:102632698 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:102632524 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:102632644 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:25773874 C>A maps to NM_018297.3 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:25761669 G>A maps to NM_018297.3 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:25770718 G>A maps to NM_018297.3 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:25781077 G>A maps to NM_018297.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:90814780 G>T maps to NM_001033088.1 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:219942060 A>C maps to NM_024782.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:116380648 C>T maps to NM_005599.3 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:18121745 C>T maps to NM_198586.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:18121925 G>A maps to NM_198586.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:18122474 G>T maps to NM_198586.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr10:115661457 T>C maps to NM_198514.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:115662297 A>G maps to NM_198514.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:39616408 G>T maps to NM_001012754.2 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr5:177576827 T>C maps to NM_017838.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:177576740 C>T maps to NM_017838.3 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:17743973 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:17744313 C>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:17744547 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:17745605 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:17742490 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:17745908 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:17750367 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:17710471 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:17750207 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:17744784 A>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:17710557 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:17743538 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:17742543 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:17743588 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:17743915 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:17750026 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:17745587 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr23:17750486 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:17746421 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:17737523 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:17744204 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:17750533 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:17742543 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:17743607 G>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:17744821 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:17745130 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:17746167 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:17739694 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:17745254 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:71359115 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:71359561 C>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:71359717 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:71360292 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:71354387 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71354481 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71359299 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71359700 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:71358887 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:71359482 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:71359564 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:71360403 T>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:71359951 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:71359688 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:71359135 G>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:71360139 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:71359376 G>T did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:71358881 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:236144972 G>T maps to NM_002508.2 R1055R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:236189262 G>A maps to NM_002508.2 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:236187505 G>A maps to NM_002508.2 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:236192895 G>A maps to NM_002508.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:236195800 G>A maps to NM_002508.2 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:236195839 G>A maps to NM_002508.2 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:236143943 G>T maps to NM_002508.2 Y1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:236145056 A>G maps to NM_002508.2 A1027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:236175218 A>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:236189397 G>A maps to NM_002508.2 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:236156996 G>A maps to NM_002508.2 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:236205357 G>T maps to NM_002508.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:52508916 G>A maps to NM_007361.3 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:52485838 C>A maps to NM_007361.3 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:52493931 C>T maps to NM_007361.3 G887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:52534848 G>A maps to NM_007361.3 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:52534590 C>T maps to NM_007361.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:52520398 C>A maps to NM_007361.3 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:201757978 C>A maps to NM_001136039.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:201759984 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:201758039 G>T maps to NM_001136039.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:51224711 G>T maps to NM_020921.3 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:51192747 G>A maps to NM_020921.3 R2039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:51224486 T>C maps to NM_020921.3 E1087E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:51288708 C>T maps to NM_020921.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:51224264 G>A maps to NM_020921.3 S1161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:51210966 G>A maps to NM_020921.3 V1727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:51223676 G>A maps to NM_020921.3 I1357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr14:51233102 G>A maps to NM_020921.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:51223975 C>A maps to NM_020921.3 E1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:51238146 C>A maps to NM_020921.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:25456923 G>A maps to NM_025176.4 A1001A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:25472142 G>A maps to NM_025176.4 Y443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:25459650 G>A maps to NM_025176.4 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:25459710 G>A maps to NM_025176.4 H683H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:25507049 G>A maps to NM_025176.4 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:25484638 A>G maps to NM_025176.4 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:25491370 G>A maps to NM_025176.4 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:25481601 G>A maps to NM_025176.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr20:25456833 C>T maps to NM_025176.4 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr16:69373950 C>T maps to NM_016101.4 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:69375491 G>A maps to NM_016101.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:23049092 G>A maps to NM_144599.4 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:23014444 G>A maps to NM_030922.6 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:23012323 C>A maps to NM_030922.6 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:23006802 G>A maps to NM_030922.6 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:48037664 T>C maps to NM_207330.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:48037777 G>A maps to NM_207330.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:99264766 T>C maps to NM_024759.1 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:24768669 C>T maps to NM_020448.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:24776052 C>T maps to NM_020448.4 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:37022455 T>C maps to NM_133433.3 A1846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:36976271 G>A maps to NM_133433.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:36962227 G>A maps to NM_133433.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:37017255 T>C maps to NM_133433.3 L1638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:37017260 A>G maps to NM_133433.3 K1639K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:37046233 T>C maps to NM_133433.3 L2174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:36985303 T>C maps to NM_133433.3 N674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr5:36976472 G>A maps to NM_133433.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:36985594 A>G maps to NM_133433.3 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:37049387 T>C maps to NM_133433.3 L2313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:37007476 G>A maps to NM_133433.3 Q1380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:37057295 C>T maps to NM_133433.3 D2424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:37026329 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:52505887 C>T maps to NM_007184.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:52522348 G>A maps to NM_007184.3 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52521556 C>T maps to NM_007184.3 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52526122 C>A maps to NM_007184.3 I1380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:52526263 G>A maps to NM_007184.3 P1427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:52524727 G>A maps to NM_007184.3 W1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:52512258 A>G maps to NM_007184.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:161089355 G>A maps to NM_005600.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:100067689 T>C maps to NM_020202.4 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:100064473 G>T maps to NM_020202.4 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:124604203 T>C maps to NM_001040214.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:125112504 C>A maps to NM_001040214.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:63659558 T>C maps to NM_173688.2 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:63831072 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:61878932 G>A maps to NM_152864.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:119059327 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GE-01A-11W-A062-09 chr23:119077523 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:119066143 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:119068460 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:119059226 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:119064011 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:119072770 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:119066068 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:119077440 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:119077501 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:119070271 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:119070293 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr23:119059333 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:119077456 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:119070317 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119066163 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119070327 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119070594 G>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:119070642 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:119072722 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:119077321 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:28228280 C>T maps to NM_001007531.1 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:50666254 C>T maps to NM_033119.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr3:23934681 G>A maps to NM_020345.3 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:40174517 C>T maps to ENST00000316082 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:118724019 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:118724558 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:118723548 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:118723849 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118723544 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118724116 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118724851 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118725104 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr23:118724257 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118723980 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118725226 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:118723672 G>A did not map to a codon.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr23:118724249 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:118723548 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:118724044 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:118724220 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:118724851 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:118726447 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:118726362 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118723340 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118724938 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118726447 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:118726438 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:118723672 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:42679070 T>G maps to NM_005385.3 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:42678626 C>A maps to NM_005385.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:42680223 C>T maps to NM_005385.3 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:172661926 C>A maps to NM_004387.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:172661978 G>A maps to NM_004387.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:172659670 G>A maps to NM_004387.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:85416923 G>T maps to NM_006168.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:85416881 C>T maps to NM_006168.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:85416991 C>A maps to NM_006168.2 G226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:85419204 C>T maps to NM_006168.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:134598512 G>A maps to NM_177400.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr10:134598587 G>A maps to NM_177400.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr17:33466305 G>A maps to NM_018096.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr17:33463459 G>T maps to NM_018096.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:33466959 A>G maps to NM_018096.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:173998847 G>T maps to NM_014932.2 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:173996696 C>T maps to NM_014932.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:173997266 C>T maps to NM_014932.2 C492C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:173993172 A>C maps to NM_014932.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:173993120 C>T maps to NM_014932.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:173998999 C>T maps to NM_014932.2 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr3:173997311 C>T maps to NM_014932.2 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:173996951 G>T maps to NM_014932.2 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7318030 G>T maps to NM_020795.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:7317810 C>T maps to NM_020795.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:70389344 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:70367767 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:70384179 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70367944 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70367753 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70368722 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70375209 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70389536 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70368734 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70389377 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:70389867 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70375068 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70389752 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70367879 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70367958 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70387058 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70389297 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70389891 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:70373339 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:70368013 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:70389249 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70389233 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70367985 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70375197 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70389394 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:70373348 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr23:70389104 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:70389237 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:5811227 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:5811395 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:5821780 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:5821435 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:5811130 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:5811429 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:5821469 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:5811687 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:5821170 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:5821639 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr23:5821434 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:5811116 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:5811288 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:5821543 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:5811288 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:5947435 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:5810862 C>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:6069210 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:5821686 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:26449682 C>T maps to NM_016231.4 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:26370185 C>A maps to NM_016231.4 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:65081684 C>T maps to NM_020726.4 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:65105430 C>T maps to NM_020726.4 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:3599182 G>A maps to ENST00000448023 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:3615001 G>A maps to ENST00000448023 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:3594329 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:3592240 C>T maps to ENST00000448023 A1065A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:32475708 G>A maps to NM_021209.4 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:32476526 C>A maps to NM_021209.4 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:32476149 G>A maps to NM_021209.4 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:32460482 C>T maps to NM_021209.4 E923E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:32475765 G>A maps to NM_021209.4 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:32475708 G>A maps to NM_021209.4 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:32475302 C>A maps to NM_021209.4 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:32476335 G>A maps to NM_021209.4 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:32449621 C>A maps to NM_021209.4 E999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:57088720 C>T maps to NM_032206.3 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:57091997 C>T maps to NM_032206.3 G1256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:57089362 C>T maps to NM_032206.3 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:57068112 G>A maps to NM_032206.3 A859A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:57099177 C>T maps to NM_032206.3 C1403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:57099123 G>A maps to NM_032206.3 R1385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:57103771 C>T maps to NM_032206.3 T1508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr16:57059748 C>T maps to NM_032206.3 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:57059916 C>T maps to NM_032206.3 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:5442820 G>A maps to NM_033004.3 D928D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr17:5462803 C>T maps to NM_033004.3 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr17:5445177 G>A maps to NM_033004.3 Q900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:5424906 G>A maps to NM_033004.3 R1240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:5425025 C>A maps to NM_033004.3 E1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr17:5418367 C>T maps to NM_033004.3 P1376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:5421188 G>A maps to NM_033004.3 R1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:7981577 C>T maps to NM_176821.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:7982380 C>A maps to NM_176821.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:7981510 C>A maps to NM_176821.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:56320319 A>G maps to NM_145007.3 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:56297124 C>A maps to NM_145007.3 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:56300755 G>A maps to NM_145007.3 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr19:56321303 G>A maps to NM_145007.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr19:56329275 G>A maps to NM_145007.3 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr19:54314084 G>A maps to ENST00000391773 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:54313265 C>T maps to ENST00000391773 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:54314033 G>A maps to ENST00000391773 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:54314360 C>T maps to ENST00000391773 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:54327373 C>A maps to ENST00000391773 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:54297341 C>T maps to ENST00000391773 A1050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:54313400 G>T maps to ENST00000391773 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:54327314 C>T maps to ENST00000391773 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:56410297 G>T maps to NM_176810.2 S932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:56423760 G>A maps to NM_176810.2 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:56407478 C>T maps to NM_176810.2 A988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:56423964 C>T maps to NM_176810.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:56435285 C>A maps to NM_176810.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr19:56443425 C>A maps to NM_176810.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:56424168 C>T maps to NM_176810.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:56423387 C>A maps to NM_176810.2 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr19:56419303 A>G maps to NM_176810.2 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:7065059 T>C maps to NM_176822.3 C601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:7083722 T>C maps to NM_176822.3 I988I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr11:7068045 T>C maps to NM_176822.3 C702C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:7063914 G>T maps to NM_176822.3 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:7067925 G>A maps to NM_176822.3 W662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:7064669 G>A maps to NM_176822.3 E471E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:7064039 C>T maps to NM_176822.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:7063992 G>T maps to NM_176822.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:7064372 C>A maps to NM_176822.3 C372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:55494973 C>T maps to NM_017852.3 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:55501891 G>T maps to NM_017852.3 E854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:55494484 C>T maps to NM_017852.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:55496510 C>T maps to NM_017852.3 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:55493030 C>A maps to NM_017852.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:247586598 G>A maps to NM_004895.4 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:247587743 C>T maps to NM_004895.4 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:247582326 G>A maps to NM_004895.4 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:247586530 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:247588376 G>A maps to NM_004895.4 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:247587512 G>A maps to NM_004895.4 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:247582326 G>A maps to NM_004895.4 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:247582371 G>A maps to NM_004895.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr19:56382339 G>A maps to NM_134444.4 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:56369487 C>T maps to NM_134444.4 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:56370439 C>T maps to NM_134444.4 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr19:56370051 G>A maps to NM_134444.4 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56370114 C>T maps to NM_134444.4 H452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56370564 C>A maps to NM_134444.4 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56373366 C>T maps to NM_134444.4 N676N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:56369746 G>T maps to NM_134444.4 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:56363527 G>T maps to NM_134444.4 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:56369332 G>T maps to NM_134444.4 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:56369610 G>A maps to NM_134444.4 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:56369448 C>T maps to NM_134444.4 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:56369289 C>A maps to NM_134444.4 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:56388448 T>C maps to NM_134444.4 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56539845 C>T maps to NM_153447.4 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56569650 C>A maps to NM_153447.4 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:56538816 C>T maps to NM_153447.4 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr19:56539845 C>T maps to NM_153447.4 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:56538690 C>T maps to NM_153447.4 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:56539690 G>T maps to NM_153447.4 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:56565132 C>T maps to NM_153447.4 C1086C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr19:56538393 G>A maps to NM_153447.4 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:56565171 C>T maps to NM_153447.4 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr19:56538450 G>A maps to NM_153447.4 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:280978 C>A maps to NM_138329.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:55450265 C>A maps to ENST00000446217 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:55451565 C>T maps to ENST00000446217 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:55435184 C>A maps to ENST00000446217 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:55435184 C>A maps to ENST00000446217 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:55449522 G>C maps to ENST00000446217 S701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:55450500 G>T maps to ENST00000446217 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:55450365 A>G maps to ENST00000446217 C635C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:55449587 C>T maps to ENST00000446217 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr19:55453025 G>A maps to ENST00000446217 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:56467185 C>T maps to NM_176811.2 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr19:56466270 C>T maps to NM_176811.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:56466869 G>A maps to NM_176811.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:56459528 C>A maps to NM_176811.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:56466569 C>T maps to NM_176811.2 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:56467028 C>T maps to NM_176811.2 H535H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr19:56466068 A>G maps to NM_176811.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr19:56466225 C>T maps to NM_176811.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:56466746 C>T maps to NM_176811.2 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56243420 C>T maps to NM_176820.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56244101 G>T maps to NM_176820.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:56228178 A>G maps to NM_176820.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:56244281 C>T maps to NM_176820.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:56244536 T>C maps to NM_176820.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:56243470 C>A maps to NM_176820.2 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:56244077 T>C maps to NM_176820.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:56244763 G>A maps to NM_176820.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:119050973 C>T maps to NM_024618.2 V748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:119045217 C>T maps to NM_024618.2 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:119050571 C>T maps to NM_024618.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:119045751 A>G maps to NM_024618.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr11:119044725 G>A maps to NM_024618.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:142396838 C>A maps to NM_002511.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:142409750 C>T maps to NM_002511.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr6:142409501 C>T maps to NM_002511.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr6:142409552 G>A maps to NM_002511.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:160958905 C>T maps to ENST00000472947 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:49239139 C>T maps to NM_198175.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr17:49239203 T>C maps to NM_198175.1 *178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:49248917 G>T maps to ENST00000393198 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:49247314 C>T maps to ENST00000393198 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:49248890 G>T maps to ENST00000393198 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:450338 C>A maps to ENST00000382940 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:454982 C>T maps to NM_020664.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:137451380 C>A maps to NM_003551.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:48336642 G>A maps to NM_005793.3 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:169293677 G>A maps to NM_013330.3 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:169199981 G>A maps to NM_013330.3 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr2:152132031 G>A maps to NM_004688.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:152132067 G>A maps to NM_004688.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:10042449 C>A maps to NM_022787.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:10032142 C>T maps to NM_022787.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:183262857 G>A maps to NM_015039.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:183262857 G>A maps to NM_015039.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:183387372 G>T maps to NM_015039.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr3:139297816 G>A maps to ENST00000296202 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:4519409 G>A maps to NM_020677.3 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:43180479 C>T maps to NM_021079.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:15154818 G>A maps to ENST00000378143 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:15154812 C>T maps to ENST00000378143 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:15161457 G>A maps to ENST00000378143 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:56473497 C>T maps to NM_006681.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:232392962 G>A maps to NM_006056.4 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:232393434 G>T maps to NM_006056.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr2:232393146 G>A maps to NM_006056.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:151784065 G>T maps to NM_020167.4 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr5:151775074 C>T maps to NM_020167.4 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:151771982 C>T maps to NM_020167.4 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:114168751 T>C maps to NM_006169.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:114168760 C>T maps to NM_006169.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:69782868 G>A maps to NM_014062.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:144098968 G>T maps to ENST00000467773 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:144095651 A>G maps to ENST00000467773 Y499Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZP-01A-21D-A10M-09 chr7:144098553 C>T maps to ENST00000467773 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:881642 C>T maps to NM_015658.3 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:96121505 C>A maps to NM_022451.9 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:96106268 C>A maps to NM_022451.9 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:96099493 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:96121505 C>A maps to NM_022451.9 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:132632647 G>A maps to NM_024078.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr12:132632257 C>T maps to NM_024078.1 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:30491340 C>T maps to NM_006092.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:30487911 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:30494807 G>A maps to NM_006092.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:30494879 G>A maps to NM_006092.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr7:30465277 A>G maps to NM_006092.2 D946D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr7:30475651 C>T maps to NM_006092.2 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr7:30491196 G>A maps to NM_006092.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr16:50744724 G>A maps to NM_022162.1 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:50745795 C>T maps to NM_022162.1 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:50744481 G>A maps to NM_022162.1 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:50744556 G>A maps to NM_022162.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr16:50745322 C>T maps to NM_022162.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:50756616 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:54671742 C>A maps to NM_005450.4 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:10712253 G>T maps to NM_024894.2 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:10803113 G>A maps to NM_024894.2 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr2:10808814 G>T maps to NM_024894.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:10811785 C>A maps to NM_024894.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:10824708 T>C maps to NM_024894.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:10808806 C>T maps to NM_024894.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:65718701 A>G maps to NM_015462.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:65722750 A>G maps to NM_015462.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:65722741 A>G maps to NM_015462.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:65735672 C>T maps to NM_015462.3 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr22:38084896 G>A maps to NM_024313.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:67208824 C>T maps to ENST00000432069 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:31523094 G>T maps to NM_003787.4 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:31538232 G>A maps to NM_003787.4 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:31538274 G>A maps to NM_003787.4 H388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr18:31432970 T>C maps to NM_003787.4 Q584Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:33462673 C>T maps to NM_022917.4 R1143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:33462718 C>T maps to NM_022917.4 V1128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:33472105 G>A maps to NM_022917.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:13615973 G>A maps to NM_016167.3 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:95085568 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:95078276 G>A maps to NM_017948.5 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:95081580 G>A maps to NM_017948.5 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:95078393 G>A maps to NM_017948.5 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:95078322 A>C maps to NM_017948.5 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr9:95086472 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:95078287 G>A maps to NM_017948.5 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr9:95063977 C>T maps to NM_017948.5 K1010K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:6592116 G>A maps to NM_024654.4 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:103920362 G>A maps to ENST00000405356 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:103921867 C>T maps to ENST00000405356 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:156759713 G>A maps to NM_138400.1 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr7:156743390 C>T maps to NM_138400.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr16:14975508 C>T maps to ENST00000456867 D998D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:14983044 A>G maps to ENST00000456867 K1139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:14968979 C>T maps to ENST00000456867 I714I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:14932340 T>G maps to ENST00000456867 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr16:14970274 C>T maps to ENST00000456867 Q806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:14947805 C>T maps to ENST00000456867 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:14976455 A>G maps to ENST00000456867 G1011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:14978245 C>T maps to ENST00000456867 I1043I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:14969009 C>T maps to ENST00000456867 N724N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:14970237 C>T maps to ENST00000456867 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:18532184 G>A maps to NM_001004060.1 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr16:18554974 C>T maps to NM_001004060.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:16345869 C>T maps to ENST00000263012 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:16346330 G>A maps to ENST00000263012 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:16346288 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr16:16346330 G>A maps to ENST00000263012 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70511691 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70514146 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70517749 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70514378 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:70517253 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70514185 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70516824 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:70517766 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70514204 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70511777 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70514184 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70517746 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:70516426 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:70510516 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70514252 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:70511777 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:70516428 T>G did not map to a codon.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr23:70511817 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:70516831 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:70514312 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:70517750 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr4:2956222 G>A maps to NM_003703.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:2940928 T>C maps to NM_003703.1 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:175812203 G>A maps to ENST00000509257 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:175813904 C>T maps to ENST00000451293 K74K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BG-A0MQ-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr5:175815447 C>T maps to ENST00000503175 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:6669657 G>T maps to ENST00000382421 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr12:6669953 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:2637469 C>T maps to NM_006392.2 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:2637451 C>T maps to NM_006392.2 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:2637451 C>T maps to NM_006392.2 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:203157505 G>T maps to NM_015934.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:203160418 G>A maps to NM_015934.3 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:117680507 G>A maps to ENST00000338101 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:117768817 A>G maps to ENST00000338101 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:117698287 T>C maps to ENST00000338101 K783K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr12:117662908 T>C maps to ENST00000338101 Q1280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:117705853 G>A maps to ENST00000338101 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr12:117680486 G>A maps to ENST00000338101 R1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:117672460 G>A maps to ENST00000338101 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:117672547 G>A maps to ENST00000338101 F1053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:117655918 G>A maps to ENST00000338101 Y1441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:117718610 G>A maps to ENST00000338101 N481N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:117768703 G>T maps to ENST00000338101 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr12:117662862 G>A maps to ENST00000338101 R1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr12:117665446 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:117691505 G>T maps to ENST00000338101 S896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:162325136 C>A maps to NM_014697.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:162326814 G>A maps to NM_014697.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:162337121 C>T maps to NM_014697.2 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr17:26091023 G>A maps to NM_000625.4 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr17:26105787 C>T maps to NM_000625.4 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:26114852 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:150698923 C>T maps to NM_000603.4 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:150690935 C>T maps to NM_000603.4 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:50063237 G>A maps to NM_015953.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:50059076 G>A maps to NM_015953.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:50063266 G>A maps to NM_015953.3 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:50063237 G>A maps to NM_015953.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:50060500 G>A maps to NM_015953.3 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:50059576 C>T maps to NM_015953.3 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:169688034 G>A maps to NM_001171631.1 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:169721448 C>A maps to NM_001171631.1 S554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr9:139391143 C>A maps to NM_017617.3 P2349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr9:139413166 G>A maps to NM_017617.3 N325N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:139410109 G>A maps to NM_017617.3 H576H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:139417386 G>A maps to NM_017617.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:139390732 C>T maps to NM_017617.3 S2486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr9:139417611 G>A maps to NM_017617.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:139399874 C>T maps to NM_017617.3 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr9:139402445 C>T maps to NM_017617.3 G1157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:139397646 G>A maps to NM_017617.3 I1718I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr9:139417590 G>A maps to NM_017617.3 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:120480030 C>T maps to NM_024408.2 T1132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:120464409 C>A maps to NM_024408.2 E1746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:120493433 C>A maps to NM_024408.2 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:120458858 G>A maps to NM_024408.2 S2162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:120464368 G>A maps to NM_024408.2 V1759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:120512257 G>A maps to NM_024408.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr1:120512299 G>A maps to NM_024408.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:145281660 T>C maps to ENST00000454606 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr1:145281657 C>A maps to ENST00000454606 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:145273385 C>T maps to ENST00000454606 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:15281329 C>T maps to NM_000435.2 P1642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:15298093 G>A maps to NM_000435.2 C554C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:15291546 G>A maps to NM_000435.2 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:15285054 C>T maps to NM_000435.2 P1520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:15308342 G>A maps to NM_000435.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:32170166 T>C maps to NM_004557.3 S1147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:32188203 G>A maps to NM_004557.3 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr6:32165332 C>A maps to NM_004557.3 E1599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:79914808 G>A maps to NM_178493.5 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:79916863 C>T maps to NM_178493.5 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:79910911 G>A maps to NM_178493.5 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:79914799 C>T maps to NM_178493.5 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:120430322 C>T maps to NM_002514.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:120429015 C>T maps to NM_002514.3 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr8:120431464 C>T maps to NM_002514.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr8:120435252 C>T maps to NM_002514.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:26949215 G>A maps to ENST00000449198 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:26917941 G>A maps to ENST00000449198 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:26939684 G>A maps to NM_006491.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:26918115 A>G maps to ENST00000449198 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:27064754 G>A maps to ENST00000449198 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:46443261 G>A maps to NM_002516.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr19:46457127 C>T maps to NM_002516.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:46443261 G>A maps to NM_002516.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:100117553 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100118516 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:100125798 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100117725 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100105256 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr23:100117461 C>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:100118512 C>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100105164 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100117253 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100117442 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100125775 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:100106313 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:100117187 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100098944 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:100106234 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100098951 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100125754 T>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:100104923 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr23:100117471 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:155752005 G>A maps to NM_015718.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:155743923 G>A maps to NM_015718.2 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:155728349 G>A maps to NM_015718.2 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:155776036 G>A maps to NM_015718.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr6:155728361 G>A maps to NM_015718.2 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:89059916 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:89182638 A>G maps to NM_016931.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr11:89059784 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr11:89155083 C>T maps to NM_016931.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:89059868 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:89133547 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:69339820 C>T maps to NM_024505.3 I587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:69347680 C>T maps to NM_024505.3 F669F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:69340217 C>T maps to NM_024505.3 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:69348990 C>T maps to NM_024505.3 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:69339760 C>T maps to NM_024505.3 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:69327807 C>T maps to NM_024505.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:69339760 C>T maps to NM_024505.3 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:140323440 C>T maps to NM_006647.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:2030444 G>A maps to NM_172168.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:2030073 A>G maps to NM_172168.1 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:47542339 C>A maps to NM_002517.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr2:101582228 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:101591323 G>A maps to NM_002518.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:101521207 G>T maps to ENST00000427413 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:101549439 G>T maps to NM_002518.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:101549439 G>T maps to NM_002518.3 E84*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:34269057 C>T maps to NM_001164749.1 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr14:34243679 C>T maps to NM_001164749.1 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:34269486 C>T maps to NM_001164749.1 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:34269153 C>T maps to NM_001164749.1 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr14:34204507 C>T maps to NM_001164749.1 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:33525144 G>T maps to NM_001164749.1 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:34266668 T>C maps to NM_001164749.1 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:34269090 C>T maps to NM_001164749.1 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:66192547 G>A maps to NM_178864.3 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:66192007 C>T maps to NM_178864.3 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:66192013 G>A maps to NM_178864.3 E551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:66188766 C>T maps to NM_178864.3 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:66190640 C>A maps to NM_178864.3 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:66191546 G>T maps to NM_178864.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:108060040 T>C maps to NM_002519.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:108043708 C>A maps to NM_002519.2 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:108056018 C>T maps to NM_002519.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:108031837 T>C maps to NM_002519.2 E1325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:108068061 A>G maps to NM_002519.2 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:108060031 T>C maps to NM_002519.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr8:53852601 G>T maps to NM_005285.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr8:53852712 C>T maps to NM_005285.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:62738052 G>T maps to NM_005286.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:21140241 C>T maps to NM_000271.4 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:21134924 G>T maps to NM_000271.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr18:21134741 C>T maps to NM_000271.4 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:21125007 G>T maps to NM_000271.4 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:44571807 C>T maps to NM_013389.2 R806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44579245 G>A maps to NM_013389.2 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:44573449 C>T maps to NM_013389.2 R723R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr7:44579497 C>T maps to NM_013389.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:57289139 C>T maps to NM_024663.3 N431N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:57289674 C>T maps to NM_024663.3 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:57289674 C>T maps to NM_024663.3 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr20:57289001 G>A maps to NM_024663.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr20:57276070 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:57276177 C>T maps to NM_024663.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:57288655 C>A maps to ENST00000371137 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:45623285 G>A maps to NM_006310.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:45656878 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr17:45691040 C>T maps to NM_006310.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:53900914 G>A maps to NM_003717.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:72994472 C>A maps to NM_004885.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:110936073 C>T maps to NM_000272.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:110922294 G>A maps to NM_000272.3 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:132407949 G>A maps to ENST00000393156 R951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:132400930 A>G maps to ENST00000393156 Y1272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:132405171 C>T maps to ENST00000393156 K1087K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:132415579 G>A maps to ENST00000393156 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr3:132403535 T>C maps to ENST00000393156 L1144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:132418249 C>A maps to ENST00000393156 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:132427037 G>T maps to ENST00000393156 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr3:132407629 G>A maps to ENST00000393156 Q997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:132415579 G>A maps to ENST00000393156 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:132438551 G>A maps to ENST00000393156 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:132403546 G>A maps to ENST00000393156 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:132400858 T>A maps to ENST00000393156 S1296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr3:132415573 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:5927851 C>T maps to NM_015102.2 E1140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:6012819 G>T maps to NM_015102.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:5924556 G>A maps to NM_015102.2 F1279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:5925254 G>A maps to NM_015102.2 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:5924552 G>A maps to NM_015102.2 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:5950972 G>A maps to NM_015102.2 D753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr1:5933356 G>A maps to NM_015102.2 A1090A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:5927116 C>T maps to NM_015102.2 P1177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:6038331 C>A maps to NM_015102.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:5934950 G>A maps to NM_015102.2 I1009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr1:5925317 C>T maps to NM_015102.2 A1220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:36336294 G>A maps to NM_004646.3 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36317493 G>T maps to NM_004646.3 I1216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36322393 C>A maps to NM_004646.3 E1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr19:36341875 G>A maps to NM_004646.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:36338978 G>A maps to NM_004646.3 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:36336312 C>T maps to NM_004646.3 E629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:36322596 G>A maps to NM_004646.3 A1078A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:36339974 G>T maps to NM_004646.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:36339985 G>A maps to NM_004646.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:36339589 T>C maps to NM_004646.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:36336315 G>A maps to NM_004646.3 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr19:36340450 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:36341941 G>T maps to NM_004646.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:179520460 C>T maps to NM_014625.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:79575809 G>A maps to NM_017921.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:79536137 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:21882773 C>T maps to NM_182795.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:21883283 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:103542288 G>A maps to NM_006993.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:103542276 G>A maps to NM_006993.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:106859497 T>C maps to ENST00000503451 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:106819081 G>A maps to ENST00000503451 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:106890053 C>T maps to ENST00000503451 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:106888483 C>G maps to ENST00000503451 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:11918442 A>G maps to NM_002521.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:153665652 C>T maps to NM_000906.3 R1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:153661545 T>C maps to NM_000906.3 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:153661482 G>A maps to NM_000906.3 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:35809162 C>T maps to NM_003995.3 I999I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35792410 G>A maps to NM_003995.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35809391 C>T maps to NM_003995.3 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:35800117 C>T maps to NM_003995.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:35792962 C>T maps to NM_003995.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:35800722 G>A maps to NM_003995.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr5:32780846 C>T maps to ENST00000265074 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:50386910 G>A maps to NM_006545.4 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:143287 G>A maps to ENST00000399953 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:188248 G>A maps to ENST00000399953 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr16:136808 C>T maps to ENST00000399953 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr16:142707 G>A maps to ENST00000399953 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:129350792 G>T maps to NM_001030013.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr7:34724219 C>G maps to NM_207172.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:34867037 G>A maps to NM_207172.1 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:34888191 C>A maps to NM_207172.1 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:34724282 G>A maps to NM_207172.1 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr7:34851395 C>T maps to NM_207172.1 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:73889624 C>T maps to NM_012428.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr15:73866014 G>A maps to NM_012428.3 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:78449359 G>A maps to NM_002522.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:98249100 C>A maps to NM_002523.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:98254426 C>T maps to NM_002523.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr7:98249164 G>T maps to NM_002523.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:164247673 A>G maps to NM_000909.4 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:156135570 C>A maps to NM_000910.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:156136176 C>T maps to NM_000910.2 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:156136152 C>T maps to NM_000910.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr4:164272659 T>A maps to NM_006174.2 L412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:164271439 C>T maps to NM_006174.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A1DQ-01A-11D-A135-09 chr4:164272618 T>C maps to NM_006174.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:69752136 C>T maps to NM_000903.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:69744944 G>A maps to NM_000903.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:69752318 G>T maps to NM_000903.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:3015820 C>T maps to NM_000904.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:30326484 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:30327278 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:30322826 C>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:30322855 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:30326345 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:30326387 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:30322826 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:30322855 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38250216 C>T maps to NM_021724.3 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38252961 G>A maps to NM_021724.3 H147H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:38253453 G>A maps to NM_021724.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:38250183 C>T maps to NM_021724.3 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:23996190 C>T maps to NM_005126.4 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:50882353 C>T maps to NM_007121.4 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:50881526 G>A maps to NM_007121.4 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:47282071 C>T maps to NM_005693.2 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:100904866 G>T maps to ENST00000392986 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:100955768 G>A maps to ENST00000392986 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:119530521 C>T maps to NM_022002.2 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:119531657 G>A maps to NM_022002.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:119531579 G>A maps to NM_022002.2 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:119534203 G>T maps to NM_022002.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161200568 G>A maps to ENST00000506209 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:161202703 G>T maps to NM_001077482.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:95416117 C>A maps to NM_003297.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:15064782 C>A maps to NM_003298.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:19313363 C>T maps to ENST00000420605 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:108499426 G>A maps to ENST00000368983 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr6:108502143 C>T maps to ENST00000368983 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:108492734 C>T maps to ENST00000368983 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:72105730 G>T maps to NM_014249.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr5:92923707 C>T maps to NM_005654.4 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr19:17343187 G>A maps to NM_005234.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr5:142780088 G>A maps to NM_001024094.1 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:142780281 A>C maps to NM_001024094.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:142662263 C>A maps to NM_001024094.1 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:142779762 T>C maps to NM_001024094.1 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr5:142675153 G>A maps to NM_001024094.1 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:149002596 C>T maps to ENST00000511528 A955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:149035298 G>A maps to ENST00000511528 Q923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:149356635 G>T maps to ENST00000511528 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:149041368 G>A maps to ENST00000511528 R865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:149357282 G>A maps to ENST00000511528 R244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:149073675 C>T maps to ENST00000511528 S822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:149356786 G>C maps to ENST00000511528 S409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr4:149356986 G>A maps to ENST00000511528 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:149002515 C>T maps to ENST00000511528 P982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr12:52450302 G>A maps to ENST00000360284 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:52451312 C>T maps to ENST00000360284 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:52452703 C>A maps to ENST00000360284 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:52448585 C>T maps to ENST00000360284 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:157184954 G>A maps to NM_006186.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:157184463 G>A maps to NM_006186.3 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:157184500 G>A maps to NM_006186.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:102606980 A>G maps to NM_173200.1 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:200014582 C>T maps to NM_205860.1 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:200012947 A>G maps to NM_205860.1 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:200017843 C>T maps to NM_205860.1 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:200017937 G>T maps to NM_205860.1 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:127289151 G>A maps to NM_033334.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:127302466 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:127306127 C>A maps to NM_033334.2 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:127302448 G>A maps to NM_033334.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:127302448 G>A maps to NM_033334.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:115357781 C>T maps to ENST00000369358 A1434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:115401185 C>A maps to ENST00000369358 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:115373959 C>T maps to ENST00000369358 A1102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:115374705 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:115380386 C>T maps to ENST00000369358 K958K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:115401231 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:115385883 G>A maps to ENST00000369358 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:115383395 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:115251241 C>A maps to NM_002524.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:115256485 G>A maps to NM_002524.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:115256485 G>A maps to NM_002524.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:64913620 G>A maps to NM_030759.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:27663268 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:144921063 A>G maps to NM_178564.3 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:107790524 C>A maps to ENST00000379032 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:107823244 G>T maps to ENST00000379032 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:107832179 G>A maps to ENST00000379032 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:107878196 G>A maps to ENST00000379032 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:107872929 G>A maps to ENST00000379032 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:52254943 T>C maps to NM_002525.2 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:52293534 C>T maps to NM_002525.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:52301806 C>T maps to NM_002525.2 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:52344034 C>A maps to NM_002525.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:52260188 A>T maps to NM_002525.2 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:129394969 C>T maps to ENST00000393231 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:32620843 C>A maps to NM_001160004.1 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:32621514 G>A maps to NM_013956.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:32453412 G>A maps to NM_013956.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:32621397 G>A maps to NM_013956.3 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:32505463 C>A maps to NM_013959.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:32607088 G>A maps to NM_013956.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:32617883 G>T maps to NM_013956.3 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:139231241 C>T maps to NM_013982.2 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:139232129 G>A maps to NM_013982.2 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:83635659 G>A maps to ENST00000404547 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:84118493 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:84118517 C>T maps to ENST00000404547 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:83926496 C>A maps to NM_001165973.1 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr10:84745219 C>T maps to ENST00000404547 Y674Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:84498383 T>C maps to ENST00000404547 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:84745345 T>G maps to ENST00000404547 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:84118591 C>T maps to ENST00000404547 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:84745301 C>T maps to ENST00000404547 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:76254275 A>C maps to NM_138573.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:16337362 T>A maps to NM_003489.3 K1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:16337047 C>A maps to NM_003489.3 E1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:16337366 C>T maps to NM_003489.3 A1049A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:16339597 C>A maps to NM_003489.3 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:16337151 A>C maps to NM_003489.3 L1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:2939981 C>T maps to NM_031474.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:2936378 G>A maps to NM_031474.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:9009769 G>A maps to NM_020645.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:9007397 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:105150518 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:105153356 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105197082 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:105144609 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:105153157 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:105161580 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:105167344 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:105168935 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:105125752 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:105168997 C>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:105125772 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:105187943 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:105193672 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:105153818 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:105197118 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105153830 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr23:105189995 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:105153255 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:105153846 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:105179181 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:105179242 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:105169014 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr23:105168723 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr23:105168951 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:105152944 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:105150500 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:105153103 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:105168780 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:105179274 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:105190373 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:105168909 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:105181434 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr23:105167390 T>C did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:105153426 G>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:105190346 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:105150431 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:105156704 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:105178433 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:6002728 C>T maps to NM_016588.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr6:6002686 C>T maps to NM_016588.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:33475279 G>A maps to NM_003873.5 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:33474631 G>A maps to NM_003873.5 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:33619721 G>A maps to NM_003873.5 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr10:33552748 G>A maps to NM_003873.5 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:33474631 G>A maps to NM_003873.5 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:33515118 G>A maps to NM_003873.5 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:33491812 C>A maps to ENST00000374823 E624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr10:33510749 T>C maps to NM_003873.5 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:206548028 T>G maps to NM_201266.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:206659484 C>A maps to NM_201266.1 Y833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:206562277 C>T maps to NM_201266.1 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr2:206608017 C>T maps to NM_201266.1 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:206617598 C>T maps to NM_201266.1 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:206562427 C>T maps to NM_201266.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:206562358 C>T maps to NM_201266.1 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:206617598 C>T maps to NM_201266.1 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:206617691 G>A maps to NM_201266.1 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:206562373 C>T maps to NM_201266.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:206617598 C>T maps to NM_201266.1 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:206630257 C>A maps to NM_201266.1 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:206656999 G>T maps to NM_201266.1 E828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:206562436 C>T maps to NM_201266.1 H81H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:24146140 G>A maps to NM_080723.4 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr6:24145981 G>A maps to NM_080723.4 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:334236 G>A maps to NM_024958.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:50149273 G>A maps to ENST00000404971 C1484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:50692637 C>T maps to ENST00000404971 W1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:50765739 G>A maps to ENST00000404971 Y638Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:50779812 C>T maps to ENST00000404971 G597G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A056-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:51254778 G>A maps to ENST00000404971 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:51147141 A>T maps to ENST00000405581 *279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:50318574 C>A maps to ENST00000404971 E1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:51254778 G>A maps to ENST00000404971 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:50282156 C>T maps to ENST00000404971 A1288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:50779938 G>A maps to ENST00000404971 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:50724631 A>C maps to ENST00000404971 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr2:51254688 G>T maps to ENST00000404971 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr2:50463973 G>A maps to ENST00000404971 R1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:51149004 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:50464042 G>A maps to ENST00000404971 R1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:64390266 C>T maps to NM_015080.3 T1377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:64402910 G>A maps to NM_015080.3 Y1139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:64387802 G>A maps to NM_015080.3 S1405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr11:64390260 C>T maps to NM_015080.3 R1379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:64428230 C>A maps to NM_015080.3 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:64375246 G>T maps to NM_015080.3 V1520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:64453285 C>T maps to NM_015080.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:64434866 G>A maps to NM_015080.3 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:64419007 G>A maps to NM_015080.3 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:64410185 C>T maps to NM_138734.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr11:64436058 G>A maps to NM_015080.3 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:79434666 A>G maps to NM_004796.4 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:79933573 G>A maps to NM_004796.4 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:80130242 C>T maps to NM_004796.4 N816N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr14:80328222 C>T maps to NM_004796.4 N1034N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:176631232 C>T maps to NM_022455.4 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:176638934 G>T maps to NM_022455.4 E1179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:176700766 A>G maps to NM_022455.4 P1868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr5:176684063 T>G maps to NM_022455.4 T1626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:176709554 T>G maps to NM_022455.4 T1994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr5:176638604 C>T maps to NM_022455.4 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr5:176722276 C>G maps to NM_022455.4 L2636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr5:176636851 A>G maps to NM_022455.4 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:176637406 C>T maps to NM_022455.4 F669F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:176687065 C>A maps to NM_022455.4 I1681I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:176638201 C>A maps to NM_022455.4 V934V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:176673766 T>C maps to NM_022455.4 D1489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr5:176636891 C>T maps to NM_022455.4 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:176631232 C>T maps to NM_022455.4 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:152031180 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152018952 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152037623 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr23:152034404 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152014886 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152031183 C>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:152031268 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:152034373 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:152031181 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr23:152036176 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr23:152027347 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:152037636 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152031205 G>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:152031180 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:152014975 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:1433202 G>A maps to ENST00000476071 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:1426308 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:212965005 C>A maps to NM_015471.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:59522248 C>A maps to NM_001144772.1 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr8:59522168 G>C maps to NM_001144772.1 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:59496666 A>G maps to NM_001144772.1 *949Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr8:59500238 C>A maps to NM_001144772.1 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:27268864 G>A maps to NM_145080.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:6607380 A>G maps to NM_017755.5 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:6625744 G>A maps to NM_017755.5 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:6620216 A>G did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr5:6625760 C>T maps to NM_017755.5 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:93845072 A>G maps to NM_022072.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:93803122 C>T maps to NM_022072.3 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:46827306 T>G maps to NM_199044.2 L315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:18840768 G>A maps to NM_182543.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:18840886 A>G maps to NM_182543.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:18885148 T>G maps to NM_182543.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:40810679 G>A maps to NM_024677.4 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:40792737 G>T maps to NM_024677.4 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:40752618 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:40792752 G>T maps to NM_024677.4 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:40796461 G>A maps to NM_024677.4 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:40131310 G>A maps to NM_032526.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:40126807 G>A maps to NM_032526.1 H228H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:40131262 G>A maps to NM_032526.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:40131262 G>A maps to NM_032526.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:40131250 G>T maps to NM_032526.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:18745175 G>T maps to ENST00000455492 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr2:18757608 A>G maps to ENST00000455492 D467D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:18765854 G>A maps to ENST00000455492 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:18745310 A>C maps to ENST00000455492 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:104849641 C>T maps to NM_001134373.1 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:104865539 T>G maps to NM_001134373.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:104852929 G>A maps to NM_001134373.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:39981852 G>A maps to NM_052935.4 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:39991472 G>A maps to NM_052935.4 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:116560209 C>A maps to NM_152729.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:116542302 C>T maps to NM_152729.2 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:116560281 C>T maps to NM_152729.2 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52563177 G>A maps to NM_001134231.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52563249 G>A maps to NM_001134231.1 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52563282 G>A maps to NM_001134231.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr3:52559278 T>C maps to NM_001134231.1 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr3:52558747 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:104171771 C>T maps to NM_001031701.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:86176975 G>T maps to NM_002526.2 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:17250212 G>A maps to ENST00000379552 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:15133885 G>T maps to NM_173474.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:15141312 G>A maps to NM_173474.2 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:5604141 C>T maps to NM_001102654.1 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr16:2096344 G>A maps to NM_002528.5 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:131781416 C>T maps to NM_001144058.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:132177620 C>T maps to NM_001144058.1 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:132016319 C>T maps to NM_001144058.1 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:9083205 G>A maps to NM_004822.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:9143092 C>T maps to NM_004822.2 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:96104369 G>A maps to NM_021229.3 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:49167914 A>C maps to NM_145807.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:107867388 C>T maps to NM_001113226.1 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:107691409 C>T maps to NM_001113226.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:107937832 C>T maps to NM_001113226.1 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:135114518 C>T maps to NM_032536.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:156846289 C>T maps to NM_002529.3 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156843722 C>T maps to NM_002529.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:156845429 C>T maps to NM_002529.3 I491I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:156811907 G>A maps to NM_001007792.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:156849885 C>T maps to NM_002529.3 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:156851253 C>T maps to NM_002529.3 I737I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BS-A0UV-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:156811907 G>A maps to NM_001007792.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:87359924 G>A maps to NM_006180.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:87342674 C>T maps to NM_006180.3 N320N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:87636168 G>T maps to NM_006180.3 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:87482188 C>T maps to NM_006180.3 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:87285746 C>T maps to NM_006180.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr9:87636327 G>A maps to NM_006180.3 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:88472460 G>A maps to NM_001012338.1 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:88669547 G>A maps to NM_001012338.1 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr15:88483979 C>T maps to NM_001012338.1 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:88476339 C>A maps to NM_001012338.1 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr15:88726683 G>T maps to NM_001012338.1 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:86272215 G>T maps to NM_006183.3 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:61341128 C>T maps to NM_002531.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr20:61386238 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:61340981 C>T maps to NM_002531.2 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:106461142 C>A maps to NM_014840.2 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:106461182 C>T maps to NM_014840.2 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:106532358 C>A maps to NM_014840.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:106461101 C>T maps to NM_014840.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:205277831 G>A maps to ENST00000441520 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:205277342 G>A maps to ENST00000441520 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:205280954 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:151072938 G>A maps to ENST00000355851 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:151065945 G>A maps to ENST00000355851 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:10851781 C>A maps to NM_002484.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:10862938 G>T maps to NM_002484.2 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:10846483 C>T maps to NM_002484.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:1836623 C>T maps to NM_012225.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:32034244 G>A maps to NM_025152.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:32031421 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr14:32295833 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49416410 G>A maps to NM_006184.5 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr19:49422494 C>T maps to NM_006184.5 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:49407614 G>A maps to NM_006184.5 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:17332455 G>T maps to ENST00000458064 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:17332760 G>T maps to ENST00000458064 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:205687485 C>T maps to NM_022731.4 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:205688690 C>A maps to NM_022731.4 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:110257596 G>A maps to NM_032869.3 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:110257569 G>A maps to NM_032869.3 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:110287682 C>T maps to NM_032869.3 W357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:110308738 A>G maps to NM_032869.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:110308708 G>A maps to NM_032869.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:162881023 G>A maps to NM_145266.4 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr7:44467292 C>T maps to NM_015332.3 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:44425714 G>T maps to NM_015332.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:44524646 G>T maps to NM_015332.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:44431997 C>T maps to NM_015332.3 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:44467202 C>T maps to NM_015332.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:2284281 C>T maps to NM_198954.1 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:51076094 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:51075875 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:51076182 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:51075999 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:51075903 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:51238967 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:51238837 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:51239118 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:51239179 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:102887995 G>A maps to NM_031438.2 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:102890501 T>C maps to NM_031438.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:105639489 A>G maps to NM_177533.3 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:48619866 G>T maps to NM_018283.1 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:4745047 G>A maps to NM_032349.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr16:4744990 C>A maps to NM_032349.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:145588451 G>A maps to NM_001012758.2 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:33202820 C>T maps to NM_001105570.1 H362H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:34343135 G>T maps to NM_147173.1 G48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:56485036 C>T maps to NM_007006.2 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr11:63994219 C>T maps to NM_032344.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr4:123838796 G>A maps to NM_007083.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:77775564 C>T maps to NM_001105663.1 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:77775537 G>A maps to NM_001105663.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:77775868 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:88379122 C>T maps to NM_024047.3 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:163310152 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr17:27613850 G>A maps to NM_020772.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:71726136 C>T maps to ENST00000393695 E810E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:71715127 C>T maps to ENST00000393695 S2053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:71734113 C>T maps to ENST00000393695 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr11:71724509 G>A maps to ENST00000393695 Q1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:71726952 C>T maps to ENST00000393695 Q538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:71734139 G>A maps to ENST00000393695 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:71727222 C>T maps to ENST00000393695 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:71729439 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr14:73743324 G>A maps to NM_001005743.1 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr14:73743687 G>T maps to NM_001005743.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:41183160 G>A maps to NM_004756.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:41173888 C>T maps to NM_004756.3 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:69115883 C>T maps to NM_020401.2 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:69103077 C>T maps to NM_020401.2 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:69109463 G>T maps to NM_020401.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:229601164 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:229613383 G>A maps to NM_018230.2 Y572Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:229631266 G>A maps to NM_018230.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr6:17629252 T>C maps to ENST00000430136 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:17629012 C>T maps to ENST00000430136 E1170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:17637987 C>T maps to ENST00000430136 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr6:17688849 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:17648118 C>T maps to ENST00000430136 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:17629744 C>T maps to ENST00000430136 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:17669568 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr6:17629744 C>T maps to ENST00000430136 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:37310815 G>T maps to NM_153485.1 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:37314335 T>C maps to NM_153485.1 E800E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:47858498 C>T maps to NM_015231.1 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:47833687 G>A maps to NM_015231.1 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:47834489 T>C maps to NM_015231.1 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:47833883 C>A maps to NM_015231.1 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:47861854 A>G maps to ENST00000458312 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:47825012 G>A maps to NM_015231.1 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:131721109 C>A maps to NM_015354.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:131721313 T>C maps to NM_015354.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:131741548 T>C maps to NM_015354.1 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:131735485 C>T maps to NM_015354.1 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:131745253 G>A maps to NM_015354.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:131730844 G>T maps to NM_015354.1 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:131730844 G>T maps to NM_015354.1 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:135298995 G>A maps to NM_015135.2 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:135300664 A>G maps to NM_015135.2 E1104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr7:135322801 C>T maps to NM_015135.2 Q1754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:135261102 G>A maps to NM_015135.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:135286122 G>T maps to NM_015135.2 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:135285615 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:135292083 C>T maps to NM_015135.2 R1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:13376971 C>T maps to NM_024923.2 S1275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:13429928 C>T maps to NM_024923.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:13377106 C>T maps to NM_024923.2 S1230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:13441303 C>T maps to NM_024923.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr3:13360602 C>T maps to NM_024923.2 T1844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:13383334 G>A maps to NM_024923.2 R1047R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:154090290 C>T maps to NM_207308.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:154034124 C>T maps to NM_207308.2 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:154099869 G>A maps to NM_207308.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:154042812 G>A maps to NM_207308.2 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:154098921 G>A maps to NM_207308.2 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:154090208 C>A maps to NM_207308.2 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:154090286 C>A maps to NM_207308.2 G512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:154101759 T>G maps to NM_207308.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:154113925 C>A maps to NM_207308.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:154099822 G>T maps to NM_207308.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:154125308 T>C maps to NM_207308.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:134008541 T>C maps to ENST00000451030 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:134049452 C>T maps to ENST00000451030 R970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:134106124 C>T maps to ENST00000451030 S2062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr9:134004847 G>T maps to ENST00000451030 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:134103661 G>A maps to ENST00000451030 S2007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr9:134014759 C>T maps to ENST00000451030 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:134014759 C>T maps to ENST00000451030 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:134050985 G>A maps to ENST00000451030 R1100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr9:134027251 C>T maps to ENST00000451030 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr9:134038530 G>A maps to ENST00000451030 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:134002927 G>A maps to ENST00000451030 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr9:134016081 C>T maps to ENST00000451030 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:184016242 T>C maps to NM_138285.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:102505967 G>A maps to NM_024057.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr12:102471110 A>G maps to NM_024057.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:150063595 G>A maps to NM_198887.1 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:45574596 C>T maps to NM_007172.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr22:45580485 G>T maps to NM_007172.3 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:77038815 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:77055442 C>A maps to ENST00000458189 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:77053838 C>T maps to ENST00000458189 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:77039287 C>T maps to ENST00000458189 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr4:77051861 G>A maps to ENST00000458189 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:77045812 T>G maps to ENST00000458189 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:77055442 C>A maps to ENST00000458189 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:50411744 G>A maps to NM_012346.4 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:50412395 C>T maps to NM_012346.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:50412113 G>A maps to NM_012346.4 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:106397394 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:106396684 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:106418350 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:106396716 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:106397375 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:5294965 G>A maps to NM_002532.3 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:5307518 A>G maps to NM_002532.3 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:56855456 G>A maps to NM_014669.3 Q202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:56868647 C>T maps to NM_014669.3 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr16:56782201 C>T maps to NM_014669.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:56864529 C>T maps to NM_014669.3 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:56865846 C>A maps to NM_014669.3 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:56863002 T>C maps to NM_014669.3 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:3723907 G>T maps to NM_016320.4 G1099G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:3720410 C>A maps to NM_016320.4 E1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:3697754 A>G maps to NM_016320.4 D1723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:3726448 C>T maps to NM_016320.4 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:3712616 G>A maps to NM_016320.4 R1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:3797195 A>G maps to NM_016320.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:3794884 C>A maps to NM_016320.4 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:3721960 T>C maps to NM_016320.4 K1207K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D1-A16F-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:3723762 C>A maps to NM_016320.4 E1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:25912853 G>T maps to NM_014089.3 G539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:25905640 C>T maps to NM_014089.3 N460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:25895090 G>T maps to NM_014089.3 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:25901074 G>A maps to NM_014089.3 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr13:25881961 C>T maps to NM_014089.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:25905589 G>A maps to NM_014089.3 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:23224701 T>A maps to ENST00000413919 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr15:41625166 C>G maps to NM_016359.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:41672321 C>T maps to NM_016359.3 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr16:67902441 G>A maps to NM_005796.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:224468865 G>A maps to NM_002533.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:224505618 G>A maps to NM_002533.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:224482033 C>T maps to NM_002533.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:16918535 C>T maps to ENST00000438489 C1292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:16918919 C>T maps to ENST00000438489 R1420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:16884093 G>A maps to ENST00000438489 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:16918931 C>T maps to ENST00000438489 F1424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:16899871 G>A maps to ENST00000438489 W937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:16908672 G>A maps to ENST00000438489 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:16918718 C>T maps to ENST00000438489 S1353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr19:16860862 G>A maps to ENST00000438489 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:16902312 G>A maps to ENST00000438489 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:16918718 C>T maps to ENST00000438489 S1353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr11:62561743 G>A maps to NM_006362.4 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:62561827 C>T maps to NM_006362.4 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:62569082 G>A maps to NM_006362.4 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:62561845 G>A maps to NM_006362.4 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62563654 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:62568567 C>A maps to NM_006362.4 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr23:101581401 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101576774 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:101572403 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:101572037 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101572386 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:101572403 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:101581386 G>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr23:101572361 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr23:101572394 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:101576706 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr23:101572033 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:101615539 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:101619977 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:101620155 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:101624598 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:101623470 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101615527 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101622754 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101624639 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:101623451 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:101624902 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:101623488 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:102334366 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:102339642 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:102334779 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:102337961 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:102335506 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:102331220 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:102334535 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:102339673 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102334739 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102335122 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:102339379 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:102339781 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:102337968 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101096243 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101096274 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101097757 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:101093351 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:101095985 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101095493 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101096485 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101096238 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:101091776 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:101096867 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:17571441 G>T maps to NM_138454.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr2:139429094 C>T maps to NM_007226.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr17:47656115 G>A maps to ENST00000513748 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:47656418 C>A maps to ENST00000513748 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:108780176 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:108785736 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:108784715 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:108779157 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:108785764 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr14:24878719 C>T maps to NM_025081.2 R574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:24877484 C>T maps to NM_025081.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:24883906 G>A maps to NM_025081.2 E984E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:24884041 G>A maps to NM_025081.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:24877969 C>T maps to NM_025081.2 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:24886096 G>A maps to NM_025081.2 T1714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:24884932 C>T maps to NM_025081.2 G1326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:24878758 G>T maps to NM_025081.2 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:24884008 C>T maps to NM_025081.2 D1018D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:24880575 G>A maps to NM_025081.2 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr23:41307172 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41333766 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:41333722 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr23:41333518 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:41333839 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:113348943 C>T maps to NM_001032409.1 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:113346399 C>T maps to NM_001032409.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:113425159 C>T maps to NM_001032731.1 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:113445508 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:113440810 C>A maps to NM_016817.2 C361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:113424997 G>A maps to NM_016817.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:113403730 C>T maps to NM_006187.2 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:113400696 C>T maps to NM_006187.2 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:113379376 A>G maps to NM_006187.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr12:113405811 C>A maps to NM_006187.2 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:121458576 C>A maps to NM_003733.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:121476744 T>C maps to NM_003733.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:121471381 G>A maps to NM_003733.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:121471447 C>T maps to NM_003733.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:121461903 G>A maps to NM_003733.2 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:121458636 G>T maps to NM_003733.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr10:126097525 A>G maps to NM_000274.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:64982679 C>T maps to ENST00000403937 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:151739763 G>T maps to ENST00000321531 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:151742668 C>T maps to ENST00000321531 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr1:151739763 G>T maps to ENST00000321531 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:192550669 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:56619961 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr12:56620168 C>A maps to NM_024068.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:56620147 C>T maps to NM_024068.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr12:56619961 G>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:138439771 C>A maps to NM_014582.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:136083887 G>A maps to NM_014581.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr9:136081319 G>A maps to NM_014581.2 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:136083953 G>A maps to NM_014581.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:228431100 C>T maps to NM_001098623.1 A1049A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:228504533 C>T maps to NM_001098623.1 G4470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:228402133 G>A maps to NM_001098623.1 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:228437882 C>T maps to NM_001098623.1 T1417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:228471258 C>T maps to NM_001098623.1 G2931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:228482667 C>T maps to NM_001098623.1 G3861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:228494958 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:228402112 G>A maps to NM_001098623.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:228434422 C>T maps to NM_001098623.1 Q1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:228466987 C>A maps to NM_001098623.1 L2413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:228491382 G>A maps to ENST00000366707 P1272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:228522594 C>A maps to NM_001098623.1 T5389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:228433366 C>T maps to NM_001098623.1 V1245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:228506714 G>A maps to NM_001098623.1 T4754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:228538617 C>T maps to NM_001098623.1 I6131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:228559907 C>T maps to NM_001098623.1 G7143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:228521024 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:228554145 G>T maps to NM_001098623.1 E6408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:228434340 G>A maps to NM_001098623.1 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:228456342 G>A maps to NM_001098623.1 T1658T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A0JY-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:228447202 G>A maps to ENST00000359599 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:228529253 C>T maps to NM_001098623.1 I5991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:228556469 C>A maps to NM_001098623.1 I6605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:228434397 G>A maps to NM_001098623.1 A1309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:228462044 C>T maps to NM_001098623.1 P1861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:228476351 C>T maps to NM_001098623.1 L3368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:228547369 C>T maps to NM_052843.2 R6259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:228565333 G>A maps to NM_001098623.1 V7808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:228471411 C>T maps to NM_001098623.1 S2982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:228480482 C>T maps to NM_001098623.1 V3621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:228466441 G>A maps to NM_001098623.1 K2304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:228509682 C>T maps to NM_001098623.1 D5047D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:228538591 G>T maps to NM_001098623.1 E6123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:228461570 T>C maps to NM_001098623.1 S1746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:228470923 C>T maps to NM_001098623.1 D2892D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:228470926 G>A maps to NM_001098623.1 A2893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:228473932 C>T maps to NM_001098623.1 I3053I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:228525655 C>A maps to NM_001098623.1 I5604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:228403339 C>T maps to NM_001098623.1 D635D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:228565354 C>T maps to NM_001098623.1 S7815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:228560042 G>T maps to NM_001098623.1 V7188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr1:228403423 C>T maps to NM_001098623.1 R663R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:228548104 C>T maps to NM_052843.2 I6504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:228529187 C>T maps to NM_001098623.1 F5969F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:220421014 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:220422064 C>A maps to NM_015311.2 E1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:220428293 A>C maps to NM_015311.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:220428200 G>A maps to NM_015311.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:220424076 G>A maps to NM_015311.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:220427361 C>T maps to NM_015311.2 K905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:220428200 G>A maps to NM_015311.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:220432975 T>C maps to NM_015311.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr2:220432810 G>A maps to NM_015311.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:133051316 C>A maps to ENST00000262283 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:133044177 G>A maps to ENST00000262283 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr15:28202861 G>A maps to NM_000275.2 H552H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:28259960 C>T maps to NM_000275.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:28090114 C>A maps to NM_000275.2 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr15:28000587 G>A maps to NM_000275.2 C821C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr15:28326870 G>A maps to NM_000275.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:28277272 C>T maps to NM_000275.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:48901863 C>A maps to NM_001014446.1 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:70378638 G>A maps to ENST00000515515 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:70388907 G>T maps to ENST00000515515 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr7:5922121 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:128695245 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:128691368 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:128692901 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:128709143 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:128724121 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:128696421 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:128710005 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:128692646 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:128692692 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:128696670 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:128723881 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:128710405 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:128694582 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:128723898 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:128724234 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr23:128723865 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:128696372 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:128724191 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:128703342 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:128703277 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:128724241 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:128696420 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:128721047 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:128678946 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:128710311 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:128721049 G>A did not map to a codon.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr23:128696372 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:10583901 G>A maps to NM_002539.1 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr8:103572892 G>A maps to NM_024410.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr8:103564083 C>A maps to NM_024410.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:131256997 C>T maps to ENST00000372814 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:131223219 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:131247128 G>A maps to NM_153435.1 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr9:131262461 C>T maps to NM_153435.1 N870N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr9:131221914 C>T maps to NM_153435.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:131262455 C>T maps to NM_153435.1 Y868Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:86818541 A>G maps to ENST00000370567 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:86848642 C>A maps to ENST00000370567 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:86836771 C>A maps to ENST00000370567 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:86836789 C>A maps to ENST00000370567 G323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:76019676 T>C maps to NM_175881.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr17:8243824 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr17:8249079 A>G maps to NM_153007.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:8249083 G>T maps to NM_153007.4 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:8248748 G>A maps to NM_153007.4 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:123518517 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:123615601 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:123779078 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:123775790 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:124028185 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:124097521 A>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:123554246 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:123587213 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:123654409 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:124028158 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123514646 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123518489 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123519630 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123615583 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123630915 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123637511 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123680826 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123785873 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123839053 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:123514497 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:123654546 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:124097420 C>A did not map to a codon.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr23:123779055 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:124029855 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:123870944 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:124097385 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:123654619 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:123514724 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:123518084 A>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:123518514 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:123514983 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:123526177 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:123538943 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:123556298 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:123663720 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:123785782 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:123838996 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:123556288 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:123785927 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123514420 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123517811 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123518429 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123554582 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123695571 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123838973 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123839095 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:123779172 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:123838904 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:123805669 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:123518504 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:123526109 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:123514604 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:123515068 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:123637511 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:123787477 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr23:123554372 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:123514955 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:124029865 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123514838 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123516585 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123526104 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123615687 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123785873 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:123554170 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:123775651 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:123518247 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:123556484 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:123787436 A>G did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:123519700 G>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:123699280 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr23:123518365 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:123554193 T>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:123870938 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:123514603 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:123615581 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:124028190 G>T did not map to a codon.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr23:123554348 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:167671561 C>T maps to NM_001122679.1 S1877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:167642224 C>T maps to NM_001122679.1 A1333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:167674558 C>T maps to NM_001122679.1 Y2196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:167419969 C>A maps to NM_001122679.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:167674405 C>T maps to NM_001122679.1 F2145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:167674777 C>T maps to NM_001122679.1 F2269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:167645680 T>G maps to NM_001122679.1 V1586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:167674051 C>T maps to NM_001122679.1 T2027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:167689499 C>T maps to NM_001122679.1 F2661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:167545381 C>T maps to NM_001122679.1 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:167645245 G>A maps to NM_001122679.1 A1441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:167674741 C>T maps to NM_001122679.1 D2257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:167525033 C>A maps to NM_001122679.1 S572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:167674405 C>T maps to NM_001122679.1 F2145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:167689107 C>T maps to NM_001122679.1 L2531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:167653194 C>T maps to NM_001122679.1 N1728N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:166802425 G>A maps to NM_001122679.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:167551990 G>A maps to NM_001122679.1 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:167645836 T>C maps to NM_001122679.1 R1638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:167674063 C>T maps to NM_001122679.1 F2031F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:167674558 C>T maps to NM_001122679.1 Y2196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:167689424 C>T maps to NM_001122679.1 S2636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:167674054 C>T maps to NM_001122679.1 A2028A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr5:167420044 G>A maps to NM_001122679.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:167551946 C>T maps to NM_001122679.1 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:167674039 C>A maps to NM_001122679.1 V2023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:183658160 C>A maps to NM_001080477.1 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:183650142 C>T maps to NM_001080477.1 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:183675944 C>A maps to NM_001080477.1 S1475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:183714436 C>A maps to NM_001080477.1 I2204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:183652201 C>T maps to NM_001080477.1 F959F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:183714187 C>A maps to NM_001080477.1 P2121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:183713935 G>A maps to NM_001080477.1 T2037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:183594305 C>A maps to NM_001080477.1 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:183674627 A>G maps to NM_001080477.1 L1296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:183714751 T>C maps to NM_001080477.1 N2309N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:183664527 G>A maps to NM_001080477.1 R1195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:183652276 C>A maps to NM_001080477.1 I984I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:183676004 C>T maps to NM_001080477.1 I1495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:183720957 C>T maps to NM_001080477.1 N2518N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:183659621 C>T maps to NM_001080477.1 Q1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr4:183710517 A>G maps to NM_001080477.1 T1859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:183713951 C>T maps to NM_001080477.1 L2043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:183721203 C>T maps to NM_001080477.1 F2600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr11:78412982 G>A maps to NM_001098816.2 R1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:78440670 G>T maps to NM_001098816.2 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:78443429 G>T maps to NM_001098816.2 V1023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:78614413 C>T maps to NM_001098816.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:78443600 G>A maps to NM_001098816.2 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:78600872 G>A maps to NM_001098816.2 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:78497991 G>A maps to NM_001098816.2 D772D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:78369474 G>A maps to NM_001098816.2 N2646N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:78381548 G>A maps to NM_001098816.2 F1947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:78600881 C>T maps to NM_001098816.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:78516487 G>A maps to NM_001098816.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:78780875 C>T maps to NM_001098816.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:78780875 C>T maps to NM_001098816.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:78381155 G>A maps to NM_001098816.2 N2078N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:78413136 A>G maps to NM_001098816.2 A1507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:78523251 G>A maps to NM_001098816.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:78369852 G>A maps to NM_001098816.2 L2520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:78380657 G>A maps to NM_001098816.2 R2244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:78369198 G>A maps to NM_001098816.2 D2738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:78523302 G>A maps to NM_001098816.2 C614C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:13754735 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:13775906 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:13775905 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:13764553 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:13771529 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:13778757 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:13781898 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:13764498 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13757138 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:13786876 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr23:13774708 T>C did not map to a codon.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr23:13769456 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:13762556 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:13765057 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:13780499 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:13786291 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:13780490 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:13785376 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:13764498 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:13754791 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:13771529 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:44715780 C>T maps to NM_001003941.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:44721380 C>A maps to ENST00000444676 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44737347 C>T maps to ENST00000444676 I790I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44739759 C>T maps to ENST00000444676 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:44733596 C>T maps to ENST00000444676 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:44736043 C>T maps to ENST00000444676 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:44714839 C>T maps to ENST00000444676 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:50946019 C>T maps to NM_018245.2 R830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:50966467 G>A maps to NM_018245.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:50953485 C>T maps to NM_018245.2 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:56504656 C>T maps to NM_018233.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:56510059 G>A maps to NM_018233.3 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr16:56485604 G>T maps to NM_018233.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:56501899 T>C maps to NM_018233.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:123461416 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:123461268 G>A maps to ENST00000228922 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:123461500 G>A maps to ENST00000228922 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:61444485 C>T maps to NM_007346.2 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:9793508 C>A maps to NM_016821.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:9798807 A>G maps to NM_016820.3 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:9800905 C>T maps to NM_016828.2 L328L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:9807561 C>T maps to NM_016821.2 R340*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:95148027 A>G maps to NM_033014.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:95152321 G>A maps to NM_033014.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr9:95165629 T>C maps to NM_033014.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:95147919 C>T maps to NM_033014.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:70779259 T>C did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:70775051 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70757896 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70767788 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70776887 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70775086 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70781696 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70775882 A>C did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:70787445 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70756095 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70767788 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70756038 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70784535 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70784540 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:70782800 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr23:70775929 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:70783230 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70775920 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70782978 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70787406 G>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:70787477 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:70774429 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:70781712 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:70784452 C>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr15:41624642 C>T maps to NM_007280.1 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:41624627 C>T maps to NM_007280.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:74684054 C>T maps to NM_152635.1 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:74684369 C>T maps to NM_152635.1 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:74684366 C>T maps to NM_152635.1 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:174946709 A>G maps to ENST00000409546 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:15091763 G>T maps to NM_018324.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:15107752 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:15107644 C>T maps to NM_018324.2 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:15115161 G>A maps to NM_018324.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:15115212 G>A maps to NM_018324.2 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:137990193 C>T maps to NM_014279.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:138011606 C>T maps to NM_014279.4 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:9971458 C>T maps to NM_058164.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:9965026 C>T maps to NM_058164.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:102270189 G>A maps to ENST00000338858 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr13:53624653 A>G maps to NM_006418.3 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:53608623 G>T maps to NM_006418.3 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:53624836 G>A maps to NM_006418.3 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr13:53624365 A>C maps to NM_006418.3 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr11:7530981 C>T maps to NM_198474.3 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:7530689 A>G maps to NM_198474.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:7507223 C>T maps to NM_198474.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:7507121 C>T maps to NM_198474.3 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:7507121 C>T maps to NM_198474.3 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr11:7530998 G>A maps to NM_198474.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:127572585 C>T maps to NM_182487.2 N618N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:127572681 C>T maps to NM_182487.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:127572426 G>A maps to NM_182487.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:127572681 C>T maps to NM_182487.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:127572087 C>T maps to NM_182487.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:161969984 C>T maps to ENST00000451379 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161967858 C>T maps to ENST00000451379 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161987264 C>T maps to ENST00000451379 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:161967654 C>T maps to ENST00000451379 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:161987294 G>A maps to ENST00000451379 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:161953716 C>T maps to ENST00000451379 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr6:137815106 G>A maps to NM_175747.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:137814968 C>T maps to NM_175747.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:10319464 T>C maps to NM_002543.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:10319551 G>A maps to NM_002543.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:59002202 C>T maps to NM_145243.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:58999993 C>A maps to NM_145243.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:59004632 C>A maps to NM_145243.3 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:59004632 C>A maps to NM_145243.3 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:95179081 G>A maps to NM_005014.2 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:95177669 C>A maps to NM_005014.2 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:95179485 C>A maps to NM_005014.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:29622905 G>A maps to NM_002544.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:29622427 G>A maps to NM_002544.4 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:76814238 T>C maps to NM_006189.1 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:53081427 G>A maps to NM_004498.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:53049844 G>A maps to NM_004498.1 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:53081346 G>A maps to NM_004498.1 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr18:55103370 C>T maps to NM_004852.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:55143918 C>T maps to NM_004852.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr18:55103931 C>T maps to NM_004852.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:55103733 C>T maps to NM_004852.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:74079352 C>A maps to NM_001080507.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:193355803 C>T maps to NM_130837.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:193360793 C>A maps to NM_130837.2 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:46032559 C>T maps to NM_001017989.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:98105732 A>G maps to NM_033207.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:98105790 G>A maps to NM_033207.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:132307155 G>A maps to NM_002545.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:132204988 C>T maps to NM_001144058.1 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:132307179 G>A maps to NM_002545.3 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:132399018 G>A maps to NM_002545.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:67518843 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:67518843 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:67518931 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:67421495 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:67421497 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:67652806 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:67421492 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:67316725 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:67652752 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:67414306 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:67339156 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:67518843 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:67430066 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:67432022 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:67433724 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:67518842 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:67273627 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:67283779 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:67421525 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:67412827 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr23:67339172 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr8:145106346 G>A maps to ENST00000360660 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:145108231 G>A maps to ENST00000360660 H917H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:145111870 C>A maps to ENST00000360660 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153416135 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153416320 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:153416294 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153416267 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153416188 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153420105 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:153409870 T>A did not map to a codon.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr23:153420213 G>A did not map to a codon.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr23:153416177 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153458962 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153453453 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153461520 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153459110 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:153459133 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:153490517 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153496123 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153490490 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr23:153490555 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153490383 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:153496060 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:128413834 G>A maps to NM_001708.2 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:128414614 G>A maps to NM_001708.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:128415619 G>A maps to NM_001708.2 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr7:128415071 G>A maps to NM_001708.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:128415538 G>A maps to NM_001708.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:128415538 G>A maps to NM_001708.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr7:128414668 G>A maps to NM_001708.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:128415769 C>T maps to NM_001708.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:241761074 T>C maps to NM_014322.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr10:88417836 G>A maps to NM_001030015.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:47775894 G>A maps to ENST00000489301 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:47775894 G>A maps to ENST00000489301 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:47763199 C>T maps to ENST00000489301 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:47775996 T>C maps to ENST00000489301 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:29189551 C>T maps to NM_000911.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:54142027 G>A maps to NM_000912.3 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:62729950 C>T maps to NM_000913.3 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:154412541 C>T maps to NM_001145279.1 R460*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A103-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:203472712 C>T maps to NM_014359.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:13166002 C>T maps to NM_021980.4 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:13166105 G>T maps to NM_021980.4 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:13160938 C>T maps to NM_021980.4 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr10:13164417 T>C maps to NM_021980.4 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:7960476 G>T maps to NM_001003745.1 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:7960511 C>A maps to NM_001003745.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:7960485 T>C maps to NM_001003745.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:6898654 G>A maps to NM_207186.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:6866934 G>T maps to ENST00000379831 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr11:6867851 A>G maps to ENST00000379831 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:7949653 C>A maps to NM_001004461.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:48596595 G>A maps to NM_001004134.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:48596424 A>T maps to NM_001004134.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:48596883 G>A maps to NM_001004134.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:48596595 G>A maps to NM_001004134.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:55735429 A>G maps to NM_001005491.1 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:55735480 T>C maps to NM_001005491.1 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:29408526 C>T maps to NM_013941.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr6:29385253 C>T maps to ENST00000383553 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:22038632 G>A maps to NM_001005465.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:22038011 G>T maps to NM_001005465.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:22038398 G>T maps to NM_001005465.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:123887030 C>T maps to NM_001004462.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2D2-01A-11D-A17D-09 chr11:123886940 C>T maps to NM_001004462.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:123909483 C>T maps to NM_001004463.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:123909060 G>T maps to NM_001004463.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:123900550 C>T maps to NM_001004464.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:123901264 G>T maps to ENST00000375021 *312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr11:123900502 C>G maps to NM_001004464.1 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:123900583 C>T maps to NM_001004464.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:123900988 C>T maps to ENST00000375021 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:123893913 C>A maps to NM_001001953.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15918676 C>T maps to NM_013940.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:15918478 G>A maps to NM_013940.2 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:15839800 A>T maps to NM_013939.2 *316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:15853071 C>A maps to NM_013938.1 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:15853062 C>T maps to NM_013938.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:15852672 G>T maps to NM_013938.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:16059858 C>A maps to NM_001004465.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15905523 C>T maps to NM_001004466.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:15905217 C>T maps to NM_001004466.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:15904866 G>A maps to NM_001004466.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:159410399 C>A maps to NM_012351.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:159410072 C>T maps to NM_012351.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:159410453 G>A maps to NM_012351.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:159283924 G>T maps to NM_001004467.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:159284263 G>A maps to NM_001004467.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:159283831 A>G maps to NM_001004467.1 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:159249385 G>T maps to ENST00000389011 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:159505014 C>T maps to NM_001004469.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr1:158436061 C>A maps to NM_001004473.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:158390347 G>T maps to NM_001004476.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:158390485 G>T maps to NM_001004476.1 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:56031541 C>A maps to NM_206899.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:56030800 C>T maps to NM_206899.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:57995510 G>A maps to NM_001004471.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:123847933 A>G maps to NM_001004474.1 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:158368422 G>A maps to NM_001004475.1 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:158368667 C>A maps to NM_001004475.1 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:158369163 G>T maps to NM_001004475.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:59480924 G>A maps to NM_001005324.1 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:59480712 G>T maps to NM_001005324.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:59480976 G>A maps to NM_001005324.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:59481027 T>C maps to NM_001005324.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:58034736 A>G maps to NM_207374.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:20666051 C>A maps to NM_001005503.1 C186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:20665530 C>T maps to NM_001005503.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:20666237 C>A maps to NM_001005503.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:16449249 G>A maps to NM_001005239.1 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:16449561 G>A maps to NM_001005239.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:16448907 G>T maps to NM_001005239.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:19377916 C>A maps to NM_001013354.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:20711483 C>T maps to NM_001004479.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248004472 G>A maps to NM_001001959.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:248005153 T>C maps to NM_001001959.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:29342374 G>A maps to NM_030959.2 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:29342155 G>T maps to NM_030959.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:45799360 G>A maps to NM_001004297.2 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:107298224 C>T maps to NM_001001961.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:107298197 C>T maps to NM_001001961.1 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:107289097 T>C maps to NM_001001919.1 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:107288806 C>T maps to NM_001001919.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:107289159 C>A maps to NM_001001919.1 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:107361025 C>T maps to NM_001004482.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:107332409 G>T maps to NM_001004483.1 *321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:107332095 C>A maps to NM_001004483.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:107457580 A>G maps to NM_001004484.1 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:107267208 C>T maps to NM_001004485.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr9:107267038 C>T maps to NM_001004485.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr9:107267277 G>A maps to NM_001004485.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:247835788 G>T maps to NM_001005487.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:247835956 G>A maps to NM_001005487.1 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:130678058 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:130678304 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:130678420 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:130678857 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:130678729 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:130678184 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr23:130678701 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr23:130678907 G>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:130678083 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:130678103 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:35870212 G>A maps to NM_001004487.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:35869882 G>A maps to NM_001004487.1 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:35869591 G>T maps to NM_001004487.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:247978371 G>A maps to NM_001001966.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:247978791 G>A maps to NM_001001966.1 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:248512705 C>A maps to NM_001001918.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:248844675 T>C maps to NM_001004734.1 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr17:3119591 G>A maps to NM_014565.2 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:3119576 C>T maps to NM_014565.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr17:3118971 C>T maps to NM_014565.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:3101420 C>T maps to NM_012352.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:3101012 C>A maps to NM_012352.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:3100832 C>A maps to NM_012352.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:3101471 C>A maps to NM_012352.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:125391658 G>T maps to NM_001004450.1 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:247921072 G>T maps to NM_012353.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:247920952 G>A maps to NM_012353.2 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:247921141 G>A maps to NM_012353.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr1:247921195 G>A maps to NM_012353.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:2995759 G>T maps to NM_002548.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:2996011 G>T maps to NM_002548.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:2995906 G>A maps to NM_002548.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:3301145 G>A maps to NM_003553.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:3254839 A>C maps to NM_012360.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:3254944 A>G maps to NM_012360.1 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:3030188 C>T maps to ENST00000381953 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:3030569 G>T maps to ENST00000381953 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:3030794 G>A maps to ENST00000381953 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:15198857 C>T maps to NM_001004713.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15197911 C>T maps to NM_001004713.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:15197902 C>A maps to NM_001004713.1 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:125239866 G>A maps to NM_001004451.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr9:125240073 G>A maps to NM_001004451.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:125281631 C>A maps to ENST00000444856 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:125424779 C>A maps to ENST00000373686 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:125424449 A>C maps to ENST00000373686 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:125437632 A>C maps to NM_001005234.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:125437653 C>T maps to NM_001005234.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:125438185 T>C maps to NM_001005234.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:125486936 C>T maps to NM_001005235.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:125486651 C>A maps to NM_001005235.1 C128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9204747 G>T maps to ENST00000305465 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:9204849 C>T maps to ENST00000305465 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr19:9204456 C>T maps to ENST00000305465 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:125315897 C>T maps to NM_001004457.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:57982863 T>C maps to NM_001004458.1 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:57982629 G>A maps to NM_001004458.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:57970825 G>A maps to NM_001004459.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:143792269 T>C maps to NM_001004135.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:143807419 C>T maps to NM_001005480.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr7:143807097 G>A maps to NM_001005480.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:143771515 C>T maps to NM_001004488.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:132022337 G>A maps to NM_030908.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:143929690 C>T maps to NM_001005287.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:143929690 C>T maps to NM_001005287.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr7:143747685 C>T maps to NM_012365.1 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:143747769 C>A maps to NM_012365.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr7:143748063 T>C maps to NM_012365.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:143956259 T>C maps to NM_001005328.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:99474173 C>T maps to NM_001005276.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:99474602 G>A maps to NM_001005276.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:6806532 G>T maps to NM_001004489.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:6789366 G>T maps to NM_001004490.1 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr11:6790158 G>A maps to NM_001004490.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr11:6789285 C>T maps to NM_001004490.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:6790023 G>A maps to NM_001004490.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:6790023 G>T maps to NM_001004490.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:248129589 G>A maps to NM_001004491.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:74800539 G>T maps to NM_001005285.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr11:74799996 G>A maps to NM_001005285.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:247614531 G>A maps to NM_001004492.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:247615089 G>T maps to NM_001004492.1 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr1:247614572 G>A maps to NM_001004492.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:247614765 G>A maps to NM_001004492.1 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:27879095 G>A maps to NM_033057.2 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:27879580 C>A maps to NM_033057.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:29054815 A>G maps to NM_001005226.2 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr6:27925215 A>G maps to NM_012367.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:3406812 G>A maps to NM_012368.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:247694973 G>A maps to NM_198074.4 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:247695288 G>A maps to NM_198074.4 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:247695555 G>A maps to NM_198074.4 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:247695426 C>T maps to NM_198074.4 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:247695696 C>T maps to NM_198074.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:247694877 G>A maps to NM_198074.4 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:6913685 C>A maps to NM_003700.1 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:6913695 G>A maps to NM_003700.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr7:143657290 T>C maps to NM_012369.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:143657093 G>T maps to NM_012369.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:143657107 C>T maps to NM_012369.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr1:247752158 C>T maps to NM_001001915.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:247769472 G>T maps to NM_001001914.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:248685522 G>A maps to NM_001013355.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:248685366 C>T maps to NM_001013355.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:248685392 G>A maps to NM_001013355.1 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:29141741 C>T maps to NM_030905.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:29079939 G>A maps to NM_001005216.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:29080182 T>C maps to NM_001005216.2 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:29079756 C>A maps to NM_001005216.2 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:248262919 G>A maps to NM_175911.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248202004 G>T maps to NM_001004686.2 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:248202294 C>T maps to NM_001004686.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:248201922 C>T maps to NM_001004686.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:248201949 T>C maps to NM_001004686.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:248224555 C>A maps to NM_001004687.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:248224882 G>A maps to NM_001004687.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr1:248224009 T>A maps to NM_001004687.1 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:248224025 G>T maps to NM_001004687.1 G15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248112812 C>T maps to NM_001001963.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248113022 C>A maps to NM_001001963.1 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:248343829 C>T maps to NM_001004688.1 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:248343829 C>T maps to NM_001004688.1 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr1:248343316 C>T maps to NM_001004688.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:248343379 C>T maps to NM_001004688.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:248343466 C>A maps to NM_001004688.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:248343835 C>T maps to NM_001004688.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:248402679 C>A maps to NM_017504.1 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:248402829 C>T maps to NM_017504.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:248402643 G>A maps to NM_017504.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:248402985 C>T maps to NM_017504.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248308904 C>T maps to NM_001004690.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:248309054 C>T maps to NM_001004690.1 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:248308904 C>A maps to NM_001004690.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:248309150 T>C maps to NM_001004690.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:248487606 G>A maps to NM_001004691.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr1:248487036 G>T maps to NM_001004691.1 Y278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:35957921 C>T maps to NM_019897.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:248570191 C>A maps to NM_030904.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:248569365 C>A maps to NM_030904.1 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:248458301 G>A maps to NM_001004692.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:248458471 G>A maps to NM_001004692.1 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:248458025 G>A maps to NM_001004692.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:248616358 G>A maps to NM_001004136.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:248616109 G>A maps to NM_001004136.1 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:248616775 C>A maps to NM_001004136.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:248813561 G>A maps to NM_001001824.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:248813408 G>A maps to NM_001001824.1 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:248637505 C>A maps to NM_001005495.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:248637029 C>T maps to NM_001005495.1 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:248637607 G>A maps to NM_001005495.1 *319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:248637430 C>A maps to NM_001005495.1 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248436765 G>T maps to NM_001004695.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:248436531 G>A maps to NM_001004695.1 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:248436999 G>A maps to NM_001004695.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:248436681 C>T maps to NM_001004695.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr1:248737121 T>G maps to NM_001001821.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:248737908 G>A maps to NM_001001821.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:248525907 C>A maps to NM_001004696.1 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:248525193 G>A maps to NM_001004696.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:248525700 C>T maps to NM_001004696.1 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:248651993 C>A maps to NM_001004697.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:248651993 C>A maps to NM_001004697.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:248652116 G>A maps to NM_001004697.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr1:248550981 G>T maps to NM_001005471.1 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248084834 C>T maps to NM_001005522.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:248084834 C>T maps to NM_001005522.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:248084669 C>A maps to NM_001005522.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:180582031 C>T maps to NM_206880.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:180582124 C>A maps to NM_206880.1 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248059127 G>A maps to NM_001001957.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:248059206 C>T maps to NM_001001957.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:247655134 G>T maps to NM_001004698.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:247655187 G>T maps to NM_001004698.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:247654968 G>A maps to NM_001004698.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:8842034 C>T maps to NM_001004699.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:8842118 G>A maps to NM_001004699.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:8842332 T>C maps to NM_001004699.1 *315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A052-01A-11W-A027-09 chr17:3181502 G>A maps to NM_002551.3 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:3181803 G>A maps to NM_002551.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:55136018 C>A maps to NM_001005275.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr11:55111245 C>T maps to NM_001005274.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:55111176 T>C maps to NM_001005274.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:55111047 C>A maps to NM_001005274.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:55110732 T>C maps to NM_001005274.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:48510532 C>A maps to NM_001005512.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr11:48510664 G>A maps to NM_001005512.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:51412143 G>A maps to NM_001005272.3 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:51412370 C>A maps to NM_001005272.3 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:51411989 G>A maps to NM_001005272.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:55371519 G>T maps to NM_001004700.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:55371765 G>T maps to NM_001004700.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:55371785 G>A maps to NM_001004700.1 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:55371309 C>T maps to NM_001004700.1 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:50003589 C>A maps to NM_001005270.2 G150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:50003767 G>T maps to NM_001005270.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:49974717 C>A maps to NM_001001955.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:49974553 G>T maps to NM_001001955.2 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:55322198 C>A maps to NM_001001920.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:55322360 C>A maps to NM_001001920.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:55322685 T>C maps to NM_001001920.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:55322462 C>T maps to NM_001001920.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:55322522 C>A maps to NM_001001920.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:55339653 G>A maps to NM_001004701.2 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:55339914 C>A maps to NM_001004701.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:55340319 C>T maps to NM_001004701.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:55339881 C>T maps to NM_001004701.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GE-01A-11W-A062-09 chr11:48346567 G>T maps to NM_001004702.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:48346597 G>T maps to NM_001004702.1 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:48347461 A>C maps to NM_001004702.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:48346596 A>G maps to NM_001004702.1 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:48346854 C>A maps to NM_001004702.1 C121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:51515358 T>C maps to NM_001004703.1 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr11:51515904 C>T maps to NM_001004703.1 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:51515913 C>A maps to NM_001004703.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:55433151 T>C maps to NM_001004704.1 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:55432702 C>T maps to NM_001004704.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:59245633 C>A maps to NM_001004705.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr11:59245192 C>T maps to NM_001004705.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:59271078 G>T maps to NM_001004706.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:56247525 C>T maps to NM_001004707.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:123810892 A>G maps to NM_001001965.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:123811087 C>A maps to NM_001001965.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:123811213 C>A maps to NM_001001965.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:59225185 C>T maps to NM_001004708.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:59224438 C>T maps to NM_001004708.1 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:59225074 C>T maps to NM_001004708.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:59224930 C>T maps to NM_001004708.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:59282432 A>G maps to NM_001004711.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:59282858 G>A maps to NM_001004711.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:22134018 G>A maps to NM_001001912.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:22133460 C>T maps to NM_001001912.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:22133481 C>T maps to NM_001001912.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:69344 C>A maps to NM_001005484.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:20404404 G>T maps to NM_001004063.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:20404334 T>C maps to NM_001004063.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:20502002 T>G maps to NM_001004714.1 *305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:20502500 C>T maps to NM_001004714.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:20586440 C>A maps to NM_001004715.1 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:20586422 C>A maps to NM_001004715.1 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:20389556 C>A maps to NM_001005483.1 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:20388896 C>A maps to NM_001005483.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:20389169 C>A maps to NM_001005483.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:20389352 A>G maps to NM_001005483.1 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:20528973 C>A maps to NM_001004717.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:20249044 C>A maps to NM_001005500.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:20248892 C>T maps to NM_001005500.1 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:22368605 G>T maps to NM_001004719.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:22368605 G>T maps to NM_001004719.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr15:22369462 A>G maps to NM_001004719.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:22369067 C>T maps to NM_001004719.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:22368775 C>A maps to NM_001004719.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:20295615 C>T maps to NM_001004723.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr14:20296068 C>T maps to NM_001004723.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:20295870 G>A maps to NM_001004723.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:20295621 C>T maps to NM_001004723.1 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr14:20295657 G>C maps to NM_001004723.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:20296266 C>A maps to NM_001004723.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:20295909 C>A maps to NM_001004723.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:22383015 C>T maps to NM_001005241.1 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:22383242 C>A maps to NM_001005241.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:22383368 G>A maps to NM_001005241.1 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:22383236 C>A maps to NM_001005241.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:22383381 C>T maps to NM_001005241.1 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:55405979 C>T maps to NM_001004124.1 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:55405979 C>T maps to NM_001004124.1 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:55406177 G>A maps to NM_001004124.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:55406324 A>G maps to NM_001004124.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:20216131 C>T maps to NM_172194.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:20216152 C>A maps to NM_172194.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr14:20216185 G>A maps to NM_172194.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:48327821 T>C maps to NM_001004725.1 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:55418837 C>T maps to NM_001004059.2 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:55418444 G>A maps to NM_001004059.2 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:48285432 G>T maps to NM_001004726.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr11:48285999 G>T maps to NM_001004726.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:48286209 C>T maps to NM_001004726.1 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr11:4976388 A>G maps to NM_001004748.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:4976493 G>A maps to NM_001004748.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:4968228 G>A maps to NM_001005329.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr11:4967775 A>G maps to NM_001005329.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:4929189 C>A maps to NM_001004749.1 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:4929150 C>A maps to NM_001004749.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:4929106 C>T maps to NM_001004749.1 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr11:5322930 G>A maps to NM_033179.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr11:5373351 C>T maps to NM_001004750.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:4674409 C>A maps to NM_152430.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:4673932 T>C maps to NM_152430.3 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:4674454 T>C maps to NM_152430.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:4674530 G>T maps to NM_152430.3 G259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:4703151 C>A maps to NM_030774.3 G264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:4703293 G>A maps to NM_030774.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:4790325 G>A maps to ENST00000380383 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:4843088 T>A maps to NM_001004753.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:4843541 G>A maps to NM_001004753.1 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:4944786 A>G maps to NM_001005237.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr11:4944863 G>A maps to NM_001005237.1 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:4936500 G>T maps to NM_001005238.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:4936521 G>T maps to NM_001005238.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:4936032 G>T maps to NM_001005238.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:5461964 G>T maps to NM_001005288.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:5462627 G>T maps to NM_001005288.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:5475053 A>G maps to NM_001004754.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:5475299 C>A maps to NM_001004754.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:5021019 C>T maps to NM_001004755.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:5020916 G>A maps to NM_001004755.1 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:5020892 G>A maps to NM_001004755.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:5410939 C>A maps to NM_001004756.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:5443751 G>T maps to NM_001004757.2 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:5444110 C>A maps to NM_001004757.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:5444260 C>A maps to NM_001004757.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:5443537 C>T maps to NM_001004757.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:4869544 G>T maps to NM_001004758.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:4870222 G>A maps to NM_001004758.1 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:4869838 A>C maps to NM_001004758.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:4903080 G>A maps to NM_001004759.1 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:5221033 G>T maps to NM_001004760.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:5221168 G>T maps to NM_001004760.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:5142202 G>T maps to NM_001005222.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:5142289 G>T maps to NM_001005222.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:5153713 A>G maps to NM_001005160.2 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr11:6190818 G>A maps to NM_001004052.1 H246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:4388682 G>A maps to NM_001005161.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:4389330 G>T maps to NM_001005161.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:5603005 C>T maps to NM_001005162.2 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:5510619 C>A maps to NM_001005163.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr11:5510217 G>A maps to NM_001005163.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr11:5080154 G>A maps to NM_001005164.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:5080818 G>T maps to NM_001005164.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:5079920 C>A maps to NM_001005164.2 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:5080599 G>T maps to NM_001005164.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:5080386 G>A maps to NM_001005164.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:5862794 G>A maps to ENST00000379946 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:5863043 C>T maps to ENST00000379946 W32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:5862476 G>A maps to ENST00000379946 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr11:5878416 C>A maps to NM_001005168.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:5566278 G>A maps to NM_001005289.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr11:4608682 T>A maps to NM_001005170.2 L214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:4608818 C>T maps to NM_001005170.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:5068655 C>T maps to NM_001001916.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:5068312 T>C maps to NM_001001916.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:5067883 C>A maps to NM_001001916.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:5068357 G>A maps to NM_001001916.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr11:4510318 C>G maps to NM_001005171.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:4510225 C>A maps to NM_001005171.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:4471231 C>A maps to NM_001005172.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:4470955 C>A maps to NM_001005172.2 C129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:4471174 C>T maps to NM_001005172.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:6007674 G>A maps to NM_001005173.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:4566813 C>T maps to NM_001004137.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:4567356 G>T maps to NM_001004137.1 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr11:5810040 T>C maps to NM_001001913.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr11:5842474 G>T maps to NM_001005174.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:5842395 C>T maps to NM_001005174.1 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:5776482 C>A maps to NM_001005175.2 C171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:5776815 T>C maps to NM_001005175.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:5776030 G>T maps to NM_001005175.2 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:5799306 C>T maps to NM_001001922.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:4825160 G>A maps to ENST00000380382 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:6048147 G>A maps to NM_001001917.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:6048133 C>T maps to NM_001001917.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:5969479 G>T maps to NM_001003443.2 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:5968614 T>C maps to NM_001003443.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:5969493 A>G maps to NM_001003443.2 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:6023688 C>T maps to NM_001005179.2 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:6129373 C>T maps to NM_001005181.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:6129496 C>T maps to NM_001005181.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:6129367 C>A maps to NM_001005181.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:6129775 C>T maps to NM_001005181.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:59211013 C>T maps to NM_001004728.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:59211072 T>C maps to NM_001004728.1 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:59210964 C>T maps to NM_001004728.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:59189982 G>A maps to NM_001001954.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:59189493 C>A maps to NM_001001954.1 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr3:97806156 G>A maps to NM_054106.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:97806054 G>A maps to NM_054106.1 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:56756577 C>T maps to NM_001005323.1 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:59132653 C>A maps to NM_001004729.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:56409866 C>A maps to NM_001002925.1 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:56409876 T>G maps to NM_001002925.1 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:56431697 C>T maps to NM_001004730.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:56431250 C>A maps to NM_001004730.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:56431382 C>A maps to NM_001004730.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:56431808 C>A maps to NM_001004730.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:55798532 A>G maps to NM_001001921.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:21623524 G>A maps to NM_001004731.1 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr14:21623947 G>A maps to NM_001004731.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:58207348 A>G maps to NM_001004733.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:58189873 G>T maps to NM_001005566.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:58190098 G>T maps to NM_001005566.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:58170138 G>T maps to NM_001005469.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:58170626 C>A maps to NM_001005469.1 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:125551795 C>T maps to NM_001001923.1 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:125551759 C>T maps to NM_001001923.1 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:125551240 G>A maps to NM_001001923.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:55541249 G>T maps to NM_001001967.1 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr11:55541185 C>A maps to NM_001001967.1 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:55563864 A>G maps to NM_001004735.1 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:55606427 C>T maps to NM_001005496.1 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:55606563 G>T maps to NM_001005496.1 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr11:55587272 G>T maps to ENST00000395203 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr11:55587764 G>A maps to ENST00000395203 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr11:55587914 C>T maps to ENST00000395203 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:55587476 C>T maps to ENST00000395203 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:55587572 T>C maps to ENST00000395203 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:55761267 G>A maps to NM_003697.1 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:55761861 C>T maps to NM_003697.1 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:55762016 A>G maps to NM_003697.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:55761177 T>C maps to NM_003697.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:55761348 G>A maps to NM_003697.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:97868296 G>A maps to NM_001005514.1 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:97887734 G>A maps to NM_001005515.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:98002243 A>G maps to NM_001005482.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:98001805 G>A maps to NM_001005482.1 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:98002087 C>T maps to NM_001005482.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:98001736 G>A maps to NM_001005482.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:98002513 C>A maps to NM_001005482.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:97983145 C>A maps to NM_001005479.1 C6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr3:97983878 C>T maps to NM_001005479.1 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:97983590 G>T maps to NM_001005479.1 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:97983878 C>T maps to NM_001005479.1 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:55703048 G>A maps to NM_006637.1 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:55703123 C>T maps to NM_006637.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr11:55703429 C>T maps to NM_006637.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:55703123 C>T maps to NM_006637.1 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:55703009 C>T maps to NM_006637.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:55703017 G>A maps to NM_006637.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:55944428 C>G maps to NM_001005492.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:55945008 G>T maps to NM_001005492.1 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:98216964 C>T maps to NM_001004737.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:98217084 C>A maps to NM_001004737.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:98216706 C>A maps to NM_001004737.1 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:98073416 C>A maps to NM_001005517.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:98073320 C>A maps to NM_001005517.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:98073489 G>T maps to NM_001005517.1 G265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:55578959 C>T maps to NM_001004738.1 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:55579533 C>T maps to NM_001004738.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:55579874 C>A maps to NM_001004738.1 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:55594948 C>A maps to NM_001004739.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:56380879 C>T maps to NM_001004740.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:56344369 G>A maps to NM_001004741.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:56344389 C>A maps to NM_001004741.1 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:56309938 C>T maps to NM_001005245.1 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:56310487 C>T maps to NM_001005245.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:56310328 C>T maps to NM_001005245.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr11:56237487 G>A maps to NM_001004742.1 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:56237136 C>A maps to NM_001004742.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:56237724 C>T maps to NM_001004742.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:56258762 C>T maps to NM_001005282.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr11:56258123 G>T maps to NM_001005282.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:7818165 G>A maps to NM_153444.1 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr11:7846751 G>T maps to NM_153445.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr11:7847288 G>T maps to NM_153445.1 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:7846760 C>A maps to NM_153445.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:56185348 G>A maps to NM_001004744.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:56043238 T>G maps to NM_001004745.1 L42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:56043509 T>C maps to NM_001004745.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:56043797 C>A maps to NM_001004745.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr11:56044075 G>A maps to NM_001004745.1 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:56043813 C>T maps to NM_001004745.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:55999896 G>T maps to NM_001004746.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr11:55999827 G>A maps to NM_001004746.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:56000146 G>T maps to NM_001004746.1 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:56020505 A>G maps to NM_001004747.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:56019776 G>A maps to NM_001004747.1 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:56020205 T>G maps to NM_001004747.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:29323854 C>A maps to NM_030876.5 G40*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:29323930 G>T maps to NM_030876.5 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:55681786 G>T maps to NM_001001960.1 S91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:55681464 C>T maps to NM_001001960.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:6816723 G>T maps to NM_003696.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:6816846 A>C maps to NM_003696.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:6816558 G>T maps to NM_003696.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:6816636 T>C maps to NM_003696.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:143701649 C>A maps to NM_001005281.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:240969276 C>T maps to NM_001005853.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:240984994 G>A maps to NM_173351.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:240984565 C>T maps to NM_173351.1 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:240985207 G>A maps to NM_173351.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr12:55715013 T>C maps to NM_001005182.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:55714655 C>A maps to NM_001005182.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:55846077 C>A maps to NM_054105.1 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:55846863 C>A maps to NM_054105.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:55846626 T>C maps to NM_054105.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:55726084 T>C maps to NM_054104.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:55945546 T>C maps to NM_001005494.1 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:55945747 C>A maps to NM_001005494.1 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:55688127 C>A maps to NM_001005493.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:55688991 C>A maps to NM_001005493.1 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:55688436 C>A maps to NM_001005493.1 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:55688127 C>A maps to NM_001005493.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:55688436 C>A maps to NM_001005493.1 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:55795031 C>A maps to NM_001005518.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr12:55886724 A>G maps to NM_001005519.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:55863658 C>T maps to NM_001005499.1 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:55863597 C>A maps to NM_001005499.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:55641280 A>G maps to NM_001005490.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr12:55759352 C>A maps to NM_001005497.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:55820447 C>A maps to NM_001005183.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:55820393 C>A maps to NM_001005183.1 C119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:247875676 G>T maps to NM_001005286.1 C127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:247875184 C>T maps to NM_001005286.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:158669488 C>A maps to NM_001005279.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:158670088 G>T maps to NM_001005279.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:158669886 G>A maps to NM_001005279.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:158670382 G>T maps to NM_001005279.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr1:158687588 G>C maps to ENST00000368146 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:158687788 G>A maps to ENST00000368146 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:158687692 G>T maps to ENST00000368146 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:158687527 G>T maps to ENST00000368146 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:158725078 C>A maps to NM_001005184.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:158725477 C>A maps to NM_001005184.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:158725324 C>T maps to NM_001005184.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:123676549 C>A maps to NM_001005325.1 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:123676993 G>A maps to NM_001005325.1 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:123676993 G>A maps to NM_001005325.1 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:123676151 C>T maps to NM_001005325.1 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr1:158735839 G>A maps to NM_001005185.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:158736154 G>A maps to NM_001005185.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:158747104 C>T maps to NM_001005278.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:57799375 T>C maps to NM_001005186.2 *318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:57798705 G>A maps to NM_001005186.2 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:57798460 G>T maps to NM_001005186.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:57798567 T>C maps to NM_001005186.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:21108983 A>G maps to NM_001001968.1 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:123814473 C>T maps to NM_001005187.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:142750303 C>A maps to NM_001001667.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:142749541 C>T maps to NM_001001667.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:142749454 G>A maps to NM_001001667.1 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:123624467 A>G maps to NM_001005188.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr11:123624710 G>T maps to NM_001005188.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:158517682 G>A maps to NM_001005189.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:14952658 C>A maps to NM_001005190.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:14991444 A>G maps to NM_030901.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:14938633 G>T maps to NM_017506.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:14910654 G>A maps to NM_198944.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:14910579 G>A maps to NM_198944.1 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15052332 C>T maps to NM_012377.1 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:15053031 C>A maps to NM_012377.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:9296528 G>A maps to NM_175883.2 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr19:9325165 G>A maps to NM_001005191.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9325471 G>T maps to NM_001005191.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr19:9325264 C>G maps to NM_001005191.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:9324793 G>T maps to NM_001005191.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9362211 T>C maps to NM_001079935.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9362471 G>A maps to NM_001079935.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:9361973 C>A maps to NM_001079935.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:9362609 T>C maps to NM_001079935.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:9225896 G>A maps to ENST00000293614 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9213928 G>T maps to NM_001005193.1 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:9237595 C>A maps to NM_001001958.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:9237020 C>A maps to NM_001001958.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:124440110 C>T maps to NM_001005194.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:124440489 G>T maps to NM_001005194.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:124252705 C>T maps to NM_001005468.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:124266550 C>A maps to NM_001005467.1 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:124267073 T>C maps to NM_001005467.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:124293906 C>T maps to NM_001005196.1 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:124294353 C>T maps to NM_001005196.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:124293972 G>A maps to NM_001005196.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:124310426 A>G maps to NM_012378.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr11:124310939 G>A maps to NM_012378.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:124180344 G>T maps to NM_001002917.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr11:124189682 G>T maps to NM_001002918.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:124095978 C>T maps to NM_001007249.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:124095828 G>A maps to NM_001007249.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:124134925 A>C maps to NM_001005198.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:124120988 C>A maps to ENST00000341493 C189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:124135378 C>A maps to NM_001005198.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:124135561 C>A maps to NM_001005198.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr11:56057977 G>T maps to NM_001005199.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:56057552 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:55873222 G>A maps to NM_001005200.1 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:55873240 C>T maps to NM_001005200.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:55890174 T>C maps to NM_001005201.1 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:55890225 C>A maps to NM_001005201.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr11:55890222 G>A maps to NM_001005201.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:55861013 A>G maps to NM_001003750.1 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:56127751 T>C maps to NM_001005205.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr11:55904447 C>A maps to NM_001004064.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:55904693 A>C maps to NM_001004064.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:55904497 C>A maps to NM_001004064.1 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:55904828 G>A maps to NM_001004064.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:55904297 A>G maps to NM_001004064.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr11:55904465 C>T maps to NM_001004064.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:56086655 C>T maps to NM_001005202.1 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:56086682 C>T maps to NM_001005202.1 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr11:56086300 C>T maps to NM_001005202.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:55927207 C>A maps to NM_001004058.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:55927462 C>A maps to NM_001004058.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:55927346 A>C maps to NM_001004058.2 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:48921843 C>T maps to NM_001005203.2 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:142723454 G>A maps to NM_001001658.1 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:142723713 G>T maps to NM_001001658.1 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:142723967 C>T maps to NM_001001658.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr7:141619440 T>C maps to NM_001001656.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:141618908 C>T maps to NM_001001656.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:56467902 C>T maps to NM_001013358.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:56467943 C>T maps to NM_001013358.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:56467953 C>T maps to NM_001013358.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:56468663 T>C maps to NM_001013358.1 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:56510788 C>A maps to NM_001005284.1 G167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:56511050 G>A maps to NM_001005284.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:56510347 C>A maps to NM_001005284.1 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr11:57886331 G>A maps to NM_001005211.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:57886088 G>T maps to NM_001005211.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr11:57886349 G>A maps to NM_001005211.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:57947501 G>T maps to NM_001005212.3 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:57958555 G>A maps to NM_001005283.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:122064856 G>A maps to NM_032790.3 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:122079092 G>A maps to NM_032790.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:102087366 C>T maps to NM_032831.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr7:102087258 C>T maps to NM_032831.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:102087063 C>T maps to NM_032831.2 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:30964666 C>T maps to NM_152288.2 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:117085971 G>A maps to NM_000607.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:117086052 G>A maps to NM_000607.2 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr9:117085971 G>A maps to NM_000607.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:117086366 C>T maps to NM_000607.2 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:38080351 G>A maps to NM_139280.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:38080438 C>T maps to NM_139280.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:58111705 C>T maps to NM_006812.3 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:58090146 C>T maps to NM_006812.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr11:59345682 G>A maps to NM_002556.2 R667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:59369209 G>A maps to NM_002556.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:59344431 G>A maps to NM_002556.2 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:59344431 G>T maps to NM_002556.2 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:59367977 G>T maps to NM_002556.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:31283459 G>A maps to NM_030758.3 W385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:31091369 G>A maps to NM_030758.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:31286875 C>T maps to NM_030758.3 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:31289463 G>T maps to NM_030758.3 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:31091369 G>A maps to NM_030758.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:31091324 G>T maps to NM_030758.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:31725423 C>T maps to NM_017784.4 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:31871603 C>T maps to NM_017784.4 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:31871561 C>T maps to NM_017784.4 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:31725222 G>T maps to NM_017784.4 Y543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:125266398 T>C maps to NM_022776.4 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:125250856 G>A maps to NM_022776.4 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:125313545 G>A maps to NM_022776.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr18:21758053 A>G maps to NM_080597.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr20:60848387 G>A maps to NM_144498.1 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:24880315 C>T maps to NM_015550.2 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:24846504 G>A maps to NM_015550.2 G778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:24846510 C>T maps to NM_015550.2 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:24874200 G>A maps to NM_015550.2 N550N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:24905820 C>T maps to NM_015550.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:24903218 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:3141704 G>A maps to NM_020896.3 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:3121469 C>T maps to NM_020896.3 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:3115514 G>A maps to NM_020896.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179213949 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179247991 A>G maps to ENST00000392505 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179255831 C>A maps to ENST00000392505 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179259127 G>T maps to ENST00000392505 E913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:179193071 G>A maps to ENST00000392505 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr2:179226509 C>T maps to ENST00000392505 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:179247253 C>T maps to ENST00000357080 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:179247934 C>A maps to ENST00000392505 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:179197372 G>A maps to ENST00000392505 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:45886792 G>T maps to NM_145798.2 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr17:45897608 A>G maps to NM_145798.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr17:45890715 G>A maps to NM_145798.2 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:76749752 C>T maps to NM_020841.4 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:76791547 C>A maps to NM_020841.4 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:76749784 G>A maps to NM_020841.4 R852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:52237811 G>T maps to ENST00000428468 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:52238364 G>A maps to ENST00000428468 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:52250248 G>A maps to ENST00000428468 E608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:52251548 T>C maps to ENST00000428468 Y633Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:52238275 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:52246871 T>C maps to ENST00000428468 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:36883760 G>A maps to ENST00000356637 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:36886189 A>G maps to ENST00000356637 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:20920237 C>T maps to NM_017807.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:190626239 C>A maps to NM_022353.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:83992868 C>T maps to NM_013370.3 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:83999071 C>T maps to NM_013370.3 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:90926892 C>A maps to NM_001126111.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:90936994 C>T maps to NM_001126111.1 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:30660207 C>T maps to NM_020530.3 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:30661071 C>T maps to NM_020530.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:38904489 C>T maps to NM_003999.2 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:38933297 G>T maps to NM_003999.2 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:38933425 A>G maps to NM_003999.2 P940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:38885505 G>A maps to NM_003999.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:38931983 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:38925390 T>C maps to NM_003999.2 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:19552978 C>T maps to NM_145260.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:19553398 C>T maps to NM_145260.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr8:99961710 C>T maps to ENST00000457907 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:65345307 G>T maps to NM_178859.3 E65*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A5-A0R7-01A-31D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:109576774 A>G maps to ENST00000512478 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:109571816 G>A maps to ENST00000512478 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:109576813 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:108375735 A>G maps to NM_014028.3 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:190967888 G>A maps to NM_198184.1 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:195955775 C>A maps to NM_152672.5 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:38240626 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:38229106 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:38268215 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:38260636 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:38271213 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:38271191 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:38260656 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:38271205 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:38260607 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:38271191 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:21698769 C>T maps to ENST00000286149 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:21747638 G>T maps to ENST00000286149 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:26688691 G>T maps to NM_194248.2 A1549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:26702405 G>A maps to NM_194248.2 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:26682904 G>T maps to NM_194248.2 I1994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:26683737 G>A maps to NM_194248.2 N1898N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:26706386 G>A maps to NM_194248.2 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:26707451 G>T maps to NM_194248.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:26726676 G>C maps to NM_194248.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:26683821 G>A maps to NM_194248.2 T1870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr2:26700143 G>A maps to NM_194248.2 Q807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:26688697 G>A maps to NM_194248.2 I1547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr2:26705406 G>A maps to NM_194248.2 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:26705444 G>A maps to NM_194248.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:26683874 G>T maps to NM_194248.2 R1853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:26688622 G>T maps to NM_194248.2 L1572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:26684958 G>A maps to NM_194248.2 F1761F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr2:26705430 A>G maps to NM_194248.2 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr2:26739407 G>A maps to NM_194248.2 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:161214760 G>T maps to NM_001080440.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:161221184 G>T maps to NM_001080440.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:4199618 G>A maps to NM_177998.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:4199534 C>T maps to NM_177998.1 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:4199294 G>T maps to NM_177998.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:4190530 T>C maps to NM_177998.1 *613W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72921672 C>A maps to NM_178160.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72923334 C>T maps to NM_178160.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72929489 C>T maps to NM_178160.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:72926821 G>A maps to NM_178160.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:72926473 C>T maps to NM_178160.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:72929579 C>T maps to NM_178160.2 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:72923892 C>T maps to NM_178160.2 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:72929469 C>T maps to NM_178160.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:72942966 C>T maps to NM_178233.1 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:72937554 G>A maps to NM_178233.1 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:16730568 G>T maps to NM_020157.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:241078667 G>A maps to NM_148961.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr5:76932705 G>A maps to NM_032109.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:76932669 G>A maps to NM_032109.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr11:63764885 C>T maps to ENST00000422031 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:63756169 G>A maps to ENST00000422031 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr11:63765246 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:20234190 G>A maps to NM_015207.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:20230830 C>T maps to NM_015207.1 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:146073705 C>A maps to ENST00000447906 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:146059238 A>G maps to ENST00000447906 N896N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:146073718 T>G maps to ENST00000447906 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:146064546 C>T maps to ENST00000447906 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:146058958 C>A maps to ENST00000447906 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:146059261 C>A maps to ENST00000447906 E889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr4:146064537 C>T maps to ENST00000447906 E554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:146095838 G>A maps to ENST00000447906 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:146071744 A>G maps to ENST00000447906 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48814374 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:48780480 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48801513 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48781193 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48781227 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48781300 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:48792073 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48791819 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:48783166 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:69282993 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69283051 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:69282601 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:69283003 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr23:69283004 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:69282632 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:69283054 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:69283054 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:92097056 T>G maps to NM_016023.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:31818565 G>A maps to ENST00000382902 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:31818565 G>A maps to ENST00000382902 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:31851205 G>A maps to ENST00000382902 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:31862286 G>A maps to ENST00000382902 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr15:31776924 C>T maps to ENST00000382902 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr15:31818565 G>A maps to ENST00000382902 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr1:149916929 G>C maps to NM_020205.2 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:149931669 C>A maps to NM_020205.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:149916649 C>T maps to NM_020205.2 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:63282727 A>G maps to NM_014562.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:63282997 G>A maps to NM_014562.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:63283099 C>T maps to NM_014562.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:63283117 C>T maps to NM_014562.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:63280184 C>T maps to NM_014562.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:57268998 C>T maps to NM_021728.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr12:29604401 G>A maps to NM_183378.2 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:29648216 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:29629166 G>A maps to NM_183378.2 Y481Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:29604478 C>A maps to NM_183378.2 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:29624802 G>A maps to NM_183378.2 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:29648317 A>G maps to NM_183378.2 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:29649118 G>C maps to NM_183378.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:29614803 C>A maps to NM_183378.2 E755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:29649181 G>A maps to NM_183378.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:29640677 A>G maps to NM_183378.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:7727860 G>A maps to NM_198185.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:7713154 A>G maps to NM_198185.2 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:7716873 G>A maps to NM_198185.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:7716873 G>A maps to NM_198185.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:7718092 A>G maps to NM_198185.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:111964245 C>A maps to ENST00000369728 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:111968072 G>T maps to ENST00000369728 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:111957337 C>T maps to ENST00000369728 E659E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:111957934 C>T maps to ENST00000369728 W460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr1:111969381 C>T maps to ENST00000369728 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr11:65562181 C>T maps to NM_004561.2 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:41870406 G>A maps to NM_000436.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:41850133 C>A maps to NM_000436.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:40236267 G>A maps to NM_022120.1 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:42990176 G>A maps to NM_148962.4 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:97639044 C>A maps to NM_080818.3 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:97639593 G>A maps to NM_080818.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:97639986 T>C maps to NM_080818.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:97639236 G>T maps to NM_080818.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:16336461 G>T maps to NM_138381.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:16336470 G>A maps to NM_138381.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:107751789 A>G maps to NM_001198533.1 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:107722881 C>T maps to NM_001198533.1 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:107718790 C>T maps to NM_001198533.1 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:107531293 A>G maps to NM_001198533.1 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:25831627 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:25832504 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:25836008 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:25833131 A>G maps to NM_017897.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:38271861 G>T maps to NM_005109.2 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:38293862 C>T maps to NM_005109.2 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:38284248 G>T maps to NM_005109.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:8808955 C>T maps to NM_000916.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:3819477 G>A maps to NM_002558.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:3802293 G>A maps to NM_002558.2 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:3806567 G>T maps to NM_002558.2 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:133197858 G>A maps to NM_170683.2 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:57116175 G>A maps to NM_002559.2 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:57135843 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:57118324 C>T maps to NM_002559.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:3595068 T>A maps to ENST00000435558 K53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:21380165 C>T maps to NM_005446.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:21377874 C>A maps to NM_005446.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:121603213 C>T maps to NM_002562.5 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:121613247 C>T maps to NM_002562.5 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:121598721 G>A maps to NM_002562.5 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:121614954 A>C maps to NM_002562.5 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:121570883 C>A maps to NM_002562.5 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:121603920 G>A maps to NM_002562.5 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr3:152554677 A>G maps to NM_002563.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:78216614 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:78216808 T>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:78216597 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr23:78216334 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:78216771 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:78216826 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:78216981 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:78216408 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:78216161 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr23:78216295 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:78217024 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:78216324 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr19:10224759 C>T maps to NM_001040664.2 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:10224766 C>T maps to NM_001040664.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:10224712 C>T maps to NM_001040664.2 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:10225326 C>T maps to NM_001040664.2 D766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:150931531 G>A maps to NM_014879.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:150932038 C>T maps to NM_014879.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:150931810 G>A maps to NM_014879.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:72945326 C>T maps to NM_176071.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:72945824 C>T maps to NM_176071.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:72945965 C>T maps to NM_176071.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69478533 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69479139 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:69478835 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69479125 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:69479134 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:69479050 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:69479144 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:73007610 C>A maps to NM_004154.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:73007796 C>A maps to NM_004154.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:1584799 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:1584905 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:1585418 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr23:1584608 G>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:1584887 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:1585022 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:1585130 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:1585233 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:1585034 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:1585309 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:1585382 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:1584505 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:1584668 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:1584489 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:1585350 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:74810843 G>A maps to NM_000917.3 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:74804802 G>A maps to NM_001142595.1 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:131544863 G>A maps to NM_001142599.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr5:131533961 A>G maps to NM_001142599.1 N436N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:131543568 A>G maps to NM_001142599.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:131546184 A>G maps to NM_001142599.1 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:131553487 C>A maps to NM_001142599.1 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:73979255 T>G maps to NM_182904.3 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:73996901 G>A maps to NM_182904.3 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:79804939 C>T maps to NM_000918.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:79805124 G>A maps to NM_000918.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:49042338 C>T maps to NM_177938.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:56504378 C>T maps to NM_006191.2 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:73611328 A>T maps to NM_025155.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:101721359 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:43552830 C>T maps to NM_001124756.1 D302D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr20:43565342 G>A maps to NM_001124756.1 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:25671449 G>T maps to NM_030979.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:40033457 C>A maps to NM_001135653.1 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:40030779 G>A maps to NM_001135653.1 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:40041581 G>A maps to NM_001135653.1 Y14Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:90690621 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:90691295 C>A did not map to a codon.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr23:90691599 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:90691436 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:90691666 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:90690584 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:90690812 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:90691131 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:90690959 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:90691408 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:90691634 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:90691564 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:90691496 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:90691189 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:90691337 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:23793179 G>A maps to NM_004643.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:88931485 A>G maps to NM_001080487.2 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:88932033 G>A maps to NM_001080487.2 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:163735953 G>T maps to NM_152410.2 G276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr6:163510310 C>T maps to NM_152410.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:20714506 T>C maps to ENST00000503585 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:20714464 G>T maps to ENST00000503585 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:20714464 G>T maps to ENST00000503585 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:66010642 C>T maps to NM_018026.2 I928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:105859580 G>A maps to ENST00000458164 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:34500261 C>T maps to NM_020804.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:34499532 C>T maps to NM_020804.3 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:34499562 C>T maps to NM_020804.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr22:43289517 C>T maps to NM_001184970.1 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr22:43278236 G>A maps to NM_001184970.1 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:43272952 G>A maps to NM_001184970.1 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:43287042 G>A maps to NM_001184970.1 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:43284714 G>T maps to NM_001184970.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr22:43280513 C>T maps to NM_001184970.1 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:17557089 C>T maps to NM_013358.2 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:17413072 G>A maps to NM_007365.2 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:17395724 G>A maps to NM_007365.2 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr1:17401414 C>T maps to NM_007365.2 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:17690063 C>T maps to NM_012387.2 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:17690123 A>G maps to NM_012387.2 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:17690063 C>T maps to NM_012387.2 F602F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:17690186 G>T maps to NM_012387.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:17668843 G>A maps to NM_012387.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:17668534 C>T maps to NM_012387.2 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:138457352 G>A maps to NM_002571.2 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:39880007 C>T maps to NM_019088.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:39876812 C>A maps to NM_019088.2 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:39880349 G>A maps to NM_019088.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:2569383 G>A maps to NM_000430.3 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:26299106 G>T maps to NM_000437.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:26311003 G>T maps to NM_000437.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:81897532 G>A maps to NM_018440.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:81897466 G>A maps to NM_018440.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:81889138 G>T maps to NM_018440.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:81897466 G>A maps to NM_018440.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49454087 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49458715 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:49455856 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:49455894 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:55117011 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:55117021 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:55117035 T>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:55116501 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:55117770 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49595047 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49595651 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49595683 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49597194 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49595683 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:55247849 A>C did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:55247057 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:57325689 G>T maps to NM_001079525.1 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:57314965 C>T maps to NM_001079525.1 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:43535702 C>A maps to NM_006451.4 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:43529901 G>A maps to NM_006451.4 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:77103374 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:77066712 G>A maps to NM_001128620.1 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:10702629 C>A maps to NM_017906.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:10709595 G>T maps to NM_017906.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:10709636 A>G maps to NM_017906.2 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:196533550 G>A maps to NM_002577.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:196539672 C>T maps to NM_002577.4 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:196539611 T>C maps to NM_002577.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:110388118 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:110416273 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:110435813 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:110439731 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:110406190 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:110406256 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:110435826 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:110385384 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:110406148 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:110406179 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:110435373 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:110439684 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:110406903 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr23:110416267 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:110389768 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:110439163 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:110385388 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:110437631 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:110366366 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:110366479 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:39665963 G>A maps to NM_005884.3 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:40565648 C>T maps to NM_020168.4 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:40565138 C>T maps to NM_020168.4 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:40565762 G>A maps to NM_020168.4 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:9538370 C>A maps to NM_177990.2 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:9546656 G>A maps to NM_177990.2 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:9546899 C>T maps to NM_177990.2 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:9525013 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:23641266 G>T maps to NM_024675.3 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:23647098 G>A maps to NM_024675.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:23641146 G>A maps to NM_024675.3 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:169815740 C>T maps to NM_001166108.1 Y704Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:169835154 C>T maps to NM_001166108.1 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:169632939 G>A maps to NM_001166108.1 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:727033 C>T maps to NM_002579.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:727076 C>T maps to NM_002579.2 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:112705282 G>T maps to ENST00000413420 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:112899773 C>T maps to NM_007203.4 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:112778273 A>G maps to NM_007203.4 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:112899162 C>T maps to NM_007203.4 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:112898777 G>T maps to NM_007203.4 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:112778279 G>A maps to NM_007203.4 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:112918707 G>A maps to NM_007203.4 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:100154787 G>A maps to NM_017734.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:100152743 A>G maps to NM_017734.4 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr1:100154787 G>A maps to NM_017734.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:100155012 C>T maps to NM_017734.4 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:100152677 C>A maps to NM_017734.4 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr5:102342536 C>T maps to NM_000919.3 G612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:102237086 C>T maps to NM_000919.3 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:102296860 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:35454062 G>A maps to NM_015430.2 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:35463239 G>A maps to NM_015430.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:35473450 C>A maps to NM_015430.2 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:56717131 C>A maps to NM_001127460.2 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:56713761 C>T maps to NM_001127460.2 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:56716263 G>A maps to NM_001127460.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:28840855 T>C maps to NM_175854.7 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:28854576 C>T maps to NM_175854.7 R740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:28854576 C>T maps to NM_175854.7 R740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:91371470 G>A maps to NM_148977.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:91359049 G>A maps to NM_148977.1 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:91371470 G>A maps to NM_148977.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:3897572 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:3891318 G>A maps to NM_153638.2 Q359Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr20:3888789 G>A maps to NM_153638.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:3897636 G>A maps to NM_153638.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:2441346 G>A maps to ENST00000425477 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:2453200 G>A maps to ENST00000425477 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:2452730 C>T maps to ENST00000425477 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:2440303 G>A maps to ENST00000425477 Y776Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:93912851 C>A maps to NM_015368.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MU-01A-11D-A13L-09 chr11:93913199 C>T maps to NM_015368.3 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr22:50617567 C>T maps to NM_052839.3 Y632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:50616106 C>T maps to NM_052839.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:124489209 C>A maps to NM_052959.2 Y186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:124489662 C>A maps to NM_052959.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:124489503 T>G maps to NM_052959.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:135193713 G>A maps to NM_152911.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:78938656 T>C maps to NM_173797.3 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:78936766 G>T maps to NM_173797.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:78981026 G>A maps to NM_173797.3 W462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:50258832 G>T maps to NM_001040284.2 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:50258864 G>A maps to NM_001040284.2 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr16:50251522 T>C maps to NM_001040284.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:6750612 C>T maps to NM_006999.4 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr5:6748667 G>A maps to NM_006999.4 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr5:6750519 C>A maps to NM_006999.4 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:6753065 T>G maps to NM_006999.4 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:6742685 G>A maps to NM_006999.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:6753122 G>A maps to NM_006999.4 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:39589224 C>T maps to NM_001004318.2 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr14:73739248 G>A maps to ENST00000427855 Q1238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:73717619 C>T maps to ENST00000427855 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr14:73719925 T>A maps to ENST00000216658 C384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:73732176 C>T maps to ENST00000427855 I1075I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:73721258 C>T maps to ENST00000427855 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:97029170 G>T maps to NM_032632.3 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:97031384 T>C maps to NM_032632.3 *746Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr7:4901278 C>A maps to NM_020144.4 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:61002212 G>T maps to NM_022894.3 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:61021250 T>C maps to NM_022894.3 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:61021873 C>T maps to NM_022894.3 D673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:119129942 G>A maps to NM_002581.3 S1505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:118969815 C>A maps to NM_002581.3 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:119109488 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr9:118950430 G>T maps to NM_002581.3 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr9:119097221 G>A maps to NM_002581.3 Q1160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:118950360 C>T maps to NM_002581.3 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:119116065 C>A maps to NM_002581.3 A1447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:119129939 C>G maps to NM_002581.3 T1504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr9:119033681 C>A maps to NM_002581.3 S980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:176675533 C>T maps to NM_020318.2 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:176675578 C>T maps to NM_020318.2 N1150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:176709305 C>T maps to NM_020318.2 D1375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:176709230 C>T maps to NM_020318.2 V1350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:176525493 G>A maps to NM_020318.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:176668659 C>T maps to NM_020318.2 R1057R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:176708760 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:176668611 C>T maps to NM_020318.2 H1041H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr1:176564092 G>A maps to NM_020318.2 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:176738759 A>C maps to NM_020318.2 T1447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:176659366 C>A maps to NM_020318.2 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:176525562 T>C maps to NM_020318.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:108614924 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:108575877 C>T maps to NM_005443.4 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:108608203 C>A maps to NM_005443.4 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:89473938 G>T maps to NM_001015880.1 G174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:89472952 C>T maps to NM_001015880.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:89501051 A>C maps to NM_001015880.1 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr10:89472994 T>C maps to NM_001015880.1 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:3021159 C>T maps to NM_152341.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:69689851 C>A maps to NM_017705.3 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr1:156214665 G>A maps to NM_024897.2 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:142681896 C>T maps to NM_198504.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:142681065 G>A maps to NM_198504.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:142681740 C>T maps to NM_198504.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:142681356 G>A maps to NM_198504.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:34759191 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:34759033 A>G maps to NM_019619.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:34573159 G>A maps to NM_019619.3 R1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:34739376 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:34626239 G>A maps to NM_019619.3 F844F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr10:34630559 G>A maps to NM_019619.3 A804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:206480281 T>C maps to ENST00000406610 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:205986464 G>A maps to ENST00000406610 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr2:206364631 G>A maps to ENST00000406610 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:205983770 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr2:205990394 C>T maps to ENST00000406610 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:206305229 C>A maps to ENST00000406610 R960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:206057937 G>T maps to ENST00000406610 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:67696084 C>A maps to NM_016948.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr20:49366799 T>A maps to NM_032521.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:49366301 C>A maps to NM_032521.2 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:49366995 G>T maps to NM_032521.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr20:49366346 C>T maps to NM_032521.2 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:51093278 A>G maps to NM_003631.2 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:51065369 C>A maps to NM_003631.2 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:51130465 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr10:51051655 G>T maps to NM_003631.2 Y792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:51362988 G>A maps to NM_003631.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:161771175 G>A maps to NM_004562.2 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:161771163 G>A maps to NM_004562.2 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr6:162206906 G>A maps to NM_004562.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:161771139 G>A maps to NM_004562.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:183562031 C>T maps to NM_018622.5 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:183580482 A>C did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:183584517 C>T maps to NM_018622.5 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:183551359 G>A maps to NM_018622.5 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:75938360 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:75937875 G>A maps to NM_015393.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:14530582 G>A maps to NM_002582.2 D637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:14723469 G>T maps to NM_002582.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:14722026 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:14698007 C>A maps to NM_002582.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr16:14676086 G>A maps to NM_002582.2 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:226549168 G>A maps to NM_001618.3 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:226573318 C>T maps to NM_001618.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:226551738 G>A maps to NM_001618.3 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:226549731 T>G maps to NM_001618.3 V967V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:3939162 C>A maps to NM_020367.4 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:3923298 G>A maps to NM_020367.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:139754552 G>A maps to NM_022750.2 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:139757767 G>A maps to NM_022750.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:139724635 G>A maps to NM_022750.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:122432361 G>A maps to NM_017554.2 T1237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:122447443 A>G maps to NM_017554.2 *1802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:122419057 G>T maps to NM_017554.2 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:122419392 C>T maps to NM_017554.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:122437794 G>A maps to NM_017554.2 T1599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:122418534 G>A maps to NM_017554.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:122404131 C>T maps to NM_017554.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:122354664 C>A maps to NM_001113523.1 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:122354799 A>T maps to NM_001113523.1 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:122334618 T>G maps to NM_152615.1 Y21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:51978569 T>C maps to NM_001003931.2 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:51978831 G>A maps to NM_001003931.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:51978879 C>A maps to NM_001003931.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:51978145 C>T maps to NM_001003931.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:25030505 A>G maps to NM_006437.3 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr13:25075780 C>T maps to NM_006437.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:50123837 G>T maps to ENST00000505697 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:50091161 G>T maps to ENST00000505697 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:50073944 C>T maps to ENST00000505697 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:50137808 C>T maps to ENST00000505697 D825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:50123842 C>A maps to ENST00000505697 S681S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AX-A0J1-01A-11W-A062-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:50118222 G>T maps to ENST00000505697 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr5:50055549 T>C maps to ENST00000505697 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:122255170 C>A maps to NM_031458.2 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:122255057 C>T maps to NM_031458.2 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:122274417 T>C maps to NM_031458.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:122271294 T>C maps to NM_031458.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr3:122274873 T>C maps to NM_031458.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:55223922 G>A maps to NM_152268.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:55223973 C>T maps to NM_152268.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:55223652 G>A maps to NM_152268.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:12495458 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr22:44536003 G>A maps to NM_001003828.1 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr22:44536021 C>T maps to NM_001003828.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:44543753 C>T maps to NM_001003828.1 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:44589679 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:44602299 G>A maps to NM_001137606.1 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr22:44583757 C>T maps to NM_001137606.1 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:44594596 G>T maps to NM_001137606.1 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:44602299 G>A maps to NM_001137606.1 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr22:44583757 C>T maps to NM_001137606.1 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:44592080 C>T maps to NM_001137606.1 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:44583729 C>T maps to NM_001137606.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:150817103 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:150828228 A>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:150791515 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:150840885 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:150840825 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:150840893 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:150842605 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr23:150840203 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:150790021 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:150844531 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:150791502 A>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:150832668 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:150840809 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:150842651 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:150840782 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:150840978 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr23:150840886 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:150793987 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:150840090 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:150840201 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:150842553 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:150789414 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:150840761 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:150832808 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:150840746 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:242065779 C>T maps to ENST00000358649 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:242051779 G>A maps to ENST00000358649 I1143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:242065854 C>T maps to ENST00000358649 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:242065854 C>T maps to ENST00000358649 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:242051815 G>A maps to ENST00000358649 I1131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:242062182 G>A maps to ENST00000358649 F1012F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:242063485 G>A maps to ENST00000358649 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:242065628 G>A maps to ENST00000358649 R901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:242047600 C>T maps to ENST00000358649 P1223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:242065920 G>T maps to ENST00000358649 T803T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr2:242076556 G>A maps to ENST00000358649 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:125616251 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:125617641 G>T maps to NM_138294.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:125647339 C>T maps to NM_212555.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:59410432 G>A maps to NM_152716.2 R657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:59419111 G>A maps to NM_152716.2 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:59423518 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr11:59420469 A>G maps to NM_152716.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:31731714 G>A maps to NM_014323.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:31740355 C>T maps to NM_014323.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:79986415 A>G maps to NM_002583.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:79988128 C>A maps to NM_002583.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:21687361 C>A maps to NM_006192.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:21687463 C>T maps to NM_006192.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:102541072 G>A maps to NM_003987.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:223158447 C>T maps to NM_013942.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:223096868 T>C maps to NM_181459.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:223066852 G>A maps to NM_181459.3 Y410Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:127253109 C>A maps to NM_006193.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:127253873 G>A maps to NM_006193.2 H158H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:127251628 C>T maps to NM_006193.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:36846845 G>A maps to NM_016734.1 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:37020789 C>A maps to NM_016734.1 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:37015133 G>T maps to NM_016734.1 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:36966526 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:31812351 C>T maps to NM_001604.4 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:31812408 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:31832563 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:31822323 T>C maps to NM_001604.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr11:31815102 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:31815662 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:31823249 A>G maps to NM_001604.4 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:19071365 C>T maps to NM_001135254.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:18962752 C>T maps to NM_002584.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:18962812 C>T maps to NM_002584.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:19071416 C>A maps to NM_001135254.1 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:19027208 G>A maps to NM_002584.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:114004443 C>T maps to NM_003466.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:113984804 G>A maps to NM_003466.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr14:37145494 C>T maps to NM_006194.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:37145482 G>A maps to NM_006194.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:37145590 G>T maps to NM_006194.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:154768032 G>A maps to NM_007349.3 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:154739618 G>T maps to NM_007349.3 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:154760440 G>T maps to NM_007349.3 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:154755422 C>T maps to NM_007349.3 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:154767881 C>A maps to NM_007349.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr7:154775000 C>T maps to NM_007349.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:154790425 G>A maps to NM_007349.3 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:154760575 C>T maps to NM_007349.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:154767972 G>A maps to NM_007349.3 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:154767528 T>C maps to NM_007349.3 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:27667824 G>T maps to NM_018492.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr10:70048414 C>T maps to NM_022129.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:70051966 G>A maps to NM_022129.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr10:70051884 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:138539130 G>T maps to NM_021635.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52610694 G>A maps to ENST00000296302 R1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:52696199 G>A maps to ENST00000296302 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:52621391 T>A maps to ENST00000296302 K1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:52637554 G>A maps to ENST00000296302 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:52678794 G>T maps to ENST00000296302 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:164532528 T>C maps to NM_002585.2 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:164761954 G>T maps to NM_002585.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:164768974 C>T maps to NM_002585.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:128728313 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:128677962 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr9:128697852 G>A maps to ENST00000373487 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr9:128723084 T>C maps to ENST00000373487 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:128691972 C>T maps to ENST00000373487 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:19710155 G>A maps to NM_025245.1 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:154918235 G>A maps to NM_020524.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:154918946 C>T maps to NM_020524.2 Q401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:66617150 G>A maps to NM_022172.2 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:66631256 G>A maps to NM_022172.2 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:66620275 C>T maps to NM_022172.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:66616796 G>A maps to NM_022172.2 A1064A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:66617870 C>T maps to NM_022172.2 A846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr11:66631259 G>A maps to NM_022172.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:66638261 G>A maps to NM_022172.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:66637838 G>A maps to NM_022172.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:70315021 C>A maps to NM_006196.3 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:53865486 G>A maps to NM_005016.5 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:53858593 G>A maps to NM_005016.5 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:47319532 G>A maps to NM_020528.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:47350748 C>T maps to NM_020528.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr21:47316227 A>G maps to NM_020528.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:47329273 C>A maps to NM_020528.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr21:47360107 C>T maps to NM_020528.2 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:51995219 C>A maps to NM_033010.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:51994676 C>T maps to ENST00000395014 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:100809576 G>T maps to NM_000282.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:100953796 G>A maps to NM_000282.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:136035817 C>A maps to NM_001178014.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:135975423 C>T maps to NM_001178014.1 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:135979124 G>A maps to ENST00000468777 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr3:136048866 A>C maps to NM_001178014.1 *560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:135975431 A>G maps to NM_001178014.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:141237021 G>A maps to NM_032420.2 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:141248532 G>A maps to NM_032420.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:134111305 G>A maps to NM_032961.1 R1038R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:134084324 G>A maps to NM_032961.1 E997E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:134071342 C>T maps to NM_032961.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr4:134073287 C>T maps to NM_032961.1 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr4:134111313 A>G maps to NM_032961.1 *1041W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr4:134072053 C>T maps to NM_032961.1 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:134073781 C>T maps to NM_032961.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr4:134071913 G>T maps to NM_032961.1 G207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:91090944 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:91873395 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:91090754 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:91133216 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:91137924 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:91090849 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:91133597 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:91133074 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:91133598 G>A did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:91133854 G>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:91542971 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:91873799 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:91090820 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:91873632 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:91873845 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:91133379 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:91090551 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:91132556 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:91133980 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:91873469 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:91132013 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr23:91132564 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:91132424 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:91090729 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:91131800 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:91133405 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:91134111 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:91723311 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:91090728 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:91132644 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:91873470 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:91133875 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:91090573 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:91132048 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:141335625 G>A maps to NM_016580.2 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:141337194 C>T maps to NM_016580.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:141329051 G>A maps to NM_016580.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr5:141336243 G>T maps to NM_016580.2 C391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:141336189 T>C maps to NM_016580.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr10:55568711 C>A maps to NM_001142769.1 E1705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:55571351 G>A maps to ENST00000395438 I1467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:55780101 T>C maps to NM_001142763.1 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:55700628 C>A maps to NM_001142763.1 E1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:55569245 C>A maps to NM_001142769.1 E1527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:55591293 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:55892757 G>T maps to NM_001142763.1 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:55569245 C>A maps to NM_001142769.1 E1527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:55626506 G>T maps to NM_001142763.1 I1209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:55913041 G>A maps to NM_001142763.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:55566597 G>T maps to ENST00000373965 S1599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:55581853 C>A maps to NM_001142763.1 E1885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:55663053 G>A maps to NM_001142763.1 I1155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:55721534 C>A maps to NM_001142763.1 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:55566673 G>A maps to ENST00000373965 R1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:55568703 T>C maps to NM_001142769.1 G1707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:55581629 A>C maps to NM_001142763.1 S1959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr10:55587184 C>T maps to NM_001142763.1 A1450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr10:55581775 C>A maps to NM_001142763.1 E1911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:56089358 A>T maps to NM_001142763.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:55582783 C>A maps to NM_001142763.1 E1575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:55945013 C>T maps to NM_001142763.1 E445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:56138639 C>A maps to NM_001142763.1 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr10:55973782 A>G maps to NM_001142763.1 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr10:55582600 C>A maps to NM_001142763.1 E1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr10:55617017 G>A maps to NM_001142763.1 S1246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr13:58206844 C>T maps to NM_001040429.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:58208701 C>T maps to NM_001040429.2 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:58206922 C>T maps to NM_001040429.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:58208416 C>T maps to NM_001040429.2 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:58208995 C>T maps to NM_001040429.2 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:58206997 C>T maps to NM_001040429.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:58207444 C>T maps to NM_001040429.2 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:58208086 G>A maps to NM_001040429.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr13:58208383 G>A maps to NM_001040429.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:58208641 C>T maps to NM_001040429.2 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:58299079 C>T maps to NM_001040429.2 I1044I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr13:58207120 G>A maps to NM_001040429.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:58206694 C>T maps to NM_001040429.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:58206949 C>T maps to NM_001040429.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:58209073 C>T maps to NM_001040429.2 F798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:58209031 C>T maps to NM_001040429.2 N784N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr13:58206889 C>T maps to NM_001040429.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr13:58208365 C>T maps to NM_001040429.2 H562H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:58208362 G>A maps to NM_001040429.2 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:58208995 C>T maps to NM_001040429.2 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:58208242 C>T maps to NM_001040429.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr13:58207414 G>A maps to NM_001040429.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:138452717 C>T maps to NM_019035.3 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:138442833 C>T maps to NM_019035.3 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:138452414 G>A maps to NM_019035.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr4:138451838 G>A maps to NM_019035.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:138452039 T>C maps to NM_019035.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:138451583 C>T maps to NM_019035.3 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:138451868 G>T maps to NM_019035.3 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:138452933 G>A maps to NM_019035.3 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr4:138452228 G>A maps to NM_019035.3 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:99662722 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:99663256 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:99551503 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:99662947 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:99661885 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:99662367 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:99662007 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:99662371 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:99662937 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:99657818 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:99662007 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:99662107 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:99662307 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:99663411 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:99662468 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:99663084 T>C did not map to a codon.
Sequencing variant TCGA-AP-A05D-01A-11W-A027-09 chr23:99551836 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:99551652 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:99663468 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:99662007 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:99662050 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:99551652 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:99661932 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:99662677 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:99657680 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:99662007 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:99661982 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr23:99663255 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:99661800 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:99662989 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:99661504 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:99662412 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:99551337 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:99661659 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:99605688 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:99662490 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:99663213 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:99662298 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:99662905 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:61985587 C>A maps to NM_022843.3 E882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:61988012 G>A maps to NM_022843.3 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:61985626 C>A maps to NM_022843.3 E869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:61986482 G>T maps to NM_022843.3 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:61987640 G>A maps to NM_022843.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:61986308 G>A maps to NM_022843.3 N641N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:53422118 G>A maps to NM_002590.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:53422331 G>A maps to NM_002590.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr13:67801807 A>G maps to NM_203487.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr13:67800010 G>A maps to NM_203487.2 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:66878990 C>T maps to NM_203487.2 K1170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:67799826 C>A maps to NM_203487.2 G916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:67801426 C>T maps to NM_203487.2 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:67800079 G>A maps to NM_203487.2 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:67802095 G>A maps to NM_203487.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr13:67205540 C>T maps to NM_203487.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr5:140166255 C>T maps to NM_018900.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140167563 G>A maps to NM_018900.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140168274 T>C maps to NM_031410.1 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140166775 G>T maps to NM_018900.2 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140167389 G>A maps to NM_018900.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140165902 G>T maps to NM_018900.2 G10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140167950 G>A maps to NM_018900.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140168121 G>A maps to NM_018900.2 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr5:140235956 C>T maps to NM_018901.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr5:140237423 C>T maps to NM_018901.2 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140236634 G>A maps to NM_018901.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140236097 C>T maps to NM_018901.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:140236673 T>C maps to NM_018901.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr5:140237072 C>T maps to NM_018901.2 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr5:140236982 C>T maps to NM_018901.2 N450N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140250010 C>A maps to NM_018902.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140249006 G>T maps to NM_018902.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140249585 G>T maps to NM_018902.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140250841 G>A maps to NM_018902.3 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:140249383 C>G maps to NM_018902.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr5:140249147 C>T maps to NM_018902.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr5:140250259 C>T maps to NM_018902.3 H524H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140251081 G>T maps to NM_031861.1 V798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr5:140250133 C>T maps to NM_018902.3 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:140250355 C>T maps to NM_018902.3 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140256757 G>A maps to NM_018903.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr5:140255671 G>A maps to NM_018903.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140256571 G>A maps to NM_018903.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140256424 G>A maps to NM_018903.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140256571 G>A maps to NM_018903.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140257129 G>A maps to NM_018903.2 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr5:140256370 G>A maps to NM_018903.2 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:140256904 C>T maps to NM_018903.2 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140256571 G>A maps to NM_018903.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140256005 G>T maps to NM_018903.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr5:140255344 C>T maps to NM_018903.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:140262035 G>A maps to NM_018904.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:140263781 G>A maps to NM_018904.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140263211 G>A maps to NM_018904.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr5:140263205 C>T maps to NM_018904.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140262716 A>G maps to NM_018904.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr5:140263586 C>T maps to NM_018904.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140263385 C>T maps to NM_018904.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr5:140263889 G>A maps to NM_018904.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140263655 G>A maps to NM_018904.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140263460 C>T maps to NM_018904.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr5:140263406 C>T maps to NM_018904.2 Y518Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140263892 G>A maps to NM_018904.2 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:140176057 G>A maps to NM_018905.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140175139 G>A maps to NM_018905.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140174794 C>T maps to NM_018905.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140176447 G>A maps to NM_018905.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140176249 G>A maps to NM_018905.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr5:140175679 C>T maps to NM_018905.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr5:140176462 C>T maps to NM_018905.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr5:140175496 C>T maps to NM_018905.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr5:140175985 G>A maps to NM_018905.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr5:140182899 G>A maps to NM_018906.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140182239 G>A maps to NM_018906.2 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:140182515 C>T maps to NM_018906.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140181171 G>A maps to NM_018906.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140181021 G>A maps to NM_018906.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr5:140182971 C>T maps to NM_018906.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:140182164 G>A maps to NM_018906.2 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:140182230 C>T maps to NM_018906.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr5:140180964 G>A maps to NM_018906.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:140182371 G>A maps to NM_018906.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:140182539 T>C maps to NM_018906.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr5:140183010 C>T maps to NM_018906.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140188181 G>A maps to NM_018907.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:140187152 C>T maps to NM_018907.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:140188964 G>A maps to NM_018907.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140187545 A>C maps to NM_018907.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr5:140187616 C>G maps to NM_018907.2 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr5:140188391 C>T maps to NM_018907.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140187572 A>G maps to NM_018907.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:140188799 A>T maps to NM_018907.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr5:140188622 C>T maps to NM_018907.2 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140201923 G>A maps to NM_018908.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:140201402 C>T maps to NM_018908.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140203132 G>A maps to NM_018908.2 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140203360 G>A maps to NM_018908.2 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr5:140203360 G>A maps to NM_018908.2 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:140202442 C>T maps to NM_018908.2 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140207945 C>T maps to NM_018909.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140208977 G>A maps to NM_018909.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr5:140209499 G>C maps to NM_018909.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140209736 G>A maps to NM_018909.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140209889 G>A maps to NM_018909.2 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140209850 G>A maps to NM_018909.2 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr5:140209517 G>A maps to NM_018909.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr5:140209295 G>A maps to NM_018909.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:140208773 T>C maps to NM_018909.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr5:140208056 C>T maps to NM_018909.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:140215476 G>A maps to NM_018910.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr5:140216157 C>T maps to NM_018910.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr5:140214327 C>T maps to NM_018910.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:140215743 G>A maps to NM_018910.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140215446 G>A maps to NM_018910.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A053-01A-21W-A027-09 chr5:140216004 G>A maps to NM_018910.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140215215 G>A maps to NM_018910.2 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140215821 G>A maps to NM_018910.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr5:140214264 C>T maps to NM_018910.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140216142 G>A maps to NM_018910.2 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:140214438 G>A maps to NM_018910.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr5:140215137 G>A maps to NM_018910.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:140215533 G>A maps to NM_018910.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr5:140215860 C>T maps to NM_018910.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140222534 G>A maps to NM_018911.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140222705 C>T maps to NM_018911.2 D600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140223158 G>A maps to NM_018911.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140221874 G>A maps to NM_018911.2 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140222357 G>A maps to NM_018911.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140222420 G>A maps to NM_018911.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140222420 G>A maps to NM_018911.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr5:140221076 G>A maps to NM_018911.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:140222681 G>A maps to NM_018911.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:140230269 C>T maps to NM_031857.1 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr5:140229750 C>T maps to NM_031857.1 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140230008 G>A maps to NM_031857.1 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140228686 G>T maps to NM_031857.1 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr5:140229366 C>T maps to NM_031857.1 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:140228550 G>A maps to NM_031857.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:140229708 G>A maps to NM_031857.1 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr5:140229864 C>T maps to NM_031857.1 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140228982 A>G maps to NM_031857.1 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140306803 G>A maps to NM_018898.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140308057 C>T maps to NM_018898.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140308267 C>A maps to NM_018898.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140307607 T>C maps to NM_018898.3 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr5:140347034 A>G maps to NM_018899.5 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140346884 C>T maps to NM_018899.5 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:140346797 G>A maps to NM_018899.5 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140389359 C>A maps to NM_018909.2 I897I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr5:140347145 G>A maps to NM_018899.5 Q265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140347139 C>T maps to NM_018899.5 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140432326 C>A maps to NM_013340.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140432386 C>T maps to NM_013340.2 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140431958 C>T maps to NM_013340.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140431555 C>A maps to NM_013340.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:140431546 T>C maps to NM_013340.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:140432245 A>C maps to NM_013340.2 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr5:140431393 G>A maps to NM_013340.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr5:140431582 G>A maps to NM_013340.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:140572511 C>T maps to NM_018930.3 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140573705 C>T maps to NM_018930.3 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:140573816 G>A maps to NM_018930.3 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140573345 C>T maps to NM_018930.3 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:140574260 G>A maps to NM_018930.3 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:140573642 C>A maps to NM_018930.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140572814 C>T maps to NM_018930.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140580723 C>T maps to NM_018931.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140579778 G>A maps to NM_018931.2 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140580813 G>A maps to NM_018931.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140579518 G>T maps to NM_018931.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140580418 G>T maps to NM_018931.2 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140581143 C>T maps to NM_018931.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140579458 G>T maps to NM_018931.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140580244 G>T maps to NM_018931.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr5:140581425 G>A maps to NM_018931.2 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:140589330 C>A maps to NM_018932.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:140590575 G>A maps to NM_018932.3 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140589999 C>T maps to NM_018932.3 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:140589921 C>T maps to NM_018932.3 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140589501 C>T maps to NM_018932.3 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140588740 G>T maps to NM_018932.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:140588595 G>A maps to NM_018932.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140588700 T>C maps to NM_018932.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140589454 G>T maps to NM_018932.3 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140595512 G>A maps to NM_018933.2 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140594387 C>T maps to NM_018933.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140593940 C>T maps to NM_018933.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140595281 C>T maps to NM_018933.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr5:140594039 C>T maps to NM_018933.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140594975 G>A maps to NM_018933.2 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140595020 C>T maps to NM_018933.2 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr5:140595611 G>A maps to NM_018933.2 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:140595041 C>T maps to NM_018933.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140605444 C>T maps to NM_018934.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140604657 C>T maps to NM_018934.2 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr5:140604696 G>A maps to NM_018934.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140604600 G>A maps to NM_018934.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140626985 C>T maps to NM_018935.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140626262 C>T maps to NM_018935.2 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140627242 G>A maps to NM_018935.2 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140625745 G>T maps to NM_018935.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140627282 C>T maps to NM_018935.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr5:140626804 C>T maps to NM_018935.2 D553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr5:140625589 T>C maps to NM_018935.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140626810 C>T maps to NM_018935.2 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:140627398 C>T maps to NM_018935.2 Y751Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:140626687 C>T maps to NM_018935.2 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr5:140626783 G>A maps to NM_018935.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr5:140564386 C>T maps to NM_020957.1 Y751Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:140562254 A>C maps to NM_020957.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr5:140563351 G>A maps to NM_020957.1 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140563447 A>G maps to NM_020957.1 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140562478 A>G maps to NM_020957.1 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140564463 A>C maps to NM_020957.1 *777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140563213 G>A maps to NM_020957.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:140562943 C>T maps to NM_020957.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr5:140475801 C>T maps to NM_018936.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140475189 C>T maps to NM_018936.2 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140475207 A>G maps to NM_018936.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140476014 G>A maps to NM_018936.2 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140474937 C>A maps to NM_018936.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140475504 C>T maps to NM_018936.2 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140476467 G>A maps to NM_018936.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr5:140476371 C>T maps to NM_018936.2 D666D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140482329 G>A maps to NM_018937.2 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140481867 G>A maps to NM_018937.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr5:140481690 A>C maps to NM_018937.2 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140481555 C>A maps to NM_018937.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140481867 G>A maps to NM_018937.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140482356 C>T maps to NM_018937.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr5:140481579 C>T maps to NM_018937.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr5:140482413 G>A maps to NM_018937.2 V727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140481091 G>T maps to NM_018937.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:140481933 C>T maps to NM_018937.2 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr5:140482389 G>A maps to NM_018937.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:140480967 G>A maps to NM_018937.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140481609 C>T maps to NM_018937.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140501660 C>T maps to NM_018938.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140502020 G>A maps to NM_018938.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140502713 A>C maps to NM_018938.2 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr5:140502134 T>C maps to NM_018938.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K0-01A-11W-A062-09 chr5:140503754 G>T maps to NM_018938.2 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140503157 C>T maps to NM_018938.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140502212 C>T maps to NM_018938.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:140503805 G>A maps to NM_018938.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140516494 G>A maps to NM_015669.2 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140516575 C>T maps to NM_015669.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140515313 G>T maps to NM_015669.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:140515729 C>T maps to NM_015669.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140516146 C>T maps to NM_015669.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr5:140516821 G>A maps to NM_015669.2 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:140515207 G>A maps to NM_015669.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr5:140516566 G>A maps to NM_015669.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr5:140516542 C>T maps to NM_015669.2 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140516848 C>T maps to NM_015669.2 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:140516878 C>T maps to NM_015669.2 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr5:140516509 C>T maps to NM_015669.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140530608 C>A maps to NM_018939.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr5:140531728 C>T maps to NM_018939.2 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140531157 C>T maps to NM_018939.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140531523 G>A maps to NM_018939.2 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:140531613 C>T maps to NM_018939.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr5:140531268 C>T maps to NM_018939.2 D477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr5:140531370 G>T maps to NM_018939.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140530308 C>T maps to NM_018939.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140530707 C>T maps to NM_018939.2 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr5:140532009 G>A maps to NM_018939.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr5:140531172 C>T maps to NM_018939.2 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140531485 C>T maps to NM_018939.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140530006 G>T maps to NM_018939.2 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140530729 G>T maps to NM_018939.2 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140531955 C>T maps to NM_018939.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr5:140531052 C>T maps to NM_018939.2 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr5:140531968 C>T maps to NM_018939.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr5:140531157 C>T maps to NM_018939.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr5:140531241 C>T maps to NM_018939.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr5:140553909 G>T maps to NM_018940.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140554368 G>A maps to NM_018940.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140553051 C>A maps to NM_018940.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr5:140553264 C>T maps to NM_018940.2 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140553936 C>T maps to NM_018940.2 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140554629 C>T maps to NM_018940.2 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr5:140553204 C>T maps to NM_018940.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:140559774 G>A maps to NM_019120.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140558499 C>T maps to NM_019120.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140558679 C>T maps to NM_019120.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140558277 G>A maps to NM_019120.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140559510 C>T maps to NM_019120.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140557692 G>A maps to NM_019120.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:140559705 G>A maps to NM_019120.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:140559180 C>T maps to NM_019120.2 Y522Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:140712233 C>T maps to NM_018912.2 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140712377 C>T maps to NM_018912.2 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140712122 C>T maps to NM_018912.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140711177 C>T maps to NM_018912.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:140711186 C>T maps to NM_018912.2 Y312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140710860 G>T maps to NM_018912.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140712356 C>T maps to NM_018912.2 C702C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:140712176 C>T maps to NM_018912.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr5:140711774 C>T maps to NM_018912.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140711802 C>T maps to NM_018912.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:140711802 C>T maps to NM_018912.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140794313 C>T maps to NM_018913.2 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140792885 C>T maps to NM_018913.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140794421 C>T maps to NM_018913.2 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140793359 C>T maps to NM_018913.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140793563 C>T maps to NM_018913.2 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140793452 C>T maps to NM_018913.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr5:140801468 C>T maps to NM_018914.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140802647 C>T maps to NM_018914.2 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140801021 C>T maps to NM_018914.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140801516 A>T maps to NM_018914.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140803130 G>A maps to NM_018914.2 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140801247 C>T maps to NM_018914.2 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140802372 C>T maps to NM_018914.2 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140800928 C>T maps to NM_018914.2 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140801450 C>T maps to NM_018914.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr5:140802356 C>T maps to NM_018914.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140801450 C>T maps to NM_018914.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140801942 C>A maps to NM_018914.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140802372 C>T maps to NM_018914.2 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr5:140802416 G>A maps to NM_018914.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140802305 C>A maps to NM_018914.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:140812446 C>T maps to NM_003735.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:140812689 C>T maps to NM_003735.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140811762 C>T maps to NM_003735.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140812446 C>T maps to NM_003735.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140812047 C>T maps to NM_003735.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr5:140812104 G>A maps to NM_003735.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr5:140812047 C>T maps to NM_003735.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140812035 C>T maps to NM_003735.2 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140811075 C>T maps to NM_003735.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140812185 T>C maps to NM_003735.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:140811837 C>T maps to NM_003735.2 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr5:140810919 C>T maps to NM_003735.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140718669 C>T maps to NM_018915.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140720010 C>T maps to NM_018915.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:140720743 C>T maps to NM_018915.2 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140718775 C>T maps to NM_018915.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140719173 C>T maps to NM_018915.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr5:140719020 C>T maps to NM_018915.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140720592 C>T maps to NM_018915.2 N685N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140719539 C>T maps to NM_018915.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140719944 C>A maps to NM_018915.2 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140720190 C>T maps to NM_018915.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140725525 C>T maps to NM_018916.3 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr5:140724409 C>T maps to NM_018916.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140723797 C>T maps to NM_018916.3 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:140723836 G>A maps to NM_018916.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr5:140724706 C>T maps to NM_018916.3 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140725733 C>T maps to NM_018916.3 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:140725564 C>T maps to NM_018916.3 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140725273 C>T maps to NM_018916.3 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140725699 C>A maps to NM_018916.3 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140736779 C>T maps to NM_018917.2 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140735976 T>C maps to NM_018917.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr5:140735309 C>T maps to NM_018917.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140735594 C>T maps to NM_018917.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:140735051 C>A maps to NM_018917.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr5:140735921 T>C maps to NM_018917.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140745867 C>A maps to NM_018918.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140744799 C>A maps to NM_018918.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140744871 C>T maps to NM_018918.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr5:140744631 C>T maps to NM_018918.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140744193 C>T maps to NM_018918.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140745165 C>T maps to NM_018918.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140745436 C>T maps to NM_018918.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140745945 C>T maps to NM_018918.2 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:140745885 C>T maps to NM_018918.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr5:140745573 G>A maps to NM_018918.2 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:140744961 G>A maps to NM_018918.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140744631 C>T maps to NM_018918.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140745352 C>T maps to NM_018918.2 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140745768 C>T maps to NM_018918.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140755254 C>T maps to NM_018919.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr5:140753892 C>T maps to NM_018919.2 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140754084 C>T maps to NM_018919.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140754489 C>A maps to NM_018919.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140755104 C>T maps to NM_018919.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140755392 C>T maps to NM_018919.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140753925 C>T maps to NM_018919.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140754660 C>A maps to NM_018919.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:140754513 C>A maps to NM_018919.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140754183 C>T maps to NM_018919.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr5:140762900 T>C maps to NM_018920.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140764118 C>T maps to NM_018920.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140764586 C>T maps to NM_018920.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140762609 C>T maps to NM_018920.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140763845 C>T maps to NM_018920.2 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:140763275 C>T maps to NM_018920.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140772622 C>T maps to NM_032088.1 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140772727 C>A maps to NM_032088.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140774059 C>T maps to NM_032088.1 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr5:140773939 C>T maps to NM_032088.1 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:140773918 C>T maps to NM_032088.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140773792 C>A maps to NM_032088.1 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140774458 C>T maps to NM_032088.1 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:140773888 G>A maps to NM_032088.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140774650 C>A maps to NM_032088.1 V757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr5:140772868 C>T maps to NM_032088.1 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140782947 C>T maps to NM_018921.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140782953 C>T maps to NM_018921.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140783550 A>G maps to NM_018921.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:140783169 C>T maps to NM_018921.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140783437 C>T maps to NM_018921.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140730135 C>T maps to NM_018922.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr5:140730579 C>T maps to NM_018922.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr5:140730144 C>T maps to NM_018922.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140730787 G>T maps to NM_018922.2 G321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140731239 C>T maps to NM_018922.2 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140731920 C>A maps to NM_018922.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140731929 C>T maps to NM_018922.2 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140730135 C>T maps to NM_018922.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr5:140731617 C>T maps to NM_018922.2 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:140730135 C>T maps to NM_018922.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140730216 C>T maps to NM_018922.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140732208 C>T maps to NM_018922.2 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140730135 C>T maps to NM_018922.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140731398 C>T maps to NM_018922.2 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140730468 C>T maps to NM_018922.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:140739911 G>A maps to NM_018923.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140740409 C>T maps to NM_018923.2 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140741027 C>A maps to NM_018923.2 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140740950 G>T maps to NM_018923.2 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:140739908 C>T maps to NM_018923.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140740556 C>T maps to NM_018923.2 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140739725 C>T maps to NM_018923.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140740019 C>T maps to NM_018923.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140740658 C>T maps to NM_018923.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr5:140751454 G>A maps to NM_018924.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:140751310 C>T maps to NM_018924.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140750656 C>T maps to NM_018924.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140750876 G>T maps to NM_018924.2 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140751106 C>T maps to NM_018924.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140751505 C>T maps to NM_018924.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140752192 C>T maps to NM_018924.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr5:140751466 G>A maps to NM_018924.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:140750740 C>T maps to NM_018924.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140752363 C>T maps to NM_018924.2 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:140752381 T>C maps to NM_032097.1 S807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140751115 A>G maps to NM_018924.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140768191 C>T maps to NM_003736.2 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140768977 C>T maps to NM_003736.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140767819 C>T maps to NM_003736.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140769154 C>T maps to NM_003736.2 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140768977 C>T maps to NM_003736.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140769649 C>T maps to NM_003736.2 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140768384 G>T maps to NM_003736.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr5:140768185 C>T maps to NM_003736.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140767819 C>T maps to NM_003736.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr5:140767465 C>T maps to NM_003736.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr5:140779295 C>A maps to NM_018925.2 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:140780135 T>C maps to NM_032099.1 F814F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140779361 G>A maps to NM_018925.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140779580 C>T maps to NM_018925.2 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr5:140779910 C>T maps to NM_018925.2 Y739Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:140778866 C>A maps to NM_018925.2 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr5:140779637 G>A maps to NM_018925.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140778845 C>T maps to NM_018925.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:140779997 A>G maps to NM_018925.2 Q768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140777843 C>T maps to NM_018925.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140778284 G>A maps to NM_018925.2 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140778503 C>T maps to NM_018925.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140779433 C>T maps to NM_018925.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140789106 C>T maps to NM_018926.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140789739 C>T maps to NM_018926.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:140789379 C>T maps to NM_018926.2 H537H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140788638 T>C maps to NM_018926.2 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr5:140788155 C>T maps to NM_018926.2 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr5:140788504 G>T maps to NM_018926.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140789334 C>T maps to NM_018926.2 H522H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:140798772 G>A maps to NM_018927.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:140797855 G>T maps to NM_018927.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr5:140797510 C>T maps to NM_018927.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:140799150 C>T maps to NM_018927.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr5:140798160 C>T maps to NM_018927.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140799138 C>A maps to NM_018927.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:140856666 C>T maps to NM_002588.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140857143 G>A maps to NM_002588.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:140856618 C>T maps to NM_002588.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140865891 T>C maps to NM_018928.2 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140867193 G>A maps to NM_032406.1 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:140865319 C>T maps to NM_018928.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:140865291 G>A maps to NM_018928.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140865748 C>T maps to NM_018928.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140866237 C>T maps to NM_018928.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:140866768 C>T maps to NM_018928.2 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:140870770 C>A maps to NM_018929.2 S655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:140884980 C>T maps to NM_018915.2 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr5:140871068 C>T maps to NM_018929.2 D754D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:140869907 A>G maps to NM_018929.2 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:140869499 C>T maps to NM_018929.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:82882912 A>G maps to NM_015885.3 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:82892085 T>C maps to NM_015885.3 G1340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:82888853 T>C maps to NM_015885.3 L1326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:74733344 G>A maps to NM_032673.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:74732872 G>A maps to NM_032673.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:755104 C>T maps to NM_006315.4 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr4:727519 C>T maps to NM_006315.4 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:93021103 C>T maps to NM_032373.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:93024195 G>A maps to NM_032373.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:93008434 T>C maps to NM_032373.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:93038066 C>T maps to NM_032373.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:93021103 C>T maps to NM_032373.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr10:93000277 C>T maps to NM_032373.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:113838699 G>A maps to ENST00000246505 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr13:113832553 G>A maps to ENST00000246505 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:113845240 A>G maps to ENST00000246505 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:113851511 C>T maps to ENST00000246505 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:44576243 G>A maps to NM_022104.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:44574849 C>T maps to NM_022104.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr20:44576372 C>T maps to NM_022104.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:56139607 C>A maps to NM_002591.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:56136616 G>A maps to NM_002591.3 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:56139330 C>A maps to NM_002591.3 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:56140181 G>T maps to NM_002591.3 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:24566229 C>T maps to NM_004563.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:24569205 C>T maps to NM_004563.2 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:82580372 C>T maps to NM_033026.5 T3177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:82584825 G>A maps to NM_033026.5 R1815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:82584918 C>A maps to NM_033026.5 E1784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr7:82584313 C>T maps to NM_033026.5 Q1985Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:82538248 G>A maps to NM_033026.5 R4461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:82581178 A>G maps to NM_033026.5 V3030V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:82585630 G>A maps to NM_033026.5 S1546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:82785656 C>T maps to NM_033026.5 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:82545766 G>A maps to NM_033026.5 T3845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:82764108 C>T maps to NM_033026.5 Q919Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:82582135 C>T maps to NM_033026.5 E2711E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:82582380 C>A maps to NM_033026.5 E2630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:82581336 G>A maps to NM_033026.5 R2978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:82583785 C>T maps to NM_033026.5 S2161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:82595616 C>A maps to NM_033026.5 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:82583836 T>C maps to NM_033026.5 E2144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:82584921 C>A maps to NM_033026.5 E1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:82784170 C>A maps to NM_033026.5 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:82785302 C>T maps to NM_033026.5 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:82785530 A>G maps to NM_033026.5 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:82390016 G>A maps to NM_033026.5 R5076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr7:82764903 C>T maps to NM_033026.5 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:82580537 A>G maps to NM_033026.5 H3122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:82584231 C>A maps to NM_033026.5 E2013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:82586185 G>A maps to NM_033026.5 S1361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:82785343 C>A maps to NM_033026.5 G205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:82580270 C>T maps to NM_033026.5 Q3211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:82508665 C>T maps to NM_033026.5 G4547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:82583641 A>C maps to NM_033026.5 V2209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:82584510 C>A maps to NM_033026.5 E1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:82785547 C>A maps to NM_033026.5 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:82453555 T>C maps to NM_033026.5 S4864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:82581256 A>G maps to NM_033026.5 H3004H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:82583198 G>T maps to NM_033026.5 S2357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:82584936 C>A maps to NM_033026.5 E1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr7:82585186 G>A maps to NM_033026.5 D1694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:82763856 T>C maps to NM_033026.5 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:82584595 T>G maps to NM_033026.5 S1891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:82595616 C>A maps to NM_033026.5 E1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:82785547 C>A maps to NM_033026.5 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:17823648 G>A maps to NM_006197.3 W999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:17830018 G>T maps to NM_006197.3 E1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:17863812 A>G maps to NM_006197.3 S1623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:17823961 G>A maps to NM_006197.3 W1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:17796395 G>T maps to NM_006197.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:17815133 G>A maps to NM_006197.3 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr8:17863821 C>T maps to NM_006197.3 R1626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr8:17838199 C>T maps to NM_006197.3 S1348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:17814152 G>T maps to NM_006197.3 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:17843070 T>C maps to NM_006197.3 H1408H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:17851107 G>T maps to NM_006197.3 E1603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:150123391 C>T maps to NM_005389.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:52773806 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:52733044 C>A maps to NM_052937.2 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:62896670 T>C maps to NM_018257.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:62891450 G>T maps to NM_018257.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr20:62904847 G>A maps to NM_018257.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:62891425 C>T maps to NM_018257.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:62904752 G>T maps to NM_018257.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr20:5100390 T>C maps to NM_002592.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr20:5095949 G>A maps to NM_002592.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:47831243 C>T maps to NM_006031.5 L1753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr21:47767387 T>C maps to NM_006031.5 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:47746337 G>A maps to NM_006031.5 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:47850051 C>T maps to NM_006031.5 R2607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:47863789 C>T maps to NM_006031.5 P3256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:47808740 C>T maps to NM_006031.5 I1183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:47783429 A>G maps to NM_006031.5 E730E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:47860967 G>A maps to NM_006031.5 T3198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr21:47850014 C>T maps to NM_006031.5 S2594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:47786918 G>A maps to NM_006031.5 T1010T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:71575561 C>T maps to NM_014982.2 S2181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:71492877 C>T maps to NM_014982.2 C1076C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:71434937 T>C maps to NM_014982.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:71540386 C>T maps to NM_014982.2 R1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:71434931 G>A maps to NM_014982.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:71444032 G>T maps to NM_014982.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr14:71444259 T>C maps to NM_014982.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr14:71511996 C>T maps to NM_014982.2 R1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:71444032 G>T maps to NM_014982.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:233393957 G>A maps to NM_014801.3 N550N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:233136092 G>T maps to NM_014801.3 V1762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:233190116 G>A maps to NM_014801.3 G1416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:233314882 C>T maps to NM_014801.3 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:233393948 C>T maps to NM_014801.3 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:233353659 G>A maps to NM_014801.3 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:233152684 A>G maps to NM_014801.3 C1607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:233120133 G>A maps to NM_014801.3 L2110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:233372674 C>T maps to NM_014801.3 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:233190031 G>A maps to NM_014801.3 R1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:233120058 G>A maps to NM_014801.3 D2135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:233353890 G>T maps to NM_014801.3 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:65401703 G>A maps to NM_032223.2 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:65392706 G>A maps to NM_032223.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr11:65387852 C>T maps to NM_032223.2 Y684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:65392026 A>C maps to NM_032223.2 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:65396094 C>T maps to NM_032223.2 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:100205407 G>A maps to NM_002593.3 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100205144 T>C maps to NM_002593.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:7697374 G>A maps to NM_174895.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:95746543 G>A maps to NM_000439.4 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:95761521 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:95746639 C>T maps to NM_000439.4 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:95730722 T>G maps to NM_000439.4 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:95730654 C>T maps to NM_000439.4 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:95734655 C>T maps to NM_000439.4 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:95757660 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:95768620 G>A maps to NM_000439.4 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:95733078 C>T maps to NM_000439.4 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr20:17417464 C>T maps to NM_002594.2 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:17240902 C>T maps to NM_002594.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:17434457 C>T maps to NM_002594.2 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:17434457 C>T maps to NM_002594.2 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:17240913 T>C maps to NM_002594.2 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:17339013 C>T maps to NM_002594.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr20:17208057 G>T maps to NM_002594.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr20:17389939 C>T maps to NM_002594.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:17208042 G>A maps to NM_002594.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:1487788 C>T maps to NM_017573.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr9:78686657 C>T maps to NM_001190482.1 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:78686801 C>T maps to NM_001190482.1 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr9:78853911 G>A maps to NM_001190482.1 E968E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:78749090 C>T maps to NM_001190482.1 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:78601103 C>T maps to NM_001190482.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:78784710 G>T maps to NM_001190482.1 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:78686646 C>T maps to NM_001190482.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:78772079 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:78682954 C>T maps to NM_001190482.1 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:78789989 C>T maps to NM_001190482.1 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:78686646 C>T maps to NM_001190482.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:101862768 G>A maps to NM_002570.3 C806C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:101853584 G>A maps to NM_002570.3 R898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:101933416 G>A maps to NM_002570.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:101938626 G>A maps to NM_002570.3 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr15:101910711 G>A maps to NM_002570.3 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr15:101847442 G>A maps to NM_002570.3 C928C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:117077468 G>A maps to NM_004716.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:117077468 G>A maps to NM_004716.2 F642F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:55509655 T>C maps to NM_174936.3 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:55521670 G>T maps to NM_174936.3 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:55509574 G>A maps to NM_174936.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:70504040 A>G maps to NM_016297.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:148745525 C>T maps to NM_024028.3 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:148747914 C>T maps to NM_024028.3 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:148748060 C>A maps to NM_024028.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:195966530 C>A maps to NM_005017.2 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:195997384 T>C maps to NM_005017.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:195974276 C>T maps to NM_005017.2 A149A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A11Y-01A-21D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr3:195974339 G>A maps to NM_005017.2 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:24690709 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:24608195 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:24597472 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:24637153 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:24593333 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr17:79867429 C>T maps to NM_001184917.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:79862804 C>T maps to NM_001184917.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:242793419 G>A maps to NM_005018.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:242794103 G>T maps to NM_005018.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:167422641 G>A maps to NM_145859.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:167402161 G>A maps to NM_145859.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:105178303 T>C maps to NM_014976.1 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:105179314 C>A maps to NM_014976.1 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:105203012 C>T maps to NM_014976.1 R1683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:105201731 G>A maps to NM_014976.1 T1569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr10:105178196 T>C maps to NM_014976.1 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr10:105177640 G>A maps to NM_014976.1 E621E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:105187116 C>T maps to NM_014976.1 R1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:105184766 G>A maps to NM_014976.1 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr10:105182763 G>A maps to NM_014976.1 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:34900380 G>T maps to NM_032346.1 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:34916905 G>T maps to NM_032346.1 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:34912477 C>T maps to NM_032346.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:112653866 G>T maps to NM_014456.4 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:112645018 T>C maps to NM_014456.4 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:112641042 G>A maps to NM_014456.4 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr5:306867 A>G maps to NM_013232.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:33868041 A>G maps to NM_001162429.1 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:33840423 C>A maps to NM_001162429.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:33883521 G>T maps to NM_001162429.1 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:33895378 T>C maps to NM_001162429.1 H638H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:65421508 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr15:65421427 G>A maps to NM_005707.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr15:65412140 T>C maps to NM_005707.1 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:125588972 G>A maps to NM_005388.4 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:125582647 C>A maps to NM_005388.4 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:125582740 C>A maps to NM_005388.4 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:56428673 G>A maps to NM_152401.2 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:56435975 C>A maps to NM_152401.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:101183039 G>T maps to NM_024065.4 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:101188050 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:774011 G>A maps to NM_182612.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr11:775134 C>T maps to NM_182612.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:165832171 C>A maps to NM_001130690.1 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:165801864 G>A maps to NM_001130690.1 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:165827173 C>A maps to NM_001130690.1 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:165746584 G>A maps to NM_001130690.1 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr6:165829717 G>A maps to NM_001130690.1 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr6:165829769 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr6:165862454 G>A maps to NM_001130690.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:178545554 G>A maps to NM_016953.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr2:178685016 G>A maps to NM_016953.3 D502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:178592831 G>A maps to NM_016953.3 D619D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:57542789 T>C maps to NM_177966.5 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr2:183011835 A>T maps to NM_005019.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:183050649 G>A maps to NM_005019.3 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:183387039 C>A maps to NM_005019.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:183129092 G>A maps to NM_005019.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr7:31918700 C>T maps to NM_001191057.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:32209401 G>T maps to NM_001191058.1 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:31855560 G>T maps to NM_001191057.1 S597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:31890331 G>T maps to NM_001191057.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:31887646 A>C maps to NM_001191057.1 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:31862830 G>A maps to NM_001191057.1 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr7:31912928 A>C maps to NM_001191057.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:72300216 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:72292004 G>T maps to NM_002599.3 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:72292417 C>T maps to NM_002599.3 E676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:72290048 G>A maps to NM_002599.3 G787G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:20774338 C>T maps to NM_000921.3 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:20803483 G>T maps to NM_000921.3 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr12:20523069 G>A maps to NM_000921.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:20766516 G>A maps to NM_000921.3 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:20833199 C>T maps to NM_000921.3 Q1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:20803519 G>T maps to NM_000921.3 E971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr12:20782878 C>T maps to NM_000921.3 C526C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:20799802 G>A maps to NM_000921.3 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:20832991 C>A maps to NM_000921.3 I1071I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:14810771 G>T maps to NM_000922.3 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:14891032 C>T maps to NM_000922.3 R1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:14808122 C>T maps to NM_000922.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:14840738 C>A maps to NM_000922.3 C597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:14839825 T>C maps to NM_000922.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:14889258 G>T maps to NM_000922.3 E1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:14865418 G>A maps to NM_000922.3 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr11:14666367 C>T maps to NM_000922.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:10574518 G>A maps to NM_001111307.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:10578212 C>T maps to NM_001111307.1 C859C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:10574653 A>G maps to ENST00000380686 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:10570053 C>A maps to ENST00000380686 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:10570128 C>T maps to NM_001111307.1 Y385Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:66384302 T>C maps to NM_001037341.1 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:66723490 C>T maps to NM_001037341.1 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:66828885 C>A maps to NM_001037341.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:66829175 C>T maps to NM_001037341.1 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:66829175 C>T maps to NM_001037341.1 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:66798192 G>T maps to NM_001037341.1 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:66827367 C>A maps to NM_001037341.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:66828885 C>A maps to NM_001037341.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:66831423 C>A maps to NM_001037341.1 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:18327691 C>T maps to NM_000923.3 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:18329173 C>T maps to NM_000923.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:59064262 G>A maps to NM_001197218.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:58882192 G>A maps to NM_006203.4 H3H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:58511669 G>A maps to NM_001104631.1 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:58270598 C>T maps to NM_001104631.1 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:59284541 G>T maps to ENST00000502484 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:144931008 C>A maps to NM_001002811.1 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:144874006 A>G maps to NM_014644.4 H1650H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:144882448 G>A maps to NM_014644.4 H1190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:145015987 G>A maps to NM_001198832.1 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:144877174 C>T maps to NM_014644.4 R1504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:144917907 G>A maps to NM_014644.4 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:144946692 C>A maps to NM_014644.4 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:144863442 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:144916667 C>A maps to NM_014644.4 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:144879042 C>T maps to NM_014644.4 S1469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:144854517 G>A maps to NM_014644.4 L2318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:144874726 G>A maps to NM_014644.4 S1627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:144879399 G>A maps to NM_014644.4 N1350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:144879456 G>T maps to NM_014644.4 P1331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:144909927 C>A maps to NM_014644.4 E754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:144946731 C>A maps to NM_014644.4 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:144857633 C>T maps to NM_014644.4 T2140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:144903113 C>T maps to NM_014644.4 E926E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr1:144994695 G>C maps to NM_014644.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr1:144857693 A>G maps to NM_014644.4 G2120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:144879336 G>T maps to NM_014644.4 V1371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:144917573 A>G maps to NM_014644.4 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:144946731 C>A maps to NM_014644.4 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:120425695 G>A maps to NM_001083.3 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:120528076 G>A maps to NM_001083.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:120428838 G>A maps to NM_001083.3 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:120463694 G>T maps to NM_001083.3 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:120463729 G>A maps to NM_001083.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr4:120528046 G>A maps to NM_001083.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:149286907 G>A maps to NM_000440.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:149245768 G>T maps to NM_000440.2 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr4:647867 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr4:654293 C>T maps to NM_000283.3 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:649788 C>T maps to NM_000283.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:663868 C>T maps to NM_000283.3 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:650044 C>A maps to NM_000283.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:629739 C>T maps to NM_000283.3 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:648635 C>T maps to NM_000283.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:95394583 G>T maps to NM_006204.3 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:95400675 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:95422805 G>T maps to NM_006204.3 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:95372878 G>T maps to NM_006204.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:95381756 G>A maps to NM_006204.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:95372928 G>A maps to NM_006204.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:79617927 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:15132111 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr8:66639125 G>A maps to ENST00000401827 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:136512818 G>A maps to NM_018945.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:136477030 C>T maps to ENST00000446774 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:136502366 C>T maps to NM_018945.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:85660970 C>T maps to NM_002605.2 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:85666343 G>T maps to NM_002605.2 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:85664053 C>T maps to NM_002605.2 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:85664246 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:76717774 G>T maps to NM_003719.3 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:76645260 C>T maps to NM_003719.3 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:44192568 C>T maps to NM_002606.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:44151907 C>T maps to NM_002606.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr21:44180448 C>T maps to NM_002606.2 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:552066 G>A maps to NM_002607.5 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:39621766 C>T maps to NM_002608.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:103814212 G>A maps to NM_025208.4 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:103866870 C>T maps to NM_025208.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:55129832 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:55127487 G>A maps to NM_006206.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:55138645 G>A maps to NM_006206.4 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:55131210 G>T maps to NM_006206.4 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:55133596 G>T maps to NM_006206.4 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:55131210 G>T maps to NM_006206.4 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:55133487 C>A maps to NM_006206.4 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:55151575 G>T maps to ENST00000507166 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:149510216 G>A maps to NM_002609.3 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:149500462 G>T maps to NM_002609.3 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:149500491 G>A maps to NM_002609.3 R849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:149501461 G>A maps to NM_002609.3 Y775Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:149513197 C>T maps to NM_002609.3 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr5:149515295 C>T maps to NM_002609.3 W62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr8:17486233 G>A maps to NM_006207.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:17486008 C>T maps to NM_006207.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:19368113 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:19372609 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19373496 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:19369511 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:19377049 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:19372656 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:19373599 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:19368099 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:19368171 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:96762428 T>C maps to NM_005390.4 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:96761742 G>T maps to NM_005390.4 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:96762308 T>C maps to NM_005390.4 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:58417331 T>G maps to NM_000925.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:58415442 C>A maps to NM_000925.3 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:58416534 C>A maps to NM_000925.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr3:58414128 C>T maps to ENST00000474765 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:34988346 C>T maps to NM_003477.2 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:35016487 C>T maps to NM_003477.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:35016487 C>T maps to NM_003477.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:35016593 C>T maps to NM_003477.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:35016491 G>T maps to NM_003477.2 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:44048911 G>A maps to NM_005313.4 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:44061727 G>T maps to NM_005313.4 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:148716135 C>T maps to NM_004911.4 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:122808055 G>A maps to NM_006810.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:122843130 C>T maps to NM_006810.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:122865055 C>T maps to NM_006810.3 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:122880292 C>T maps to NM_006810.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:10929937 G>A maps to ENST00000381611 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:10927441 G>T maps to ENST00000381611 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr2:10927560 G>A maps to ENST00000381611 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:26449100 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:26448948 C>T maps to NM_152835.3 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:26440916 C>T maps to NM_152835.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:20371960 C>A maps to NM_174924.1 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:20380849 C>T maps to NM_174924.1 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:173423505 T>C maps to ENST00000392571 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr17:48185984 C>A maps to NM_002611.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:48183362 G>A maps to NM_002611.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:48184446 C>T maps to NM_002611.3 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:48184203 C>T maps to NM_002611.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:24516995 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:24545774 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:24544313 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:24552115 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:24546222 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:24545732 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:24521501 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:24557270 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:24512885 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:24516956 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:24521469 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:24545704 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:24523329 T>C did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:24521540 G>C did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr7:95224434 G>T maps to NM_002612.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:95224470 C>A maps to NM_002612.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:95222230 G>A maps to NM_002612.3 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:97007014 C>T maps to NM_020992.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:96998377 C>T maps to NM_020992.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:97007026 C>T maps to NM_020992.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:97007026 C>T maps to NM_020992.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:97007026 C>T maps to NM_020992.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr8:22451332 C>T maps to NM_021630.5 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:186435954 G>A maps to NM_001114107.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:186446223 C>T maps to NM_014476.4 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:186427696 C>A maps to NM_014476.4 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr4:186423510 G>A maps to NM_014476.4 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:131607780 C>T maps to NM_003687.3 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr5:131606679 G>T maps to NM_003687.3 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:95585305 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:95575653 G>T maps to NM_006457.3 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:95497059 C>T maps to NM_006457.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr5:176918824 G>A maps to NM_005451.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:176910930 G>A maps to NM_005451.3 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:176917868 A>G did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr5:176910897 G>A maps to NM_005451.3 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:94935366 G>A maps to NM_001161778.1 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:94934568 C>T maps to NM_001161778.1 Y153Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr8:94934859 G>A maps to NM_001161778.1 Q250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:94934550 C>T maps to NM_001161778.1 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZP-01A-21D-A10M-09 chr8:94930117 G>C maps to NM_001161778.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:66918570 C>A maps to NM_020786.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:66919296 C>T maps to NM_020786.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:13940870 C>T maps to NM_006474.4 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:13936892 T>C maps to NM_006474.4 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:13933759 G>T maps to NM_006474.4 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:13933680 G>A maps to NM_006474.4 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:70190673 C>T maps to NM_017990.3 I844I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:70166117 C>T maps to NM_017990.3 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:39910113 A>G maps to NM_001100399.1 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:39929622 G>T maps to NM_001100399.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:39899993 G>T maps to NM_001100400.1 Y595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:39846301 C>T maps to NM_001100399.1 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:39846282 G>A maps to NM_001100399.1 R1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:33320216 G>A maps to ENST00000400481 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:33316752 C>T maps to ENST00000400481 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr13:33258136 A>T maps to ENST00000400481 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr13:33233386 G>A maps to ENST00000400481 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:33334729 T>G maps to ENST00000400481 V1130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:33316752 C>T maps to ENST00000400481 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:33225999 T>G maps to ENST00000400481 Y56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:27012808 A>C maps to NM_014317.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:27009167 C>A maps to NM_014317.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:27024209 C>T maps to NM_014317.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:107655451 G>A maps to NM_020381.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr6:107780272 G>A maps to NM_020381.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:28498639 C>T maps to NM_000209.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr16:15127222 G>A maps to NM_015027.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:15100249 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:45153947 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:45165993 C>T maps to NM_003681.4 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr21:45161451 A>G maps to ENST00000467908 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:45165993 C>T maps to NM_003681.4 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:1963658 C>T maps to NM_024411.4 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:69507146 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:69506957 G>A did not map to a codon.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr23:69507629 T>G did not map to a codon.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr5:31799763 C>T maps to NM_178140.2 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:32074100 C>A maps to NM_178140.2 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:32088656 C>T maps to NM_178140.2 S1701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:32088080 C>T maps to NM_178140.2 P1509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:32101301 G>A maps to NM_178140.2 S2770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:31983426 C>T maps to NM_178140.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:32074688 C>T maps to NM_178140.2 V1159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:31799558 C>A maps to NM_178140.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:32087469 C>T maps to NM_178140.2 R1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:32088587 T>G maps to NM_178140.2 T1678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:32071493 C>T maps to NM_178140.2 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr5:32053972 C>T maps to NM_178140.2 D628D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:31799711 C>A maps to NM_178140.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:32088636 G>T maps to NM_178140.2 E1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:31799456 C>T maps to NM_178140.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:32087480 G>A maps to NM_178140.2 S1309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:31799519 T>C maps to NM_178140.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:32090727 T>C maps to NM_178140.2 L2392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153070656 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153070250 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153072226 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:153069031 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153070052 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:153069157 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr23:153070283 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr23:153069727 C>G did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:153073997 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:153069914 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153069399 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153070249 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153069192 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:153069505 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr10:102789871 T>C maps to NM_001195263.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:102782015 G>A maps to NM_001195263.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:119042997 T>C maps to NM_173791.3 E1082E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:119049714 G>A maps to NM_173791.3 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:119043230 C>A maps to NM_173791.3 E1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:22000058 C>A maps to ENST00000424898 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:22000035 A>G maps to ENST00000424898 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:145762127 C>A maps to NM_002614.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:145762179 C>T maps to NM_002614.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:47650690 C>T maps to NM_005764.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:47649648 C>T maps to NM_005764.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:47650690 C>T maps to NM_005764.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:73432935 G>A maps to NM_015009.1 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:73432614 G>A maps to NM_015009.1 F1034F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:73433280 C>T maps to NM_015009.1 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:73433568 G>A maps to NM_015009.1 R716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:73657760 G>A maps to NM_015009.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:73440207 C>T maps to NM_015009.1 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:41900430 C>A maps to NM_001164595.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:41967265 C>T maps to NM_001164595.1 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:41966950 G>A maps to NM_001164595.1 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:41967364 C>T maps to NM_001164595.1 D928D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:41967268 C>T maps to NM_001164595.1 D896D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:41961613 G>A maps to NM_001164595.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:41967169 C>T maps to NM_001164595.1 V863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:41967265 C>T maps to NM_001164595.1 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:41966765 G>T maps to NM_001164595.1 E729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:41585298 G>T maps to NM_001164595.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:41831758 T>C maps to NM_013377.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:41967523 C>G maps to NM_001164595.1 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:41903640 G>T maps to NM_001164595.1 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156879654 C>A maps to NM_001080471.1 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156880107 C>A maps to NM_001080471.1 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:156876427 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:156883040 G>A maps to NM_001080471.1 S826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:118575869 G>A maps to NM_002567.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:32096372 G>A maps to NM_012392.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr7:94293619 G>A maps to NM_001172437.1 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:94293190 C>T maps to NM_001172437.1 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:94293413 C>T maps to NM_001172437.1 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:94293044 C>T maps to NM_001172437.1 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:94293685 C>T maps to NM_001172437.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:57325627 A>G maps to NM_006210.2 A1394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:57335807 G>A maps to NM_006210.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:57328600 C>T maps to NM_006210.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:57325288 G>A maps to NM_006210.2 C1507C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:57325944 C>A maps to NM_006210.2 E1289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:57327231 C>A maps to NM_006210.2 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:57328293 C>A maps to NM_006210.2 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:57327757 G>A maps to NM_006210.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:57326653 G>T maps to NM_006210.2 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:64322144 G>A maps to NM_020651.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr2:64322228 T>A maps to NM_020651.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:56763604 G>A maps to NM_021255.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:66240743 C>T maps to NM_145065.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:52096873 C>T maps to NM_015946.4 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:4574796 G>A maps to ENST00000301396 A1254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:4578896 G>T maps to ENST00000301396 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:4579049 A>G maps to ENST00000301396 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:57354490 G>A maps to NM_001135690.1 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:57353920 G>A maps to NM_001135690.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:57354328 G>A maps to NM_001135690.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:57353998 G>T maps to NM_001135690.1 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:33892708 G>A maps to NM_000285.3 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:33892768 G>A maps to NM_000285.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:33902606 G>A maps to NM_000285.3 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:34003549 G>A maps to NM_000285.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:8053375 G>A maps to NM_002616.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:8052891 G>A maps to NM_002616.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:8044490 G>A maps to NM_002616.2 G1256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:239177589 C>T maps to NM_022817.2 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:239159250 G>T maps to NM_022817.2 I1136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:239155018 C>T maps to NM_022817.2 T1255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr2:239161837 G>T maps to NM_022817.2 A942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:7845626 C>A maps to ENST00000377532 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:7886574 C>T maps to ENST00000377532 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:7895930 C>T maps to ENST00000377532 V1108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:7863903 C>T maps to ENST00000377532 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:7845552 G>T maps to ENST00000377532 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr6:138417629 C>A maps to NM_022121.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr22:30975267 C>T maps to NM_014303.2 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr22:30976110 A>G maps to NM_014303.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:92147066 G>T maps to NM_000466.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr7:92148362 T>G maps to NM_000466.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:92130835 G>A maps to NM_000466.2 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:92116799 G>A maps to NM_000466.2 R1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:92147523 G>A maps to NM_000466.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:92147348 T>G maps to NM_000466.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:92148326 T>C maps to NM_000466.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:92116850 C>A maps to NM_000466.2 E1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:2338298 C>T maps to NM_153818.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:2339888 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:145522768 C>T maps to NM_003846.2 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:145517351 C>T maps to NM_003846.2 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr17:33904280 C>T maps to NM_000286.2 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr17:33904175 C>T maps to NM_000286.2 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:33904321 C>A maps to NM_000286.2 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:10683164 C>T maps to NM_004565.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:45932473 G>A maps to NM_057174.2 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:45935951 G>A maps to NM_057174.2 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:160253318 C>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:160253337 C>T maps to NM_002857.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:160252818 G>A maps to NM_002857.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:160253412 G>A maps to NM_002857.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:160253412 G>A maps to NM_002857.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:160252818 G>A maps to NM_002857.3 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:77896102 G>T maps to NM_001172087.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:77896041 G>A maps to NM_001172087.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr8:77895793 G>A maps to NM_001172087.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:77896041 G>A maps to NM_001172087.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:143810356 G>A maps to NM_003630.2 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:143792692 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:7361624 G>A maps to NM_001131023.1 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:179537754 C>A maps to NM_016559.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:179593236 G>A maps to NM_016559.1 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:179593214 G>A maps to NM_016559.1 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:179526112 C>A maps to NM_016559.1 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:179519818 C>A maps to NM_016559.1 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:179526065 C>T maps to NM_016559.1 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:179597885 G>A maps to NM_016559.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr3:179533660 A>G maps to NM_016559.1 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr6:42942665 G>A maps to NM_000287.3 Y331Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:137147486 G>A maps to NM_000288.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:137166790 G>A maps to NM_000288.3 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:74846959 C>T maps to NM_002619.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:74846959 C>T maps to NM_002619.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:74719814 C>A maps to NM_002620.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr17:8170104 C>T maps to NM_012393.2 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:8172122 C>T maps to NM_012393.2 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:8160199 C>T maps to NM_012393.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:8170431 G>T maps to NM_012393.2 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:8160222 C>T maps to NM_012393.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:8172025 G>A maps to NM_012393.2 Q1186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr17:8158878 G>A maps to NM_012393.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr20:52835580 C>T maps to NM_002623.3 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53689657 C>T maps to NM_002624.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54971911 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54978507 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54985325 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54987280 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54978348 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:54985327 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:54978530 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:54982652 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr23:54960313 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:207245616 G>A maps to NM_006212.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:207235989 T>C maps to NM_006212.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:207242776 T>C maps to NM_006212.2 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:207237134 C>T maps to NM_006212.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:207245616 G>A maps to NM_006212.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:6263662 G>A maps to NM_004566.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:6261578 A>G maps to NM_004566.3 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr10:6261657 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:6263366 C>T maps to NM_004566.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:48563099 G>A maps to NM_004567.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:48563042 G>T maps to NM_004567.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:48573874 G>T maps to NM_004567.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr21:45746761 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr21:45745047 C>T maps to NM_002626.4 C630C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:48529157 A>T maps to NM_001166686.1 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:48535134 C>T maps to NM_001166686.1 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:48537585 C>A maps to NM_001166686.1 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:48539355 C>T maps to NM_001166686.1 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:48534623 T>C maps to NM_001166686.1 H508H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:3175484 C>T maps to NM_002627.3 N667N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:3141501 C>T maps to NM_002627.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:3161048 C>T maps to NM_002627.3 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr10:3143744 C>T maps to NM_002627.3 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:3175484 C>T maps to NM_002627.3 N667N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:149686142 A>G maps to ENST00000461868 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:149686232 G>A maps to NM_053024.3 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:149686330 C>A maps to NM_053024.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:61018605 C>T maps to ENST00000422676 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:61017449 C>T maps to ENST00000422676 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:61018710 C>T maps to ENST00000422676 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr10:99190262 G>A maps to NM_002629.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:44102512 C>T maps to NM_000290.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77224401 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77224825 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:77225099 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:77224438 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:77225003 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:77224950 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:77224703 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:77224480 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:77225073 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:77224877 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:197757936 A>G maps to NM_024989.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:197755584 G>T maps to NM_024989.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:3845198 C>T maps to NM_014489.2 H145H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr17:37840942 G>A maps to NM_033419.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:28269251 G>T maps to NM_032507.3 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:28269620 G>T maps to NM_032507.3 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:249211947 G>T maps to NM_170725.2 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:249210978 C>T maps to NM_170725.2 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:249210939 G>T maps to NM_170725.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:249211079 G>A maps to NM_170725.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:249211485 G>T maps to NM_170725.2 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr1:249211988 C>T maps to NM_170725.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:249211485 G>T maps to NM_170725.2 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:249212391 C>T maps to NM_170725.2 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:249211653 C>T maps to NM_170725.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:34396247 C>T maps to NM_152595.4 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:34395739 T>G maps to NM_152595.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr15:34395597 G>A maps to NM_152595.4 W289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:34395898 C>T maps to NM_152595.4 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:34396247 C>T maps to NM_152595.4 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:230468626 G>A maps to ENST00000321327 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:230459356 A>G maps to ENST00000321327 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:230472878 C>T maps to ENST00000321327 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:230468773 G>A maps to ENST00000321327 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:230459239 G>A maps to ENST00000321327 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:230468599 C>T maps to ENST00000321327 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr1:230492669 G>A maps to ENST00000321327 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:41710062 G>T maps to NM_002630.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:41704637 G>A maps to NM_002630.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:41712252 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:10471500 C>T maps to NM_002631.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:10479703 C>T maps to NM_002631.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:114557702 C>A maps to NM_005023.3 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:77378835 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:77372890 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77372820 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77378736 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:77369531 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:77380409 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr23:77380398 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr6:49754594 T>C maps to NM_138733.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:49754597 G>A maps to NM_138733.4 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:17627004 G>A maps to NM_012088.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:17628608 C>T maps to NM_012088.2 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:46522895 A>G maps to NM_005091.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:15579485 T>G maps to NM_052890.3 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:15580622 G>A maps to NM_052890.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:15586937 G>A maps to NM_052890.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:15586619 G>A maps to NM_052890.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:153276339 G>T maps to NM_052891.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:153283135 C>T maps to NM_052891.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:153270503 G>A maps to NM_052891.1 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:153315684 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:64097419 C>T maps to NM_002633.2 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:64100677 T>C maps to NM_002633.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:64095097 C>T maps to NM_002633.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:64095097 C>T maps to NM_002633.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr11:74058191 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:74081994 T>C maps to NM_173582.3 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:74056610 G>T maps to NM_173582.3 S374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:74082760 G>A maps to NM_173582.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:83900662 G>A maps to ENST00000416472 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:83889563 A>G maps to ENST00000416472 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr6:83892649 G>A maps to ENST00000416472 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:83900641 C>T maps to ENST00000416472 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr9:71098927 C>T maps to NM_021965.3 Y481Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:71098963 G>A maps to NM_021965.3 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:71098927 C>T maps to NM_021965.3 Y481Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:71006576 G>A maps to NM_021965.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr9:71114228 C>T maps to NM_021965.3 Y522Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr15:99512804 G>T maps to NM_001102612.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:100996849 G>A maps to NM_000926.4 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:100920776 C>A maps to NM_000926.4 E791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:100999719 G>A maps to NM_000926.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:118370487 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118370503 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:118370466 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118377181 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:118370539 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:76399859 C>T maps to NM_024419.3 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr17:76410963 C>G maps to NM_024419.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr6:13228266 C>T maps to NM_030948.1 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:13283790 C>T maps to NM_030948.1 D549D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:13206248 C>T maps to NM_030948.1 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:144070120 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:144093491 G>T maps to NM_001100164.1 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:58416500 C>T maps to NM_080672.3 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:58342310 C>A maps to NM_080672.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:58420269 G>A maps to NM_080672.3 E538E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:58318214 C>T maps to NM_080672.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr20:58349366 C>T maps to NM_080672.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:28786745 C>T maps to NM_023923.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:28733919 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:28802769 C>T maps to NM_023923.3 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:28817494 C>T maps to NM_023923.3 R627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr17:47489168 G>A maps to NM_002634.2 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:47486755 G>A maps to NM_002634.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:7076359 G>A maps to NM_001144831.1 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:7077627 G>A maps to NM_001144831.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:7079402 A>T maps to NM_001144831.1 G56G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:9087074 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:9089467 G>A maps to ENST00000433083 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:9085435 T>G maps to ENST00000433083 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:33833029 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:33790579 G>T maps to ENST00000419414 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:33799729 G>A maps to ENST00000419414 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr1:33838021 C>T maps to ENST00000419414 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:169815158 G>A maps to NM_024947.3 I949I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:169820610 C>T maps to NM_024947.3 A860A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:22095597 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:22112103 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:22094543 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:22115084 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:22129663 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:22065219 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:22245664 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:22095807 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:22129610 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:22239762 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:22244606 C>G did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:22186488 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:22065219 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:22263473 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:22237174 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:22117234 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:22095739 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:33382519 G>A maps to NM_024165.2 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:33383411 C>T maps to NM_024165.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr6:33381250 A>G maps to NM_024165.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr6:170104122 C>T maps to NM_018288.3 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:170118934 C>A maps to NM_018288.3 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:170118908 C>T maps to NM_018288.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:50080831 C>T maps to NM_001040443.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:50080819 C>A maps to NM_001040443.1 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:50092273 C>T maps to NM_001040443.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:50100565 C>T maps to NM_001040443.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr13:50092189 G>T maps to NM_001040443.1 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:50087278 G>T maps to NM_001040443.1 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:50092273 C>T maps to NM_001040443.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:27238153 G>A maps to NM_001033561.1 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:27240274 C>T maps to NM_001033561.1 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:27240237 G>A maps to NM_001033561.1 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:27238153 G>A maps to NM_001033561.1 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr17:27239530 G>A maps to NM_001033561.1 N686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:27237196 G>A maps to ENST00000378879 Y802Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:6680348 C>T maps to NM_153812.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:6680291 G>T maps to NM_153812.2 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:11022147 G>T maps to ENST00000303905 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:11151055 G>T maps to ENST00000303905 G912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:11030442 G>A maps to ENST00000303905 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr7:11022444 C>T maps to ENST00000303905 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:133909366 C>T maps to ENST00000448712 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:133887800 G>A maps to ENST00000448712 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:133901966 C>A maps to ENST00000448712 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:133902203 G>A maps to ENST00000448712 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:133897982 C>T maps to ENST00000448712 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:46845187 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:46898450 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:46887474 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:46913929 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:46917781 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr23:46917817 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:46918036 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:46918110 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:46913649 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:46913744 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:46913820 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:46857552 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:46887352 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:46857617 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:46844337 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:129770293 A>G maps to NM_199320.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr4:129793185 C>T maps to NM_199320.2 H766H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr4:129783193 T>G maps to NM_199320.2 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:96415577 C>T maps to NM_005392.3 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:96411440 C>T maps to NM_005392.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:96428006 C>T maps to NM_005392.3 F659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:96437248 T>C maps to NM_005392.3 F889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:96422511 C>T maps to NM_005392.3 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:96438038 C>T maps to NM_005392.3 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:34435356 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:34526918 G>A maps to NM_016436.4 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:34501267 T>C maps to NM_016436.4 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:133811102 G>A maps to ENST00000395386 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:133848921 C>T maps to ENST00000395386 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:133844573 C>T maps to ENST00000395386 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:133811336 C>T maps to ENST00000395383 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:133816966 C>T maps to ENST00000395386 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:133854868 C>T maps to ENST00000395386 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:45955584 C>T maps to ENST00000257821 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:45959705 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr11:45967527 G>A maps to ENST00000257821 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:45986913 G>A maps to ENST00000257821 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:45312462 G>A maps to NM_138415.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr22:45283872 G>A maps to NM_138415.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:7139747 G>T maps to NM_024297.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:64394169 G>T maps to NM_015153.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:64421966 G>T maps to NM_015153.2 E1495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:64422268 A>G maps to NM_015153.2 R1595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:64422703 G>A maps to NM_015153.2 Q1740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:64423289 G>T maps to NM_015153.2 E1936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:64394051 G>A maps to NM_015153.2 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:64395140 G>A maps to NM_015153.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:64401723 G>T maps to NM_015153.2 E763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:64390063 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:64395140 G>A maps to NM_015153.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:64421205 T>G maps to NM_015153.2 P1315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:64421668 A>G maps to NM_015153.2 E1395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:64423532 G>T maps to NM_015153.2 E2017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr6:64356461 T>C maps to NM_015153.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:41864134 A>G maps to NM_032758.3 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:133551260 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:133551317 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:133547853 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:133511651 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:133527959 G>T did not map to a codon.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr23:133547668 A>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:133527636 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:133527978 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:52455723 G>T maps to ENST00000454052 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:54022169 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:54028587 C>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53966898 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:54037691 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53965595 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53966753 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54012331 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54044222 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:54012294 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:54029032 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:54043098 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr23:54044119 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:54019238 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:54014210 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:54011424 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr23:53970622 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53965595 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54012213 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54028588 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:53965673 G>A did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:54037559 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:120286593 C>A maps to NM_006623.3 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:120269482 C>T maps to NM_006623.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:120279852 C>T maps to NM_006623.3 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:120284438 C>T maps to NM_006623.3 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:120286530 G>A maps to NM_006623.3 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr1:120263914 C>T maps to NM_006623.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:79735658 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:79655852 C>A maps to NM_017934.5 E1499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:79668220 G>A maps to NM_017934.5 F1251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:79668220 G>A maps to NM_017934.5 F1251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr6:79770484 A>G maps to NM_017934.5 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:79679563 G>A maps to NM_017934.5 R1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:71933700 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:71864320 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:71802441 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:71856148 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71812994 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71830891 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:71825456 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:71813023 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:71838686 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:71875990 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:71876082 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:71802310 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:71846846 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:71870281 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:71802448 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:71843049 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:71802267 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:71802424 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:71823030 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:71886004 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:71829489 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:71839136 G>T did not map to a codon.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr23:71840621 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:71846859 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr23:18943865 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:18956801 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:18972475 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:18970628 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18912320 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18912486 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18923935 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18926924 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18956756 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:18944612 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:18947400 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:18970640 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:18912470 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:18942594 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:18938221 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:18958167 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:18958125 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:18944663 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:18959760 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:18959750 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:18911621 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:18958137 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:19002003 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:18924630 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:18912486 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:18923935 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:18926137 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:47644794 G>A maps to NM_000293.2 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:47703320 C>T maps to NM_000293.2 R875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:47684813 T>G maps to NM_000293.2 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:47621610 C>T maps to NM_000293.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:47730389 C>T maps to NM_000293.2 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:47628126 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr16:47698876 T>C maps to NM_000293.2 H806H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:47684807 C>A maps to NM_000293.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:47727312 C>T maps to NM_000293.2 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:47695649 C>T maps to NM_000293.2 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:56154685 A>T maps to NM_006213.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:56156592 C>T maps to NM_006213.3 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr7:56149624 C>T maps to NM_006213.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:30768327 G>A maps to NM_000294.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr16:30767996 C>T maps to NM_000294.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:201437662 G>A maps to NM_012396.3 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:118502928 G>A maps to NM_015157.2 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:118516455 G>A maps to NM_015157.2 A1140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:118499173 C>T maps to NM_015157.2 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:118501934 C>T maps to NM_015157.2 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:111604253 C>T maps to NM_001134438.1 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:111658392 C>T maps to NM_001134438.1 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:111603010 C>T maps to NM_001134438.1 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:111604253 C>T maps to NM_001134438.1 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:111603770 C>T maps to NM_001134438.1 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:111639199 G>A maps to NM_001134438.1 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:111685471 A>G maps to NM_001134438.1 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:111667825 G>A maps to NM_001134438.1 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44006255 G>A maps to NM_198850.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:43983601 G>A maps to NM_198850.3 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:43982214 A>T maps to NM_198850.3 L591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr19:43999419 C>T maps to NM_198850.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:60630706 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:60506127 C>T maps to NM_194449.2 R629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:60642665 C>T maps to NM_194449.2 A1264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:60645922 C>T maps to NM_194449.2 S1471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:60642762 C>T maps to NM_194449.2 R1297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:60646445 C>T maps to NM_194449.2 R1646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:60646138 C>T maps to NM_194449.2 N1543N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:60562355 C>T maps to NM_194449.2 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:71683713 C>T maps to NM_015020.2 A1017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:71683604 C>A maps to NM_015020.2 G1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:71682986 C>A maps to NM_015020.2 E1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:71686694 C>A maps to NM_015020.2 E939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:71712838 C>A maps to NM_015020.2 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr16:71692624 C>T maps to NM_015020.2 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:71682986 C>A maps to NM_015020.2 E1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:71682987 T>G maps to NM_015020.2 T1259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr16:71683656 A>G maps to NM_015020.2 G1036G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:71682807 G>A maps to NM_015020.2 F1319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:170557987 G>A maps to NM_001008489.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:170557501 T>C maps to NM_001008489.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:41749464 G>T maps to NM_003924.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:41748255 G>T maps to NM_003924.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr4:41748144 G>A maps to NM_003924.3 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr4:41749671 C>T maps to ENST00000510424 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:610556 C>T maps to ENST00000264555 C1491C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:601668 C>T maps to ENST00000264555 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:582049 G>A maps to ENST00000264555 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:607786 C>T maps to ENST00000264555 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:608848 G>A maps to ENST00000264555 R1131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:609172 C>T maps to ENST00000264555 P1239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr11:606567 C>T maps to ENST00000264555 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:611773 C>A maps to ENST00000264555 G1649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:114246777 T>C maps to NM_006608.2 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:77549646 C>A maps to ENST00000427986 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:77572075 C>A maps to ENST00000427986 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:77538251 A>G maps to ENST00000427986 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:77583129 G>A maps to ENST00000427986 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:13323038 G>A maps to NM_006214.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr10:13330464 G>A maps to NM_006214.3 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:61005348 T>G maps to NM_032439.3 *377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr10:60996340 G>A maps to NM_032439.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:75757428 T>C maps to NM_015886.3 Y153Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:75757648 C>T maps to NM_015886.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:75761360 G>A maps to NM_015886.3 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:36929306 C>T maps to NM_153370.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr6:36931623 C>T maps to NM_153370.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:25258263 A>C maps to NM_018323.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:21098924 G>A maps to NM_058004.2 Y1091Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:21068775 G>A maps to NM_058004.2 R1753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr22:21063600 G>A maps to NM_058004.2 S2022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:151266605 G>A maps to NM_002651.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:151288272 G>A maps to NM_002651.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:151288384 A>G maps to NM_002651.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr1:151271405 G>C maps to NM_002651.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:151265333 G>T maps to NM_002651.2 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:68378831 G>A maps to NM_016166.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:68475966 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:44470549 C>T maps to NM_004671.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:44470802 G>T maps to NM_004671.2 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:44470866 C>A maps to NM_004671.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr18:44470615 G>A maps to NM_004671.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:44497292 C>A maps to NM_004671.2 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:44470842 G>A maps to NM_004671.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:145581450 C>A maps to NM_006099.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:4013180 G>T maps to NM_015897.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:4013192 G>A maps to NM_015897.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:4012976 C>T maps to NM_015897.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:73357819 T>G maps to NM_006346.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr13:73401174 A>T maps to NM_006346.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:73409468 C>T maps to NM_006346.2 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:73372122 G>T maps to NM_006346.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr11:85701335 T>C maps to ENST00000393343 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:85723422 C>A maps to ENST00000393343 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:85723422 C>A maps to ENST00000393343 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:85712095 T>C maps to ENST00000393343 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:38470321 C>T maps to NM_012407.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr22:38468493 C>T maps to NM_012407.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr2:229890503 G>A maps to NM_017933.4 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:15349369 A>C did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:15339760 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:15344162 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:15342917 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:15349659 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:15344080 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:15349657 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:15349810 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:15349823 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:15349443 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:55643035 T>G maps to ENST00000164305 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:55643035 T>C maps to ENST00000164305 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:55612483 G>T maps to ENST00000164305 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:172411113 G>A maps to NM_153747.1 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:46842078 G>A maps to NM_002643.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:517561 C>T maps to NM_001127178.1 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:509771 A>G maps to NM_001127178.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:68059435 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:68060600 C>A maps to NM_004569.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:77632516 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:77629585 C>A maps to NM_005482.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:77627341 T>C maps to NM_005482.2 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:16120680 A>C maps to NM_004278.3 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:160000656 T>C maps to NM_145167.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:59742035 G>A maps to NM_176787.4 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:59774318 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:59756029 G>A maps to NM_176787.4 R777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35091479 G>A maps to NM_032634.2 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr16:633129 T>C maps to NM_148920.1 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:207112776 G>T maps to NM_002644.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:207109101 C>G maps to NM_002644.3 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:207105097 G>A maps to NM_002644.3 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:207112734 C>T maps to NM_002644.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr1:207107918 G>A maps to NM_002644.3 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:207109014 C>T maps to NM_002644.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:26881880 G>A maps to NM_033198.3 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:44045190 G>A maps to NM_015937.4 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:44047896 C>T maps to ENST00000372689 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:44053135 C>T maps to NM_015937.4 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:44047542 C>T maps to NM_015937.4 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:33173278 G>A maps to NM_080476.4 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr20:33222425 C>T maps to NM_080476.4 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:34893858 C>T maps to NM_178517.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr17:34892970 G>A maps to NM_178517.3 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:34893630 A>G maps to NM_178517.3 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:34894112 T>G maps to NM_178517.3 L388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:196674558 A>G maps to NM_025163.2 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:111943843 G>A maps to NM_138789.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:98416608 C>T maps to NM_152309.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:98380158 C>A maps to NM_152309.2 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:98469723 G>A maps to NM_152309.2 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:98412545 C>T maps to NM_152309.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:98412584 G>T maps to NM_152309.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:98411318 C>A maps to NM_152309.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:98416629 C>T maps to NM_152309.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:98386570 G>T maps to NM_152309.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:17134129 G>T maps to NM_002645.2 V1135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:17139103 C>T maps to NM_002645.2 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:17190349 C>T maps to NM_002645.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:17191093 T>C maps to NM_002645.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr11:17115923 T>C maps to NM_002645.2 V1445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:17132000 A>G maps to NM_002645.2 C1174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:204424994 G>T maps to NM_002646.3 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:204425120 G>A maps to NM_002646.3 N602N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:204403700 G>T maps to NM_002646.3 C1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:204433608 C>T maps to NM_002646.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:204438624 C>T maps to NM_002646.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:204409359 G>A maps to NM_002646.3 R1113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:18649003 A>T maps to NM_004570.4 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:18443881 G>A maps to NM_004570.4 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:18658287 A>G maps to NM_004570.4 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:18446949 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:18716365 C>A maps to NM_004570.4 S1238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr18:39575939 C>A maps to ENST00000398870 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:178916536 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:178921543 C>A maps to NM_006218.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:178916822 C>T maps to NM_006218.2 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr3:178921519 C>T maps to NM_006218.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr3:138417834 G>A maps to NM_006219.1 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:138383890 C>A maps to NM_006219.1 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:138417900 C>A maps to NM_006219.1 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:9782085 T>G maps to ENST00000361110 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:9784470 A>G maps to ENST00000361110 K976K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:9783209 C>T maps to ENST00000361110 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr1:9778876 C>T maps to ENST00000361110 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr1:9778813 G>A maps to ENST00000361110 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:106523505 G>A maps to NM_002649.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:106526694 A>G maps to NM_002649.2 G996G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:106526601 C>T maps to NM_002649.2 F965F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:106508824 C>T maps to NM_002649.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:106545738 C>T maps to NM_002649.2 I1072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr7:106508875 C>T maps to NM_002649.2 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr7:106509865 T>C maps to NM_002649.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:106509543 C>A maps to NM_002649.2 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:106545757 G>T maps to NM_002649.2 G1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:106508836 G>A maps to NM_002649.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:31685194 C>T maps to ENST00000402249 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:31685649 C>A maps to NM_052880.4 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr5:67592107 C>T maps to ENST00000396611 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr5:67589167 C>T maps to ENST00000396611 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:67586618 T>C maps to NM_181504.2 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:67589617 C>T maps to ENST00000396611 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:67589617 C>T maps to ENST00000396611 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:67590425 A>G maps to ENST00000396611 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr5:67589235 C>A maps to ENST00000396611 Y408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:67592107 C>T maps to ENST00000396611 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr5:67591036 A>T maps to ENST00000396611 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:67522656 G>T maps to ENST00000396611 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:67591245 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:67592160 C>A maps to ENST00000396611 C667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr5:67591245 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:67588950 C>T maps to ENST00000396611 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:18277022 C>A maps to NM_005027.2 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:18272781 G>A maps to NM_005027.2 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:18276971 G>A maps to NM_005027.2 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr19:18271915 C>T maps to NM_005027.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:46511693 C>T maps to NM_001114172.1 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:46521643 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:46531835 C>A maps to NM_001114172.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:46597551 C>A maps to NM_001114172.1 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:46527649 C>A maps to NM_001114172.1 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:130454819 C>A maps to NM_014602.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:130409455 C>T maps to NM_014602.2 T1047T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:130442276 G>A maps to NM_014602.2 Y654Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:8791957 G>A maps to NM_001142633.1 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:8784103 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:8790505 G>T maps to NM_001142633.1 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:8791555 C>T maps to NM_001142633.1 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr17:8784027 C>A maps to NM_001142633.1 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr17:8791756 C>T maps to NM_001142633.1 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr2:209167078 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:209169028 C>T maps to NM_015040.3 D485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:209168980 C>T maps to NM_015040.3 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:209168944 C>T maps to NM_015040.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:209193005 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:209189702 G>A maps to NM_015040.3 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:209190651 G>A maps to NM_015040.3 K1039K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:209189702 G>A maps to NM_015040.3 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:209190823 G>T maps to NM_015040.3 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:209169568 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:209204754 C>T maps to NM_015040.3 L1611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:209217385 G>A maps to NM_015040.3 T1908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:99971333 C>T maps to NM_013439.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr7:99964996 C>T maps to ENST00000413850 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:99956425 G>T maps to ENST00000413850 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:48771422 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48772383 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:48772312 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48776110 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48775919 C>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:48772299 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:71406382 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:71406133 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:20964486 G>A maps to NM_032409.2 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:20975573 C>A maps to NM_032409.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:20975079 C>T maps to NM_032409.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:20975576 C>T maps to NM_032409.2 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:10623135 G>A maps to NM_017884.4 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:10690467 G>T maps to ENST00000354846 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:10677738 G>A maps to NM_017884.4 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:76957929 T>C maps to NM_017439.3 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:77010671 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr10:22880677 G>A maps to NM_005028.4 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:22862254 C>T maps to NM_005028.4 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr10:22896909 C>T maps to NM_005028.4 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:36936743 G>A maps to NM_003559.4 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:36943125 A>G maps to NM_003559.4 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:57994112 G>T maps to NM_024779.4 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:151206803 A>G maps to NM_001135638.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:71504007 G>T maps to NM_003558.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:71532489 T>C maps to NM_003558.2 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:71504033 G>A maps to NM_003558.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:71549845 C>T maps to NM_003558.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:3661080 G>A maps to NM_012398.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3643341 G>A maps to NM_012398.2 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3656477 G>A maps to NM_012398.2 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:3653503 G>A maps to NM_012398.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:3664846 G>A maps to NM_012398.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:3638917 C>T maps to NM_012398.2 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:3664857 G>A maps to NM_012398.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:130687414 C>T maps to NM_001135219.1 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:130692023 G>A maps to NM_001135219.1 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr17:27372016 A>G maps to NM_016518.2 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:27370348 C>T maps to NM_016518.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:27380453 C>T maps to NM_016518.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:27380108 C>T maps to NM_016518.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:27381633 G>A maps to NM_016518.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:27380439 C>T maps to NM_016518.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:15497926 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15403222 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:15444028 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:15474092 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:15509287 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr23:15474137 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:15408362 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:15477832 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:10728740 G>T maps to NM_001101387.1 C74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr17:10728851 G>A maps to NM_001101387.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:1437515 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:1438502 C>T maps to ENST00000313486 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:65688751 C>T maps to NM_012417.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:65628317 C>T maps to NM_012417.2 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:65688719 C>T maps to NM_012417.2 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr11:67266089 G>A maps to NM_004910.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:67260518 G>A maps to NM_004910.2 I1119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:67269405 G>T maps to NM_004910.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:67269543 G>A maps to NM_004910.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:67267197 C>T maps to NM_004910.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:123485628 G>A maps to NM_020845.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:123479486 G>A maps to NM_020845.2 R698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:6387538 G>A maps to NM_031220.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:6367602 G>A maps to NM_031220.3 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:6367608 G>A maps to NM_031220.3 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:6374577 C>T maps to NM_031220.3 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:6367494 G>A maps to NM_031220.3 V717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:6367614 C>T maps to NM_031220.3 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:6381944 G>A maps to NM_031220.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr17:6371604 T>C maps to NM_031220.3 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr17:6361006 C>T maps to NM_031220.3 T842T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr10:3208419 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:3181219 C>T maps to ENST00000380989 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:3202074 T>C maps to ENST00000380989 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:3189805 C>T maps to ENST00000380989 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:3207720 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:3190224 G>A maps to ENST00000380989 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:3201217 C>A maps to ENST00000380989 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr5:134364918 G>A maps to NM_002653.4 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr5:134367187 G>A maps to NM_002653.4 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:111539442 G>A maps to NM_153426.1 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:111539583 G>T maps to NM_153426.1 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr4:111539616 T>C maps to NM_153426.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:111539757 C>T maps to NM_153426.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:111542466 C>T maps to NM_153426.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr10:103990447 G>C maps to NM_005029.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:130831535 G>A maps to NM_004764.4 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:130841498 G>T maps to NM_004764.4 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:130833782 G>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:22140606 T>A maps to NM_001135721.1 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:22173828 C>T maps to NM_001135721.1 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:22145124 A>G maps to NM_001135721.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:22147806 C>T maps to NM_001135721.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:25120864 G>A maps to NM_001008496.2 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:25130059 T>C maps to NM_001008496.2 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:25147449 G>T maps to NM_001008496.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:94341804 C>T maps to NM_152431.2 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:94340606 A>G maps to NM_152431.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:94310652 G>T maps to NM_152431.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:94310652 G>T maps to NM_152431.2 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:68382876 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:68382064 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:68381994 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:68382827 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:68382139 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:68381998 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:68382136 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:68381692 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:68382238 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:68382309 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:68382282 T>G did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:68382671 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr23:68381423 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:68381346 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:68381243 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:68382670 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:108714326 G>T maps to NM_014819.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:108680445 A>G maps to NM_014819.4 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr5:108673057 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:2150070 G>A maps to NM_001009944.2 S3238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:2150454 G>A maps to NM_001009944.2 I3170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:2158297 G>A maps to NM_001009944.2 D2290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:2158463 G>T maps to NM_001009944.2 S2235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:2139982 G>A maps to NM_001009944.2 F4219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr16:2140507 C>T maps to NM_001009944.2 L4074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:2158837 G>A maps to NM_001009944.2 A2110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr16:2152546 C>T maps to NM_001009944.2 T3012T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr16:2160331 C>T maps to NM_001009944.2 T1612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:47876560 G>A maps to NM_138295.3 Y1967Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr7:47886655 G>A maps to NM_138295.3 G1658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:47852786 G>A maps to NM_138295.3 N2426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:47876571 G>A maps to NM_138295.3 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:47930345 G>A maps to NM_138295.3 C823C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr7:47921618 C>G maps to NM_138295.3 G1110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:47968882 G>A maps to NM_138295.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr7:47870858 G>A maps to NM_138295.3 T2143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:47937617 G>T maps to NM_138295.3 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr7:47876560 G>T maps to NM_138295.3 Y1967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:47852825 G>A maps to NM_138295.3 G2413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:47872762 G>A maps to NM_138295.3 L2088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:47906069 G>A maps to NM_138295.3 R1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:47945515 G>A maps to NM_138295.3 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:47860723 A>G maps to NM_138295.3 F2305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:81187675 C>T maps to NM_052892.3 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:81232528 G>T maps to NM_052892.3 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:81183466 C>T maps to NM_052892.3 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr16:81157274 C>T maps to NM_052892.3 T2154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:81198247 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:81232572 C>A maps to NM_052892.3 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:81185370 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:81213292 C>T maps to NM_052892.3 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:81180924 A>C maps to NM_052892.3 T1722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:81208318 G>A maps to ENST00000378597 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:81204679 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr4:88940680 G>T maps to NM_000297.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:88986977 G>T maps to NM_000297.2 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr4:88986630 C>T maps to NM_000297.2 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:88957422 C>A maps to NM_000297.2 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:102089039 G>T maps to NM_016112.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:102052760 G>A maps to NM_016112.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:102055986 C>A maps to NM_016112.2 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:102089695 A>G maps to NM_016112.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr10:102052702 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:137226176 G>A maps to ENST00000230643 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:137261579 T>C maps to ENST00000230643 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:137228172 T>C maps to ENST00000230643 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr5:137271496 C>T maps to ENST00000230643 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr5:137257411 C>T maps to ENST00000230643 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:137235300 G>A maps to ENST00000230643 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:137242063 G>T maps to ENST00000230643 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:46653123 C>T maps to NM_006071.1 S2032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:46652658 C>T maps to NM_006071.1 S2187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:46653594 G>T maps to NM_006071.1 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:46656942 A>G maps to NM_006071.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr22:46656705 T>C maps to NM_006071.1 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:46658043 G>T maps to NM_006071.1 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:46658013 C>T maps to NM_006071.1 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:46653951 C>T maps to NM_006071.1 K1756K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:46656809 C>A maps to NM_006071.1 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr22:46654758 G>A maps to NM_006071.1 Y1487Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:46652916 G>A maps to NM_006071.1 F2101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:51611649 G>A maps to NM_138694.3 S3289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:51613374 G>T maps to NM_138694.3 S3013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:51776732 C>T maps to NM_138694.3 E2118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:51890682 C>A maps to NM_138694.3 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:51949677 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr6:51799028 G>A maps to NM_138694.3 S2000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:51524426 G>A maps to NM_138694.3 F3499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr6:51524036 A>G maps to NM_138694.3 S3629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:51491846 G>T maps to NM_138694.3 S3911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:51613341 A>G maps to NM_138694.3 C3024C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:51751971 C>T maps to NM_138694.3 P2356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:51893102 C>T maps to NM_138694.3 T1137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr6:51889574 G>C maps to NM_138694.3 S1678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:51929822 C>T maps to NM_138694.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:51619635 C>A maps to NM_138694.3 E2915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr6:51924833 C>T maps to NM_138694.3 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:51523871 G>A maps to NM_138694.3 N3684N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:51771022 C>T maps to NM_138694.3 A2266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:51938331 T>G maps to NM_138694.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr6:51618013 G>A maps to NM_138694.3 R2979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:51930772 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:51890887 C>A maps to NM_138694.3 V1240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr8:110439283 G>T maps to ENST00000426474 E967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:110424601 A>C maps to ENST00000426474 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:110425753 C>T maps to ENST00000426474 Y780Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:110454374 A>G maps to ENST00000426474 V1448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:110451282 C>A maps to ENST00000426474 I1306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:110441616 A>C maps to ENST00000426474 R1017R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:110442243 C>A maps to ENST00000426474 V1069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:110503227 C>T maps to ENST00000426474 R3338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:110519969 C>T maps to ENST00000426474 S3692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr8:110456915 C>T maps to ENST00000426474 V1606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr8:110502265 G>A maps to ENST00000426474 T3322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:110535016 C>T maps to ENST00000426474 H4077H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr8:110499006 C>T maps to ENST00000426474 R3279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:110456077 G>T maps to ENST00000426474 E1580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:110527509 G>T maps to ENST00000426474 E3890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr8:110471928 G>A maps to ENST00000426474 T2370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:110408290 C>T maps to ENST00000426474 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:110539059 G>T maps to ENST00000426474 E4179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:110455326 G>T maps to ENST00000426474 E1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:79510759 C>A maps to NM_181839.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:43243208 C>T maps to NM_181805.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:155270071 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:155263330 G>A maps to ENST00000423816 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:155265335 G>A maps to ENST00000423816 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:72500984 G>A maps to ENST00000419739 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:3026880 C>T maps to NM_004203.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:14568873 C>T maps to NM_213560.1 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:14578405 C>A maps to NM_213560.1 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:14578528 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:14580563 C>T maps to NM_213560.1 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:14580221 C>T maps to NM_213560.1 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr1:89236087 A>G maps to NM_006256.2 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:89225903 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:89237365 A>G maps to NM_006256.2 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:131476566 G>A maps to NM_013355.3 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr9:131480609 C>G maps to NM_013355.3 Y664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:44427618 T>C maps to NM_004571.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:44427615 G>T maps to NM_004571.3 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:44433266 T>C maps to NM_004571.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:125255524 C>T maps to NM_022062.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:125298942 C>T maps to NM_022062.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr11:125301143 C>T maps to NM_022062.2 H425H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr1:201288982 G>A maps to NM_000299.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:201252880 C>T maps to NM_000299.3 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:201252973 C>T maps to NM_000299.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:201285704 C>A maps to NM_000299.3 C242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:201291203 C>T maps to NM_000299.3 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:201294879 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:33030913 C>T maps to NM_004572.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:32949047 G>A maps to NM_004572.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:33030912 G>A maps to NM_004572.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:32994139 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:403709 G>A maps to NM_007183.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:399131 C>T maps to NM_007183.2 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:159488367 C>A maps to NM_003628.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:159499084 C>T maps to NM_003628.3 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr2:159481934 G>T maps to NM_003628.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:159477865 C>A maps to NM_003628.3 S179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:159481877 C>T maps to NM_003628.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:159514692 C>T maps to NM_003628.3 R654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:159530190 C>A maps to NM_003628.3 S976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:159481853 G>A maps to NM_003628.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr2:159481457 T>A maps to NM_003628.3 Y224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:119334898 C>T maps to NM_015900.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:119337022 C>T maps to NM_015900.2 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:74695491 G>T maps to NM_032562.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:74700925 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:74714296 G>A maps to NM_032562.2 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:74714385 G>A maps to NM_032562.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:68289681 C>A maps to NM_012320.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:68289849 G>A maps to NM_012320.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:20499296 G>A maps to NM_001105572.1 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:20440659 G>A maps to ENST00000442610 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:20249176 G>A maps to NM_014589.1 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:20474812 G>A maps to NM_022819.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:186862207 A>C maps to NM_024420.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr1:186957570 T>C maps to NM_024420.2 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:186948475 G>T maps to NM_024420.2 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:186946762 G>A maps to NM_024420.2 K601K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:186908253 G>A maps to NM_024420.2 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:186839634 C>A maps to NM_024420.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:186880449 G>T maps to NM_024420.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:186957517 G>T maps to NM_024420.2 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:48565257 G>A maps to NM_003706.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:48558204 G>A maps to NM_003706.2 C453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr15:42361122 G>A maps to NM_178034.3 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:42377687 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:42361086 C>T maps to NM_178034.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr15:42375407 G>A maps to NM_178034.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:42363055 G>A maps to NM_178034.3 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:42362935 G>A maps to NM_178034.3 Y674Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:42281667 G>A maps to NM_001080490.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:42293400 G>A maps to NM_001080490.1 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:42292153 G>A maps to NM_001080490.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:42276163 G>A maps to NM_001080490.1 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:42279474 C>A maps to NM_001080490.1 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:42276651 G>A maps to NM_001080490.1 R761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:42434304 G>T maps to ENST00000397272 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:42442639 G>A maps to ENST00000397272 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:42436340 G>A maps to ENST00000397272 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr15:42446525 A>G maps to ENST00000397272 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:20416365 C>T maps to NM_000929.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:20412579 G>C maps to NM_000929.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:20416365 C>T maps to NM_000929.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:38524420 C>T maps to NM_003560.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr22:38565394 G>A maps to NM_003560.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:46672308 C>T maps to NM_001168357.1 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr6:46680049 A>G maps to NM_001168357.1 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:46690524 G>T maps to NM_001168357.1 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:46672296 C>A maps to NM_001168357.1 *442Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:46679235 C>T maps to NM_001168357.1 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:160873151 G>A maps to NM_007366.4 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:160832604 C>A maps to NM_007366.4 E857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:160832722 G>T maps to NM_007366.4 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:160889518 T>G maps to NM_007366.4 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:160840541 C>A maps to NM_007366.4 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:26923307 G>A maps to NM_001031689.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:26923268 C>A maps to NM_001031689.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr9:26905721 A>G maps to NM_001031689.2 C725C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:133700566 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:133700328 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:59807946 C>A maps to NM_173801.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:59811020 G>A maps to NM_173801.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:84026108 G>A maps to NM_001130715.1 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:84028957 G>A maps to NM_001130715.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:145464035 C>A maps to NM_001029869.1 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:57079500 C>A maps to NM_002655.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:57078942 G>A maps to NM_002655.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:144262860 C>T maps to NM_001080951.1 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:144263556 G>A maps to NM_001080951.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:144263438 G>A maps to NM_001080951.1 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:30784821 C>T maps to NM_002657.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:30784627 G>C maps to NM_002657.3 S373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:30784581 C>T maps to NM_002657.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:42033666 G>A maps to NM_000930.3 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:42048919 G>A maps to NM_000930.3 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:42033666 G>A maps to NM_000930.3 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr8:42037772 G>A maps to NM_000930.3 Y403Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:75675090 C>T maps to NM_002658.3 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:75673382 G>T maps to NM_002658.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:75672051 G>A maps to NM_002658.3 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:44160709 C>T maps to NM_002659.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:44160751 G>A maps to NM_002659.2 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:28854922 C>A maps to NM_153021.4 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:28763247 C>A maps to NM_153021.4 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:28808688 G>T maps to NM_153021.4 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr2:28761169 G>A maps to NM_001170585.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:28843190 C>A maps to NM_153021.4 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr12:14695179 C>T maps to NM_024829.5 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr12:14706299 T>C maps to NM_024829.5 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:113824841 C>A maps to NM_173542.3 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:113826406 G>A maps to NM_173542.3 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr20:8630053 A>C maps to NM_015192.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:8639182 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:8862336 C>T maps to NM_015192.2 F1164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:8721036 G>A maps to NM_015192.2 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:8769318 G>A maps to NM_015192.2 R1076R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:8769163 C>A maps to NM_015192.2 I1060I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr20:8665627 C>T maps to NM_015192.2 N304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:8782722 C>T maps to NM_182734.1 F1148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:8717718 C>T maps to NM_015192.2 Y696Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr20:8862336 C>T maps to NM_015192.2 F1164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:40589025 G>T maps to NM_004573.2 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:40594678 G>A maps to NM_004573.2 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:40594693 G>T maps to NM_004573.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:40583362 G>A maps to NM_004573.2 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:40590453 G>A maps to NM_004573.2 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:40594541 A>G maps to NM_004573.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr11:64022488 C>T maps to NM_000932.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:64024145 C>T maps to NM_000932.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:64026071 C>T maps to NM_000932.2 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:64029077 G>A maps to NM_000932.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:64029918 C>T maps to NM_000932.2 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:64029897 C>T maps to NM_000932.2 N686N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:64030267 C>T maps to NM_000932.2 F781F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr11:64024174 G>A maps to NM_000932.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:64022873 G>A maps to NM_000932.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:9376257 C>T maps to NM_001172646.1 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:9449233 C>T maps to NM_001172646.1 R1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:9365023 G>T maps to NM_001172646.1 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:9360699 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:9416240 T>C maps to NM_001172646.1 F853F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr20:9351881 G>A maps to NM_001172646.1 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:38061814 C>T maps to NM_001130964.1 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:38050578 G>T maps to NM_001130964.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:38050089 G>A maps to NM_001130964.1 D608D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr3:38052852 G>A maps to NM_001130964.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr3:38053061 G>A maps to NM_001130964.1 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:38052852 G>A maps to NM_001130964.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:43190565 G>A maps to NM_133373.3 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:43195393 G>A maps to NM_133373.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:43190532 G>A maps to NM_133373.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:219483488 G>T maps to ENST00000432688 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:219492800 C>A maps to ENST00000432688 C274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:219495467 G>A maps to ENST00000432688 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:219486298 G>T maps to ENST00000432688 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:96084726 C>T maps to ENST00000371380 R2267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:95994017 C>T maps to ENST00000371380 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:96039633 C>T maps to ENST00000371380 D1587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:96084683 C>T maps to ENST00000371380 F2252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:95790931 T>C maps to ENST00000371380 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:96014743 G>A maps to ENST00000371380 T1164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr10:96025409 G>T maps to ENST00000371380 E1354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr10:96084104 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:95987083 C>T maps to ENST00000371380 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:96018574 C>T maps to ENST00000371380 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr10:95987094 G>A maps to ENST00000371380 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:96066182 G>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr10:96066254 C>T maps to ENST00000371380 G1898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr10:96043586 T>C maps to ENST00000371380 N1612N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:96030347 G>T maps to ENST00000371380 E1499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr10:95993910 G>T maps to ENST00000371380 E686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:39794394 C>T maps to NM_002660.2 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:39794301 C>T maps to NM_002660.2 H545H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:39801480 C>T maps to NM_002660.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:39795390 C>T maps to NM_002660.2 F731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:39798785 C>T maps to NM_002660.2 F895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:39794394 C>T maps to NM_002660.2 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:39802888 G>A maps to NM_002660.2 P1257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:81934315 G>A maps to NM_002661.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr16:81990346 G>A maps to NM_002661.2 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:81942052 G>A maps to NM_002661.2 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr16:81946259 C>A maps to NM_002661.2 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:81888068 G>T maps to NM_002661.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:81934351 G>A maps to NM_002661.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:155203409 T>A maps to ENST00000340059 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:155198927 G>A maps to ENST00000340059 G1637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:155311973 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr3:155199314 C>T maps to ENST00000340059 E1508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:155314138 G>A maps to ENST00000340059 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:155199719 G>T maps to ENST00000340059 T1373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:155200460 G>A maps to ENST00000340059 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:155303983 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:155203156 C>A maps to ENST00000340059 E996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr1:2418790 C>T maps to NM_014638.2 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:2418807 C>T maps to NM_014638.2 C369C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:2415978 G>A maps to NM_014638.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:2418744 C>T maps to NM_014638.2 D348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:198950304 C>T maps to NM_006226.3 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:198950754 C>T maps to NM_006226.3 H838H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:198948513 G>A maps to NM_006226.3 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:199011545 G>T maps to NM_006226.3 E1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:198949563 C>T maps to NM_006226.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:198968591 G>T maps to NM_006226.3 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:198950517 G>A maps to NM_006226.3 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:198948733 G>T maps to NM_006226.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:198950116 G>T maps to NM_006226.3 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:17052088 C>T maps to NM_001144382.1 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:17052334 C>A maps to NM_001144382.1 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:17052196 C>A maps to NM_001144382.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:17056366 G>A maps to NM_001144382.1 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:17051777 G>T maps to NM_001144382.1 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:17052010 C>A maps to NM_001144382.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:17052046 C>T maps to NM_001144382.1 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:17051945 G>T maps to NM_001144382.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:17051892 C>A maps to NM_001144382.1 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:207317 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:205490 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr23:205501 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:215972 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:215848 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:215987 C>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:215941 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:111427052 G>A maps to ENST00000312791 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr3:111426959 G>A maps to ENST00000312791 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:41381943 C>A maps to NM_001005473.2 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:41382553 G>T maps to NM_001005473.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:18876400 C>A maps to ENST00000266505 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr12:18849093 A>G maps to ENST00000266505 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:18854529 C>A maps to ENST00000447925 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:18872474 A>C maps to ENST00000266505 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:18876260 G>A maps to ENST00000266505 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr3:171410199 G>A maps to NM_002662.3 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:171395476 C>T maps to NM_002662.3 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:171330196 G>A maps to NM_002662.3 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr3:171455751 C>T maps to NM_002662.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:171410195 C>A maps to NM_002662.3 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:171427437 C>A maps to NM_002662.3 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:4712816 C>A maps to NM_002663.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:4721298 C>A maps to NM_002663.3 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:4722098 G>T maps to NM_002663.3 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:4725127 C>T maps to NM_002663.3 R835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:4721890 C>T maps to NM_002663.3 H704H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:4720042 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:4722487 C>T maps to NM_002663.3 I761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr19:40873683 G>A maps to NM_012268.2 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:105397116 C>T maps to NM_138790.2 H252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:242271076 G>A maps to NM_152666.2 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:242271076 G>A maps to NM_152666.2 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:242383316 G>A maps to NM_152666.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:242271076 G>A maps to NM_152666.2 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:45884412 G>T maps to NM_012388.2 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:45898631 G>T maps to NM_012388.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:45895321 C>T maps to NM_012388.2 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:144995291 G>A maps to NM_201380.2 S3036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr8:145024637 G>A maps to NM_201380.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr8:144995411 G>A maps to NM_201380.2 H2996H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:145004569 G>A maps to NM_201380.2 C950C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:144997577 G>A maps to NM_201380.2 F2310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:144991292 G>A maps to NM_201380.2 F4369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:144990902 T>C maps to NM_201380.2 P4499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:144996866 C>T maps to NM_201380.2 A2547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr8:145005755 A>G maps to NM_201380.2 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:124184472 C>T maps to NM_021622.4 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:124189423 C>T maps to NM_021622.4 D395D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:124172443 G>A maps to NM_021622.4 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:124189331 G>T maps to NM_021622.4 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr10:124189204 C>A maps to NM_021622.4 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:38803739 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr8:38814897 C>A maps to NM_021623.1 Y277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179365839 C>T maps to NM_019091.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr2:179365845 C>T maps to NM_019091.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:179367201 C>A maps to ENST00000421187 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:49348777 G>A maps to NM_020904.2 H554H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:49363674 G>A maps to NM_020904.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:19475255 C>T maps to ENST00000429027 R744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:19427588 G>T maps to ENST00000429027 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:19427828 C>T maps to ENST00000429027 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr12:19427701 T>C maps to ENST00000429027 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr12:19282694 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:204230537 G>A maps to ENST00000367191 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:204192621 G>A maps to ENST00000367191 D1061D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:16810797 G>A maps to ENST00000448080 R1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:16848082 G>T maps to ENST00000448080 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:16863104 C>T maps to ENST00000448080 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:16816193 C>T maps to ENST00000448080 P862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:16876465 G>A maps to ENST00000448080 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:30090048 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:30094382 C>T maps to ENST00000440706 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:131904259 C>T maps to ENST00000409158 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:96166862 C>A maps to NM_024613.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:151153216 G>A maps to NM_001029884.1 A990A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:151152619 G>A maps to NM_001029884.1 Q791Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:151055144 A>T maps to NM_001029884.1 K110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:151161365 C>T maps to NM_001029884.1 N1164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr19:39909462 C>T maps to NM_022835.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:39912916 C>T maps to NM_022835.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:39913865 G>A maps to NM_022835.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:39914565 C>T maps to NM_022835.2 H931H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:39904749 G>C maps to NM_022835.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:39909387 C>T maps to NM_022835.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:39906076 C>T maps to NM_022835.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:39912756 C>T maps to NM_022835.2 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:65198134 G>A maps to ENST00000394691 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:65207827 G>A maps to ENST00000394691 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr14:65210120 C>T maps to ENST00000394691 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:65210240 G>A maps to ENST00000394691 E1160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:67316643 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr16:67316108 C>T maps to NM_001129729.1 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:161897 C>T maps to NM_052909.3 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:169625 C>T maps to NM_052909.3 D860D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:151675 G>T maps to NM_052909.3 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:163444 C>T maps to NM_052909.3 F730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:156217 G>A maps to NM_052909.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:171405 C>T maps to NM_052909.3 Y943Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:163459 C>T maps to NM_052909.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:6556582 G>A maps to NM_198681.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:6422878 C>T maps to NM_001144856.1 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:6425462 C>T maps to NM_001144856.1 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:93150096 A>G maps to NM_001004330.2 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:93135292 C>A maps to NM_001004330.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:93155549 T>G maps to NM_001004330.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:93157878 A>G maps to NM_001004330.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:93157970 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:43921626 G>T maps to NM_172069.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:43924456 C>A maps to NM_172069.3 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:43927266 T>C maps to NM_172069.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:43921650 G>T maps to NM_172069.3 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:43927014 C>T maps to NM_172069.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:43927452 A>C maps to NM_172069.3 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:43921626 G>T maps to NM_172069.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:43937713 G>A maps to NM_172069.3 Q767Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:43937647 C>T maps to NM_172069.3 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:40823040 G>A maps to NM_024927.4 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr17:43553040 G>A maps to NM_014798.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:43528085 G>T maps to NM_014798.2 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:43535655 T>C maps to NM_014798.2 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:43522966 C>T maps to NM_014798.2 Q902Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:43535706 C>T maps to NM_014798.2 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:16057199 G>A maps to ENST00000420314 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:16043303 G>A maps to ENST00000420314 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:16051896 C>A maps to ENST00000420314 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:16060341 C>T maps to ENST00000420314 F1094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:16055610 G>A maps to ENST00000420314 Q770Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:208811147 A>G maps to NM_001080475.2 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:208693096 G>A maps to NM_001080475.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:208842185 G>A maps to NM_001080475.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:208773239 G>A maps to NM_001080475.2 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:208841984 G>A maps to NM_001080475.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr2:208795719 G>A maps to NM_001080475.2 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:906208 G>A maps to ENST00000379409 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr1:908962 C>T maps to ENST00000379409 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:161139850 G>A maps to NM_000301.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:161155112 T>C maps to NM_000301.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:161162341 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:161174008 C>T maps to NM_000301.3 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:161160208 C>T maps to NM_000301.3 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:161139745 C>T maps to NM_000301.3 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:87243503 T>C maps to NM_002665.4 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:19116428 C>T maps to NM_001122.2 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:19121073 C>T maps to NM_001122.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:4512549 G>A maps to NM_001080400.1 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:4510485 G>T maps to NM_001080400.1 I1148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:4511070 T>C maps to NM_001080400.1 G953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:4511412 C>T maps to NM_001080400.1 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:4510505 A>G maps to NM_001080400.1 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:4508803 G>T maps to NM_001080400.1 A1212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:4531744 G>A maps to NM_001013706.2 H50H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:4531783 G>A maps to NM_001013706.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:23692346 C>T maps to NM_005030.3 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:23700903 C>T maps to NM_005030.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr5:57752345 C>T maps to NM_006622.2 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:45266754 C>T maps to NM_004073.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:45271169 C>T maps to NM_004073.2 Y587Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr1:45270452 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:128807127 T>C maps to NM_014264.4 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr4:128814570 G>T maps to NM_014264.4 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:12009828 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:12027051 G>A maps to ENST00000376369 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:12034840 C>T maps to ENST00000376369 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:12027090 T>C maps to ENST00000376369 C613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:145788911 G>A maps to NM_182943.2 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:145788559 C>A maps to NM_182943.2 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:145796907 C>A maps to NM_182943.2 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:145839026 A>G maps to NM_182943.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:145878680 C>T maps to NM_182943.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:145804577 C>A maps to NM_182943.2 G375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:100854987 G>A maps to NM_001084.4 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:100849678 G>A maps to NM_001084.4 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:100853833 G>A maps to NM_001084.4 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:100849708 G>A maps to NM_001084.4 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:100853626 G>T maps to NM_001084.4 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100853820 G>A maps to NM_001084.4 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:103041574 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:103045490 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:103041424 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:103041429 C>A did not map to a codon.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr23:49031028 G>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49028439 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49029474 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49030741 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:49029823 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:49028357 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:49030741 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:49029778 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:155463403 G>A maps to NM_002669.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:155463410 G>A maps to NM_002669.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:155458496 G>A maps to NM_002669.2 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:155461762 G>A maps to NM_002669.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:155463403 G>A maps to NM_002669.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:155457810 A>G maps to ENST00000503251 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:155461948 G>A maps to NM_002669.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr4:155462020 G>A maps to NM_002669.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:155463419 C>T maps to NM_002669.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr3:142422825 A>G maps to NM_001172312.1 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:142389876 C>T maps to NM_001172312.1 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:142430716 C>T maps to NM_001172312.1 Y586Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:142430827 A>G maps to NM_001172312.1 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:142423409 T>G maps to NM_001172312.1 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:114874746 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:114863564 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:114880495 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:114869320 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:114871166 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:114879418 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:114863532 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:114877645 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:114871256 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:114864196 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:114863547 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:146239684 C>A maps to NM_021105.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:146251311 C>T maps to NM_021105.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:146173171 C>A maps to ENST00000497985 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:146167087 C>A maps to ENST00000497985 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:146159543 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:146173093 G>A maps to ENST00000497985 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:146177733 A>G maps to ENST00000497985 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr3:146177697 T>C maps to ENST00000497985 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:7296825 A>G maps to NM_020360.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:7296250 T>C maps to NM_020360.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:145914483 C>A maps to NM_020353.2 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr3:146311730 G>A maps to NM_001085420.1 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:146309629 G>A maps to NM_001085420.1 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:146307529 G>T maps to NM_001085420.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:17476485 G>T maps to NM_031310.1 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:37265500 C>T maps to NM_020405.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:20500655 G>T maps to NM_032812.7 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:20290839 C>T maps to NM_032812.7 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:20466339 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:20453446 C>T maps to NM_032812.7 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr10:20534319 C>T maps to NM_032812.7 H453H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr3:126736461 C>G maps to NM_032242.3 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:126708272 G>A maps to NM_032242.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:126751633 C>T maps to NM_032242.3 S1850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:126708350 G>A maps to NM_032242.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:126741654 C>T maps to NM_032242.3 F1452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:126747902 C>T maps to NM_032242.3 N1579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:126710378 C>T maps to NM_032242.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:126733389 C>T maps to NM_032242.3 R892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:126733574 C>T maps to NM_032242.3 D926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:126708281 C>T maps to NM_032242.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:126708491 A>G maps to NM_032242.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:126736614 A>G maps to NM_032242.3 A1180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr3:126733175 G>A maps to NM_032242.3 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:126747139 C>T maps to NM_032242.3 G1542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:126737186 G>A maps to NM_032242.3 S1237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:126708317 G>A maps to NM_032242.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:126730880 C>T maps to NM_032242.3 N731N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:126708140 G>A maps to NM_032242.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr3:126733131 C>T maps to NM_032242.3 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr3:126722310 C>T maps to NM_032242.3 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:126707993 C>T maps to NM_032242.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:208225777 G>A maps to NM_025179.3 R963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:208205080 G>A maps to NM_025179.3 D1693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:208213028 G>A maps to NM_025179.3 G1479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:208315745 G>A maps to NM_025179.3 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:208391195 G>T maps to NM_025179.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:208212266 G>A maps to NM_025179.3 N1521N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:208227843 G>T maps to NM_025179.3 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:208216455 G>A maps to NM_025179.3 R1323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:208218447 G>A maps to NM_025179.3 C1201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:208390388 G>A maps to NM_025179.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:208217897 G>A maps to NM_025179.3 Q1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:208212320 G>A maps to NM_025179.3 N1503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:208227855 G>A maps to NM_025179.3 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153695647 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153699879 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153689078 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153694177 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153695443 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153695711 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153698801 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:153689948 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153689605 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153694325 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr23:153699493 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:153700939 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:153699458 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153688731 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153688842 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153689821 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:153692556 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153690557 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:153689811 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:153695632 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153693830 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153689467 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153694581 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153698801 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:153694104 T>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:132192960 G>A maps to NM_020911.1 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:131887518 G>T maps to NM_020911.1 G824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr7:131866876 A>G maps to NM_020911.1 H1077H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:132192612 G>A maps to NM_020911.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr7:131913110 G>A maps to NM_020911.1 N574N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:131832743 G>A maps to NM_020911.1 S1593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:132169655 G>T maps to NM_181775.3 C496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:131913110 G>A maps to NM_020911.1 N574N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:132193203 C>T maps to NM_020911.1 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:131883311 G>A maps to NM_020911.1 I890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:132193203 C>T maps to NM_020911.1 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:131912336 C>T maps to NM_020911.1 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr7:132174137 G>A maps to NM_020911.1 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:132192603 A>G maps to NM_020911.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:132192873 G>A maps to NM_020911.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:131895761 G>A maps to NM_020911.1 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:131865476 G>A maps to NM_020911.1 I1169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr7:131844253 G>A maps to NM_020911.1 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:48451073 C>T maps to NM_001130082.1 P1948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:48450802 C>T maps to NM_001130082.1 A2007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:48456704 C>T maps to NM_001130082.1 T1282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:48462778 C>T maps to NM_001130082.1 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:48463103 G>A maps to NM_001130082.1 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:48450832 G>A maps to NM_001130082.1 F1997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:48465756 G>A maps to NM_001130082.1 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:48460727 A>C maps to NM_001130082.1 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:50728215 G>T maps to NM_012401.2 C266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50718187 G>A maps to NM_012401.2 P1420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr22:50728515 G>A maps to NM_012401.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr22:50714389 C>T maps to NM_012401.2 A1780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:50728644 G>A maps to NM_012401.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:153037411 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:153031020 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153032393 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153035823 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153040369 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:153037424 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153036336 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153041422 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153043458 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153043656 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr23:153034622 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153032713 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153035588 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153039999 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153041530 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153043053 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153043530 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:153032620 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:153040440 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:153040796 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:153040816 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:153035875 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153032417 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153035630 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153040260 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153043005 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153036323 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153033216 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153034456 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153041461 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:153043437 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:153043104 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153032362 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:94603462 C>T maps to NM_005761.1 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:94654591 C>T maps to NM_005761.1 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:94676113 C>T maps to NM_005761.1 I1272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:94691200 T>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:94634434 G>A maps to NM_005761.1 W765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:94673352 G>T maps to NM_005761.1 E1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:94676099 G>T maps to NM_005761.1 E1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:94575304 C>T maps to NM_005761.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:94692547 C>T maps to NM_005761.1 V1405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:94543430 C>T maps to NM_005761.1 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr12:94543465 G>A maps to NM_005761.1 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:129291780 G>A maps to NM_015103.2 I947I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:129302993 G>A maps to NM_015103.2 R704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:129280491 G>A maps to NM_015103.2 R1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr3:129294623 G>A maps to NM_015103.2 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:205811842 G>A maps to NM_152491.4 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:205819185 G>A maps to NM_152491.4 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:205797819 C>A maps to NM_152491.4 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:89871871 C>T maps to NM_001010853.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:89868139 G>T maps to NM_001010853.1 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:102590807 C>A maps to NM_002674.2 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:56227144 G>A maps to NM_020182.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr20:56234685 C>T maps to NM_020182.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:156202161 G>A maps to NM_007221.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:156203454 G>T maps to NM_007221.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:72162648 G>A maps to NM_031293.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:72163132 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:72174370 G>T maps to NM_031293.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:72174339 G>A maps to NM_031293.2 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:72153906 G>A maps to NM_031293.2 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:72188117 C>A maps to NM_031293.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr15:74290466 G>A maps to NM_033238.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:74325571 G>T maps to NM_033238.2 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:74290676 A>G maps to NM_033238.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:74327565 G>A maps to NM_033239.2 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:41974873 G>A maps to NM_002676.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:8895685 C>T maps to NM_000303.2 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr8:82356796 G>A maps to NM_002677.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:15134374 C>T maps to NM_000304.2 A114A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BS-A0UJ-01A-12D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:102950917 G>T maps to NM_004279.2 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:190656630 C>A maps to NM_000534.4 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:190717472 T>C maps to NM_000534.4 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:190738243 C>A maps to NM_000534.4 Y832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:6022615 C>T maps to NM_000535.5 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:6026708 G>T maps to NM_000535.5 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:6022615 C>T maps to NM_000535.5 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:6038759 G>A maps to NM_000535.5 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:6043623 C>A maps to NM_000535.5 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:154897627 C>A maps to NM_006556.3 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:154901595 A>G maps to NM_006556.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:152938100 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152936434 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152938716 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr23:152937104 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:152936263 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:152936961 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152936825 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152938463 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:152937460 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:152936841 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:152936948 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:219206334 C>T maps to NM_015488.4 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:219209223 G>A maps to NM_015488.4 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:219209647 C>A maps to NM_015488.4 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:50364948 G>A maps to NM_007254.3 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:50365986 G>A maps to NM_007254.3 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:160239685 C>T maps to NM_173516.1 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr6:160221853 C>T maps to NM_173516.1 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:118313333 C>A maps to NM_000936.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:118306830 C>T maps to NM_000936.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:118306830 C>T maps to NM_000936.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:118315011 C>A maps to NM_000936.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr10:118315630 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:118319997 C>T maps to NM_000936.2 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:118389517 C>T maps to NM_005396.4 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:118390842 T>C maps to NM_005396.4 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:118404580 C>T maps to NM_005396.4 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr14:74180252 A>G maps to NM_006029.4 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr14:74179646 C>T maps to NM_006029.4 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:74179577 C>T maps to NM_006029.4 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:26365707 G>T maps to NM_007257.5 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr8:26366265 C>T maps to NM_007257.5 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:26365742 C>A maps to NM_007257.5 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:152226035 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152225698 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152226564 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152225898 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:152226340 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:152226516 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:152226303 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:152226882 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152226666 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:152226588 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:152159590 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:152159037 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152159136 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152159241 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152159298 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152159654 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152159898 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:152159628 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:152158982 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:152159782 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:152160100 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:152159569 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:152159517 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152159383 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152159440 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152159166 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152160138 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:46997630 G>A maps to NM_020709.1 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:46997755 C>A maps to NM_020709.1 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:46997312 G>A maps to NM_020709.1 N470N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BS-A0TE-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr19:46997285 G>T maps to NM_020709.1 Y479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr14:39650748 T>C maps to NM_002687.3 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:39648299 G>A maps to NM_002687.3 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr14:39650457 A>G maps to NM_002687.3 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:68385652 G>T maps to NM_020143.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr14:20943403 C>T maps to NM_000270.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:36259160 G>A maps to ENST00000457797 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:36270233 G>T maps to ENST00000457797 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:36259298 A>G maps to ENST00000457797 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:36260896 C>T maps to ENST00000457797 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:822401 C>T maps to NM_020376.3 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:823778 C>T maps to NM_020376.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr11:824409 G>A maps to NM_020376.3 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:44323034 C>T maps to NM_025225.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:44324765 C>T maps to NM_025225.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:44342153 G>A maps to NM_025225.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:44328870 G>A maps to NM_025225.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:44323040 C>T maps to NM_025225.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:7870046 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:7889812 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:7880130 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:7893991 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:7894048 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:7889874 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:7868790 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:7889751 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:44285367 G>T maps to ENST00000216177 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:7620211 G>A maps to NM_001166111.1 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:7623967 C>T maps to NM_001166111.1 Y1220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7615270 C>T maps to NM_001166111.1 F643F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:7614875 C>T maps to NM_001166111.1 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:7621376 G>A maps to NM_001166111.1 T1054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:7605049 C>T maps to NM_001166111.1 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:7625637 C>T maps to NM_001166111.1 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:7620238 C>T maps to NM_001166111.1 G984G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:140374829 G>A maps to NM_001098537.1 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:140361801 G>A maps to NM_001098537.1 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:140400170 G>A maps to NM_001098537.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:140441760 G>A maps to NM_001098537.1 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:140357193 C>T maps to NM_001098537.1 A1145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:140409960 G>A maps to NM_001098537.1 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr9:140361771 G>A maps to NM_001098537.1 A1012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:140396179 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:140391644 G>A maps to NM_001098537.1 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:140395198 G>A maps to NM_001098537.1 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:140437201 G>A maps to NM_001098537.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:140392578 G>A maps to NM_001098537.1 R626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:108128201 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:46022935 C>A maps to NM_018129.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:46023709 G>T maps to NM_018129.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:46019115 G>T maps to NM_018129.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:55872516 G>A maps to NM_033109.3 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr6:89793611 T>A maps to NM_006813.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:89815022 G>T maps to NM_172240.2 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:89861453 G>T maps to NM_172240.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:75008687 C>T maps to NM_001099271.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:53546512 C>T maps to NM_153703.4 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:53542921 C>T maps to NM_153703.4 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:53542933 C>T maps to NM_153703.4 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:53546474 C>T maps to NM_153703.4 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:131195586 G>A maps to NM_001018111.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr7:131191401 G>A maps to NM_001018111.2 C395C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:131196151 C>T maps to NM_001018111.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:127379725 A>G maps to NM_015720.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:127379518 G>A maps to NM_015720.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:127379728 C>T maps to NM_015720.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:127390311 C>T maps to NM_015720.2 C487C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:84537312 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:84634300 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:84560851 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:84634288 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:84561193 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:84634326 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:84634237 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr23:84600883 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:84537292 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:84561278 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:84606418 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:84614614 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:84622760 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:84561223 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:84614573 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:84622694 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:84570732 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:84600943 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:84606373 C>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:84622742 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:30797901 C>T maps to NM_015352.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:46687548 G>A maps to NM_133635.4 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:166810318 C>T maps to NM_017542.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:166818509 C>T maps to NM_017542.3 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:151396425 G>A maps to NM_015100.3 R508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:151380716 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:151396425 G>A maps to NM_015100.3 R508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:151396464 G>A maps to NM_015100.3 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:151413449 G>A maps to NM_015100.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:151396579 G>A maps to NM_015100.3 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:151395900 T>C maps to NM_015100.3 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:151397475 A>G maps to NM_015100.3 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:151413407 G>A maps to NM_015100.3 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr1:151381038 G>A maps to NM_015100.3 R694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr1:151381277 T>C maps to NM_015100.3 K651K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:151384858 G>A maps to NM_015100.3 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:151396749 C>A maps to NM_015100.3 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr1:151380589 G>T maps to NM_015100.3 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GX-01A-11W-A062-09 chr23:24828014 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:24732780 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:24744108 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:24757654 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:24760154 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:24828893 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:24906159 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:24861771 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24732688 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24735423 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24735717 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24751887 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24763627 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:24721417 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:24732734 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:24734565 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:24859882 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr23:24745998 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr23:25014018 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr23:24766991 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:24833181 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:24732726 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:24732773 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:24746000 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:24761440 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:24735003 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:24745073 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:24833168 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:24760154 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:24830964 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:24761361 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:24861699 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:24722536 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:24745085 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:24839594 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:65048543 C>A maps to NM_002689.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr8:42196186 C>T maps to NM_002690.1 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr8:42229165 G>C maps to NM_002690.1 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:50917084 G>A maps to ENST00000391817 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:50917039 C>T maps to ENST00000391817 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr19:50919777 G>T maps to ENST00000391817 V1008V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr19:50905594 C>T maps to ENST00000391817 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44157610 G>T maps to NM_006230.2 C91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:44156577 G>A maps to NM_006230.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:74329804 G>T maps to NM_006591.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr11:74329632 C>A maps to NM_006591.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:74329804 G>T maps to NM_006591.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:26677486 G>A maps to NM_015584.3 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:42981816 C>A maps to ENST00000415122 E433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr22:42999128 G>A maps to ENST00000415122 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:133208981 G>A maps to ENST00000455752 L2086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:133220437 G>A maps to ENST00000455752 G1428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:133202290 G>A maps to ENST00000455752 I2202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:133249236 G>A maps to ENST00000455752 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:133212499 G>T maps to ENST00000455752 S1933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:133226289 C>T maps to ENST00000455752 G1259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:133201523 G>A maps to ENST00000455752 C2241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:133219468 A>C maps to ENST00000455752 V1558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:133238264 G>T maps to ENST00000455752 G907G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:133218273 C>T maps to ENST00000455752 P1782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:133214682 G>A maps to ENST00000455752 Y1868Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr12:133249803 G>A maps to ENST00000455752 Y476Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:133219474 G>A maps to ENST00000455752 F1556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr12:133201327 C>T maps to ENST00000455752 E2275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:133244972 T>C maps to ENST00000455752 E717E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:50118022 G>T maps to NM_002692.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:116171187 G>T maps to NM_017443.4 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:116171016 A>C did not map to a codon.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr2:75187230 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:89872059 G>T maps to NM_002693.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:89869916 G>A maps to NM_002693.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:89876724 G>T maps to NM_002693.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr15:89876721 G>A maps to NM_002693.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:89876787 G>A maps to NM_002693.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:62492921 C>T maps to NM_007215.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:43581897 G>A maps to NM_006502.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:43565514 C>T maps to NM_006502.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:51810357 G>T maps to NM_007195.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:51820557 T>C maps to NM_007195.2 N648N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:51804083 G>T maps to NM_007195.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:51820531 G>T maps to NM_007195.2 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr18:51800392 T>C maps to NM_007195.2 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:74886192 G>A maps to NM_016218.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:74892497 G>A maps to NM_016218.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:74842946 G>T maps to NM_016218.2 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:74882874 C>T maps to NM_016218.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:103342452 C>A maps to ENST00000416979 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44119489 C>T maps to NM_013284.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:44116210 G>A maps to NM_013284.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:2083386 G>A maps to NM_181808.2 R761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:2230910 C>T maps to NM_181808.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:121248605 C>A maps to ENST00000393672 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr3:121208591 C>T maps to ENST00000393672 A1198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:121151778 C>A maps to ENST00000393672 E2686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:121229024 C>T maps to ENST00000393672 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:121208057 T>G maps to ENST00000393672 I1376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr3:121178941 A>G maps to ENST00000393672 I2505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:121207646 A>G maps to ENST00000393672 A1513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:121206739 C>A maps to ENST00000393672 E1816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:86317034 G>A maps to NM_015425.3 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:86305238 G>A maps to NM_015425.3 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:86258455 G>A maps to NM_015425.3 C1525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:86297361 G>A maps to NM_015425.3 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr2:86297158 C>T maps to NM_015425.3 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:86302260 G>A maps to NM_015425.3 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr2:86308803 C>T maps to NM_015425.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:113317032 T>C maps to NM_019014.4 C498C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:113332501 C>T maps to NM_019014.4 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:113315623 C>T maps to NM_019014.4 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:113309452 T>C maps to NM_019014.4 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:113308543 G>T maps to NM_019014.4 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr2:113310278 C>T maps to NM_019014.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:113332675 T>C maps to NM_019014.4 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:43497008 G>A maps to NM_004875.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:37487879 C>A maps to NM_022490.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr17:7406809 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7405939 C>T maps to NM_000937.4 G892G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7415604 G>A maps to NM_000937.4 E1478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr17:7399262 C>T maps to NM_000937.4 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7400988 T>C maps to NM_000937.4 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:7401403 G>T maps to NM_000937.4 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:7416820 G>A maps to NM_000937.4 P1746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7404317 G>A maps to NM_000937.4 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:7400676 T>C maps to NM_000937.4 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:7416820 G>A maps to NM_000937.4 P1746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:57889619 G>A maps to NM_000938.1 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:57856934 C>T maps to NM_000938.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:57888375 G>T maps to NM_000938.1 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:57857058 G>T maps to NM_000938.1 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:57865842 G>T maps to NM_000938.1 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:57896507 G>A maps to NM_000938.1 A1126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:57888372 G>T maps to NM_000938.1 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:57503666 C>T maps to NM_032940.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:1091826 G>A maps to NM_002695.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:1091901 C>T maps to NM_002695.3 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr22:38363690 G>A maps to NM_021974.3 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:184084503 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:36605707 G>A maps to NM_006233.4 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr10:79785935 C>T maps to NM_007055.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:79782102 G>A maps to NM_007055.3 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr10:79739976 G>A maps to NM_007055.3 L1316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr10:79781725 G>A maps to NM_007055.3 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:79769400 G>A maps to NM_007055.3 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:79743719 G>A maps to NM_007055.3 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:79781378 C>T maps to NM_007055.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr10:79745860 T>C maps to NM_007055.3 K986K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr10:79741953 G>A maps to NM_007055.3 H1239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr10:79781630 C>T maps to NM_007055.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:106821136 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:106751666 C>T maps to NM_018082.5 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:106821007 A>T maps to NM_018082.5 K379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:106890684 C>T maps to NM_018082.5 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:145606307 G>A maps to NM_006468.6 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:145608132 G>A maps to NM_006468.6 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:145601613 G>A maps to NM_006468.6 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:22106819 C>A maps to NM_001722.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:22105448 C>T maps to NM_001722.2 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:22337235 C>T maps to NM_018119.2 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:22319509 G>A maps to NM_018119.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:22337520 C>T maps to NM_018119.2 H596H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:22328486 G>A maps to NM_018119.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:22319509 G>A maps to NM_018119.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:22337082 G>A maps to NM_018119.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:22334209 C>T maps to NM_018119.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:18455765 G>T maps to NM_006466.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:145456651 G>A maps to NM_032305.1 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:41925340 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:41940057 C>T maps to NM_138338.3 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:623480 C>T maps to NM_005035.3 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr19:629935 C>T maps to NM_005035.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:618522 G>A maps to NM_005035.3 S1129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:621774 G>A maps to NM_005035.3 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:619597 G>A maps to NM_005035.3 S1018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:624850 G>A maps to NM_005035.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr7:72413471 G>A maps to ENST00000434423 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:72411053 C>T maps to ENST00000434423 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:72416155 C>T maps to ENST00000434423 T1187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:72413591 G>A maps to ENST00000434423 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:72413792 G>A maps to ENST00000434423 S1087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr7:72398920 A>G did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr7:72400576 C>T maps to ENST00000434423 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:75052178 G>A maps to ENST00000257665 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:75053497 C>T maps to ENST00000257665 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:75051182 G>A maps to ENST00000257665 F1026F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:75048603 G>A maps to ENST00000257665 F1197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:75051281 C>T maps to ENST00000257665 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:75052112 C>T maps to ENST00000257665 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr7:75051539 C>T maps to ENST00000257665 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:53103957 C>T maps to NM_182595.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr7:53104002 G>A maps to NM_182595.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:53103699 C>A maps to NM_182595.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:53103948 G>A maps to NM_182595.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:53104224 C>T maps to NM_182595.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr7:53103789 G>A maps to NM_182595.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:25384102 G>A maps to NM_001035256.1 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:25384261 G>A maps to NM_001035256.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:46655227 G>A maps to ENST00000371986 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:46657799 G>A maps to ENST00000371986 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:46663531 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:46655561 T>C maps to ENST00000371986 K583K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:46663513 A>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:29246474 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr13:29238678 T>C maps to NM_015932.5 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:134385744 C>A maps to NM_007171.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:134394818 G>A maps to NM_007171.3 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:134396773 G>A maps to NM_007171.3 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:134398378 C>T maps to NM_007171.3 C710C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:77769268 G>A maps to NM_013382.5 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:77769182 G>A maps to NM_013382.5 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:76240877 G>A maps to NM_012230.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:94947667 C>A maps to NM_000446.5 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr7:94931624 G>A maps to NM_000446.5 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:95045609 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:95045601 G>A maps to NM_000305.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:94996744 C>T maps to NM_000940.2 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:94993365 G>A maps to NM_000940.2 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:95001574 G>A maps to NM_000940.2 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:99146259 C>T maps to NM_015029.2 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:99139823 G>A maps to NM_015029.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:99146250 T>C maps to NM_015029.2 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:99158877 T>C maps to NM_015029.2 C559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:99170198 T>C maps to NM_015029.2 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:99140662 G>A maps to NM_015029.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:99153051 G>A maps to NM_015029.2 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:30106169 C>A maps to NM_006627.2 C182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:30099570 C>A maps to NM_006627.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:30106208 T>C maps to NM_006627.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:121017687 G>A maps to NM_015918.3 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:121017723 G>A maps to NM_015918.3 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:119379024 G>A maps to NM_022135.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:105609850 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:105606226 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:75615355 C>T maps to NM_000941.2 N595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:75615475 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:75615340 G>A maps to NM_000941.2 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:48369746 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:48372701 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr23:48370810 C>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48369770 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48370748 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48375653 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:48372643 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:48374135 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48378849 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48369728 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48370822 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:48368227 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:48368316 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48369714 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:38144728 G>A maps to NM_006475.2 R753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr13:38154759 G>A maps to NM_006475.2 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:38153218 C>A maps to NM_006475.2 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:38161043 G>A maps to NM_006475.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:38158931 G>T maps to NM_006475.2 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:38158865 T>G maps to NM_006475.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:124463993 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:124503424 G>A maps to NM_015450.2 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:43159840 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:14542878 G>T maps to ENST00000444806 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:14530523 C>A maps to ENST00000444806 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:14542890 G>A maps to ENST00000444806 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:14530552 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:132021142 C>T maps to NM_001083538.1 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:132020987 G>T maps to NM_001083538.1 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr2:132010543 C>T maps to NM_001083538.1 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:132021700 G>A maps to NM_001083538.1 K891K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:131985925 G>T maps to NM_001083538.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:131976292 C>T maps to NM_001083538.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:131976386 G>T maps to NM_001083538.1 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:130865652 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:130832047 C>T maps to NM_001099771.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:130859723 C>A maps to NM_001099771.2 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr2:130832650 G>A maps to NM_001099771.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:130872452 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr14:19571394 G>T maps to NM_001005356.2 G392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:19553676 C>T maps to NM_001005356.2 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:19571348 A>G maps to NM_001005356.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:16287588 G>A maps to NM_001136213.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:16287420 G>A maps to NM_001136213.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:16287694 C>T maps to NM_001136213.1 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:16258284 A>G maps to NM_001136213.1 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:16287789 G>A maps to NM_001136213.1 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:20019851 G>A maps to ENST00000439503 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr14:19990655 T>C maps to ENST00000439503 Q558Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:87309171 C>A maps to NM_001122757.1 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:87309171 C>A maps to NM_001122757.1 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr3:87322578 C>T maps to NM_001122757.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:87313485 C>A maps to NM_001122757.1 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:87309192 C>A maps to NM_001122757.1 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:167358896 C>T maps to NM_002697.3 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:167353142 A>G maps to NM_002697.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:167341273 G>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:42626316 G>T maps to ENST00000342301 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:42598023 C>T maps to ENST00000342301 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:42599554 C>T maps to ENST00000342301 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:42600377 C>T maps to ENST00000342301 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:42599720 G>A maps to ENST00000342301 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:42626334 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:120176369 G>A maps to NM_014352.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:120178281 C>T maps to NM_014352.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:120187971 G>A maps to NM_014352.2 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:38511641 G>A maps to NM_002699.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:38511641 G>A maps to NM_002699.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:99283973 G>T maps to NM_005604.2 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr2:105473101 G>A maps to NM_006236.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr2:105473056 C>T maps to NM_006236.1 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:105473056 C>T maps to NM_006236.1 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:105473128 G>A maps to NM_006236.1 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:105473017 C>A maps to NM_006236.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:105473056 C>T maps to NM_006236.1 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:82764002 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:82763696 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:82764362 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:82763942 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:82763923 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:82764062 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:82764159 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:82764108 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:82764245 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:82763800 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:82764335 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:82763668 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:82764317 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:82763490 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:82763945 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr23:82763621 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:82764245 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:82763389 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr13:79175714 G>A maps to NM_006237.3 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr4:147561401 C>A maps to NM_004575.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:147561857 C>T maps to NM_004575.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:147561143 G>A maps to NM_004575.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:147561857 C>T maps to NM_004575.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:147561629 C>T maps to NM_004575.2 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:147561581 C>A maps to NM_004575.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:147560579 G>A maps to NM_004575.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:147561617 G>A maps to NM_004575.2 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr4:147561188 C>T maps to NM_004575.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:147561806 G>A maps to NM_004575.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr4:147561806 G>A maps to NM_004575.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr5:145719175 G>A maps to NM_002700.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:145719403 G>A maps to NM_002700.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:145719826 G>A maps to NM_002700.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:31137990 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:128428977 C>T maps to NM_001159542.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:93076768 G>A maps to NM_153216.1 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:93076768 G>A maps to NM_153216.1 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:93076843 G>A maps to NM_153216.1 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51584311 C>T maps to NM_002702.3 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:51590652 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr12:51583974 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:51583850 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:39491185 C>T maps to NM_007252.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:39500251 T>G maps to NM_007252.3 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr7:39379595 G>A maps to NM_007252.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:39504071 C>T maps to NM_007252.3 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:39472879 C>T maps to NM_007252.3 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr7:39504197 G>A maps to NM_007252.3 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:106320207 C>A maps to ENST00000357415 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:106307786 G>A maps to ENST00000357415 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:106345479 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:10224480 C>T maps to NM_001040664.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:10218209 C>T maps to NM_001040664.2 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr1:57002629 G>A maps to NM_003713.4 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:287667 G>A maps to NM_177543.1 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:291318 G>T maps to NM_003712.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:122334703 C>T maps to NM_001030059.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:4663001 C>A maps to NM_203453.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:46627960 C>T maps to NM_001001928.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr22:46614296 C>T maps to NM_001001928.2 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:46611073 G>A maps to NM_001001928.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:46627846 C>T maps to NM_001001928.2 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr22:46614185 C>A maps to NM_001001928.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:35393813 G>A maps to NM_006238.4 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:12393127 G>T maps to NM_015869.4 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:12447549 G>A maps to NM_015869.4 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:23814705 C>T maps to NM_013261.3 T612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:23833275 C>T maps to NM_013261.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:23814748 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr4:23830041 C>T maps to NM_013261.3 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:23814462 G>A maps to NM_013261.3 H642H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:23816019 T>G maps to NM_013261.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:149216481 G>T maps to NM_133263.3 E822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:149216159 G>A maps to NM_133263.3 P714P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:57267603 T>G maps to NM_002703.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:57267647 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:57272693 G>A maps to NM_002703.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr4:57272684 T>C maps to NM_002703.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:18725943 A>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:18768031 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:18767972 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18775774 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18836164 C>A did not map to a codon.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr23:18836171 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:18748383 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:18807245 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:18748329 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:18767977 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:18842041 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:18775788 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:18807277 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:18775756 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:18725933 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:18845432 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:18797189 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:18725907 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:18768004 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:76794278 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:76793278 G>A maps to NM_006239.2 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:76781990 G>T maps to NM_006239.2 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:76811166 G>T maps to NM_006239.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:76809433 T>C maps to NM_006239.2 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr11:70172753 G>T maps to NM_003626.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:70200468 G>A maps to NM_003626.2 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:70118319 C>T maps to NM_003626.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:70183485 G>T maps to NM_003626.2 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:81732957 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:81769670 C>T maps to NM_003625.2 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:81719593 G>A maps to NM_003625.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:81741407 C>T maps to NM_003625.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:81851581 C>A maps to NM_003625.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:81693161 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:81851623 C>A maps to NM_003625.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:81688700 G>A maps to NM_003625.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:81688675 G>A maps to NM_003625.2 R955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:81732958 G>A maps to NM_003625.2 R850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:81777836 C>A maps to NM_003625.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr12:81719571 G>A maps to NM_003625.2 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:81833825 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr12:81777849 G>A maps to NM_003625.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49632241 C>T maps to NM_003660.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49645289 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr19:49637370 C>T maps to NM_003660.2 N442N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:203040887 C>T maps to ENST00000367238 D1110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:203013081 C>T maps to ENST00000367238 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:203024598 G>A maps to ENST00000367238 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:27841308 G>T maps to NM_003622.3 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:7674304 C>T maps to NM_003621.2 F829F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:7674304 C>T maps to NM_003621.2 F829F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:7647052 G>T maps to NM_003621.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:143767580 G>A maps to NM_001123068.1 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:122364502 C>A maps to NM_000943.4 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:122364491 G>T maps to NM_000943.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:122372308 A>G maps to NM_000943.4 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:40214722 C>T maps to NM_006112.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:81112118 G>A maps to NM_005729.3 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:81112145 C>T maps to NM_005729.3 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:81113526 G>T maps to NM_005729.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:170493861 C>T maps to NM_004792.2 D698D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:170489706 C>T maps to NM_004792.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:170493912 A>G maps to NM_004792.2 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:170489742 G>T maps to NM_004792.2 G335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:170492645 A>G maps to NM_004792.2 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:170487392 C>T maps to NM_004792.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:170493733 G>T maps to NM_004792.2 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:170493170 C>A maps to NM_004792.2 S468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:170487477 C>T maps to NM_004792.2 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:170493789 A>G maps to NM_004792.2 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr2:170493460 C>T maps to NM_004792.2 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:170493493 C>T maps to NM_004792.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:43132227 C>T maps to NM_006347.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:43125144 C>T maps to ENST00000436387 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr22:22049096 C>T maps to NM_148175.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr22:22043054 C>T maps to NM_148175.2 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:149854643 C>A maps to NM_139126.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:149855845 G>A maps to NM_139126.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr6:149855845 G>A maps to NM_139126.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:109748082 G>A maps to NM_001111298.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:109748082 G>A maps to NM_001111298.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:109748350 G>A maps to NM_001111298.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr5:102518984 G>A maps to ENST00000451606 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:102522051 G>A maps to ENST00000451606 S1082S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:102484894 C>A maps to ENST00000451606 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:102537302 G>T maps to ENST00000451606 E1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:102522057 C>T maps to ENST00000451606 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:102530628 A>C maps to ENST00000451606 I1209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr16:4934329 G>A maps to NM_002705.4 T1442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:4933729 G>A maps to NM_002705.4 S1642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:4939014 G>T maps to NM_002705.4 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr16:4934259 G>A maps to NM_002705.4 L1466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:4960946 G>T maps to NM_002705.4 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:4934125 G>A maps to NM_002705.4 G1510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:4934239 C>T maps to NM_002705.4 R1472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:4940727 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:4933909 G>T maps to NM_002705.4 L1582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:4934869 G>A maps to NM_002705.4 I1262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:4947714 G>A maps to NM_002705.4 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:60749552 C>T maps to NM_177952.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr14:60752340 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:60712595 G>T maps to NM_177952.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:58740708 A>G maps to NM_003620.3 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:58740667 G>T maps to NM_003620.3 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:58740748 C>T maps to NM_003620.3 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:58740667 G>T maps to NM_003620.3 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:58740478 C>T maps to NM_003620.3 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:58740369 T>C maps to NM_003620.3 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:58740813 G>A maps to NM_003620.3 K573K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:58740667 G>T maps to NM_003620.3 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:57049633 G>T maps to NM_014906.3 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:57033115 G>T maps to NM_014906.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:57058136 C>T maps to NM_014906.3 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr22:22300345 C>T maps to NM_014634.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr22:22280023 C>T maps to NM_014634.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:22287812 C>A maps to NM_014634.3 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27607602 G>T maps to NM_177983.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27608637 C>A maps to NM_177983.1 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:27605373 C>A maps to NM_177983.1 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:27607946 C>A maps to NM_177983.1 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:27607749 G>A maps to NM_177983.1 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:63182106 T>G maps to NM_020700.1 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:63114003 C>T maps to NM_020700.1 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:63042336 G>A maps to NM_020700.1 R493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:113253143 G>A maps to NM_005167.5 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:113253098 C>T maps to NM_005167.5 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:89198352 G>T maps to NM_152542.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr4:89183812 T>C maps to NM_152542.3 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:89183866 G>A maps to NM_152542.3 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:160679598 G>T maps to NM_139245.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:160679654 C>T maps to NM_139245.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:160786804 C>T maps to NM_139245.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:160786804 C>T maps to NM_139245.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:160786804 C>T maps to NM_139245.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:52282676 G>A maps to NM_144641.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:52282670 G>A maps to NM_144641.2 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:46005309 G>A maps to NM_001080401.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:46003205 G>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:73936302 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:73936271 T>C maps to NM_016147.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161140453 C>A maps to NM_001122764.1 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:161138867 G>A maps to NM_001122764.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:161137243 C>T maps to NM_001122764.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:161136960 C>A maps to NM_001122764.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:29022132 T>C maps to NM_002709.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:29022063 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:29011566 G>A maps to NM_002709.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:30573697 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:30572488 C>T maps to NM_002714.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:80169709 T>A maps to NM_001143885.1 *1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:80203757 T>C maps to NM_001143885.1 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:202418185 G>A maps to ENST00000367270 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:202399914 G>A maps to ENST00000367270 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:202409886 C>T maps to ENST00000367270 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:202394733 G>A maps to ENST00000367270 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:55606124 G>T maps to NM_017607.2 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:55606834 C>T maps to NM_017607.2 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:55604153 C>T maps to NM_017607.2 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:55603226 G>A maps to NM_017607.2 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:55606087 C>T maps to NM_017607.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:104263819 C>T maps to NM_015316.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr14:104206406 G>A maps to NM_015316.2 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr14:104212710 G>A maps to NM_015316.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr14:104206649 C>T maps to NM_015316.2 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:104220487 C>A maps to NM_015316.2 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:45883480 G>A maps to NM_001142502.1 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:45899488 C>T maps to NM_001142502.1 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:45888874 G>A maps to NM_001142502.1 F731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:49376810 C>A maps to NM_014330.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:49378881 C>T maps to NM_014330.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:49379178 C>T maps to NM_014330.3 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:49376699 C>T maps to NM_014330.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:204379443 C>A maps to NM_032833.3 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:145727126 C>T maps to NM_032902.5 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr8:145724195 C>T maps to NM_032902.5 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr20:37536697 G>A maps to NM_015568.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:54978105 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:37790281 G>T maps to ENST00000394271 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:182928486 G>A maps to ENST00000280295 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:113519229 A>G maps to NM_002711.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:113558816 C>A maps to NM_002711.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:113558744 C>A maps to NM_002711.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:113519906 C>A maps to NM_002711.3 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:113517855 G>A maps to NM_002711.3 G1097G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:113517797 C>A maps to NM_002711.3 E1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:113518716 A>G maps to NM_002711.3 C810C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:113558829 A>G maps to NM_002711.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:113518607 C>A maps to NM_002711.3 E847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr7:113519094 G>A maps to NM_002711.3 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:8998501 C>T maps to NM_024607.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:8998765 G>A maps to NM_024607.2 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:8999143 G>A maps to NM_024607.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:8998915 G>A maps to NM_024607.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr10:93390250 G>A maps to NM_005398.4 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:49137914 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49142861 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49127039 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49127109 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49142463 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49143080 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:49142932 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr23:49157908 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49143299 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:49127167 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:49143006 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49157906 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:49142426 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:94540229 G>T maps to NM_001166160.1 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:94897955 C>A maps to NM_001166160.1 P920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:94540297 G>A maps to NM_001166160.1 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:94913590 C>A maps to NM_001166160.1 I1186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:94539734 G>T maps to NM_001166160.1 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:94539976 T>C maps to NM_001166160.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:94881344 C>A maps to NM_001166160.1 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:94919404 T>C maps to NM_001166160.1 A1305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:94539734 G>T maps to NM_001166160.1 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:94540568 G>T maps to NM_001166160.1 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:94540511 G>T maps to NM_001166160.1 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:133537681 G>A maps to NM_002715.2 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:30643750 T>G maps to NM_001009552.1 *310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:30651483 G>A maps to NM_001009552.1 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr19:52705195 G>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:52724322 G>A maps to NM_014225.5 K485K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr19:52719117 G>A maps to NM_014225.5 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:52719326 G>A maps to NM_014225.5 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:111630560 A>G maps to NM_181699.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr11:111622912 A>G maps to NM_181699.2 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:111631717 C>A maps to NM_181699.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr8:26227856 G>A maps to NM_001177591.1 W434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:26223850 T>C maps to NM_001177591.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:145979871 G>A maps to ENST00000394414 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:146077635 G>A maps to ENST00000394414 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:146070774 G>A maps to ENST00000394414 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:146077607 C>A maps to ENST00000394414 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:146017937 C>T maps to ENST00000394414 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr5:145979958 C>T maps to ENST00000394414 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:145969653 C>A maps to ENST00000394414 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:6380161 G>A maps to NM_181876.2 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:6349717 C>T maps to NM_181876.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:6349699 A>G maps to NM_181876.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:133761256 C>A maps to ENST00000455566 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:133761247 C>T maps to ENST00000455566 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:135721827 C>T maps to NM_002718.4 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:135721566 C>T maps to NM_002718.4 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:135809479 C>A maps to NM_002718.4 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr3:135742044 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:135822142 C>T maps to NM_002718.4 H1049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:135789363 T>C maps to NM_002718.4 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:306303 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:306334 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:308377 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:308341 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:299560 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:295122 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:306356 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:306356 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:306356 G>T did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:308047 T>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:299398 G>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:306398 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:301564 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:322317 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:35557155 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:212530530 C>T maps to NM_006243.3 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:212532090 C>T maps to NM_006243.3 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:212502577 G>T maps to NM_006243.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:212530306 G>T maps to NM_006243.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:212502577 G>T maps to NM_006243.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr1:212530626 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:212532090 C>T maps to NM_006243.3 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr11:64694307 C>T maps to NM_006244.3 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:64695546 G>T maps to NM_006244.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:102348515 C>T maps to NM_002719.3 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:102372813 C>T maps to NM_002719.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:102391578 C>T maps to NM_002719.3 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr14:102384271 C>T maps to NM_002719.3 D477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:42976483 G>T maps to NM_006245.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:42974217 G>A maps to NM_006245.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:42974718 C>T maps to NM_006245.2 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:42974214 C>G maps to NM_006245.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:64006313 C>T maps to ENST00000422769 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:102117234 C>A maps to NM_000944.4 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:75231342 A>G maps to NM_001142353.1 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:75239075 T>C maps to NM_001142353.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:22368600 C>T maps to ENST00000397775 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:22398194 T>C maps to ENST00000397775 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr8:22386043 C>G maps to ENST00000397775 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:68414432 G>A maps to ENST00000406334 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:104356945 G>A maps to NM_147180.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:104357026 G>A maps to NM_147180.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr9:104357044 C>T maps to NM_147180.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:104356906 G>A maps to NM_147180.2 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:9562040 G>A maps to NM_001042388.1 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:9550052 G>A maps to NM_001042388.1 C848C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr18:9549315 G>A maps to NM_001042388.1 C856C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:9593847 G>A maps to NM_001042388.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr18:9559584 C>T maps to NM_001042388.1 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:9588140 G>A maps to NM_001042388.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:73114186 G>T maps to NM_174907.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:73112848 C>T maps to NM_174907.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:73096444 C>T maps to NM_174907.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:94718098 A>G maps to NM_058237.1 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:94708293 G>T maps to NM_058237.1 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:94732159 C>T maps to NM_058237.1 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:94744970 C>A maps to NM_058237.1 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:94703941 G>T maps to NM_058237.1 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:94716579 A>G maps to NM_058237.1 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:94722795 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:94703941 G>T maps to NM_058237.1 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:46890428 C>T maps to NM_006247.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:46878958 C>T maps to NM_006247.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:46887077 C>T maps to NM_006247.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:46893579 C>T maps to NM_006247.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:127951936 C>A maps to NM_001123355.1 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:244855247 G>T maps to NM_016076.3 G93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:244868994 C>A maps to NM_016076.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:103906832 C>T maps to NM_015062.3 Q1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:103899563 C>T maps to NM_015062.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:103901696 C>T maps to NM_015062.3 S1144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:103899383 G>A maps to NM_015062.3 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:103904779 C>T maps to NM_015062.3 G1204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr10:103899008 A>G maps to NM_015062.3 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:103907015 C>T maps to NM_015062.3 R1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:40555166 G>A maps to ENST00000372783 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:40546146 G>A maps to ENST00000372783 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:110983689 G>A maps to NM_139283.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:110976078 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:64881995 G>T maps to NM_015342.2 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:64872842 C>T maps to NM_015342.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:64863427 T>C maps to NM_015342.2 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:47087703 C>T maps to NM_005972.4 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:47087145 G>A maps to NM_005972.4 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:47087703 C>T maps to NM_005972.4 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:48759748 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48759862 C>A did not map to a codon.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr23:48759801 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48755854 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48755849 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:48759871 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48929605 G>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:8564294 G>A maps to NM_032152.4 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:8563553 G>A maps to NM_032152.4 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:8563791 G>A maps to NM_032152.4 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:8555222 G>A maps to NM_032152.4 C658C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:8563566 G>A maps to NM_032152.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr19:8555631 C>T maps to NM_032152.4 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:8563566 G>A maps to NM_032152.4 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:22890680 C>T maps to NM_206954.1 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:22890514 G>A maps to NM_206954.1 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:22890989 G>A maps to NM_206954.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:12856003 G>A maps to NM_023013.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:12854204 G>A maps to NM_023013.2 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:12953076 T>C maps to NM_001039361.3 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:12884844 G>A maps to NM_001146344.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:12888615 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr1:12837210 G>A maps to NM_001080830.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr1:12835285 G>A maps to NM_001080830.1 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:12918989 G>A maps to NM_023014.1 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:12921144 T>C maps to NM_023014.1 C312C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:12921438 G>A maps to NM_023014.1 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:12919079 G>A maps to NM_023014.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:12920112 G>T maps to NM_023014.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:13052803 G>T maps to ENST00000414205 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:12943094 G>A maps to NM_001009611.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:12942093 G>A maps to ENST00000376192 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:12979707 C>T maps to NM_001012277.1 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:12979719 G>C maps to NM_001012277.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:12979698 C>T maps to NM_001012277.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:11506874 T>G maps to NM_005039.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:11546090 T>C maps to NM_006248.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:11421587 C>A maps to NM_006249.4 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:11461753 C>A maps to NM_002723.3 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr12:11461655 G>A maps to NM_002723.3 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:91513663 G>A maps to NM_003981.2 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:91519937 G>A maps to NM_003981.2 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr15:91517380 C>G maps to NM_003981.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:156756455 T>C maps to NM_005973.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:82561469 T>C maps to NM_199418.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:82595870 A>G maps to NM_199418.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr11:82564221 G>A maps to NM_199418.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:106553145 C>A maps to NM_001198.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:106553387 C>T maps to NM_001198.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:106553744 C>T maps to NM_001198.3 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:106543510 G>T maps to NM_001198.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:129814884 C>T maps to NM_020228.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:129800984 G>A maps to NM_020228.2 Q486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:129781997 C>T maps to NM_020228.2 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:129817094 C>T maps to NM_020228.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:129784891 G>A maps to NM_020228.2 R854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:129784673 G>A maps to NM_020228.2 Y926Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:45204610 C>A maps to NM_020229.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:45203865 C>T maps to NM_020229.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:70978614 C>T maps to NM_024504.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:70980716 C>A maps to NM_024504.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:70981759 C>T maps to NM_024504.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr8:70964323 A>G maps to NM_024504.2 H568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:43240514 G>A maps to NM_022115.3 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:43246375 G>A maps to NM_022115.3 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:43230644 G>A maps to NM_022115.3 Y1205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:43230569 G>A maps to NM_022115.3 C1230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:43259753 G>A maps to NM_022115.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:43230617 G>A maps to NM_022115.3 H1214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr21:43259891 G>A maps to NM_022115.3 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr21:43281686 G>A maps to NM_022115.3 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:3347576 C>T maps to NM_022114.3 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:3348550 C>T maps to NM_022114.3 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr1:3334390 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:3350323 C>A maps to NM_022114.3 V1260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:3328185 C>T maps to NM_022114.3 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:3313068 C>T maps to NM_022114.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr1:3329208 C>T maps to NM_022114.3 N816N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:14105516 G>A maps to NM_012231.4 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:14108472 C>T maps to NM_012231.4 R1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:14108975 G>A maps to NM_012231.4 S1562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:14105786 A>G maps to NM_012231.4 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:14106626 C>T maps to NM_012231.4 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:14068615 G>A maps to NM_012231.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:14106626 C>T maps to NM_012231.4 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:14107334 C>A maps to NM_012231.4 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:108134870 G>T maps to NM_012406.3 C592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:108128096 C>A maps to NM_012406.3 E766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:108145246 C>T maps to NM_012406.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:108135008 G>T maps to NM_012406.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:108128058 A>G maps to NM_012406.3 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr12:108133179 C>T maps to NM_012406.3 Q691Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:108128013 C>T maps to NM_012406.3 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:108147731 C>T maps to NM_012406.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr12:108133320 C>T maps to NM_012406.3 K644K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:121631519 G>A maps to NM_018699.2 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:121702378 A>G maps to NM_018699.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:121702333 G>A maps to NM_018699.2 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:121739565 C>A maps to NM_018699.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:81123179 T>C maps to NM_001099403.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:23510083 C>T maps to NM_020227.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:23527086 C>T maps to NM_020227.2 H630H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:23510114 G>T maps to NM_020227.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:23526540 T>C maps to NM_020227.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:23521145 G>T maps to NM_020227.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr5:23521145 G>A maps to NM_020227.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:23523423 G>T maps to NM_020227.2 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr5:23526585 G>A maps to NM_020227.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr5:23522863 C>G maps to NM_020227.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:23526438 G>A maps to NM_020227.2 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:23522456 G>T maps to NM_020227.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr5:23526954 G>T maps to NM_020227.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:45980633 T>C maps to NM_181697.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:45980597 G>T maps to NM_181697.1 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:12907945 C>T maps to NM_005809.4 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr19:12911686 T>G maps to NM_181738.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:120933305 G>A maps to NM_006793.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:120931928 G>A maps to NM_006793.2 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:23685839 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:173454532 G>T maps to NM_004905.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:27354654 A>G maps to NM_013388.4 D348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:27354538 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:176732930 C>T maps to NM_013237.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:176732883 C>T maps to NM_013237.2 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:145197493 C>A maps to NM_182960.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:203452842 G>A maps to NM_201348.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr1:203452494 C>T maps to NM_201348.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:203452872 G>A maps to NM_201348.1 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:105845793 A>G maps to NM_002726.4 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:105729748 G>T maps to NM_002726.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:105726222 G>A maps to NM_002726.4 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:105824092 G>A maps to NM_002726.4 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:44586755 G>A maps to NM_001171603.1 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr2:44556233 T>G maps to NM_001171603.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr20:47248965 G>T maps to ENST00000396220 S1493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr20:47351100 G>T maps to NM_020820.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:47246158 G>A maps to NM_020820.3 L1532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:47267433 C>A maps to NM_020820.3 E939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:47307578 C>T maps to NM_020820.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:47248858 G>A maps to NM_020820.3 N1494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:68989630 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:68992690 C>T maps to NM_024870.2 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:68934336 G>T maps to NM_024870.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:68972980 C>T maps to NM_024870.2 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:69020447 C>T maps to NM_024870.2 V940V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:69017482 G>A maps to NM_025170.4 E942E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:69058534 A>G maps to NM_024870.2 Q1393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr8:69104649 T>C maps to NM_024870.2 C1498C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:68992729 G>A maps to NM_024870.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:69017564 G>T maps to NM_025170.4 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:69009354 G>A maps to NM_024870.2 E824E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:72360352 G>A maps to NM_005041.4 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:72358726 C>T maps to NM_005041.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:57147250 C>A maps to NM_006093.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:57147248 C>T maps to NM_006093.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr11:57147229 G>A maps to NM_006093.3 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:186276212 C>A maps to NM_005807.3 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:186275669 G>A maps to NM_005807.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:186275523 G>T maps to NM_005807.3 G225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:186276791 G>A maps to NM_005807.3 E647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:186275712 G>T maps to NM_005807.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:186269221 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:11034970 G>A maps to NM_006250.2 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:62192177 G>A maps to NM_001037335.2 D2417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:62200850 G>A maps to NM_001037335.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:62195719 G>A maps to NM_001037335.2 C1485C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:62195167 C>T maps to NM_001037335.2 T1669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:62198703 C>T maps to NM_001037335.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:62192731 C>T maps to NM_001037335.2 G2308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:62198256 C>T maps to NM_001037335.2 W818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr12:42863293 A>G maps to NM_153026.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:64084882 T>C maps to NM_198859.3 E793E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:64184495 C>T maps to NM_198859.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr3:64132682 G>T maps to NM_198859.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:49032264 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:49034347 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:49034396 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:49034342 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:49034396 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49032194 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49034342 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49040321 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49032169 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:49034793 C>T did not map to a codon.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr23:49032262 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49033461 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:49032030 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr23:49033257 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:49033355 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:49034528 C>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:49032131 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:41753217 A>G maps to NM_013397.5 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr6:41751309 G>A maps to NM_013397.5 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:41753915 G>A maps to NM_013397.5 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr6:41754696 G>T maps to NM_013397.5 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:57246833 T>C maps to NM_000947.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:40762926 C>A maps to NM_206907.3 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:40764940 C>T maps to NM_206907.3 W422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:40762926 C>A maps to NM_206907.3 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:40777566 C>T maps to NM_206907.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:57169916 T>C maps to NM_006252.3 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:57158173 C>T maps to NM_006252.3 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:57157065 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:57169667 T>C maps to NM_006252.3 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:120106177 C>T maps to NM_006253.4 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr12:120117781 C>T maps to NM_006253.4 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:146639476 C>T maps to NM_005399.3 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:14208184 G>A maps to NM_002730.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:14208659 G>T maps to NM_002730.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:14208250 G>T maps to NM_002730.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:84700970 G>T maps to NM_182948.2 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:84668409 C>A maps to NM_182948.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:71628096 G>A maps to NM_002732.3 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:71628498 G>A maps to NM_002732.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:71628876 G>A maps to NM_002732.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:71628876 G>A maps to NM_002732.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:71628951 G>A maps to NM_002732.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:49397645 G>A maps to NM_002733.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:49398772 C>T maps to NM_002733.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:151372574 G>A maps to NM_016203.3 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:151292507 G>A maps to NM_016203.3 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:151273505 G>A maps to NM_016203.3 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr7:151483612 G>A maps to NM_016203.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:219693290 G>A maps to NM_017431.2 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:66511611 G>A maps to NM_212472.1 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:66511702 G>T maps to NM_212472.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:635851 C>T maps to NM_002735.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr7:716924 C>T maps to NM_002735.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:618895 C>T maps to NM_002735.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:48802466 G>A maps to NM_004157.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:48831471 C>T maps to NM_004157.2 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:106781368 C>T maps to NM_002736.2 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:106710739 C>T maps to NM_002736.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:106768680 C>T maps to NM_002736.2 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:106797672 C>T maps to NM_002736.2 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:64683343 C>T maps to NM_002737.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:64770133 T>C maps to NM_002737.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:64685161 C>T maps to NM_002737.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:64685161 C>T maps to NM_002737.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:64731713 G>A maps to NM_002737.2 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:64785096 G>A maps to NM_002737.2 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr16:23999886 C>T maps to NM_002738.6 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:24105582 G>T maps to NM_002738.6 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:24104184 T>C maps to NM_002738.6 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:24226082 C>T maps to NM_002738.6 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:23847555 C>T maps to NM_002738.6 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:24192158 G>A maps to NM_002738.6 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr16:24046788 G>A maps to NM_002738.6 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:24166144 C>T maps to NM_002738.6 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:53220660 C>T maps to NM_212539.1 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr3:53215568 C>T maps to NM_212539.1 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:53226260 C>T maps to NM_212539.1 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:46234650 C>T maps to NM_005400.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:46207513 C>T maps to NM_005400.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:46231740 C>T maps to NM_005400.2 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:46411872 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:46372291 C>T maps to NM_005400.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr19:54403572 T>C maps to NM_002739.3 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:54393164 C>A maps to NM_002739.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:54403512 C>T maps to NM_002739.3 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:54385906 C>T maps to NM_002739.3 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:54395879 G>A maps to NM_002739.3 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:54407962 G>A maps to NM_002739.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:61917576 C>T maps to NM_006255.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:61952329 C>A maps to NM_006255.3 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:61919966 C>T maps to NM_006255.3 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:61995852 C>T maps to NM_006255.3 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr14:61857944 G>C maps to NM_006255.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr14:61909893 C>T maps to NM_006255.3 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:170011255 C>T maps to NM_002740.5 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:170009667 C>G maps to NM_002740.5 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr3:170015153 G>C maps to NM_002740.5 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr10:6527123 C>T maps to NM_006257.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:6525476 T>C maps to NM_006257.2 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:6498674 C>T maps to NM_006257.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:6556986 G>A maps to NM_006257.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:6470297 G>A maps to NM_006257.2 F664F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr10:6506333 G>A maps to NM_006257.2 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:11547246 C>A maps to ENST00000436195 C39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr19:11548936 C>T maps to ENST00000436195 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:2077530 C>T maps to NM_002744.4 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:30135355 G>A maps to NM_002742.2 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:30046481 C>A maps to NM_002742.2 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:30105518 G>A maps to NM_002742.2 H389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:30107758 G>A maps to NM_002742.2 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:30068325 G>A maps to NM_002742.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr14:30103719 G>A maps to NM_002742.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:30100143 G>A maps to NM_002742.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:47214209 G>A maps to ENST00000449438 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:47178364 G>T maps to ENST00000449438 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:47181764 G>A maps to ENST00000449438 Y742Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:47204102 C>T maps to ENST00000449438 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:47197138 C>T maps to ENST00000449438 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:47197300 G>A maps to ENST00000449438 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:37501726 G>A maps to NM_005813.3 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:48762031 C>T maps to NM_006904.6 A2345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:48690333 T>C maps to NM_006904.6 V3984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:48691037 C>T maps to NM_006904.6 A3944A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:48715999 A>G maps to NM_006904.6 H3262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:48798618 G>T maps to NM_006904.6 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:48811030 G>A maps to NM_006904.6 R1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:48848993 C>T maps to NM_006904.6 Q399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr8:48686734 C>A maps to NM_006904.6 *4128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:48802880 G>A maps to NM_006904.6 T1335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:48706962 C>A maps to NM_006904.6 E3519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:48752647 G>A maps to NM_006904.6 F2460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:48855903 C>T maps to NM_006904.6 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:48697865 C>A maps to NM_006904.6 E3638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:48710932 C>T maps to NM_006904.6 A3440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:48771529 C>T maps to NM_006904.6 T2074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:48825008 C>T maps to NM_006904.6 T965T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:48843347 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:48869956 G>A maps to NM_006904.6 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:48798573 C>T maps to NM_006904.6 T1568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:48815247 C>T maps to NM_006904.6 E1050E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:48848298 A>G maps to NM_006904.6 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:48691058 G>A maps to NM_006904.6 I3937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:48866930 C>A maps to NM_006904.6 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:48715978 G>A maps to NM_006904.6 D3269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:48749007 G>A maps to NM_006904.6 G2613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:48845713 C>A maps to NM_006904.6 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:48711894 C>T maps to NM_006904.6 A3390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:53921651 T>G maps to NM_001098512.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:82092922 G>A maps to NM_006259.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:82056346 C>A maps to NM_006259.1 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:82095959 G>T maps to NM_006259.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr2:179306375 G>C maps to NM_003690.4 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:76063703 C>A maps to NM_004705.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:76063167 A>G maps to NM_004705.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:3530317 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:3530336 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:3559906 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:3530279 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:3559971 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:22294637 G>A maps to ENST00000397199 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:22294637 G>A maps to ENST00000397199 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:22297202 G>A maps to ENST00000397199 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:22294637 G>A maps to ENST00000397199 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:35086413 G>T maps to NM_000949.4 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:35068365 C>A maps to NM_000949.4 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:35066122 C>A maps to NM_000949.4 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:35089665 G>A maps to NM_000949.4 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:35072708 G>A maps to NM_000949.4 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:11369731 G>A maps to ENST00000435245 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:11370140 G>A maps to ENST00000435245 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:50188200 C>T maps to NM_001536.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:50189880 G>A maps to NM_001536.3 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr19:50189970 C>T maps to NM_001536.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:148591789 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:148563979 A>C maps to NM_138364.2 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:148591847 C>A maps to NM_138364.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:48071896 C>T maps to ENST00000397634 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:48083405 G>A maps to NM_206962.1 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:48068476 C>A maps to NM_206962.1 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:48083315 G>A maps to NM_206962.1 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:20411319 A>G maps to NM_005788.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:20419170 G>A maps to NM_005788.3 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:20429518 G>A maps to NM_005788.3 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:23395505 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:23397340 G>A maps to NM_006109.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr14:23393477 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:23391450 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:107600413 C>A maps to NM_018137.2 Y359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:68380159 C>T maps to NM_019023.2 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:68358584 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:68373256 C>T maps to NM_019023.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:68391084 C>T maps to NM_019023.2 G679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr16:68386281 C>T maps to NM_019023.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:68391084 C>T maps to NM_019023.2 G679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:3677989 G>T maps to NM_019854.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr12:3701430 C>T maps to NM_019854.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:4680429 G>A maps to NM_001080123.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:4680288 C>T maps to NM_001080123.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:4680597 C>A maps to NM_001080123.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:128180916 C>T maps to ENST00000409048 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr2:128183781 G>A maps to ENST00000409048 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:128180682 C>T maps to ENST00000409048 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:27031739 G>A maps to ENST00000415329 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:27031106 C>T maps to ENST00000415329 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr22:18913198 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr22:18905899 G>T maps to NM_016335.4 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:18910681 G>A maps to NM_016335.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:18912669 G>A maps to NM_016335.4 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:36303434 G>A maps to NM_021232.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:110996587 T>C maps to NM_032414.2 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr3:71821940 T>C maps to NM_001126128.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:68882626 C>T maps to NM_138964.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:68882681 G>T maps to NM_138964.2 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:68882461 C>T maps to NM_138964.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr20:5282793 C>T maps to NM_144773.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:71275581 A>G maps to NM_021225.4 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:16077473 G>C maps to NM_006017.2 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr4:15995678 A>G maps to NM_006017.2 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:95952595 G>A maps to NM_144707.2 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:177419967 G>A maps to NM_006261.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:177420045 G>T maps to NM_006261.4 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr5:177419919 G>A maps to NM_006261.4 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:93593097 C>T maps to NM_000313.3 K674K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:93593226 T>C maps to NM_000313.3 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:93598158 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:93615492 C>A maps to NM_000313.3 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:93646099 C>T maps to NM_000313.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:93595918 C>T maps to NM_000313.3 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:93619773 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:93595918 C>T maps to NM_000313.3 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:93624879 C>A maps to NM_000313.3 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:93593205 G>T maps to NM_000313.3 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:37635576 C>T maps to NM_007198.3 C261C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A052-01A-11W-A027-09 chr1:214171026 C>T maps to NM_002763.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:214184961 C>T maps to NM_002763.3 N644N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:214170987 C>A maps to NM_002763.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr1:214178605 C>T maps to NM_002763.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:214170574 C>T maps to NM_002763.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:214171173 C>T maps to NM_002763.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:214170906 G>A maps to NM_002763.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:75321888 C>T maps to ENST00000445876 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:75329877 T>G maps to ENST00000445876 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:75330051 C>T maps to ENST00000445876 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:75321888 C>T maps to ENST00000445876 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr13:113814464 G>T maps to ENST00000342783 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:113818923 G>A maps to ENST00000342783 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:113819409 G>A maps to ENST00000342783 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr13:113826046 G>A maps to ENST00000342783 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:13656079 C>T maps to NM_003675.3 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:13642284 G>A maps to NM_003675.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr10:13658483 C>T maps to NM_003675.3 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:13642284 G>A maps to NM_003675.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:60666050 C>A maps to NM_014502.4 G368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:60666024 G>T maps to NM_014502.4 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:60666752 G>A maps to NM_014502.4 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:150310700 G>A maps to NM_004698.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:150300832 C>T maps to NM_004698.2 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:150316692 G>A maps to NM_004698.2 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:150316731 A>G maps to NM_004698.2 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:54626939 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:54621753 C>T maps to NM_015629.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:54631561 C>T maps to NM_015629.3 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:54625260 G>A maps to NM_015629.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:54627196 C>A maps to NM_015629.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:54625966 G>A maps to NM_015629.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:52880494 C>T maps to NM_032864.3 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:52870537 C>A maps to NM_032864.3 C39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:52878211 G>A maps to NM_032864.3 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr1:52879630 C>T maps to NM_032864.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:52880432 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:109242528 C>T maps to NM_018061.2 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:109238667 C>T maps to NM_018061.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:109241946 C>T maps to NM_018061.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:109242528 C>T maps to NM_018061.2 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:109238742 C>T maps to NM_018061.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:109242414 C>T maps to NM_018061.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:45578917 C>T maps to NM_017922.3 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr14:45577688 G>A maps to NM_017922.3 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr14:45564522 T>C maps to NM_017922.3 H27H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:45571878 G>A maps to NM_017922.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:116038991 T>C maps to NM_004697.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:116041387 G>A maps to NM_004697.3 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:116038823 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:153526817 G>T maps to ENST00000410080 Y583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:50030622 G>A maps to NM_001031698.1 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr12:50031302 C>G maps to NM_001031698.1 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr12:50031272 T>C maps to NM_001031698.1 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:50027855 C>T maps to NM_001031698.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:50029726 G>A maps to NM_001031698.1 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr6:4049305 C>G maps to NM_003913.4 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:4041036 C>T maps to NM_003913.4 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:4044124 C>T maps to NM_003913.4 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:4032371 C>T maps to NM_003913.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:4032425 C>T maps to NM_003913.4 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr20:62626420 T>C maps to NM_012469.3 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:62664258 C>T maps to NM_012469.3 C913C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:62642792 C>T maps to NM_012469.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:62654210 C>T maps to NM_012469.3 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:1557249 G>A maps to NM_006445.3 I2016I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:1565228 G>T maps to NM_006445.3 G1331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:1565372 C>T maps to NM_006445.3 E1283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:1557249 G>T maps to NM_006445.3 I2016I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:1577959 C>A maps to NM_006445.3 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:1577886 A>G maps to NM_006445.3 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:1582174 C>A maps to NM_006445.3 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:1582964 C>T maps to NM_006445.3 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:1554823 G>T maps to NM_006445.3 I2178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:1576785 G>A maps to NM_006445.3 F1174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:1561585 G>A maps to NM_006445.3 I1822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:1585430 G>A maps to NM_006445.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:1554501 G>A maps to NM_006445.3 Y2251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:1554106 G>A maps to NM_006445.3 L2333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:49690962 C>T maps to ENST00000451891 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:106871946 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:106884313 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:106882702 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:106890931 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:18066811 C>T maps to NM_175886.2 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:18067213 G>A maps to NM_175886.2 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr23:12837721 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12817417 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12828145 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12828246 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12838852 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:12828324 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:12828324 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:12817517 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:18832161 A>G maps to NM_002767.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:57247131 C>T maps to NM_018304.3 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:57262417 C>T maps to NM_018304.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50102761 G>A maps to NM_020719.1 T1304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:50128231 C>T maps to NM_020719.1 S1951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:50103064 C>T maps to NM_020719.1 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:30664067 C>A maps to NM_024031.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr16:30667467 C>T maps to NM_024031.2 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:46030399 G>A maps to NM_024320.2 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:120021929 A>C maps to NM_016644.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:120021794 G>A maps to NM_016644.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:42813939 G>A maps to NM_199285.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:240981422 G>T maps to NM_001080835.1 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:5783261 G>A maps to NM_001134316.1 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:5783603 G>A maps to NM_001134316.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:5783660 C>T maps to NM_001134316.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:138724663 G>A maps to NM_001134659.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr3:138724642 G>A maps to NM_001134659.1 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:138724462 G>A maps to NM_001134659.1 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:138739101 G>A maps to NM_001013650.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr3:138739155 G>A maps to NM_001013650.2 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:138738765 C>A maps to NM_001013650.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:138738768 G>A maps to NM_001013650.2 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:138763171 G>A maps to NM_001134657.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V7-01A-21D-A122-09 chr3:138762997 G>A maps to NM_001134657.1 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:10999862 A>G maps to NM_007244.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:10999732 G>A maps to NM_007244.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr22:45128210 G>A maps to ENST00000352766 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr22:45133112 C>T maps to NM_001198721.1 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:45218316 C>T maps to ENST00000352766 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:36467950 G>A maps to NM_001160167.1 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:126874754 C>T maps to ENST00000330542 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:37285111 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr23:37312735 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:37312718 C>A did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:37312840 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:150869124 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:150869311 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:150873775 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:150869131 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:150869136 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:150873843 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:150868542 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:150869030 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:150869465 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:150873794 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr23:150868654 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:150873800 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:170695425 C>T maps to NM_022716.2 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:170688904 C>T maps to NM_022716.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:142458436 C>T maps to ENST00000486171 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:142460771 C>A maps to ENST00000486171 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr7:142459720 C>T maps to ENST00000486171 Y113Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:119239662 G>A maps to NM_003619.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:119204000 C>A maps to NM_003619.3 G769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:119229693 C>A maps to NM_003619.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:27222906 C>T maps to NM_005865.3 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:27222601 C>A maps to NM_005865.3 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:27220720 C>T maps to NM_005865.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr6:27222550 G>A maps to NM_005865.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:27220720 C>T maps to NM_005865.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:27215727 C>T maps to NM_005865.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:2905692 G>A maps to NM_022119.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:86519542 A>G maps to NM_007173.4 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:86519255 C>T maps to NM_007173.4 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:86518777 T>C maps to NM_007173.4 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:2763672 G>A maps to NM_031948.3 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:33795588 C>T maps to NM_002771.3 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:84234197 C>T maps to NM_153362.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:84233721 T>C maps to NM_153362.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:84234101 C>T maps to NM_153362.2 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr16:31159944 G>A maps to NM_173502.3 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:31154787 G>A maps to NM_173502.3 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:31151683 G>T maps to NM_173502.3 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:228004927 C>A maps to NM_183062.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:228004927 C>A maps to NM_183062.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:228033773 C>A maps to NM_183062.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:228033726 C>T maps to NM_183062.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:228005170 C>A maps to NM_183062.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:228003869 C>T maps to NM_183062.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:152204387 G>T maps to NM_183375.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:31097750 G>T maps to NM_001039503.2 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:58324966 G>A maps to NM_001080492.1 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:58318586 G>T maps to NM_001080492.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:58318586 G>A maps to NM_001080492.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:58314649 T>C maps to NM_001080492.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:10388873 C>T maps to NM_198464.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:10388876 C>T maps to NM_198464.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr8:10396218 G>A maps to NM_198464.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr8:10388837 C>T maps to NM_198464.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:31143833 G>A maps to NM_002773.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:31144177 G>A maps to NM_002773.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:25226196 G>A maps to NM_020200.5 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:25231293 C>T maps to NM_020200.5 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:25226157 T>A maps to NM_020200.5 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:55933314 G>A maps to NM_173814.4 C711C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:55964706 C>T maps to NM_173814.4 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:55971562 C>A maps to NM_173814.4 G352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:56032721 G>A maps to NM_173814.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:56032578 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:151006280 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:79322689 C>T maps to NM_015225.2 V1500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:79320709 G>A maps to NM_015225.2 L2160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:79323979 G>A maps to NM_015225.2 D1070D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:79324125 G>A maps to NM_015225.2 R1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:79267456 G>T maps to NM_015225.2 I2833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:79270372 G>A maps to NM_015225.2 G2774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:79320988 C>T maps to NM_015225.2 A2067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:79322131 A>C maps to NM_015225.2 G1686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:79322515 G>T maps to NM_015225.2 S1558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr9:79320471 G>A maps to NM_015225.2 Q2240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr9:79259685 G>A maps to NM_015225.2 I2899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:79319791 G>T maps to NM_015225.2 S2466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:79320910 G>A maps to NM_015225.2 C2093C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:79322527 T>C maps to NM_015225.2 S1554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:79318530 G>A maps to NM_015225.2 L2666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr9:79322614 G>A maps to NM_015225.2 A1525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:40904490 G>A maps to NM_020956.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:40904649 G>A maps to NM_181882.2 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:40901300 C>T maps to NM_181882.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:40902278 C>T maps to NM_181882.2 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:40901777 G>A maps to NM_181882.2 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:40902655 C>A maps to NM_181882.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:40902659 C>T maps to NM_181882.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:40901828 C>T maps to NM_181882.2 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:40903084 G>A maps to NM_181882.2 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:73585486 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:73590887 C>A maps to ENST00000373120 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:80919839 A>G maps to ENST00000421149 K172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:80923404 C>T maps to ENST00000421149 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr9:80932597 C>T maps to ENST00000421149 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:80923440 C>T maps to ENST00000421149 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr8:143763381 G>A maps to ENST00000301258 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:104163160 C>T maps to NM_002779.3 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:104170823 G>A maps to NM_002779.3 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr10:104164483 C>A maps to NM_002779.3 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:104173860 G>A maps to NM_002779.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:104174836 C>A maps to NM_002779.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:104163633 C>A maps to NM_002779.3 E937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr5:139193807 C>A maps to NM_032289.2 S292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:139216554 G>T maps to NM_032289.2 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:18725214 T>A maps to ENST00000440756 K535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:18656819 G>A maps to ENST00000440756 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:18729178 G>A maps to ENST00000440756 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:18432687 G>A maps to ENST00000440756 N865N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:18623005 G>A maps to ENST00000440756 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:18725355 C>A maps to ENST00000440756 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:18729949 C>A maps to ENST00000440756 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr8:18729299 C>T maps to ENST00000440756 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:18490284 C>A maps to ENST00000440756 E752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr2:113956356 T>C maps to NM_012455.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:113955138 A>G did not map to a codon.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr2:113956733 G>A maps to NM_012455.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:113951181 C>A maps to NM_012455.2 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:113940359 C>T maps to NM_012455.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:73683936 C>T maps to NM_000021.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr14:73659519 G>A maps to NM_000021.3 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:73653577 T>G maps to NM_000021.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:227083145 C>T maps to ENST00000391872 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:227075811 C>T maps to ENST00000391872 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:43382341 A>G maps to NM_006905.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:43348514 G>T maps to ENST00000449000 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr19:43528918 T>C maps to ENST00000306308 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:43528849 G>T maps to ENST00000306308 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:43519484 G>T maps to ENST00000306308 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:43570711 T>C maps to NM_031246.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:43585056 C>A maps to ENST00000449000 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:43234002 T>G maps to NM_021016.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:43233452 G>A maps to NM_021016.3 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:43234055 G>A maps to NM_021016.3 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:43233350 G>A maps to NM_021016.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr19:43242874 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:43233278 G>T maps to NM_021016.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:43698747 T>C did not map to a codon.
Alternatively spliced codon TCGA-D1-A103-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr19:43420280 T>C maps to NM_002782.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr19:43268332 G>A maps to NM_182707.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:43763080 C>A maps to NM_002784.3 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:43762513 C>T maps to NM_002784.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:15471301 G>A maps to ENST00000380715 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:15472666 G>A maps to NM_001128217.1 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr9:15474201 C>T maps to NM_001128217.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:15486002 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:87076214 G>A maps to ENST00000276616 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:87076850 G>T maps to ENST00000276616 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:14535412 G>A maps to NM_148976.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:14535994 G>A maps to NM_148976.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:14535412 G>A maps to NM_148976.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:14539449 A>G maps to NM_148976.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:14540583 G>A maps to NM_148976.2 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:42957375 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:42964340 C>A maps to NM_002787.4 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:58727702 C>T maps to NM_002788.2 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr14:58724680 T>C maps to NM_002788.2 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:58738594 A>T maps to NM_002788.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:58734217 C>T maps to NM_002788.2 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:58727738 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:109953691 G>A maps to NM_002790.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:60712431 A>G maps to NM_002792.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:23713973 C>T maps to NM_144662.2 D15D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:170844376 G>A maps to NM_002793.3 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr16:67968567 G>A maps to NM_002801.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:36101916 G>A maps to NM_002794.4 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:151372944 A>G maps to NM_002796.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:23502643 C>T maps to NM_002797.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr17:4701063 G>A maps to NM_002798.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr17:4700731 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:4701344 C>A maps to NM_002798.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:127115900 T>C maps to NM_002799.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:32809341 A>C maps to NM_148919.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:90730064 A>G maps to NM_002802.2 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:90729660 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:90729735 G>T maps to NM_002802.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:103008399 C>T maps to NM_002803.2 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:103004747 C>T maps to NM_002803.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:47441876 C>T maps to NM_002804.4 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:47446716 G>T maps to NM_002804.4 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:47440466 C>T maps to NM_002804.4 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:40729245 G>T maps to NM_016556.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:40725567 G>A maps to NM_016556.2 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:40480304 C>T maps to NM_006503.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:61907803 C>T maps to NM_002805.5 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:61907803 C>T maps to NM_002805.5 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:61907824 T>C maps to NM_002805.5 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:53175534 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:53175043 G>T maps to NM_002806.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:231941834 C>T maps to NM_002807.3 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:232035368 C>T maps to NM_002807.3 I935I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:231949807 C>T maps to NM_002807.3 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:231937052 C>T maps to NM_002807.3 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:107331303 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107330976 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:107331185 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:107330980 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr23:107328208 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:30804555 C>T maps to NM_002815.2 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:65344683 G>T maps to NM_002816.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:65346382 G>A maps to NM_002816.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:65346382 G>A maps to NM_002816.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:65337162 G>A maps to NM_002816.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:65344740 C>T maps to NM_002816.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:248824 C>T maps to NM_002817.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:162242048 G>A maps to NM_005805.4 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:162224371 C>A maps to NM_005805.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:162251666 G>T maps to NM_005805.4 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr2:162175371 T>C maps to NM_005805.4 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:184023647 G>A maps to NM_002808.3 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:184026567 T>C maps to NM_002808.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:184022092 C>T maps to NM_002808.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:38151781 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:38146392 G>A maps to NM_002809.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:38140707 C>T maps to NM_002809.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr9:123580189 G>A maps to NM_005047.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:123583116 C>T maps to NM_005047.2 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:123586958 G>A maps to NM_005047.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:123589135 G>A maps to NM_005047.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:123589135 G>A maps to NM_005047.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:123586958 G>A maps to NM_005047.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:123595732 C>A maps to NM_005047.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:123589148 A>G maps to NM_005047.2 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr3:64008409 C>T maps to ENST00000492933 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:74338217 G>A maps to NM_002811.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:74334090 G>A maps to NM_002811.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:74334090 G>A maps to NM_002811.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr16:74338293 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:38869924 C>T maps to NM_002812.4 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:38872858 C>T maps to NM_002812.4 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr12:122340976 G>A maps to NM_002813.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24613225 T>C maps to ENST00000429021 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:24615431 C>T maps to ENST00000429021 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:54125011 G>A maps to NM_014614.2 R1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:54159831 G>A maps to NM_014614.2 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:54119979 A>G maps to NM_014614.2 L1386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:54146298 T>C maps to NM_014614.2 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:54135702 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:54114531 A>G maps to NM_014614.2 P1531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:1106169 G>A maps to NM_006814.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr20:1108136 G>A maps to NM_006814.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:40550510 G>A maps to NM_003720.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr13:20346593 A>G maps to NM_001042414.1 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:20251930 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:20346536 C>T maps to NM_001042414.1 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:20315771 C>A maps to NM_001042414.1 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:20346380 C>T did not map to a codon.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr13:20346551 G>A maps to NM_001042414.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr13:20279933 A>G maps to NM_001042414.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:20304416 G>A maps to NM_001042414.1 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:20356737 C>A maps to NM_001042414.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:109823731 G>T maps to ENST00000409138 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:109824252 G>A maps to ENST00000409138 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:77317659 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:77310517 C>T maps to NM_003978.3 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:43591154 G>A maps to NM_024430.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:43571881 C>T maps to NM_024430.3 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:28477016 G>A maps to NM_001164721.1 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:72347117 G>A maps to NM_001099666.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:807900 C>T maps to NM_002819.4 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:806557 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:804204 C>T maps to NM_002819.4 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:804371 C>T maps to NM_002819.4 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:805010 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:804914 C>T maps to NM_002819.4 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:97272006 C>T maps to ENST00000370197 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:97217024 G>A maps to ENST00000370197 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:97216991 C>T maps to ENST00000370197 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:99030945 G>A maps to NM_001198879.1 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:99032598 A>G maps to NM_001198879.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:99022549 G>A maps to NM_001198879.1 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:71622475 G>A maps to NM_024754.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:86360380 T>C did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:86364215 C>A maps to NM_017952.5 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:86335627 G>T maps to NM_017952.5 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr2:86350883 C>T maps to NM_017952.5 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:86359496 C>T maps to NM_017952.5 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:98224212 T>A maps to NM_000264.3 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:98211389 G>A maps to NM_000264.3 I1255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:98224161 G>A maps to NM_000264.3 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:98242842 G>A maps to NM_000264.3 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:98215884 G>A maps to NM_000264.3 I1108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr9:98231084 G>T maps to NM_000264.3 S733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:98209262 C>T maps to NM_000264.3 S1425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:98220555 G>A maps to NM_000264.3 I969I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:98209226 G>A maps to NM_000264.3 C1437C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:98218602 G>A maps to NM_000264.3 I1087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:98215773 G>A maps to NM_000264.3 F1145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:98232137 G>A maps to NM_000264.3 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:98209262 C>T maps to NM_000264.3 S1425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:98244447 C>A maps to NM_000264.3 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:98231278 G>A maps to NM_000264.3 Y668Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:45293862 A>G maps to NM_003738.4 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:45294719 G>A maps to NM_003738.4 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:45292044 C>T maps to NM_003738.4 A997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:45294915 G>T maps to NM_003738.4 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:23397777 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:23411078 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:23398110 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:23398343 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:23411152 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:23397826 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:23411465 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:23412225 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:23397873 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:23410773 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:23412218 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:23412107 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:23397938 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:23411554 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:23411963 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:23410888 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:23411150 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:23353268 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:23410761 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:23411050 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:23411059 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:23411728 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:11579453 C>T maps to NM_020780.1 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:11596622 G>A maps to NM_020780.1 R1353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:11562050 G>A maps to NM_020780.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:11562864 C>A maps to NM_020780.1 Y409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:11584047 C>A maps to NM_020780.1 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:11561153 G>A maps to NM_020780.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:11590006 T>C maps to NM_020780.1 I1031I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:11594592 C>T maps to NM_020780.1 I1177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:11594484 G>A maps to NM_020780.1 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr1:11580753 C>A maps to NM_020780.1 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:27702801 G>T maps to NM_001034842.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:27702264 G>T maps to NM_001034842.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr10:27702858 G>A maps to NM_001034842.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:27700741 G>T maps to NM_001034842.3 C402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr10:27703017 G>A maps to NM_001034842.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr10:27703173 C>T maps to NM_001034842.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr10:27702984 A>G maps to NM_001034842.3 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:27702915 C>T maps to NM_001034842.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:27687294 G>T maps to NM_001034842.3 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:97316405 G>A maps to NM_014754.1 W297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:97274423 C>T maps to NM_014754.1 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:97316363 T>C maps to NM_014754.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:488254 C>T maps to NM_030783.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:473909 T>C maps to NM_030783.1 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:488239 C>T maps to NM_030783.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr10:89717608 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:89692923 T>A maps to NM_000314.4 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:89653779 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr10:89653828 G>T maps to NM_000314.4 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:89720740 C>T maps to NM_000314.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr10:89720740 C>T maps to NM_000314.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr10:89725042 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:89711982 G>T maps to NM_000314.4 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:89720748 C>T maps to NM_000314.4 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr10:89717777 T>C did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr10:89692963 G>T maps to NM_000314.4 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr10:89690800 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JS-01A-11D-A10B-09 chr10:89692934 T>G maps to NM_000314.4 L140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:89624244 G>T maps to NM_000314.4 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr10:89725042 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr10:89692963 G>T maps to NM_000314.4 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:89717712 G>A maps to NM_000314.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:89720743 G>T maps to NM_000314.4 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr10:89685299 C>G maps to NM_000314.4 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:89624244 G>T maps to NM_000314.4 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:89725042 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr10:89692960 C>T maps to NM_000314.4 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr10:89717608 G>C did not map to a codon.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr10:89692995 C>G maps to NM_000314.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr10:89692786 G>T maps to NM_000314.4 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr10:89720649 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:89692952 T>G maps to NM_000314.4 L146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr10:89653819 G>T maps to NM_000314.4 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:89720748 C>T maps to NM_000314.4 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:89717694 C>A maps to NM_000314.4 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:89720748 C>T maps to NM_000314.4 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr10:89717752 A>T maps to NM_000314.4 K260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr10:89720856 C>G maps to NM_000314.4 Y336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:89624244 G>T maps to NM_000314.4 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr10:89692952 T>A maps to NM_000314.4 L146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr10:89720669 G>A maps to NM_000314.4 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr10:89692934 T>G maps to NM_000314.4 L140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:89711982 G>T maps to NM_000314.4 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:89692774 C>T maps to NM_000314.4 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr10:89624273 T>G maps to NM_000314.4 Y16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr10:89717694 C>G maps to NM_000314.4 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:89720856 C>A maps to NM_000314.4 Y336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr10:89690801 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr10:89712016 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:16526440 C>T maps to NM_030664.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:52741529 C>T maps to NM_000953.2 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr9:139875306 G>T maps to ENST00000224167 *225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr14:52781994 C>T maps to NM_000956.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:71512840 G>A maps to ENST00000354608 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:71513071 G>A maps to ENST00000354608 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr1:71478026 G>A maps to ENST00000354608 Y346Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:71512570 G>A maps to ENST00000354608 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:71512792 C>T maps to ENST00000354608 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:71513049 G>A maps to ENST00000354608 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:71478167 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:79002176 G>A maps to NM_000959.3 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:79002278 C>T maps to NM_000959.3 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:117503974 C>T maps to NM_020440.2 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:117529453 C>T maps to NM_020440.2 I835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr1:117509897 C>T maps to NM_020440.2 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:48164424 C>T maps to NM_000961.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:48156258 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr9:114348375 C>T maps to NM_001146108.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:114348375 C>T maps to NM_001146108.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr9:114348275 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:114348402 A>G maps to NM_001146108.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:74340772 G>A maps to NM_152444.2 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:125148755 C>T maps to NM_000962.2 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:125145786 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:125148812 C>T maps to NM_000962.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:186648496 G>A maps to NM_000963.2 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:186645266 G>T maps to NM_000963.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:13514032 G>T maps to NM_000315.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr3:46940034 C>A maps to ENST00000313063 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:46939866 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:46940058 G>T maps to ENST00000313063 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr3:46942521 C>T maps to NM_000316.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:46939387 G>A maps to NM_000316.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:209308222 A>G maps to NM_005048.2 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:209358023 G>A maps to NM_005048.2 W431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:28116380 G>A maps to ENST00000354417 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:141900788 C>T maps to NM_005607.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:141716244 C>T maps to NM_005607.4 Q756Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:141900821 G>T maps to NM_005607.4 Y27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:141753326 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:141762394 A>G maps to NM_005607.4 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:141745479 G>A maps to NM_005607.4 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr8:27308360 G>A maps to NM_004103.3 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:27297823 C>T maps to NM_004103.3 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:27288436 C>T maps to NM_004103.3 Y238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:27277503 C>A maps to NM_004103.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:27296577 C>A maps to NM_004103.3 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:27291043 C>A maps to NM_004103.3 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:27293269 C>T maps to NM_004103.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:27289826 G>A maps to NM_004103.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:27287615 C>T maps to NM_004103.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:62164011 C>T maps to NM_005975.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:62162251 C>T maps to NM_005975.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr6:43098060 G>A maps to NM_002821.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:43099885 C>T maps to NM_002821.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:43111239 C>T maps to NM_002821.3 A711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:43111254 C>A maps to NM_002821.3 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:43126670 G>A maps to NM_002821.3 V946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:43106920 C>T maps to NM_002821.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:43126631 G>A maps to NM_002821.3 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:6878782 G>A maps to NM_002824.4 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr12:6879329 A>G maps to NM_002824.4 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:136936136 C>T maps to NM_002825.5 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr19:50363364 C>T maps to NM_017432.3 N388N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr19:50363334 C>T maps to NM_017432.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:50361834 G>A maps to NM_017432.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:50361819 G>A maps to NM_017432.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:64289209 C>T maps to NM_003463.3 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:96857614 C>T maps to ENST00000434261 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:96863861 C>T maps to ENST00000434261 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:96857614 C>T maps to ENST00000434261 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:96870207 C>A maps to ENST00000434261 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:96860862 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:17641287 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:65864666 C>A maps to NM_016395.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:21015925 G>A maps to NM_001010915.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:123219413 G>A maps to NM_198402.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:49197850 C>T maps to NM_002827.2 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:49197867 C>T maps to NM_002827.2 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:49197897 C>T maps to NM_002827.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:49197850 C>T maps to NM_002827.2 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr12:112893821 T>C maps to ENST00000392596 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr12:112940030 G>A maps to ENST00000392596 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:77200460 G>T maps to NM_002835.3 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:77200463 G>T maps to NM_002835.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:77240120 G>T maps to NM_002835.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:87622953 G>T maps to NM_080685.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:87686579 C>T maps to NM_080685.2 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:87690980 C>T maps to NM_080685.2 R1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr4:87684280 G>T maps to NM_080685.2 G1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:87671635 T>C maps to NM_080685.2 F888F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr4:87672019 A>G maps to NM_080685.2 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:87655926 C>T maps to NM_080685.2 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:87662970 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:87695569 C>T maps to NM_080685.2 S1803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:87728797 C>T maps to NM_080685.2 F2282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:87728965 C>G maps to NM_080685.2 V2338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr4:87687591 C>T maps to NM_080685.2 R1422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:87720313 T>C maps to NM_080685.2 D2159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:87637690 C>T maps to NM_080685.2 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:87655549 T>C maps to NM_080685.2 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:87728978 C>T maps to NM_080685.2 R2343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:214557295 G>A maps to NM_005401.4 H634H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:214557373 G>T maps to NM_005401.4 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:214588019 G>A maps to NM_005401.4 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:214557277 G>T maps to NM_005401.4 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:214558057 A>G maps to NM_005401.4 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:214542937 G>A maps to NM_005401.4 R1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr1:214557613 C>T maps to NM_005401.4 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr1:214549669 G>A maps to NM_005401.4 N933N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:214638038 C>T maps to NM_005401.4 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:131117065 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:131128788 C>T maps to NM_014369.3 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:131128342 C>T maps to NM_014369.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:12794464 G>A maps to NM_002828.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr18:12817301 A>G maps to NM_002828.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:12802120 G>A maps to NM_002828.2 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr14:88945617 G>A maps to NM_007039.3 F719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:88951468 C>T maps to NM_007039.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:88935996 C>T maps to NM_007039.3 K1027K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:88974354 A>C maps to NM_007039.3 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:88946508 G>T maps to NM_007039.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:114380395 T>C maps to NM_015967.5 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:114362220 G>A maps to NM_015967.5 N779N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:114380973 C>A maps to NM_015967.5 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:114380973 C>A maps to NM_015967.5 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:47437677 G>T maps to NM_015466.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr3:47448221 G>A maps to NM_015466.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:112219589 G>A maps to NM_002829.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:112141790 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:112144048 G>T maps to NM_002829.3 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:112182878 G>A maps to NM_002829.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:112143963 G>A maps to NM_002829.3 R878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:112153416 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:112168787 G>A maps to NM_002829.3 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:112182741 G>A maps to NM_002829.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:112141679 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:112153771 G>A maps to NM_002829.3 R675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:112144048 G>A maps to NM_002829.3 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:112143963 G>A maps to NM_002829.3 R878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:120677643 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:120690014 C>A maps to NM_002830.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:120702817 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:120714640 G>A maps to NM_002830.2 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:120677745 G>A maps to NM_002830.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:120702777 G>T maps to NM_002830.2 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:120635107 G>T maps to NM_002830.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:120702655 G>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:120712790 T>C maps to NM_002830.2 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:18751284 T>C maps to NM_032781.3 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:18750528 G>A maps to NM_032781.3 H550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:18751320 G>T maps to NM_032781.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:18751410 C>A maps to ENST00000396166 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr11:18762245 G>A maps to NM_032781.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:18754195 G>T maps to NM_032781.3 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:18762296 C>T maps to NM_032781.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:18764892 C>T maps to NM_032781.3 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:18765570 G>A maps to NM_032781.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:18754805 G>T maps to NM_032781.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:7066905 C>T maps to ENST00000416215 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:202124737 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr1:202119437 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:75761274 G>A maps to NM_002833.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:75762283 A>G maps to NM_002833.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:75798323 A>G maps to NM_002833.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr15:75815502 T>C maps to NM_002833.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:3008483 C>T maps to NM_002836.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:2998525 C>T maps to NM_002836.3 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:3003364 C>T maps to NM_002836.3 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:3005227 C>T maps to NM_002836.3 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr20:3016503 C>T maps to NM_002836.3 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:2967462 C>T maps to NM_002836.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:2985770 C>T maps to NM_002836.3 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:3018745 T>C maps to NM_002836.3 I792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:3002791 C>T maps to NM_002836.3 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:2968578 C>T maps to ENST00000358719 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:71016382 C>T maps to NM_001109754.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:70990063 C>T maps to NM_001109754.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:70949045 A>G maps to NM_001109754.1 D1679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr12:70970309 A>G maps to NM_001109754.1 H898H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:71003572 A>G maps to NM_002837.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:198671582 C>A maps to ENST00000271610 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:198718617 C>A maps to ENST00000271610 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:198703467 G>T maps to ENST00000271610 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:198721724 G>A maps to ENST00000271610 R1111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:198687382 C>T maps to ENST00000271610 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:198665929 G>T maps to ENST00000271610 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:198719712 C>T maps to ENST00000271610 V1055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:8404585 C>T maps to NM_002839.3 A1387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr9:8528596 G>A maps to NM_002839.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:8518042 C>A maps to NM_002839.3 G450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:8319962 C>T maps to NM_002839.3 A1846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:8485846 G>A maps to NM_002839.3 Y990Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr9:8460541 G>A maps to NM_002839.3 D1248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:8465626 C>A maps to NM_002839.3 E1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:8376021 T>C maps to NM_002839.3 P1525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:8504273 T>C maps to NM_002839.3 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:129868018 G>A maps to NM_006504.4 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:129866454 C>T maps to NM_006504.4 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:129861419 A>G maps to NM_006504.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr10:129877826 C>T maps to NM_006504.4 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:129859201 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:129870442 G>T maps to NM_006504.4 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:129866454 C>T maps to NM_006504.4 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:44019190 G>A maps to NM_002840.3 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:44069100 C>T maps to NM_002840.3 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:44075092 G>A maps to NM_002840.3 S1299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:44058141 C>T maps to NM_002840.3 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:44071036 G>A maps to NM_002840.3 P1104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:44084834 C>T maps to NM_002840.3 C1536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:61975326 G>A maps to NM_002841.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:62248537 G>A maps to NM_002841.3 K875K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:62204615 C>T maps to NM_002841.3 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:61975386 G>A maps to NM_002841.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:62180830 G>A maps to NM_002841.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:62229529 C>T maps to NM_002841.3 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:62142876 C>T maps to NM_002841.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:62229544 G>T maps to NM_002841.3 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:62267267 C>T maps to NM_002841.3 R1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr3:62257125 G>A maps to NM_002841.3 W1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:55707971 C>A maps to NM_002842.3 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:55711613 G>A maps to NM_002842.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:55713637 G>A maps to NM_002842.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr19:55696970 G>A maps to NM_002842.3 H987H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:48149330 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:48185152 G>A maps to NM_002843.3 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr11:48146704 G>T maps to NM_002843.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:48161227 G>A maps to NM_002843.3 T781T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:48177583 G>A maps to NM_002843.3 P1117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr11:48157627 C>A maps to NM_002843.3 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:128643329 C>A maps to ENST00000368210 G117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:128312531 G>A maps to ENST00000368210 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr6:128840282 G>T maps to ENST00000368202 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr6:128319978 C>T maps to ENST00000368210 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr6:128505747 G>A maps to ENST00000368210 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr18:8406144 C>T maps to NM_001105244.1 Y1461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:8069819 T>C maps to NM_001105244.1 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:8069786 T>C maps to NM_001105244.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:8069838 C>T maps to NM_001105244.1 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:8076492 C>A maps to NM_001105244.1 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:8376501 C>A maps to NM_001105244.1 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr18:7955149 C>T maps to NM_001105244.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:8113645 G>A maps to NM_001105244.1 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:8253246 C>T maps to NM_001105244.1 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:7774264 A>G maps to NM_001105244.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr18:8296436 C>T maps to NM_001105244.1 Y942Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr18:8376549 C>T maps to NM_001105244.1 C1139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:8113687 C>T maps to NM_001105244.1 Y687Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:220166334 C>T maps to NM_002846.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:220160949 C>A maps to NM_002846.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:220161021 G>A maps to NM_002846.3 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:220167423 G>T maps to NM_002846.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:220167213 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr2:220172183 G>A maps to NM_002846.3 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:157341693 G>A maps to NM_002847.3 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:157691370 G>A maps to NM_002847.3 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:157997903 C>T maps to NM_002847.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:157396767 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:157414108 G>A maps to NM_002847.3 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:157475479 C>T maps to NM_002847.3 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:157341654 G>A maps to NM_002847.3 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr7:157449063 G>A maps to NM_002847.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:157341693 G>A maps to NM_002847.3 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:15704515 C>A maps to NM_030667.1 I823I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:15650275 T>G maps to NM_030667.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:15656963 C>T maps to NM_030667.1 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr12:15636975 C>T maps to NM_030667.1 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:15637131 A>G maps to NM_030667.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:71095096 C>T maps to NM_002849.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:71155264 C>A maps to NM_002849.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:71139847 C>A maps to NM_002849.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:71139847 C>A maps to NM_002849.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:71139847 C>A maps to NM_002849.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:5212059 G>A maps to NM_002850.3 P1657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:5212185 G>A maps to NM_002850.3 V1615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:5244287 G>A maps to NM_002850.3 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:5262974 C>A maps to NM_002850.3 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:5273522 G>A maps to NM_002850.3 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:5245952 T>C maps to NM_002850.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:5220021 G>A maps to NM_002850.3 F1231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:5231336 G>A maps to NM_002850.3 V713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:5245886 G>A maps to NM_002850.3 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:5256124 G>A maps to NM_002850.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:5210527 G>A maps to NM_002850.3 Y1813Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr20:40877409 G>A maps to ENST00000373198 N762N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:41408885 G>A maps to ENST00000373198 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:41306566 T>C maps to ENST00000373198 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:41408894 G>A maps to ENST00000373198 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr20:40730843 G>A maps to ENST00000373198 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:41306638 G>A maps to ENST00000373198 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:40980829 G>T maps to ENST00000373198 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:40714412 G>A maps to ENST00000373198 D1331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:40714424 G>A maps to ENST00000373198 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:40714424 G>A maps to ENST00000373198 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:40735479 G>A maps to ENST00000373198 I1134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr20:40735539 G>T maps to ENST00000373198 G1114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr1:29649896 C>A maps to NM_005704.4 Y1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:29602074 G>A maps to NM_005704.4 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:29606137 G>A maps to NM_005704.4 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:29651768 C>T maps to NM_005704.4 H1403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:29585170 C>T maps to NM_005704.4 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:29631891 G>A maps to NM_005704.4 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:29606137 G>A maps to NM_005704.4 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:29609286 G>A maps to NM_005704.4 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:29633658 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr7:121668611 C>A maps to NM_002851.2 C1665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:121650584 T>C maps to NM_002851.2 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:121652756 T>C maps to NM_002851.2 S1219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:121650422 T>G maps to NM_002851.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:121671534 C>T maps to NM_002851.2 V1696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:121695023 T>C maps to NM_002851.2 N2137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:121623863 C>T maps to NM_002851.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:121651424 G>A maps to NM_002851.2 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:121681021 C>T maps to NM_002851.2 V1930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:121682688 T>C maps to NM_002851.2 Y1943Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:121671534 C>T maps to NM_002851.2 V1696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:121616297 A>G maps to NM_002851.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr7:121638060 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr7:121612688 C>T maps to NM_002851.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:121652175 G>T maps to NM_002851.2 E1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:121650411 G>T maps to NM_002851.2 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:121671534 C>T maps to NM_002851.2 V1696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:121638046 T>C maps to NM_002851.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:159849388 C>T maps to NM_004219.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:159855639 G>A maps to NM_004219.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:46271540 G>A maps to NM_004339.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:157154736 G>A maps to NM_002852.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:1537464 G>T maps to NM_001013658.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:31465332 G>A maps to ENST00000373741 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr1:31465244 G>A maps to ENST00000373741 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:31452999 G>A maps to ENST00000373741 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:31478707 C>A maps to ENST00000373741 G274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:31426817 C>T maps to ENST00000373741 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:31479912 C>A maps to ENST00000373741 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:31465299 C>T maps to ENST00000373741 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:31454253 T>C did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:20494157 T>C maps to ENST00000361078 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:20507832 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:20483242 A>C maps to ENST00000361078 Y432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:20478389 T>C maps to ENST00000361078 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr2:20508089 G>A maps to ENST00000361078 Y258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr2:20463060 G>A maps to ENST00000361078 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44924203 G>A maps to NM_033224.3 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:30889260 G>A maps to NM_013357.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:30889533 G>A maps to NM_013357.2 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:132426054 C>T maps to NM_025215.5 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:61235924 C>A maps to NM_144709.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:61172244 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:61180143 T>C maps to NM_144709.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:125765267 A>G maps to NM_031307.3 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:125763750 C>A maps to NM_031307.3 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:125765681 C>A maps to NM_031307.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:105111265 C>A maps to NM_019042.3 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:105105796 G>T maps to NM_019042.3 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:105103128 G>A maps to NM_019042.3 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:105103128 G>A maps to NM_019042.3 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:44148232 C>T maps to NM_031292.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:44136325 C>T maps to NM_031292.3 Q432Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr12:44124340 G>T maps to NM_031292.3 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:44124466 C>T maps to NM_031292.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:1244875 T>C maps to NM_153339.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:45153327 C>T maps to NM_006505.3 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:99818807 C>T maps to NM_024070.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr7:99817896 A>G maps to NM_024070.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:99818868 C>T maps to NM_024070.3 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:119549236 A>G maps to NM_002855.4 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:119535723 G>A maps to NM_002855.4 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:45389192 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:45391389 G>A maps to NM_001042724.1 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:45381609 G>A maps to NM_002856.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:45389418 G>A maps to NM_001042724.1 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:45368669 G>A maps to NM_001042724.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:110845069 C>T maps to NM_015480.1 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:110852558 G>T maps to NM_015480.1 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:110852765 G>T maps to NM_015480.1 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:110830979 G>A maps to NM_015480.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161049491 G>A maps to NM_030916.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr1:161043569 G>T maps to NM_030916.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:108082571 T>C maps to NM_007062.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr12:108102921 C>T maps to NM_007062.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr21:45535192 C>T maps to NM_005049.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr21:45535213 C>T maps to NM_005049.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:45537716 G>T maps to NM_005049.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr21:45548492 C>T maps to NM_005049.2 D857D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:159520915 C>T maps to NM_001130864.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:159520999 C>T maps to NM_001130864.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:159519685 G>A maps to NM_001130864.1 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:134219443 C>T maps to NM_138499.3 C480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:1652392 G>A maps to NM_012293.1 Y1053Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:1647348 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:1652065 G>A maps to NM_012293.1 G1162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:1657453 G>A maps to NM_012293.1 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:1664725 G>A maps to NM_012293.1 D588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:1677538 G>A maps to NM_012293.1 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:1653181 G>A maps to NM_012293.1 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:1652404 C>T maps to NM_012293.1 E1049E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:1652662 C>T maps to NM_012293.1 E963E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr2:1652992 G>A maps to NM_012293.1 N853N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:1643194 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:1687499 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:1652896 G>A maps to NM_012293.1 C885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr8:52320919 C>T maps to NM_144651.4 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:52320931 C>T maps to NM_144651.4 A1084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:52232512 C>A maps to NM_144651.4 G1444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr8:52321075 G>T maps to NM_144651.4 Y1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:52321054 G>A maps to NM_144651.4 G1043G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:52320649 T>C maps to NM_144651.4 S1178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:52287203 A>C maps to NM_144651.4 L1215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:52323840 C>T maps to NM_144651.4 K677K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:52567294 C>A maps to NM_144651.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:58351612 C>T maps to NM_017771.3 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr3:58380795 C>T maps to NM_017771.3 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:58410680 C>T maps to NM_017771.3 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr20:32295751 G>A maps to NM_007238.4 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:120660723 G>A maps to NM_001080855.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:120651737 G>A maps to NM_001080855.1 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr12:120650353 G>A maps to NM_001080855.1 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:120650155 C>T maps to NM_001080855.1 K579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr12:120651942 G>A maps to NM_001080855.1 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:31213055 G>A maps to NM_013258.4 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:79893353 C>T maps to ENST00000432920 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:79893242 C>T maps to ENST00000432920 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:144689239 G>A maps to NM_023078.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr20:25255331 C>T maps to NM_002862.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:25257334 C>T maps to NM_002862.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr20:25274856 C>T maps to NM_002862.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr20:25261706 T>C maps to NM_002862.3 N454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:25260899 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:51376794 C>T maps to NM_002863.4 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:51379845 T>C maps to NM_002863.4 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:64518836 G>T maps to NM_005609.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:64525930 G>A maps to NM_005609.2 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:64519512 C>A maps to NM_005609.2 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:64514145 C>T maps to NM_005609.2 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:55838598 G>A maps to NM_015617.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:55838475 C>T maps to NM_015617.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:55881016 T>A maps to NM_015617.1 K12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:55838258 C>A maps to NM_015617.1 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr15:55838481 G>A maps to NM_015617.1 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:55838835 C>T maps to NM_015617.1 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:154931521 G>A maps to NM_138300.3 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:154931374 C>T maps to NM_138300.3 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:158911852 A>G maps to NM_152501.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:158906747 C>A maps to NM_152501.3 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:158911834 C>T maps to NM_152501.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:158906910 G>T maps to NM_152501.3 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:158913693 C>T maps to NM_152501.3 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:158943537 C>A maps to NM_152501.3 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:158908890 G>T maps to NM_152501.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:158908913 T>C maps to NM_152501.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:158913693 C>T maps to NM_152501.3 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:21614990 C>T maps to NM_024854.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:21598279 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:21608084 G>T maps to NM_024854.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:100144782 G>A maps to NM_032709.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:100152743 G>A maps to NM_032709.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr10:100159900 T>C maps to NM_032709.2 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:100159989 G>A maps to NM_032709.2 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:100150368 G>A maps to NM_032709.2 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:100159861 G>A maps to NM_032709.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:100157252 G>T maps to NM_032709.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:9311045 G>A maps to NM_002864.2 S1088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:9307427 G>A maps to NM_002864.2 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:9311057 G>A maps to NM_002864.2 G1084G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:9348973 G>A maps to NM_002864.2 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:9312535 A>G maps to NM_002864.2 T1045T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:9317963 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr12:9345290 T>A maps to NM_002864.2 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr20:3145117 A>G maps to NM_014731.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:49136578 T>C maps to NM_005051.1 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:49137862 C>T maps to NM_005051.1 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:49135853 C>T maps to NM_005051.1 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:49135654 C>T maps to NM_005051.1 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:163899876 C>T maps to ENST00000361752 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:37594508 G>A maps to NM_012413.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:37594508 G>A maps to NM_012413.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr2:37596907 C>T maps to NM_012413.3 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:37594547 C>T maps to NM_012413.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:37594508 G>A maps to NM_012413.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:37596907 C>T maps to NM_012413.3 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:37586916 T>C maps to NM_012413.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:46198902 C>A maps to NM_017659.3 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:133769000 C>T maps to NM_198180.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr9:133769000 C>T maps to NM_198180.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:133768892 C>T maps to NM_198180.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:122254181 T>C maps to NM_198179.2 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:122257961 C>T maps to NM_198179.2 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:122301667 C>T maps to NM_198179.2 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:122253994 C>A maps to NM_198179.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:122251586 C>A maps to NM_198179.2 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:122250726 T>C maps to NM_198179.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr3:49083878 A>G maps to NM_198880.1 Y550Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:49114381 C>T maps to NM_198880.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:74276782 G>A maps to NM_032134.1 L1305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:74287324 G>A maps to NM_032134.1 V995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:74276740 G>A maps to NM_032134.1 I1319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:74289247 G>A maps to NM_032134.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:74274254 G>A maps to NM_032134.1 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr17:74274128 G>A maps to NM_032134.1 S1520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:74276133 G>A maps to NM_032134.1 D1410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:74288461 T>G maps to NM_032134.1 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:74275152 C>A maps to NM_032134.1 E1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:74274149 G>A maps to NM_032134.1 F1513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr17:74271927 G>A maps to NM_032134.1 S1652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:107100260 T>C did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:107097073 C>T maps to NM_018292.4 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:107090881 T>G maps to NM_018292.4 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:32954117 T>G maps to NM_001076786.1 Y309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:32975577 T>C maps to NM_001076786.1 G1322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:32956713 A>C maps to NM_001076786.1 R1175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:32954657 G>A maps to NM_001076786.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:32976922 C>T maps to NM_001076786.1 R1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr11:32955236 C>A maps to NM_001076786.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:180151337 C>T maps to NM_002826.4 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr1:180151343 G>A maps to NM_002826.4 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:180163426 C>T maps to NM_002826.4 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:180163426 C>T maps to NM_002826.4 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:139103193 C>A maps to NM_181701.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:139103122 G>A maps to NM_181701.3 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:113789535 C>T maps to ENST00000485050 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:113786841 G>T maps to ENST00000485050 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:136473139 C>T maps to ENST00000409606 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr2:136396588 G>T maps to ENST00000409606 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:136362498 A>G maps to ENST00000409606 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr2:136409416 C>T maps to ENST00000409606 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:136399193 T>G maps to ENST00000409606 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr2:136409469 A>G maps to ENST00000409606 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:57648611 G>A maps to ENST00000438036 R1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:57648611 G>A maps to ENST00000438036 R1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr12:57663633 C>T maps to ENST00000438036 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:42969909 G>A maps to NM_178491.2 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:26332690 C>T maps to NM_016131.4 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:37729301 G>T maps to NM_001002814.2 P1006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:37729010 G>T maps to NM_001002814.2 I1103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:37732352 G>T maps to NM_001002814.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:37732817 C>T maps to NM_001002814.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:37734870 G>A maps to NM_001002814.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:37730048 C>T maps to NM_001002814.2 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:37732283 C>T maps to NM_001002814.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr10:119799985 G>A maps to ENST00000369199 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:119798619 G>A maps to ENST00000369199 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:119768654 C>A maps to ENST00000369199 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:119798664 T>C maps to ENST00000369199 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:119798705 C>A maps to ENST00000369199 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:570823 C>T maps to NM_014700.3 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:532622 T>C maps to NM_014700.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:521367 C>T maps to NM_014700.3 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:29849022 G>A maps to NM_032932.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:29848210 G>A maps to NM_032932.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr17:29848989 T>G maps to NM_032932.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:29855768 C>T maps to NM_032932.3 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:73316112 C>T maps to NM_015470.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:73315538 G>A maps to NM_015470.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:73315740 C>T maps to NM_015470.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr2:73315307 G>T maps to NM_015470.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr2:73302804 G>A maps to NM_015470.2 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:8638253 C>A maps to NM_001025300.2 C243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:8636336 C>T maps to NM_001025300.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr1:153955754 G>T maps to NM_002870.2 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:65415098 C>T maps to ENST00000436278 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:65419254 G>A maps to NM_198686.2 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:65417854 G>A maps to NM_198686.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:238483763 C>T maps to NM_022449.3 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:27793919 G>T maps to ENST00000423465 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:27822880 G>T maps to NM_021252.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:27822775 C>T maps to NM_021252.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:65318184 G>A maps to NM_004161.4 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:65316075 C>T maps to NM_004161.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:65315767 C>T maps to NM_004161.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:65318184 G>A maps to NM_004161.4 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:111176268 G>A maps to NM_017817.1 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr13:111176302 C>T maps to NM_017817.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr20:56928526 C>T maps to NM_020673.2 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:56928573 A>G maps to NM_020673.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr20:56929277 C>T maps to NM_020673.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:57072498 T>C maps to NM_016277.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:57061345 A>C maps to NM_016277.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:176729179 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:156039960 G>A maps to NM_020387.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:55497736 C>A maps to NM_183235.1 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:52546598 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr4:13462368 G>A maps to NM_004249.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TD-01A-11D-A10B-09 chr4:13462413 G>A maps to NM_004249.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:13371493 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:21943025 C>T maps to NM_032846.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr18:9775297 C>T maps to NM_006868.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr18:9775345 T>C maps to NM_006868.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:129318674 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129318524 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:129306242 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:140393922 C>A maps to NM_031296.1 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:27041669 A>G maps to NM_001144943.1 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:27041618 G>A maps to ENST00000413526 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:120535081 C>T maps to NM_006861.6 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:120534944 C>A maps to ENST00000427416 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72739297 C>T maps to NM_001006638.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr17:72725495 C>T maps to NM_175738.4 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:87847221 C>T maps to NM_022337.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:87883055 G>A maps to NM_022337.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:154490100 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:154490500 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154490100 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:154493496 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154490266 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:18308465 G>A maps to NM_002866.4 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:52442681 G>T maps to NM_002867.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:58147069 C>T maps to NM_138453.2 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr19:11447997 T>G maps to NM_004283.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:135809896 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:135851218 T>C maps to NM_001172435.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:135893132 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:135872872 C>T maps to NM_001172435.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:220340661 G>A maps to ENST00000358951 Y1020Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:220324640 G>T maps to ENST00000358951 A1378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:220369720 G>T maps to ENST00000358951 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:220356239 C>A maps to ENST00000358951 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:220355696 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:220363445 C>T maps to ENST00000358951 K558K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:220330695 G>A maps to ENST00000358951 H1157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:220340694 G>A maps to ENST00000358951 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:220364575 C>A maps to ENST00000358951 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:220330776 C>T maps to ENST00000358951 A1130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:220364441 T>C maps to ENST00000358951 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:61674153 G>A maps to NM_013401.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:70194050 G>A maps to NM_175623.2 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:70194053 T>C maps to NM_175623.2 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:70149203 T>C maps to NM_175623.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:102755442 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:102754974 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:102755247 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:102755471 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102755389 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:102755288 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:102755392 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:102192552 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:102192653 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102192372 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:102192747 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102192976 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr23:102192540 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:102192954 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:102192997 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69504448 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69502431 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:69503874 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:69503806 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:69504448 G>A did not map to a codon.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr23:69502148 T>C did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:69502143 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:69502189 C>T did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:69504462 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:128810154 G>T maps to NM_198490.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:229438699 G>A maps to NM_004578.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:41292603 C>T maps to ENST00000419646 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:41292639 C>T maps to ENST00000419646 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:41292615 G>A maps to ENST00000419646 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr19:41289891 C>T maps to ENST00000419646 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:41286314 C>T maps to ENST00000419646 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:56385187 G>A maps to NM_002868.2 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:56380819 C>T maps to NM_002868.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:133557033 C>T maps to NM_016577.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:133553424 C>A maps to NM_016577.3 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:130738189 C>T maps to NM_032144.2 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:128516800 A>G maps to NM_004637.5 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:128532243 G>A maps to NM_004637.5 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:63548720 C>T maps to NM_016530.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:63541879 G>A maps to NM_016530.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:13727065 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:13727373 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:13726991 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13727373 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:13727052 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:13727252 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:13727257 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:103080497 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:103080649 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:103080469 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:103080168 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:103080465 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:103080519 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:103080473 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:5276634 G>A maps to NM_004703.4 Q637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:5250090 G>T maps to NM_004703.4 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:5250207 G>T maps to NM_004703.4 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:5268523 G>A maps to NM_004703.4 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:5212065 G>T maps to NM_004703.4 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:5238552 G>T maps to NM_004703.4 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:5250090 G>T maps to NM_004703.4 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:5280482 G>T maps to NM_004703.4 E700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:5212065 G>T maps to NM_004703.4 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:28925592 G>A maps to NM_024816.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:28919974 C>T maps to NM_024816.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:127969872 C>A maps to NM_005833.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:127975773 C>T maps to NM_005833.3 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:127982956 G>A maps to NM_005833.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:127996156 A>G maps to NM_005833.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:127965345 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:125782657 C>T maps to NM_012197.3 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:125852093 C>T maps to NM_012197.3 Q828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:125852603 C>T maps to NM_012197.3 N856N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:125748492 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:125772638 C>T maps to NM_012197.3 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:125835910 C>T maps to NM_012197.3 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:125752435 C>A maps to NM_012197.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:174668742 C>T maps to NM_014857.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:174210749 G>A maps to NM_014857.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:174606539 C>T maps to NM_014857.3 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:174200460 G>A maps to NM_014857.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:174668742 C>T maps to NM_014857.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:174363156 G>T maps to NM_014857.3 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:174671315 C>T maps to NM_014857.3 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:174340132 C>A maps to NM_014857.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:174247838 T>A maps to NM_014857.3 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:66236963 C>T maps to ENST00000451741 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:66273955 C>T maps to ENST00000451741 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:66270130 C>A maps to ENST00000451741 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr7:66273874 C>T maps to ENST00000451741 C577C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:24738117 A>C maps to NM_182836.1 L266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:24735636 G>A maps to NM_182836.1 N518N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr14:24737768 G>A maps to NM_182836.1 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:24738313 C>T maps to NM_182836.1 W229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:202850312 A>G maps to NM_002871.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:114398524 G>T maps to ENST00000409875 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:51208417 G>A maps to NM_001130923.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr22:51220635 G>A maps to NM_001130923.1 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:6441971 G>A maps to NM_018890.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:6438342 G>A maps to NM_018890.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:79991386 C>T maps to NM_005052.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:50386108 G>T maps to NM_013277.3 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr12:50400225 G>A maps to NM_013277.3 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:50393509 C>A maps to NM_013277.3 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:50387961 C>A maps to NM_013277.3 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:34908819 G>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:34914819 G>A maps to NM_002853.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:68695961 C>A maps to NM_133339.1 Y564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:68669670 T>C maps to NM_133339.1 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:8983270 C>A maps to NM_020165.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:8940614 C>A maps to NM_020165.3 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:117861196 A>G maps to NM_006265.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr8:117859870 C>T maps to NM_006265.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:117868975 G>T maps to NM_006265.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr19:13063594 C>T maps to NM_005053.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr19:13060222 G>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:110081147 G>A maps to NM_002874.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:110068823 G>A maps to NM_002874.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:110074007 G>A maps to NM_002874.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:110064334 T>C maps to NM_002874.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:131915614 G>T maps to NM_005732.3 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:131953873 C>T maps to NM_005732.3 R1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:131931410 C>T maps to NM_005732.3 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:131939091 G>T maps to NM_005732.3 E770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:131939632 A>C maps to NM_005732.3 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:4657955 C>T maps to NM_001130862.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:4652993 C>T maps to NM_001130862.1 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr12:4653046 A>G maps to NM_001130862.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr2:17698752 T>C maps to NM_001099218.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:17695302 C>A maps to NM_001099218.2 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:17698530 G>A maps to NM_001099218.2 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:17699117 C>A maps to NM_001099218.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:17695281 C>A maps to NM_001099218.2 G1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:17697675 G>T maps to NM_001099218.2 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:17695302 C>A maps to NM_001099218.2 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:56770149 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr12:1023672 C>T maps to NM_134424.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:95479761 T>C maps to NM_012415.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:95406083 C>A maps to NM_012415.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:95470576 C>A maps to NM_012415.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:95392608 G>A maps to NM_012415.2 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:95470505 T>C maps to NM_012415.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:46740344 C>T maps to NM_003579.3 R609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:46738373 G>A maps to NM_003579.3 K425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:46739887 G>T maps to NM_003579.3 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:46725744 C>T maps to NM_003579.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:46726622 C>T maps to NM_003579.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr1:46714182 G>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:51673505 C>T maps to NM_015106.2 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:51669728 G>A maps to NM_015106.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:51696691 C>T maps to NM_015106.2 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:51673631 C>T maps to NM_015106.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:51664397 C>T maps to NM_015106.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:51697405 C>T maps to NM_015106.2 D1458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:51675864 C>T maps to NM_015106.2 R778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:67163282 C>T maps to NM_004584.2 H182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:4856057 C>T maps to NM_018059.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr7:4874345 G>A maps to NM_018059.4 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:4875988 G>A maps to NM_018059.4 H261H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:55941949 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr20:55929872 G>T did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr20:55948637 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr20:55941930 C>T maps to NM_001015885.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:150240217 A>G maps to NM_001001788.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:150238092 G>A maps to NM_001001788.2 N320N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:150343350 G>A maps to NM_130900.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:150342233 C>T maps to NM_130900.2 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:150342212 T>C maps to NM_130900.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:12633235 C>T maps to ENST00000415519 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:12626117 C>T maps to ENST00000415519 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:12641190 G>A maps to ENST00000415519 H389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr3:12626105 C>T maps to ENST00000415519 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:36597013 C>T maps to NM_000448.2 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:36596126 G>T maps to NM_000448.2 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:36595937 G>T maps to NM_000448.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:36596003 G>T maps to NM_000448.2 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:36597628 G>A maps to NM_000448.2 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:36597695 G>T maps to NM_000448.2 E948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:36595981 C>A maps to NM_000448.2 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:36615379 A>G maps to NM_000536.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:36614194 T>C maps to NM_000536.3 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:36614848 G>A maps to NM_000536.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:17697344 G>A maps to ENST00000395776 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:17700293 C>T maps to ENST00000395776 F1344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:17701172 G>A maps to ENST00000395776 S1637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:17699828 C>A maps to ENST00000395776 V1189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:17699774 C>T maps to ENST00000395776 C1171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:17700053 G>A maps to ENST00000395776 E1264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:34796115 A>G maps to NM_001145521.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr5:34824013 C>T maps to NM_001145521.1 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:34824553 C>T maps to NM_001145521.1 Y869Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:34823798 C>T maps to NM_001145521.1 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:34823926 G>A maps to NM_001145521.1 E660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:17818976 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:17819457 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:17819982 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:17818976 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:17818544 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:17818976 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:17819856 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:17819662 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr23:17819514 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:17819573 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:17819908 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZP-01A-21D-A10M-09 chr23:17819812 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:17820052 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:39745748 C>T maps to NM_005402.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:39745748 C>T maps to NM_005402.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:39745742 G>T maps to NM_005402.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:39745748 C>T maps to NM_005402.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:121043569 C>T maps to NM_002881.2 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr2:121047206 C>T maps to NM_002881.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr18:9524623 A>G maps to NM_006788.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:9517300 G>T maps to NM_006788.3 G235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:9524600 C>T maps to NM_006788.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:9513180 G>A maps to NM_006788.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr14:36041792 G>A maps to NM_194301.2 F1941F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr14:36008843 A>G maps to NM_194301.2 D2052D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:36154162 A>C maps to NM_194301.2 A916A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:36143791 G>T maps to NM_194301.2 S1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:36155764 G>A maps to NM_194301.2 R848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:36096434 C>A maps to NM_194301.2 E1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:36097065 G>A maps to NM_194301.2 S1523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:36143907 A>G maps to NM_194301.2 S1038S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:36240205 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr20:20563838 G>A maps to NM_020343.3 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:20484006 G>T maps to NM_020343.3 S1732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:20493272 G>A maps to NM_020343.3 F1580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:20553674 G>A maps to NM_020343.3 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:20601238 T>C maps to NM_020343.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:20505472 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr20:20596787 A>G maps to NM_020343.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:20571958 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:20601237 T>G maps to NM_020343.3 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr20:20618075 G>A maps to NM_020343.3 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr20:20553671 G>A maps to NM_020343.3 A916A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr20:20493272 G>A maps to NM_020343.3 F1580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr20:37161461 C>T maps to NM_020336.2 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr20:37150143 T>C maps to NM_020336.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:37174999 T>C maps to NM_020336.2 H943H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr20:37154551 A>G maps to NM_020336.2 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:129728196 C>T maps to NM_014636.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:129815211 C>T maps to NM_014636.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:129831561 G>A maps to NM_014636.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:178875974 T>C maps to NM_152663.3 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:178855202 G>A maps to NM_152663.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:178780472 G>A maps to NM_152663.3 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:178846733 C>T maps to NM_152663.3 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:178846733 C>T maps to NM_152663.3 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:32664565 C>T maps to NM_016732.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:32664565 C>T maps to NM_016732.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:85799837 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:85799947 C>T maps to NM_001100391.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr8:85441645 G>A maps to NM_001100391.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:40914632 A>G maps to ENST00000456272 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:40914460 C>T maps to ENST00000456272 C89C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:67778251 G>A maps to NM_020850.1 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:67761725 G>A maps to NM_020850.1 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:170343497 G>A maps to NM_022897.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:170648816 G>T maps to NM_022897.3 E799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr5:170351477 C>T maps to NM_022897.3 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:109370340 G>T maps to NM_006267.4 E706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:109371462 C>T maps to NM_006267.4 R769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:109400236 G>A maps to NM_006267.4 K3185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:109381653 A>G maps to NM_006267.4 L1553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:109399205 C>A maps to NM_006267.4 S3086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:109383154 G>T maps to NM_006267.4 E2054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:109381386 T>C maps to NM_006267.4 L1464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:109370331 G>T maps to NM_006267.4 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:109380661 A>C maps to NM_006267.4 R1223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:109374978 G>A maps to NM_006267.4 Q859Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:109388277 C>T maps to NM_006267.4 F2657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:5925721 G>A maps to NM_007322.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:5918572 G>A maps to NM_007322.2 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:5941689 G>A maps to NM_007322.2 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:36251469 G>A maps to NM_001161429.1 C458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:36260952 C>A maps to NM_001161429.1 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr9:6012535 G>C maps to NM_012416.2 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:6012448 T>C maps to NM_012416.2 G1053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:6013425 G>A maps to NM_012416.2 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:6015091 G>A maps to NM_012416.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:6015300 G>A maps to NM_012416.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:6014707 C>T maps to NM_012416.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:6012212 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:6013450 C>T maps to NM_012416.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:13642737 C>A maps to NM_005493.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr6:13622614 T>C maps to NM_005493.2 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr22:41650389 C>T maps to NM_002883.2 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:41645344 C>T maps to NM_002883.2 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr17:8192117 G>A maps to NM_016492.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:112240088 T>A maps to NM_002884.2 C51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:112238013 G>T maps to NM_002884.2 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:69044197 G>T maps to NM_015646.4 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:69044217 C>T maps to NM_015646.4 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr12:69042551 G>A maps to NM_015646.4 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:69042542 C>T maps to NM_015646.4 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr1:21936747 G>A maps to NM_001145658.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:21938261 G>A maps to NM_001145658.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:21940144 G>A maps to NM_001145658.1 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:21940546 G>A maps to NM_001145658.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:2894656 C>T maps to NM_015085.4 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:2934291 G>A maps to NM_015085.4 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:99325713 G>T maps to NM_001100426.1 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:131348372 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:131351271 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:131348310 G>A did not map to a codon.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr23:131348374 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:131351259 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:131348203 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:131351068 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:134455675 G>A maps to NM_198679.1 L1037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:134465301 G>A maps to NM_198679.1 F778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr9:134467550 C>T maps to NM_198679.1 E735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr9:134504616 G>A maps to NM_198679.1 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:134526259 C>T maps to NM_198679.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:134463343 G>T maps to NM_198679.1 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:134471751 G>A maps to NM_198679.1 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr9:134514083 C>A maps to NM_198679.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr9:134497215 C>T maps to NM_198679.1 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:134459919 G>A maps to NM_198679.1 F931F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr9:134526253 T>C maps to NM_198679.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:134497311 G>A maps to NM_198679.1 N593N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:134514178 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:160252897 A>C maps to NM_014247.2 G403G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:160273837 C>T maps to ENST00000505026 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr4:160273950 C>A maps to NM_014247.2 S1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr4:160268127 C>T maps to NM_014247.2 P1069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:160251114 C>T maps to NM_014247.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:160253610 G>T maps to NM_014247.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:160253610 G>T maps to NM_014247.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:160251520 A>G maps to NM_014247.2 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:160253610 G>T maps to NM_014247.2 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr2:173830319 C>T maps to NM_007023.3 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:173659857 A>G maps to NM_007023.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr2:173883402 C>T maps to NM_007023.3 C676C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:173883522 C>A maps to NM_007023.3 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:173882185 C>T maps to NM_007023.3 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr2:173679122 C>T maps to NM_007023.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:22194136 G>A maps to ENST00000344041 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:22206737 C>T maps to ENST00000344041 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:22270523 C>A maps to ENST00000344041 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:22270532 C>A maps to ENST00000344041 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:22348028 T>C maps to ENST00000344041 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:22202098 A>G maps to ENST00000344041 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:22184732 C>A maps to ENST00000344041 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:22348030 C>A maps to ENST00000344041 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:130771675 G>A maps to NM_001164389.1 R1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:130883835 A>T maps to ENST00000514667 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr5:130764604 G>A maps to ENST00000514667 S1640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:130841145 A>G maps to ENST00000514667 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:130828286 T>C maps to ENST00000514667 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:130771775 T>C maps to NM_001164389.1 K1348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:130766822 G>A maps to ENST00000514667 D1448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:130797437 G>A maps to ENST00000514667 R992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38346999 C>T maps to ENST00000456989 R440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:204322266 C>A maps to ENST00000374493 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:204354747 C>T maps to ENST00000374493 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:25638037 G>A maps to NM_000965.3 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:25611345 G>A maps to NM_000965.3 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:25635011 A>C maps to NM_000965.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:25502751 C>T maps to NM_000965.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:25637917 G>A maps to NM_000965.3 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:53607926 C>T maps to NM_000966.4 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:53608384 G>A maps to NM_000966.4 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:158422609 G>T maps to NM_206963.1 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:150036170 C>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:150035811 C>A maps to NM_002889.3 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:167915735 C>T maps to NM_002887.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:167937679 G>T maps to NM_002887.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:167944984 C>A maps to NM_002887.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:88255352 G>A maps to NM_020320.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:88231219 G>A maps to NM_020320.3 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:88234360 C>T maps to NM_020320.3 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:88226594 G>A maps to NM_020320.3 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:88226546 G>A maps to NM_020320.3 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:86685340 G>A maps to NM_002890.1 Q1019Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:86649004 G>T maps to NM_002890.1 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:86667933 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr5:86672236 T>A maps to NM_002890.1 L680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:86672208 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:86672808 G>T maps to NM_002890.1 E766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:86645107 G>T maps to NM_002890.1 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:86649004 G>T maps to NM_002890.1 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:86679577 G>A maps to NM_002890.1 R913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:86645119 C>T maps to NM_002890.1 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:86674232 C>T maps to NM_002890.1 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:86637123 A>C maps to NM_002890.1 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:86665696 G>T maps to NM_002890.1 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:86685311 C>T maps to NM_002890.1 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:141289843 C>T maps to ENST00000452898 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:141299274 G>A maps to ENST00000452898 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr13:114793351 G>A maps to ENST00000389544 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:114782718 G>A maps to ENST00000389544 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:114751210 G>A maps to ENST00000389544 F775F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:113557226 G>T maps to NM_001193520.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:113539773 C>A maps to NM_001193520.1 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:178412232 G>T maps to ENST00000263528 E433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:178427225 T>C maps to ENST00000263528 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:178269182 G>A maps to ENST00000263528 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:178425911 A>C maps to ENST00000263528 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:178420746 G>T maps to ENST00000263528 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:178427460 C>A maps to ENST00000263528 R1001R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:178427156 C>A maps to ENST00000263528 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr1:178389707 C>T maps to ENST00000263528 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:178421572 G>T maps to ENST00000263528 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15565330 G>A maps to NM_022904.1 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:15562668 C>T maps to NM_022904.1 T991T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:15566940 G>T maps to NM_022904.1 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:15571018 C>T maps to NM_022904.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr19:15574875 C>T maps to NM_022904.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr22:35943098 C>T maps to NM_014310.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:85613320 T>C maps to NM_152573.2 E588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:85615855 T>C maps to NM_152573.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:85622385 G>A maps to NM_152573.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:85615381 G>T maps to NM_152573.2 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:85630719 C>T maps to NM_152573.2 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:85627405 G>A maps to NM_152573.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:85615939 G>A maps to NM_152573.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:85615852 G>A maps to NM_152573.2 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:85615863 G>A maps to NM_152573.2 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr9:85620366 G>A maps to NM_152573.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:43693553 A>G maps to ENST00000374459 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:82355801 G>A maps to NM_152545.1 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:179538514 G>A maps to NM_175062.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:179546376 G>A maps to NM_175062.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:79350699 G>A maps to NM_002891.4 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:79296447 C>T maps to NM_002891.4 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:79327524 G>T maps to NM_002891.4 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:79282602 T>C maps to NM_002891.4 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:79310204 G>A maps to NM_002891.4 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:80508285 C>T maps to NM_006909.1 C1086C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:80382719 C>T maps to NM_006909.1 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:80376532 C>A maps to NM_006909.1 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:80497243 C>T maps to NM_006909.1 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:80408452 C>T maps to NM_006909.1 D621D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:80388671 C>T maps to NM_006909.1 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr5:80369247 C>T maps to NM_006909.1 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:38791087 G>A maps to NM_005739.3 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:38852034 G>A maps to NM_005739.3 C69C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:38803815 C>A maps to NM_005739.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:38818584 G>A maps to NM_005739.3 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:38791058 C>T maps to NM_005739.3 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr15:38786723 A>G maps to NM_005739.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:64507149 C>T maps to ENST00000320253 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr11:64508415 G>A maps to ENST00000394430 C125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:64503025 C>T maps to ENST00000320253 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr11:64503136 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:33783811 G>A maps to NM_170672.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:33745703 T>C maps to NM_170672.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:33784045 G>A maps to NM_170672.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:38910637 G>T maps to ENST00000405332 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:38912675 G>A maps to ENST00000405332 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49228157 C>T maps to NM_017805.2 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr19:49230660 A>G maps to NM_017805.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:34068161 C>T maps to NM_033315.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:34067549 G>A maps to NM_033315.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:27847447 C>T maps to NM_206827.1 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:65357570 T>C maps to NM_016563.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr15:65350832 G>A maps to NM_016563.2 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:4766953 G>A maps to NM_014737.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:4771126 G>A maps to NM_014737.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:4766953 G>A maps to NM_014737.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:4771114 G>A maps to NM_014737.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr10:45479481 G>A maps to NM_032023.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:45487427 G>T maps to NM_032023.3 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:206757804 G>A maps to NM_182663.2 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:206757933 C>T maps to NM_182663.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:206760286 G>T maps to NM_182663.2 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:74450941 T>C maps to NM_201431.1 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:74447585 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:74442343 C>A maps to NM_201431.1 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr4:74459181 G>A maps to NM_201431.1 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:74442008 C>T maps to NM_201431.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:74453611 A>G maps to NM_201431.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:26217803 C>T maps to NM_001164747.1 C159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr12:26220563 C>T maps to NM_001164747.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:26217609 C>T maps to NM_001164747.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:86198959 G>A maps to NM_005447.3 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:86198962 A>C maps to NM_005447.3 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:86199529 G>A maps to NM_005447.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:86198721 C>A maps to NM_005447.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr12:86198605 A>G maps to NM_005447.3 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:86199678 C>A maps to NM_005447.3 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:86198721 C>A maps to NM_005447.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:86199123 G>A maps to NM_005447.3 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:10428162 C>T maps to NM_133452.2 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:10433410 G>C maps to NM_133452.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:10434173 C>T maps to NM_133452.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:65273142 G>T maps to ENST00000294428 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:56939652 C>T maps to NM_013435.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:56939637 G>A maps to NM_013435.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:56939763 C>T maps to NM_013435.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:56939700 C>T maps to NM_013435.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr13:48954197 C>T maps to NM_000321.2 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr13:48941647 C>T maps to NM_000321.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr13:49039505 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:48919243 G>T maps to NM_000321.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:48939040 T>C maps to NM_000321.2 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:49030384 G>A maps to NM_000321.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:49037928 C>A maps to NM_000321.2 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr13:49030384 G>A maps to NM_000321.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr13:49039205 C>T maps to NM_000321.2 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:48951074 G>T maps to NM_000321.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:48955516 G>T maps to NM_000321.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:48919243 G>T maps to NM_000321.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:48955516 G>T maps to NM_000321.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:53568593 T>C maps to NM_014781.4 K1265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:53574278 C>A maps to NM_014781.4 G392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:53586652 C>A maps to NM_014781.4 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr8:53536365 G>A maps to NM_014781.4 A1587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:53558287 G>A maps to NM_014781.4 R1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:53589008 G>A maps to NM_014781.4 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:53558287 G>A maps to NM_014781.4 R1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:53596248 C>A maps to NM_014781.4 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:53558287 G>A maps to NM_014781.4 R1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:5105036 C>A maps to NM_021163.3 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:33117530 A>G maps to NM_005610.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:205069346 C>A maps to NM_005057.3 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:205068200 C>A maps to NM_005057.3 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205057914 T>G maps to NM_005057.3 *539C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:205068200 C>A maps to NM_005057.3 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr16:24574803 C>T maps to NM_006910.4 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:24567768 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:24567140 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:24573143 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:24580273 C>T maps to NM_006910.4 R755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:24580684 C>T maps to NM_006910.4 R892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:24583225 G>A maps to NM_006910.4 K1613K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:24566994 G>A maps to NM_006910.4 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:24582751 A>G maps to NM_006910.4 K1455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:24582254 C>T maps to NM_006910.4 R1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:24573338 G>A maps to NM_006910.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:24582254 C>T maps to NM_006910.4 R1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:24578821 G>T maps to NM_006910.4 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:24564850 G>A maps to NM_006910.4 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:24582236 G>T maps to NM_006910.4 E1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:24583346 G>T maps to NM_006910.4 E1654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:24583346 G>T maps to NM_006910.4 E1654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:24582875 C>T maps to NM_006910.4 R1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:24581698 G>T maps to NM_006910.4 E1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:16871855 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:16875812 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:16876912 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:16871953 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:16887276 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:16870184 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:16871928 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:16887334 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr23:16875774 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:16867362 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:16871941 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:16870695 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:16876912 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:20573116 C>T maps to ENST00000360790 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:20602121 G>T maps to ENST00000360790 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr18:20576373 G>A maps to ENST00000360790 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:20516898 G>T maps to ENST00000360790 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:18474612 G>A maps to NM_006606.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr20:18476488 G>A maps to NM_006606.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:400054 C>A maps to NM_031229.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:28050541 G>A maps to NM_022128.1 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:35661094 A>G maps to NM_002895.2 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:35675476 C>T maps to NM_002895.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:35646735 C>A maps to NM_002895.2 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:53515636 C>T maps to NM_005611.3 R1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:53495698 G>T maps to NM_005611.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:53480954 C>T maps to NM_005611.3 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:53495698 G>T maps to NM_005611.3 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:53496516 G>T maps to NM_005611.3 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:53515708 G>T maps to NM_005611.3 E1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr16:53503979 C>T maps to NM_005611.3 Q710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:47041379 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47039842 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47045708 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:47030472 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:47039372 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47041362 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47044501 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47045564 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:47044741 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:47030497 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:47044712 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr23:47034470 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:47045695 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47006894 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:47045763 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47045662 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47006895 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:47039366 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr21:15599470 C>T maps to NM_144770.3 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:34241498 C>T maps to NM_001198838.1 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr20:34240547 T>C maps to NM_001198838.1 E899E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:34243010 T>C maps to NM_001198838.1 E78E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D1-A103-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr20:34242509 C>T maps to NM_001198838.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:94748136 C>A maps to NM_203390.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:94748071 A>G maps to NM_203390.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:66392816 G>A maps to NM_006328.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:66393143 G>A maps to NM_006328.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:66392336 C>A maps to NM_006328.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:66394093 C>A maps to NM_006328.3 Y655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:110884672 T>G maps to NM_022768.4 T882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:51430236 C>A maps to NM_013286.4 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:51430938 C>T maps to NM_013286.4 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr3:51430209 C>T maps to NM_013286.4 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:51430839 C>T maps to NM_013286.4 H670H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:51431058 C>T maps to NM_013286.4 D743D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:51430380 C>G maps to NM_013286.4 Y517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:6143328 G>A maps to NM_001145547.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:125004183 T>A maps to NM_033117.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:125014160 G>A maps to NM_033117.3 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:125014176 A>C maps to NM_033117.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:114358445 C>T maps to NM_016196.3 E785E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:114356246 G>A maps to NM_016196.3 H797H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:114383707 T>C maps to NM_016196.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr12:114377917 C>T maps to NM_016196.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:150072502 G>A maps to NM_018047.2 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:150076243 C>T maps to NM_018047.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:23371497 G>A maps to NM_001077351.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:23375465 C>T maps to NM_001077351.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:17281910 C>A maps to NM_001143942.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:17292145 C>T maps to NM_001143942.1 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr6:17292139 C>T maps to NM_001143942.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:73577663 G>A maps to NM_021239.2 E606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr14:73550245 C>T maps to NM_021239.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:73544151 G>T maps to NM_021239.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:79951536 C>A maps to ENST00000438737 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:79940774 A>G maps to ENST00000438737 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr13:79911349 G>A maps to ENST00000438737 R875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:145613011 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:145603075 G>T maps to NM_018989.1 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:145610218 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr5:145610440 C>T maps to NM_018989.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:145608583 G>T maps to NM_018989.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:145651213 G>T maps to NM_018989.1 E989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:127965929 G>A maps to NM_018077.2 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48433979 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:48435515 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48433957 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr23:48434774 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr7:155559267 C>T maps to NM_053043.2 C1098C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:155559267 C>T maps to NM_053043.2 C1098C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:155530775 G>A maps to NM_053043.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr7:155499635 G>A maps to NM_053043.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr7:155532605 G>A maps to NM_053043.2 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:155503967 G>A maps to NM_053043.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:155457911 G>A maps to NM_053043.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:235318411 C>T maps to NM_015014.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:34292629 A>G maps to NM_184234.1 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:34312575 G>A maps to NM_184234.1 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:66411236 T>C maps to NM_001198845.1 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:66407464 C>T maps to NM_002896.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:66411458 A>G maps to NM_001198845.1 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr11:66407319 G>A maps to NM_002896.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:66411419 C>T maps to NM_001198845.1 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:106359129 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:106331956 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:106332017 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:106310805 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:106359124 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:106331786 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:106331766 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:106312531 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:106332055 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:36124671 G>A maps to NM_024321.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:36125186 G>A maps to NM_024321.3 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr2:152107914 C>T maps to NM_198557.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:152108028 T>G maps to NM_198557.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:238726725 G>A maps to NM_001080504.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:238738021 G>A maps to NM_001080504.2 S922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:238726386 C>T maps to NM_001080504.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:238726663 G>T maps to NM_001080504.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:238742662 G>A maps to NM_001080504.2 Q971Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:238725760 G>T maps to NM_001080504.2 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr2:238726204 G>T maps to NM_001080504.2 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:178988952 G>T maps to ENST00000456670 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:178988318 G>A maps to ENST00000456670 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:178988969 G>A maps to ENST00000456670 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:155719111 C>T maps to NM_144979.3 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:155749197 C>A maps to NM_144979.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr4:155719155 A>G maps to NM_144979.3 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr4:155720030 T>A maps to NM_144979.3 Y239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:40428046 G>A maps to NM_001098634.1 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:40440316 G>A maps to NM_001098634.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:40440442 G>A maps to NM_001098634.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:40438529 C>A maps to NM_001098634.1 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:40440205 G>A maps to NM_001098634.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr4:40440651 G>A maps to NM_001098634.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:40440108 G>A maps to NM_001098634.1 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:40440445 G>A maps to NM_001098634.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:66436582 G>A maps to NM_031492.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:66436111 G>T maps to NM_031492.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:50148202 A>G maps to NM_005778.2 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:50151654 C>T maps to NM_005778.2 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr3:50151504 C>T maps to NM_005778.2 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:50091791 C>T maps to NM_005777.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:50095877 G>A maps to NM_005777.2 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:50112663 C>T maps to NM_005777.2 I1049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:50114527 C>T maps to NM_005777.2 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:50005100 G>A maps to NM_005777.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:50005970 G>A maps to NM_005777.2 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:50012814 G>A maps to NM_005777.2 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:50005748 G>A maps to NM_005777.2 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:114276433 C>T maps to NM_016090.2 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:161132195 G>A maps to NM_016836.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:161135121 G>A maps to NM_016836.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:56981447 G>A maps to NM_002898.3 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:29476238 C>A maps to NM_001003793.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:135956458 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135957423 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135961236 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135961578 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:135957702 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:135956317 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:135961585 T>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:135958687 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129546567 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129543229 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129545340 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:129545444 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:129546643 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:129536328 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:129546622 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:129543250 T>C did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:129546814 G>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:129546700 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:89448539 G>A maps to NM_019610.5 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:89448636 T>C maps to NM_019610.5 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:89448558 A>G maps to NM_019610.5 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:139173579 C>T maps to NM_004164.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:139195244 G>A maps to NM_004164.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:48382045 C>T maps to NM_002900.2 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:48383865 G>T maps to NM_002900.2 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr10:48383961 G>A maps to NM_002900.2 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:48382177 G>T maps to NM_002900.2 I1157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:48383976 G>A maps to NM_002900.2 I1085I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:48389545 G>A maps to NM_002900.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr10:48383987 T>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:48390466 G>A maps to NM_002900.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:7280846 G>A maps to NM_031491.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr20:43945484 C>T maps to NM_014276.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:43945223 C>T maps to ENST00000372741 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:43945427 C>T maps to NM_014276.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:43940865 C>T maps to NM_014276.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:173951906 A>G maps to NM_172071.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:173950063 G>A maps to NM_172071.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:173933138 C>T maps to NM_172071.2 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:173952772 A>T maps to NM_172071.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:173930904 T>C maps to NM_172071.2 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:125621234 G>A maps to NM_001100588.1 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:125652723 T>C maps to NM_001100588.1 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:125627701 G>A maps to NM_001100588.1 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:125611950 G>A maps to NM_001100588.1 N1177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr9:125613436 A>G maps to NM_001100588.1 N1101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:125611950 G>A maps to NM_001100588.1 N1177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:125612055 C>T maps to NM_001100588.1 Q1142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:125613502 G>T maps to NM_001100588.1 I1079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:125621358 C>T maps to NM_001100588.1 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr9:125642035 G>A maps to NM_001100588.1 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:35895990 G>T maps to NM_004414.5 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:46293150 G>T maps to NM_005822.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr6:46214542 G>A maps to ENST00000405162 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:24857724 C>A maps to NM_013441.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:24857808 G>A maps to NM_013441.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:50115932 C>T maps to NM_018191.3 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:50115125 C>T maps to NM_018191.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:50115949 G>A maps to NM_018191.3 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:50115947 T>C maps to NM_018191.3 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:50118957 C>A maps to NM_018191.3 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:49077013 C>T maps to NM_001268.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:28862488 C>A maps to NM_001048194.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:28863272 C>T maps to NM_001048194.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:28864438 C>T maps to NM_001048194.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:17755625 G>A maps to NM_018715.2 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr1:17743014 G>A maps to NM_018715.2 N329N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr1:17740147 G>A maps to NM_018715.2 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:17735629 C>A maps to NM_018715.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:76434126 C>A maps to NM_015436.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:4834226 C>G maps to NM_005772.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:4834208 C>A maps to NM_005772.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:4823587 G>A maps to NM_005772.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:32118702 C>T maps to NM_002901.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:50040294 G>T maps to NM_020650.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:50045996 C>T maps to NM_020650.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:103180846 G>T maps to NM_015156.2 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:103188615 C>T maps to NM_015156.2 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:103187379 G>T maps to NM_015156.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:167653238 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:167666383 C>T maps to NM_052862.3 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:167666433 G>A maps to NM_052862.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:167663455 C>T maps to NM_052862.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:167663514 C>T maps to NM_052862.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:9808263 G>A maps to NM_002903.2 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:9801503 C>A maps to NM_002903.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:9808122 G>A maps to NM_002903.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:9808122 G>A maps to NM_002903.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr6:31922643 G>A maps to ENST00000375425 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:74231398 C>A maps to NM_172037.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:74231353 G>A maps to NM_172037.3 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:74234917 G>T maps to NM_172037.3 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:74233304 C>T maps to NM_172037.3 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:74231353 G>A maps to NM_172037.3 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:68191258 C>T maps to NM_152443.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:68195906 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:55568111 G>A maps to NM_001145971.1 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:18736489 A>G maps to NM_020905.3 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:18737041 G>A maps to ENST00000444297 N454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:56117833 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:56115653 C>T maps to NM_002905.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:56115653 C>T maps to NM_002905.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:56117723 C>T maps to NM_002905.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:56115036 C>T maps to NM_002905.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:10132277 G>A maps to NM_015725.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr19:10131448 C>T maps to NM_015725.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:34247232 G>A maps to NM_145654.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:110108240 G>A maps to ENST00000405097 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:110143260 C>T maps to ENST00000405097 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:110134829 C>A maps to ENST00000405097 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:110134829 C>A maps to ENST00000405097 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:110134865 C>A maps to ENST00000405097 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24649225 G>A maps to NM_005132.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:36100438 T>G maps to NM_021111.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:36108126 C>T maps to NM_021111.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:36083482 C>T maps to NM_021111.2 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:21636460 C>T maps to NM_032941.2 E183E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:21624396 C>T maps to NM_032941.2 K544K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr12:21628400 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:21652549 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:21630873 G>A maps to NM_032941.2 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:21623995 C>T maps to NM_032941.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:21643312 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:145742454 G>A maps to ENST00000428558 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:145739581 G>A maps to ENST00000428558 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr8:145740618 C>A maps to ENST00000428558 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr8:145740585 C>G maps to ENST00000428558 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:145738263 C>T maps to ENST00000428558 Q907Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:73626323 T>C maps to NM_004259.5 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr2:86481860 G>A maps to NM_022912.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:137781175 T>C maps to ENST00000378339 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:137780136 C>T maps to ENST00000378339 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:137780447 C>T maps to ENST00000378339 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr10:65379553 C>T maps to NM_001001330.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:65326132 C>A maps to NM_001001330.2 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:79350040 T>C maps to NM_002909.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:79385535 A>G maps to NM_138937.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:79255018 C>A maps to NM_001008387.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:120342395 G>T maps to NM_032044.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:61147228 C>T maps to NM_002908.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:61118894 C>T maps to NM_002908.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65423206 G>A maps to NM_021975.3 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:45525372 G>A maps to ENST00000221452 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:45537511 C>T maps to ENST00000221452 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:45535972 G>A maps to ENST00000221452 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:141019528 A>G maps to NM_173828.4 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:141019612 G>A maps to NM_173828.4 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:141018368 C>T maps to NM_173828.4 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr7:103292124 G>T maps to ENST00000428762 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:103194141 G>A maps to ENST00000428762 I1978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:103214696 G>A maps to ENST00000428762 F1451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:103179612 G>A maps to ENST00000428762 Y2364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:103194176 C>A maps to ENST00000428762 E1967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:103206668 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:103301964 G>A maps to ENST00000428762 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:103124179 G>A maps to ENST00000428762 N3367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:103243780 G>T maps to ENST00000428762 I1101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:103276010 G>A maps to ENST00000428762 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:103293080 G>T maps to ENST00000428762 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:103138294 G>A maps to ENST00000428762 G2974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:103175898 A>G maps to ENST00000428762 L2405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:103207068 G>A maps to ENST00000428762 R1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:103136268 G>T maps to ENST00000428762 S3090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:73101934 C>T maps to NM_152222.1 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:73106159 C>A maps to NM_152222.1 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:73105539 G>A maps to NM_152222.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr11:73101855 A>G maps to NM_152222.1 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:30070154 C>T maps to NM_014012.4 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:30070154 C>T maps to NM_014012.4 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr20:30064256 C>G maps to NM_014012.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:23354009 C>T maps to NM_173527.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:204129789 G>A maps to NM_000537.3 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:153206945 G>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153205591 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153209389 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:153205672 A>G did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:153206985 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:153209093 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153208501 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:139235833 C>T maps to ENST00000367663 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:139266425 G>A maps to ENST00000367663 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:139228652 G>A maps to ENST00000367663 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:139241430 T>C maps to ENST00000367663 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:17047722 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr23:17043252 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:17080606 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:17092257 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:17157039 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:17070538 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:17165583 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:17065475 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:17070551 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:2328607 C>A maps to NM_007033.4 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr1:2334499 G>A maps to NM_007033.4 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:8422898 C>T maps to NM_012102.3 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:8684437 G>A maps to NM_012102.3 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:8557478 G>A maps to NM_012102.3 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:8526065 G>A maps to NM_012102.3 Y374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:8716050 A>G maps to NM_012102.3 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:8418862 G>A maps to NM_012102.3 P1244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr12:15262108 G>A maps to NM_032918.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:15262186 C>A maps to NM_032918.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:18238552 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:57796164 G>T maps to NM_005612.4 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:57797472 C>T maps to NM_005612.4 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:57798144 G>T maps to NM_005612.4 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:57796739 T>C maps to NM_005612.4 N572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:57797925 G>T maps to NM_005612.4 E968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:57797429 G>A maps to NM_005612.4 E802E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr10:43613824 C>T maps to NM_020975.4 N763N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:43606665 C>A maps to NM_020975.4 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:43623617 C>T maps to NM_020975.4 G1082G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:43612093 C>T maps to NM_020975.4 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:43615599 C>T maps to NM_020975.4 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:43596114 C>T maps to NM_020975.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:43604666 C>T maps to NM_020975.4 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:43609967 C>T maps to NM_020975.4 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:43597793 C>T maps to NM_020975.4 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:43615087 C>T maps to NM_020975.4 N834N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:43604575 C>A maps to NM_020975.4 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:7734705 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:108475403 G>T maps to NM_032579.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr3:108476023 C>T maps to NM_032579.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:85570843 A>T maps to NM_017750.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:100055195 G>A maps to NM_016316.2 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:100037985 C>T maps to NM_016316.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:100081430 G>A maps to NM_016316.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:100037994 T>C maps to NM_016316.2 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:100019259 C>A maps to NM_016316.2 E1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:100019263 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:100022485 C>T maps to NM_016316.2 P899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:100065843 C>A maps to NM_016316.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:100055063 T>G maps to NM_016316.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:100029222 A>G maps to NM_016316.2 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:111688744 C>T maps to NM_002912.3 T2082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:111698984 C>A maps to NM_002912.3 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:111650872 C>T maps to NM_002912.3 K2701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:111726751 C>T maps to NM_002912.3 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:111694204 C>A maps to NM_002912.3 E1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:111680075 C>A maps to NM_002912.3 E2341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:111698984 C>A maps to NM_002912.3 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:111695023 G>A maps to NM_002912.3 R1512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr6:111696315 G>C maps to NM_002912.3 S1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr6:111688527 A>G maps to NM_002912.3 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:111694780 C>A maps to NM_002912.3 E1593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:1828259 C>T maps to NM_020695.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:1816082 G>A maps to NM_020695.3 D1216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:1827391 G>A maps to NM_020695.3 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:136279819 C>T maps to NM_020385.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:136277527 G>A maps to NM_020385.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:136278001 G>A maps to NM_020385.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:39310547 C>T maps to ENST00000381897 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:39318545 C>A maps to ENST00000381897 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:39322969 C>A maps to ENST00000381897 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:39304176 C>T maps to ENST00000381897 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:39329344 C>T maps to ENST00000381897 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:39344022 T>C maps to ENST00000381897 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:39322116 C>T maps to ENST00000381897 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:73654305 C>A maps to NM_181471.1 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:73654381 C>T maps to NM_181471.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr7:73668698 G>A maps to NM_181471.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:186510633 C>T maps to NM_181573.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:186515333 C>A maps to NM_181573.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:118457549 G>T maps to NM_007370.4 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:118457527 G>A maps to NM_007370.4 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:118457549 G>T maps to NM_007370.4 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr5:94989940 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:33348659 C>T maps to NM_001017368.1 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:29834902 C>T maps to NM_021026.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:29837751 G>T maps to NM_021026.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:32587001 G>A maps to NM_001098527.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:32756500 G>A maps to NM_001098535.1 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:112671440 G>A maps to NM_001013734.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:53155780 G>A maps to NM_052859.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr3:53159944 G>T maps to NM_052859.3 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:53159971 A>G maps to NM_052859.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:53164351 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:16358556 G>A maps to NM_015150.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:16411712 A>G maps to NM_015150.1 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:16364885 C>T maps to NM_015150.1 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:16358729 G>A maps to NM_015150.1 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:16535267 C>A maps to NM_015150.1 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:16399519 G>T maps to NM_015150.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:198508989 C>T maps to NM_144629.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:198511351 G>A maps to NM_144629.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:198480649 G>A maps to NM_144629.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:198480649 G>A maps to NM_144629.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:198495918 G>T maps to NM_144629.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:198436962 T>C maps to NM_144629.2 K425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:198498486 C>A maps to NM_144629.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:198480649 G>A maps to NM_144629.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:175958604 G>T maps to NM_022457.5 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:176085768 G>A maps to NM_022457.5 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:176050292 G>A maps to NM_022457.5 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:176054996 C>T maps to NM_022457.5 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:175957508 T>C maps to NM_022457.5 K629K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:74664716 C>T maps to NM_018124.3 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr16:74683059 A>G maps to NM_018124.3 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:74695152 C>T maps to NM_018124.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:14094040 G>A maps to NM_002918.4 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:14092935 T>C maps to NM_002918.4 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr19:14076299 G>A maps to NM_002918.4 H724H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr19:14074786 C>T maps to NM_002918.4 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:14076531 G>A maps to NM_002918.4 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:6004310 T>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:6002803 C>T maps to NM_000635.3 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:6026191 G>A maps to NM_000635.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:3247979 C>A maps to NM_002919.2 E674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr9:3330444 A>C maps to NM_134428.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:3293150 T>C maps to NM_134428.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:107002657 G>T maps to ENST00000357881 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:107105267 A>G maps to ENST00000357881 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:107103189 C>T maps to ENST00000357881 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:107109322 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:107048038 C>A maps to ENST00000357881 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:107114604 C>T maps to ENST00000357881 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:151317005 G>T maps to NM_000449.3 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:151318402 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:151316920 G>A maps to NM_000449.3 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:117250118 C>T maps to NM_173560.3 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:117198957 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:117243296 G>T maps to NM_173560.3 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:117250060 C>T maps to NM_173560.3 D846D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:117248340 C>A maps to NM_173560.3 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:56387540 A>G maps to NM_022841.5 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:56387600 G>A maps to NM_022841.5 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:56387723 G>T maps to NM_022841.5 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:56386691 A>G maps to NM_022841.5 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:56388239 G>A maps to NM_022841.5 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:56385785 G>A maps to NM_022841.5 F1380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:56386802 G>T maps to NM_022841.5 V1041V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:56385596 T>G maps to NM_022841.5 S1443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:56385857 T>C maps to NM_022841.5 G1356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr15:56535450 C>T maps to NM_022841.5 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:56390308 G>T maps to NM_022841.5 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:19308339 C>T maps to NM_003721.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:19309476 G>A maps to NM_003721.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:19312470 C>T maps to NM_003721.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:37394090 C>T maps to NM_000538.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:101284279 G>T maps to NM_017819.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr3:101283741 C>T maps to NM_017819.2 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:101283657 C>A maps to NM_017819.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:101283870 C>T maps to NM_017819.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:100474947 A>G maps to NM_001134666.1 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:100477319 C>A maps to NM_001134666.1 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:37777656 G>T maps to NM_144964.2 G302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:37761988 G>T maps to NM_144964.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr9:37763697 C>G maps to NM_144964.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:109695530 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:109695734 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:109693939 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:109696751 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:109695547 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:109696561 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:109696620 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:109695498 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr23:109697236 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:109695861 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:109697259 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:109697453 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:109696276 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:109697345 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr23:109697387 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:109694306 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:109695631 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:109693978 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:109697237 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:109697520 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr23:109696150 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:109695578 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:109694751 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:109696358 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:109694333 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:109697261 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:109696386 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:109697529 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:71350302 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:71350445 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:71350783 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:71351348 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:71350168 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:71351310 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:71350529 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr23:71350298 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:71349919 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:71350234 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:71350799 G>A did not map to a codon.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr23:71350837 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:71349919 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:71350055 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:183885603 T>C maps to NM_015149.3 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:183885835 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:183861232 G>T maps to NM_015149.3 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:183854065 C>T maps to NM_015149.3 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:11517268 G>A maps to NM_001161616.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr19:11515997 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:24036574 C>T maps to ENST00000382833 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:93588737 G>A maps to NM_020211.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:98115323 C>T maps to NM_001012761.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:98128880 C>A maps to NM_001012761.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:98129336 G>A maps to NM_001012761.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:46949304 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:46951088 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:46940547 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:46949213 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:73142254 C>A maps to NM_001080479.2 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:73189113 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:73190251 G>A maps to NM_001080479.2 A1231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:73181687 A>G maps to NM_001080479.2 E1023E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr5:73187962 T>G maps to NM_001080479.2 A1158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:73069791 C>T maps to NM_001080479.2 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:107049638 G>A maps to ENST00000304514 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:107064044 C>T maps to ENST00000304514 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:107040420 G>T maps to ENST00000304514 Y1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:107069226 G>A maps to ENST00000304514 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:107041368 G>A maps to ENST00000304514 S1018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:107049684 G>A maps to ENST00000304514 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:107041131 T>C maps to ENST00000304514 R1097R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:107007934 C>A maps to ENST00000452099 *1016Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:107040324 T>C maps to ENST00000304514 R1366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:107040335 C>A maps to ENST00000304514 E1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:107052982 G>A maps to ENST00000304514 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:107084677 G>A maps to ENST00000304514 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:107042524 T>C maps to ENST00000304514 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:108487477 A>G maps to NM_182588.2 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:108475702 A>G maps to NM_182588.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:108443504 C>T maps to NM_182588.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr2:113161750 C>T maps to NM_005054.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:113157316 G>A maps to NM_005054.2 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr2:113147500 G>A maps to NM_005054.2 Y1007Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:86014144 G>A maps to ENST00000358110 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:192548338 G>T maps to NM_002922.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr16:321411 G>A maps to NM_183337.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr16:323525 C>T maps to NM_183337.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:3416528 C>A maps to NM_198229.2 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:3424131 G>A maps to NM_198229.2 E956E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:3318061 C>T maps to NM_198229.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:3419134 C>T maps to NM_198229.2 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:3415868 C>T maps to NM_198229.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:192628556 C>A maps to NM_144766.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:192627409 C>A maps to NM_144766.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:192627356 T>C maps to NM_144766.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:192613506 G>T maps to NM_144766.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:182569516 C>T maps to NM_002928.3 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:153345471 C>T maps to NM_012419.4 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:192127818 G>T maps to NM_130782.2 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:192779334 A>G maps to NM_002923.3 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:54866761 C>A maps to NM_170587.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr8:54791978 C>A maps to NM_170587.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr1:192316469 G>A maps to NM_001039152.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:101016299 G>A maps to NM_015668.3 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:100994290 A>G maps to NM_015668.3 T1078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:101083706 C>A maps to NM_015668.3 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:101076164 C>T maps to NM_015668.3 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:101054037 C>A maps to NM_015668.3 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:101083614 G>A maps to NM_015668.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:101117606 C>A maps to NM_015668.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:101074918 C>A maps to NM_015668.3 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:101117606 C>A maps to NM_015668.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:101020697 C>A maps to NM_015668.3 E756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:101014533 G>A maps to NM_015668.3 R896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:116359226 G>A maps to NM_144488.4 P1197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr9:116346502 G>A maps to NM_144488.4 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:116246416 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:116359067 G>A maps to NM_144488.4 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:116291525 C>T maps to NM_144488.4 C632C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:163117161 G>A maps to NM_003617.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:163131753 G>A maps to NM_003617.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:72926359 G>A maps to NM_004296.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:72985220 G>T maps to NM_004296.4 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:72961964 G>A maps to NM_004296.4 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:72926359 G>A maps to NM_004296.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:72961861 T>G maps to NM_004296.4 L286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:240969577 T>C maps to ENST00000407727 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:240977028 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:240969481 C>T maps to ENST00000407727 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:240990433 C>T maps to ENST00000407727 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:241146387 C>A maps to ENST00000407727 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:240966278 T>C maps to ENST00000407727 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:63894201 G>T maps to NM_001029875.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:63803659 T>C maps to NM_001029875.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:63803629 G>A maps to NM_001029875.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:182640796 T>C maps to NM_033345.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:63193349 G>T maps to NM_003835.3 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:63159208 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr17:63164390 C>A maps to NM_003835.3 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:63206716 C>T maps to NM_003835.3 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:63173899 G>A maps to NM_003835.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:49604471 A>T maps to NM_000324.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:49583448 G>A maps to NM_000324.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:49583350 A>T maps to NM_000324.2 L209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:227731980 G>A maps to NM_001167608.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:227729564 C>A maps to NM_001167608.1 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:75513121 C>T maps to NM_001040456.1 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:114986 C>T maps to NM_022450.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:112991 C>G maps to NM_022450.3 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:39377087 C>T maps to ENST00000372985 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:39384829 C>A maps to ENST00000372985 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:30648199 C>T maps to NM_138328.2 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:156348179 C>T maps to NM_020407.3 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:156347819 C>T maps to NM_020407.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:156347981 G>A maps to ENST00000400992 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:156354848 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:25718593 G>A maps to NM_020485.4 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:90026323 C>A maps to NM_016321.1 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:90026302 G>A maps to NM_016321.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:90021066 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:25611169 G>A maps to ENST00000357542 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:129251518 C>A maps to NM_000539.3 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:129249824 C>T maps to NM_000539.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:129251135 C>T maps to NM_000539.3 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:129247605 C>T maps to NM_000539.3 Y10Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:129251377 C>T maps to NM_000539.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:129249800 C>T maps to NM_000539.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:129247647 C>T maps to NM_000539.3 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:62647996 C>A maps to NM_014836.4 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:62631204 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:62631392 G>A maps to NM_014836.4 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:62632024 G>A maps to NM_014836.4 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:62648591 G>T maps to NM_014836.4 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:62648102 C>T maps to NM_014836.4 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:62637804 C>T maps to NM_014836.4 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:22862015 C>T maps to NM_001160036.1 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:22862039 C>A maps to NM_001160036.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:95128826 G>A maps to NM_014899.3 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr5:95115959 G>A maps to NM_014899.3 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:3849086 C>T maps to NM_001665.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr11:3849020 C>T maps to NM_001665.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:40245551 C>T maps to NM_004310.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:63747756 C>T maps to NM_020663.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:63757597 C>T maps to NM_020663.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:63671709 C>T maps to NM_020663.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:63747756 C>T maps to NM_020663.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:30551677 C>T maps to NM_001033568.1 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr17:30538194 C>T maps to NM_001033568.1 N632N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr16:722302 C>T maps to NM_138769.1 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:720751 C>T maps to NM_138769.1 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:722746 C>T maps to NM_138769.1 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:228879201 T>C maps to NM_021205.4 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:119249615 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:119249467 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr23:119249400 G>T did not map to a codon.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr23:119249508 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:119249587 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:119293185 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:119293293 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr23:119293081 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:119293162 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:119294299 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:119293257 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:119211124 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:119209877 T>G did not map to a codon.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr23:119211109 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:144462126 C>T maps to ENST00000422773 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:144457751 C>T maps to ENST00000422773 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:33498965 C>T maps to NM_033103.4 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:33481509 C>T maps to NM_033103.4 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:33486950 G>A maps to NM_033103.4 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:33502679 G>A maps to NM_033103.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:33502616 C>T maps to NM_033103.4 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:33481509 C>T maps to NM_033103.4 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53455490 A>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:53457515 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:53454995 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53456821 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:8161623 C>A maps to ENST00000309737 G81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:8148241 C>A maps to ENST00000309737 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:211297 T>C maps to NM_021932.4 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr11:209504 C>T maps to NM_021932.4 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:209484 C>T maps to NM_021932.4 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:107268288 T>C maps to ENST00000355478 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:38949525 G>A maps to ENST00000296782 I1380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:38982000 G>A maps to ENST00000296782 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:38945075 G>A maps to ENST00000296782 C1600C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:38991159 A>G maps to ENST00000296782 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr5:38950097 C>T maps to ENST00000296782 S1284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:152308205 G>A maps to NM_018151.4 Q777Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:152320435 C>T maps to NM_018151.4 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:152267786 G>T maps to NM_018151.4 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:152319987 T>C maps to NM_018151.4 V1318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:152321755 G>T maps to NM_018151.4 E1908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:152314403 C>T maps to NM_018151.4 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:152273409 C>T maps to NM_018151.4 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:152292041 G>A maps to NM_018151.4 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr2:152279513 C>T maps to NM_018151.4 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:152314403 C>T maps to NM_018151.4 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:152285409 T>G maps to NM_018151.4 L300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:152320360 C>T maps to NM_018151.4 R1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:152298447 T>C maps to NM_018151.4 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:1549776 C>A maps to NM_031430.2 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:1550249 G>A maps to NM_031430.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:123957132 G>A maps to NM_178314.3 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:123983140 G>A maps to NM_178314.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:130935763 G>A maps to NM_015347.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:130926789 G>T maps to NM_015347.4 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:130897302 G>A maps to NM_015347.4 F894F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:130926552 G>A maps to NM_015347.4 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:130926744 G>A maps to NM_015347.4 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:130929801 G>A maps to NM_015347.4 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:130935763 G>A maps to NM_015347.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:130892333 C>T maps to NM_015347.4 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr12:130921737 G>A maps to NM_015347.4 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:130926552 G>A maps to NM_015347.4 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:130926558 G>A maps to NM_015347.4 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:130934791 G>A maps to NM_015347.4 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr12:130921587 G>A maps to NM_015347.4 H618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr12:130941155 G>A maps to NM_015347.4 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:20457005 G>A maps to NM_015672.1 S1432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:20457632 C>T maps to NM_015672.1 P1223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:20457733 G>A maps to NM_015672.1 R1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:20458826 G>A maps to NM_015672.1 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:20458931 C>T maps to NM_015672.1 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:20457596 G>A maps to NM_015672.1 C1235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:20458024 G>A maps to NM_015672.1 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:20458732 G>A maps to NM_015672.1 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:20457632 C>T maps to NM_015672.1 P1223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:42880414 G>T maps to NM_173642.3 G316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:42880422 G>A maps to NM_173642.3 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:42865150 G>A maps to NM_173642.3 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr1:42880383 T>C maps to NM_173642.3 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:8902617 C>T maps to NM_020734.2 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:72806762 T>A maps to NM_014989.4 C119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:72889318 C>A maps to NM_014989.4 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:72889486 C>A maps to NM_014989.4 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:73110295 C>T maps to NM_014989.4 I1653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:72806726 C>T maps to NM_014989.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:72960723 G>T maps to NM_014989.4 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:72806738 C>T maps to NM_014989.4 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:72892166 G>A maps to NM_014989.4 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:72960768 G>T maps to NM_014989.4 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:72960728 A>G maps to NM_014989.4 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr6:72889460 C>T maps to NM_014989.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:72892166 G>A maps to NM_014989.4 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:72892799 G>A maps to NM_014989.4 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:72889549 G>A maps to NM_014989.4 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:104987662 A>C maps to NM_001100117.2 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:105026800 C>T maps to NM_001100117.2 R1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:41101685 C>T maps to NM_014747.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr1:41107588 G>A maps to NM_014747.2 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr20:43384831 C>T maps to NM_182970.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:66100857 G>T maps to NM_004292.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr20:19955328 C>A maps to ENST00000255006 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:19977393 C>T maps to ENST00000255006 R807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr20:19955571 G>A maps to ENST00000255006 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:19972896 C>T maps to ENST00000255006 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:93043757 C>T maps to NM_024832.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:93118824 C>A maps to NM_024832.3 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:93043733 G>A maps to NM_024832.3 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr14:93118515 G>A maps to NM_024832.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:93022110 T>C maps to NM_024832.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr6:33178979 A>C maps to NM_002931.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:33177557 G>A maps to NM_002931.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:105207700 A>G maps to NM_021930.4 Q774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:105190605 C>T maps to NM_021930.4 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:105187706 C>T maps to NM_021930.4 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:105195514 G>A maps to NM_021930.4 Q504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:105205786 G>A maps to NM_021930.4 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:7405480 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:7405180 C>T maps to NM_031480.2 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:96503655 G>T maps to NM_018343.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:96503535 T>C maps to NM_018343.2 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr5:96500767 G>T maps to NM_018343.2 S494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:21044218 C>T maps to NM_003831.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:21046198 C>T maps to NM_003831.3 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:21059319 C>T maps to NM_003831.3 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr18:21042999 G>T maps to NM_003831.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:21046198 C>T maps to NM_003831.3 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:3111038 G>T maps to NM_003804.3 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr6:3105899 G>A maps to NM_003804.3 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:3111189 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr8:90782097 A>G maps to NM_003821.5 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:90802518 G>T maps to NM_003821.5 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24806336 G>A maps to NM_006871.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24805598 G>A maps to NM_006871.3 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:24805598 G>A maps to NM_006871.3 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr14:24808367 G>A maps to NM_006871.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr14:24807177 G>A maps to NM_006871.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr21:43161263 G>A maps to ENST00000352483 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:43161177 G>A maps to ENST00000352483 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr21:43176747 C>T maps to ENST00000352483 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:106145431 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:106144109 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:106146366 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:106144086 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:106144745 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:84566958 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr15:89753548 G>A maps to NM_000326.4 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:89753602 G>A maps to NM_000326.4 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:40703169 C>A maps to NM_012421.3 V932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:40706114 C>A maps to NM_012421.3 S1914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:40668268 G>T maps to NM_012421.3 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:40701727 C>T maps to NM_012421.3 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:40703622 G>A maps to NM_012421.3 G1083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:40661411 C>T maps to NM_012421.3 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:40697312 A>C maps to NM_012421.3 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:73812164 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:73811845 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:73815708 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:73811555 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:73812850 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:73812695 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:73812117 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:73812202 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:73812729 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:73811326 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:73812449 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr23:73815790 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:73811357 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:73811612 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:73812742 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:73811736 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:73811990 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:5335426 C>A maps to NM_006911.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr19:14141675 G>C maps to NM_080864.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:14139127 G>T maps to NM_080864.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:67686230 G>T maps to NM_001013838.1 E936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:86617667 C>T maps to NM_024945.2 C589C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:86616828 G>T maps to NM_024945.2 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:86616458 C>T maps to NM_024945.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:86617655 A>G maps to NM_024945.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:151744666 G>A maps to NM_017909.2 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:177569911 G>A maps to NM_022762.3 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:177570961 C>T maps to NM_022762.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:177574773 C>T maps to NM_022762.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:177574602 C>T maps to NM_022762.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr5:177565137 C>A maps to NM_022762.3 C6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr5:177574767 C>A maps to NM_022762.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:20979241 C>A maps to ENST00000430083 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:20979106 T>C maps to ENST00000430083 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:20978683 C>T maps to ENST00000430083 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:21052621 A>G maps to NM_145250.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:21052555 A>G maps to NM_145250.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:21052294 C>T maps to NM_145250.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr14:21058855 C>T maps to NM_001024822.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:21058833 C>A maps to NM_001024822.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:21424307 G>A maps to NM_002934.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:21511501 G>A maps to NM_032572.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:21526156 C>T maps to NM_138331.1 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:21024772 C>T maps to NM_001110361.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:21025041 C>A maps to NM_001110361.1 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr2:3595519 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:3599782 C>T maps to NM_002936.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:12924189 C>A maps to NM_006397.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:12918271 C>G maps to NM_006397.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:51519600 G>A maps to NM_024570.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:51522141 C>T maps to NM_024570.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr13:51501539 C>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:182550479 C>T maps to NM_021133.3 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:182554537 T>A maps to NM_021133.3 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:182554653 A>G maps to NM_021133.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:182554498 G>A maps to NM_021133.3 Y481Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:182554462 T>G maps to NM_021133.3 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:182555659 C>T maps to NM_021133.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:182554716 G>A maps to NM_021133.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:182555077 G>A maps to NM_021133.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:49251993 C>A maps to NM_014470.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:49251931 C>T maps to NM_014470.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr2:151343805 G>C maps to NM_005168.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:121014432 G>A maps to ENST00000458409 K805K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:121014453 C>T maps to ENST00000458409 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:121000845 G>A maps to ENST00000458409 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:121000803 T>C maps to ENST00000458409 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:120995215 G>A maps to ENST00000458409 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:120995113 C>T maps to ENST00000458409 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:86831123 G>A maps to NM_005667.3 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr2:86831568 G>A maps to NM_005667.3 D485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:86831640 C>T maps to NM_005667.3 W461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:51736865 C>T maps to NM_014372.4 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:59323857 T>C maps to ENST00000434298 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:59323276 G>T maps to ENST00000434298 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:59347880 G>A maps to ENST00000434298 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:59376432 G>A maps to ENST00000434298 Q810Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:59377945 C>T maps to ENST00000434298 R847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:59323498 G>T maps to ENST00000434298 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr15:59344631 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:59323815 C>A maps to ENST00000434298 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:19317772 C>T maps to NM_007148.4 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:19315843 C>T maps to NM_007148.4 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr17:19318130 C>T maps to NM_007148.4 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:19316975 G>A maps to NM_007148.4 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:119005321 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:119005120 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:119005255 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119005308 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119005431 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:119005192 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:119004937 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:119005479 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:119005559 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119005116 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:119004651 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:98829331 G>A maps to NM_178861.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr13:98829136 G>A maps to NM_178861.4 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:98829148 G>A maps to NM_178861.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:98829331 G>A maps to NM_178861.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr13:98829331 G>A maps to NM_178861.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:145686991 T>A maps to NM_014455.2 C228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:71707390 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:71701699 C>A maps to NM_018320.4 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:33407001 G>A maps to NM_024787.2 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49758003 C>A maps to NM_022064.2 C1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:49749943 C>T maps to NM_022064.2 R843R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:49728900 C>A maps to NM_022064.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:49728900 C>A maps to NM_022064.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:49753083 C>T maps to NM_022064.2 F1029F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr3:49739801 T>C maps to NM_022064.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr3:49735316 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:29622213 G>T maps to NM_017831.3 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:106016374 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:106016319 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:105937373 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:105937521 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:105970442 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:106016207 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr3:149613257 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:149678833 C>T maps to NM_007282.4 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:149563869 G>A maps to NM_007282.4 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:149589851 G>T maps to NM_007282.4 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:149613336 A>C maps to NM_007282.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr3:149589883 T>C maps to NM_007282.4 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:179393883 G>A maps to NM_018434.4 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:179405222 G>A maps to NM_018434.4 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:29311658 G>T maps to NM_032322.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:29315014 C>T maps to NM_032322.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:29709126 G>T maps to NM_001191324.1 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:141354399 C>T maps to NM_183399.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:141353305 C>T maps to NM_183399.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr5:141359764 A>G maps to NM_183399.1 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:10555653 C>A maps to NM_016422.3 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:7154889 A>G maps to NM_014746.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:7154896 G>T maps to NM_014746.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:18465258 T>A maps to NM_182757.3 C291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:18465267 G>A maps to NM_182757.3 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr5:158634775 A>C maps to NM_144726.2 L11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:127608739 C>T maps to ENST00000368314 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr6:127608678 C>A maps to ENST00000368314 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:127608730 C>T maps to ENST00000368314 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:127608585 C>T maps to ENST00000368314 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:122341976 G>A maps to NM_198085.1 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:122342774 C>T maps to NM_198085.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr7:122342249 C>T maps to NM_198085.1 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:141832469 G>A maps to NM_020724.1 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:2017279 C>T maps to NM_174903.4 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:2017300 C>T maps to NM_174903.4 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:59483686 G>A maps to NM_173557.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:74151331 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:74154582 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:44035936 C>T maps to NM_152470.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:43914288 C>T maps to NM_152470.2 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:44027524 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:44013366 C>T maps to NM_152470.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:4845731 C>T maps to NM_015528.1 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:196215476 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:196202170 C>T maps to NM_152617.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:196199136 T>G maps to NM_152617.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:74521324 G>T maps to NM_001098638.1 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:74521237 G>T maps to NM_001098638.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:25363556 T>C maps to ENST00000381927 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:25376658 T>C maps to ENST00000381927 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:25367209 G>A maps to ENST00000381927 Q322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:25356007 G>A maps to ENST00000381927 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:25436906 G>A maps to ENST00000381927 K1366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:25418796 G>T maps to ENST00000381927 E996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:25424528 C>A maps to ENST00000381927 S1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:25416215 C>T maps to ENST00000381927 F889F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:25425701 G>T maps to ENST00000381927 E1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:25453359 C>T maps to ENST00000381927 D1652D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:25428091 C>T maps to ENST00000381927 N1189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:42711367 G>T maps to NM_030954.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:42729096 G>A maps to NM_030954.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:42720612 G>A maps to NM_030954.3 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:154636775 C>T maps to ENST00000274068 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:63509983 C>T maps to NM_001113561.1 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:63496649 G>T maps to NM_001113561.1 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:13977578 G>T maps to NM_001165033.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:13977800 G>T maps to NM_001165033.1 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:13978018 C>T maps to NM_001165033.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:31600505 G>A maps to NM_152267.3 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:31601192 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr22:31601134 A>C did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr22:31601283 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr22:31601319 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:20141383 G>A maps to NM_019062.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:20141039 G>A maps to NM_019062.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:20141513 A>G maps to NM_019062.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:101271191 C>T maps to NM_183419.1 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:101299856 C>T maps to NM_183419.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:101271181 C>A maps to NM_183419.1 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:101271290 C>A maps to NM_183419.1 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A121-01A-31D-A122-09 chr1:33415338 C>T maps to NM_153341.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:33415181 C>A maps to NM_153341.2 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:104319830 G>T maps to NM_019592.5 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:104324595 C>A maps to NM_019592.5 V940V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr9:104312895 G>A maps to NM_019592.5 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr9:104314838 C>T maps to NM_019592.5 R569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr9:104319830 G>T maps to NM_019592.5 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:6270961 G>A maps to NM_207396.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:6270288 C>T maps to NM_207396.2 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:6272335 C>T maps to NM_207396.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:6270306 C>A maps to NM_207396.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:6272391 C>T maps to NM_207396.2 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:6271106 C>T maps to NM_207396.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:1075398 G>T maps to NM_001131034.3 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:1067426 C>T maps to NM_001131034.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:1067392 G>A maps to NM_001131034.3 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:78319973 C>T maps to NM_020914.4 R2662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:78269613 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:78317011 C>T maps to NM_020914.4 R2073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:78265609 A>G maps to NM_020914.4 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:78302194 G>A maps to NM_020914.4 E1194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:78282934 G>A maps to NM_020914.4 E922E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:78346925 G>A maps to NM_020914.4 P4350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:78335564 G>A maps to NM_020914.4 Q3793Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:78263499 G>T maps to NM_020914.4 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:78343455 A>C maps to NM_020914.4 R4153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:78269421 G>A maps to NM_020914.4 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:78320270 G>A maps to NM_020914.4 P2761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:78268741 G>A maps to NM_020914.4 Q614Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:78359416 G>A maps to NM_020914.4 T4894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr17:78321263 C>T maps to NM_020914.4 L3092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:78343364 G>A maps to NM_020914.4 V4122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:78308011 G>A maps to NM_020914.4 G1466G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BS-A0UF-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:78327453 C>T maps to NM_020914.4 L3571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:78320348 G>T maps to NM_020914.4 L2787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr17:78360197 C>T maps to NM_020914.4 Y4945Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:78320402 C>T maps to NM_020914.4 V2805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:78360621 C>T maps to NM_020914.4 F5000F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:78363969 C>T maps to NM_020914.4 T5197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr17:78311743 C>T maps to NM_020914.4 L1643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:78319964 C>T maps to NM_020914.4 N2659N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:78291022 G>A maps to NM_020914.4 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr17:78306007 C>T maps to NM_020914.4 A1289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr17:78320687 C>T maps to NM_020914.4 D2900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:117115291 G>A maps to NM_207343.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:30782610 G>T maps to NM_001017981.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:5754773 G>A maps to NM_207111.2 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:5752343 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:5781074 G>A maps to NM_207111.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:5752359 G>A maps to NM_207111.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:125379110 C>T maps to NM_152553.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:79191010 G>A maps to NM_024546.3 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:79190751 C>A maps to NM_024546.3 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:79212996 G>T maps to NM_024546.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:79189855 G>A maps to NM_024546.3 H680H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:79190281 G>T maps to NM_024546.3 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:79189918 T>C maps to NM_024546.3 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr13:79190387 G>C maps to NM_024546.3 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:45088412 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:44878146 C>T maps to ENST00000453887 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:45079861 C>T maps to ENST00000453887 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:44877783 G>A maps to ENST00000453887 R5R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DI-A0WH-01A-12D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:119206725 G>A maps to NM_032015.3 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:119206935 G>A maps to NM_032015.3 W368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:119206364 G>A maps to NM_032015.3 W178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24629121 C>T maps to NM_017999.4 D983D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:24619329 C>T maps to NM_017999.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:24629073 C>T maps to NM_017999.4 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24618718 G>T maps to NM_017999.4 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:24629122 G>T maps to NM_017999.4 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr14:24627348 A>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:24624466 C>T maps to NM_017999.4 C744C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:24619302 G>A maps to NM_017999.4 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:24620579 C>T maps to NM_017999.4 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr14:24624841 C>T maps to NM_017999.4 Q812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:156469038 G>A maps to ENST00000432459 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:156447396 C>T maps to NM_001184997.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:156450916 C>A maps to NM_001184997.1 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr7:156469253 C>T maps to NM_001184997.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:121861192 C>T maps to NM_194271.1 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:121855614 G>A maps to NM_194271.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:36357879 A>G maps to NM_022781.4 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:36375991 G>A maps to NM_022781.4 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:36351114 G>A maps to NM_022781.4 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr6:30043428 C>T maps to NM_025236.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr4:2515434 C>T maps to NM_002938.4 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:30780223 C>T maps to NM_014771.2 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr16:30774875 G>C maps to NM_014771.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr16:30779623 C>A maps to NM_014771.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:56601529 G>A maps to NM_194359.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:56604187 G>A maps to NM_194359.1 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:56601952 C>A maps to NM_194359.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr17:56439943 C>T maps to NM_017763.4 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr17:56440644 G>A maps to NM_017763.4 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:56435581 G>A maps to NM_017763.4 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:56435789 G>A maps to NM_017763.4 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:56440942 G>A maps to NM_017763.4 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:56492874 G>A maps to NM_017763.4 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:56436127 G>A maps to NM_017763.4 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr17:56440010 T>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:175956243 G>A maps to ENST00000506378 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:26788658 G>A maps to NM_005977.3 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:26789202 C>T maps to NM_005977.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr13:26789361 T>A maps to NM_005977.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:37336152 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:37336984 G>A maps to NM_003958.3 Q322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:89511326 C>A maps to NM_003800.3 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:89600275 C>T maps to NM_003800.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:89563346 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:90332759 C>T maps to NM_001031709.2 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:90034735 C>T maps to NM_018363.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:90074234 C>T maps to NM_001031709.2 W288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:90122414 G>T maps to NM_001031709.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:13737010 G>T maps to NM_003799.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:13734531 A>T maps to NM_003799.1 K163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:686544 C>T maps to NM_018146.2 L179L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AP-A0LD-01A-11W-A062-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:694837 C>G maps to NM_018146.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:104087651 G>T maps to NM_017619.3 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:104076395 T>C maps to NM_017619.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:201966518 C>T maps to NM_020216.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:201972378 C>T maps to NM_020216.3 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:241517179 C>T maps to NM_018226.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:78655918 G>A maps to NM_002941.3 R1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:78795966 G>A maps to NM_002941.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:78717177 C>T maps to NM_002941.3 W607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:78706322 G>A maps to NM_002941.3 R847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:78649333 G>A maps to NM_002941.3 R1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:78719421 G>A maps to NM_002941.3 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:78708862 A>G maps to NM_002941.3 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:78649333 G>A maps to NM_002941.3 R1624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr3:78649388 G>A maps to NM_002941.3 S1605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:78666965 C>T maps to NM_002941.3 T1367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:78683186 G>A maps to NM_002941.3 R1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:78717411 T>C maps to NM_002941.3 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr3:78711140 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:78663873 G>A maps to NM_002941.3 A1453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:78680339 G>A maps to NM_002941.3 S1199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:77638007 C>A maps to ENST00000332191 C869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:77614131 C>T maps to ENST00000332191 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:77666777 C>T maps to ENST00000332191 G1136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:77684172 C>T maps to ENST00000332191 R1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:77684172 C>T maps to ENST00000332191 R1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:77600081 C>T maps to ENST00000332191 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr3:77607267 G>T maps to ENST00000332191 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:77629267 C>T maps to ENST00000332191 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:124747172 G>A maps to NM_022370.3 P938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:124744109 C>A maps to NM_022370.3 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr11:124742858 G>A maps to NM_022370.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr11:124747920 G>A maps to NM_022370.3 A1025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr11:124755023 G>A maps to NM_019055.5 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:124754982 G>T maps to NM_019055.5 I985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:124756459 G>T maps to NM_019055.5 G898G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:124756465 G>A maps to NM_019055.5 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:124765380 G>A maps to NM_019055.5 N336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:124756588 G>T maps to NM_019055.5 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:124764159 G>A maps to NM_019055.5 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:124761393 G>A maps to NM_019055.5 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:18572880 G>A maps to NM_005406.2 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:18619433 G>A maps to NM_005406.2 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:18564336 C>A maps to NM_005406.2 E822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:18595405 C>A maps to NM_005406.2 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:18546979 C>A maps to NM_005406.2 E1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:18564313 C>T maps to NM_005406.2 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:11337449 G>A maps to NM_004850.3 R1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:11334415 C>A maps to NM_004850.3 E1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:11367485 C>T maps to NM_004850.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:11332798 C>A maps to NM_004850.3 E1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr16:4848646 G>A maps to NM_024589.1 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr11:62381190 C>T maps to NM_000327.3 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62381259 C>T maps to NM_000327.3 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr11:62382115 G>A maps to NM_000327.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:62381289 G>A maps to NM_000327.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:123699276 G>A maps to NM_017578.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:123694387 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:125701289 T>C did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:125702135 C>T maps to NM_001012337.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:10442410 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:10461309 G>A maps to NM_031916.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr5:10448389 G>A maps to NM_031916.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:64515424 G>T maps to NM_005012.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:64643331 C>A maps to NM_005012.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:64643952 C>T maps to NM_005012.2 H743H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr1:64515549 G>T maps to NM_005012.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:64643244 C>A maps to NM_005012.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:94488849 T>C maps to NM_004560.2 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr9:94487152 G>A maps to NM_004560.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:60850429 G>A maps to NM_134260.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:60803734 G>A maps to NM_134260.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr15:60803743 C>T maps to NM_134260.2 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:77282716 C>T maps to ENST00000396204 D348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:77277433 C>T maps to ENST00000396204 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:77282782 C>T maps to ENST00000396204 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:77257642 C>A maps to ENST00000396204 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:77257358 C>T maps to ENST00000396204 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:151780016 G>T maps to ENST00000392697 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:151787533 G>A maps to ENST00000392697 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:151785742 G>A maps to ENST00000392697 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:151780028 G>A maps to ENST00000392697 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:117674264 G>A maps to NM_002944.2 D1403D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:117679090 C>A maps to NM_002944.2 E1244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:117681538 T>C maps to NM_002944.2 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:117706995 G>T maps to NM_002944.2 Y718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:117662295 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:117746807 A>G maps to NM_002944.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:117725514 T>G maps to NM_002944.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:117609783 T>C maps to NM_002944.2 E2305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:117647492 C>T maps to NM_002944.2 W1817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:117709018 C>T maps to NM_002944.2 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:117710656 C>A maps to NM_002944.2 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr6:117662778 C>T maps to NM_002944.2 Q1562Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:117647425 C>A maps to NM_002944.2 E1840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:55541145 A>G maps to NM_006269.1 E1568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:55538697 G>A maps to NM_006269.1 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:55534750 A>G maps to NM_006269.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:55541299 G>T maps to NM_006269.1 E1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:55534723 G>A maps to NM_006269.1 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:55538572 G>T maps to NM_006269.1 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:55542259 G>T maps to NM_006269.1 E1940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:55538092 G>T maps to NM_006269.1 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:55540654 G>T maps to NM_006269.1 E1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:55541766 A>G maps to NM_006269.1 L1775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr8:55534729 A>G maps to NM_006269.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:55542702 A>G maps to NM_006269.1 V2087V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:55541107 G>T maps to NM_006269.1 E1556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:10474034 G>T maps to NM_178857.5 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:10467571 C>A maps to NM_178857.5 G1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr8:10469810 C>T maps to NM_178857.5 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:10465975 C>A maps to NM_178857.5 E1878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:10466258 C>T maps to NM_178857.5 A1783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:10467227 C>T maps to NM_178857.5 T1460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr8:10466258 C>T maps to NM_178857.5 A1783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:46737003 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:46713475 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:46713288 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:46719465 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:46696580 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:46719460 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:46713438 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:46712961 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:46713114 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:46713188 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:46719516 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:46713137 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:46713159 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:46713335 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:33138994 G>A maps to NM_203288.1 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:33136123 G>A maps to NM_203288.1 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:1782920 A>G maps to NM_002945.3 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:1792102 C>T maps to NM_002945.3 C503C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:1747884 G>A maps to NM_002945.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:1783901 C>T maps to NM_002945.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:7678705 C>A maps to NM_002947.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr7:7677604 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:96139731 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:96139731 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:96140002 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:96139433 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:96139332 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:5331596 A>C maps to NM_001160243.1 *232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:41819229 G>A maps to NM_015540.2 R595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:41828412 G>A maps to NM_015540.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:41812990 C>T maps to NM_015540.2 R1131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:41822147 C>A maps to NM_015540.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr15:41827749 T>C maps to NM_015540.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:41815133 C>T maps to NM_015540.2 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr1:92846377 G>T maps to NM_024813.2 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:92789025 G>A maps to NM_024813.2 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:92798994 T>C maps to NM_024813.2 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:92789058 C>T maps to NM_024813.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:92789200 C>T maps to NM_024813.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:48057296 G>A maps to NM_024604.2 Y663Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:210880778 C>T maps to NM_199229.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:210881335 C>T maps to NM_199229.1 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:68904978 A>G maps to NM_000329.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:68910231 G>T maps to NM_000329.2 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:68896847 C>T maps to NM_000329.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:68896748 A>G maps to NM_000329.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:68905293 G>A maps to NM_000329.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:84961116 T>C maps to NM_025065.6 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:84946688 C>T maps to NM_025065.6 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:84956010 C>T maps to NM_025065.6 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:84956093 A>G maps to NM_025065.6 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:84962013 C>A maps to NM_025065.6 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:84961129 G>T maps to NM_025065.6 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:111320936 C>T maps to NM_032194.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:38147137 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:38146512 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:38156697 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:38128997 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:38163919 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:38169920 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:38169957 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:38145281 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:38145401 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:38147248 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:38176605 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr23:38146240 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:38147173 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:38129022 C>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:38145179 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:38145081 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:38147137 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:38158318 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:38163929 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:38146198 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:38150691 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:38146001 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:38146423 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:38178170 C>A did not map to a codon.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr23:38156697 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:21819294 G>T maps to NM_020366.3 G1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:21816376 G>T maps to NM_020366.3 E1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:21794289 C>T maps to NM_020366.3 R890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:21798505 T>C maps to NM_020366.3 H1066H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:21793104 T>G maps to NM_020366.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr16:53674995 T>C maps to NM_015272.2 T969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:53674971 G>A maps to NM_015272.2 F977F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:53653023 G>A maps to NM_015272.2 R1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:53686477 G>A maps to NM_015272.2 S707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:53686794 G>A maps to NM_015272.2 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:53706832 A>G maps to NM_015272.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:53636047 G>A maps to NM_015272.2 V1296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr16:53686653 G>A maps to NM_015272.2 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:53686794 G>A maps to NM_015272.2 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:53705429 A>C maps to NM_015272.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:53720481 G>A maps to NM_015272.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:53691409 T>C maps to NM_015272.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:53720369 G>A maps to NM_015272.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:113306257 G>A maps to NM_001143854.1 W156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:113332451 C>T maps to NM_001143854.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:113285582 G>T maps to NM_001143854.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:113285590 C>A maps to NM_001143854.1 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:113328799 C>T maps to NM_001143854.1 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:89036172 C>T maps to NM_144563.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153628931 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153627715 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153628885 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153631276 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153627879 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153628223 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:153627723 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153629056 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:35437208 G>A maps to NM_007104.4 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:47120324 G>T maps to NM_080746.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:24022838 T>C maps to NM_000975.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:130211897 T>C maps to NM_000976.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:130211948 C>T maps to NM_000976.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr19:49993145 C>T maps to NM_012423.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:49994114 C>T maps to NM_012423.2 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:49993540 C>T maps to NM_012423.2 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:49994338 C>T maps to NM_012423.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:23959934 C>A maps to NM_002948.2 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr3:23960715 G>T maps to NM_002948.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:17973793 C>T maps to NM_000980.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:37358640 C>T maps to NM_000981.3 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:27830371 C>T maps to NM_000982.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:170584254 G>A maps to NM_001099645.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:172396496 G>T maps to NM_016093.2 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:55899310 T>C maps to NM_001136135.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:52028046 A>G maps to NM_000992.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:39711491 C>A maps to NM_000967.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:39709297 C>T maps to NM_000967.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:12880924 C>T maps to ENST00000273223 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr9:127620292 G>A maps to NM_007209.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr23:100650474 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:50085519 G>A maps to NM_001001.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72205369 C>T maps to NM_001035258.1 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:118923905 G>T did not map to a codon.
Sequencing variant TCGA-AX-A062-01A-11W-A027-09 chr23:118923931 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118923916 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:118923916 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:118920673 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118923896 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr16:1997324 G>A maps to NM_005061.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:1997345 G>A maps to NM_005061.2 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:66795004 G>A maps to NM_000968.2 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:66795843 C>T maps to NM_000968.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:93298989 C>T maps to NM_000969.3 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:93303150 G>A maps to NM_000969.3 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:112843671 G>A maps to NM_001024662.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:74205016 C>T maps to ENST00000396470 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:42854003 C>T maps to NM_198486.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:69745319 C>T maps to NM_001003.2 Y11Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr20:35857116 C>A maps to NM_002951.3 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:92660426 T>C maps to NM_006413.4 C266C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:92631781 T>A maps to ENST00000458617 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:92635815 A>G maps to ENST00000458617 L99L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A0JY-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr10:15145709 C>T maps to NM_183005.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:5004146 C>T maps to NM_006638.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:5002392 C>T maps to NM_006638.2 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:36694549 C>T maps to NM_021215.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150444468 C>T maps to NM_015203.3 N1015N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150444621 C>T maps to NM_015203.3 R1066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150445791 C>T maps to NM_015203.3 F1456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:150444615 A>G maps to NM_015203.3 E1064E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:150444918 A>G maps to NM_015203.3 A1165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:150444738 C>T maps to NM_015203.3 T1105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr6:34392482 G>A maps to NM_001014.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:18794396 G>A maps to NM_001030009.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr19:42373816 C>G maps to NM_001022.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:2012498 G>A maps to NM_002952.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr16:2012221 G>A maps to NM_002952.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:60963563 T>C maps to ENST00000337102 *97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr20:60963411 C>T maps to NM_001024.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:81572315 T>C maps to NM_001025.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:55460515 G>A maps to NM_001177413.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:75111791 C>T maps to NM_001005.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:75115192 C>T maps to NM_001005.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:75115079 C>T maps to NM_001005.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:75113454 G>A maps to NM_001005.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:71495439 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:71493731 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:71493732 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:71493123 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:58904470 C>T maps to NM_001009.3 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:58904473 C>A maps to NM_001009.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:58904548 C>T maps to NM_001009.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr9:19376328 G>A maps to NM_001010.2 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:26898371 C>T maps to NM_001006665.1 C604C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:26873395 C>T maps to NM_001006665.1 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:166902390 C>T maps to ENST00000510118 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:166952239 G>A maps to ENST00000510118 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:166827368 C>T maps to ENST00000510118 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:166862307 G>A maps to ENST00000510118 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:166836821 G>A maps to ENST00000510118 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr6:166862262 T>C maps to ENST00000510118 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:166952272 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:166864701 C>T maps to ENST00000510118 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:20179839 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:20193390 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:20185714 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:20213225 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:20173603 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:20213260 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:20204441 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:20227434 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:20185792 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:20204441 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:20187557 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:20183053 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:20179806 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:20194404 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:20212319 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:20194573 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:20185778 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:20204432 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:20222221 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:20185715 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:64138774 G>A maps to NM_003942.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:64126758 G>T maps to NM_003942.2 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:64127680 G>A maps to NM_003942.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:91356875 G>A maps to NM_004755.2 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:91356869 G>A maps to NM_004755.2 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:91389510 A>C maps to NM_004755.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:91360783 T>A maps to NM_004755.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:91413894 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:91339999 A>G maps to NM_004755.2 H712H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:83319303 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:83374938 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr23:83362039 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:83319322 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:83400516 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:83361978 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:83361978 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:83374997 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:83419346 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:83390129 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:83359616 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:83400506 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83361978 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83372109 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83372418 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:83375032 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0V7-01A-21D-A122-09 chr23:83390201 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr23:83351249 T>C did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:83361409 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:83402050 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:83352817 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:83357168 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:58011821 C>T maps to NM_003161.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:58013874 G>A maps to NM_003161.2 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:58024037 T>C maps to NM_003161.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:67202552 G>A maps to NM_003952.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:67200129 T>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr11:67201700 C>T maps to NM_003952.2 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:213414366 C>T maps to NM_012424.3 C516C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:213341223 G>T maps to NM_012424.3 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:213415539 A>G maps to NM_012424.3 Q907Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:213415960 C>A maps to NM_012424.3 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:213414090 T>C maps to NM_012424.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:213414982 G>T maps to NM_012424.3 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:213434920 G>T maps to NM_012424.3 E978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr14:75388103 A>T maps to NM_031464.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:75378029 G>A maps to NM_031464.3 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:3623179 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:45242366 C>T maps to NM_001012.1 H44H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr3:39453846 T>C maps to ENST00000443003 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr1:152127254 G>A maps to NM_001122965.1 Q774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:152128001 G>A maps to NM_001122965.1 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:78704478 C>T maps to NM_020761.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:78811748 C>A maps to NM_020761.2 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:78938084 C>T maps to NM_020761.2 N1321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr17:78617611 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:78796928 C>T maps to NM_020761.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:78811748 C>T maps to NM_020761.2 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr17:78727892 C>T maps to NM_020761.2 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:78796918 T>G maps to NM_020761.2 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:836201 G>T maps to NM_058192.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr16:837434 G>A maps to NM_058192.2 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr16:836266 G>A maps to NM_058192.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:9883731 C>T maps to NM_173659.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:126075477 G>A maps to NM_032795.2 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr11:126081473 G>A maps to NM_032795.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:219457376 C>T maps to NM_005444.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr2:219445457 T>C maps to NM_005444.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:19050247 C>A maps to NM_006570.4 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:55758003 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:55777542 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:55782316 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:55782280 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:55755740 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:55784682 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:55757863 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:55757951 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:55748675 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:55745777 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:55757992 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:39305278 A>G maps to NM_022157.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:39318044 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:90089927 G>A maps to NM_021244.4 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:50138847 G>T maps to NM_006270.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:14316022 T>C maps to NM_012250.5 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr20:17600997 C>T maps to ENST00000377813 K1175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:17602337 G>T maps to ENST00000377813 S1107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:17623772 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:17600358 C>T maps to ENST00000377813 T1198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:17639427 A>G maps to ENST00000377813 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr20:17597403 C>T maps to ENST00000377813 A1280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr6:7229955 C>T maps to NM_001003699.3 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:7211138 C>T maps to NM_001003699.3 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:7231049 C>A maps to NM_001003699.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr6:7246810 G>A maps to NM_001003699.3 P1376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr6:7231193 C>T maps to NM_001003699.3 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:7211816 C>T maps to NM_001003699.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:4142937 T>C maps to NM_001033.3 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:4139573 T>C maps to NM_001033.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:103231056 G>T maps to NM_015713.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:15179552 G>A maps to NM_018427.3 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:99133589 C>T maps to NM_015179.3 W620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:99132883 G>A maps to NM_015179.3 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr10:99129214 G>A maps to NM_015179.3 D974D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr10:99129322 A>G maps to NM_015179.3 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr10:99160848 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr21:45096646 C>A maps to NM_015056.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:45096649 C>T maps to NM_015056.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:42914088 G>A maps to NM_015703.4 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:42908975 G>A maps to NM_015703.4 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:51969627 C>T maps to NM_004704.3 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:51971580 G>A maps to NM_004704.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:51967608 G>T maps to NM_004704.3 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:51970560 C>T maps to NM_004704.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:67341476 C>T maps to NM_015169.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:67341788 G>A maps to NM_015169.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr23:18660233 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18665379 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr23:18690185 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:18674830 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:18662662 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:18665352 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:18690181 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:7018011 C>T maps to NM_080657.4 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:7018218 A>G maps to NM_080657.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:114340490 C>A maps to NM_018364.3 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:114309072 G>A maps to NM_018364.3 C646C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:114319974 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:77325855 G>T maps to NM_198467.2 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:77365790 A>G maps to NM_198467.2 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:77365773 G>T maps to NM_198467.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:77365773 G>T maps to NM_198467.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:77402274 G>A maps to NM_016578.3 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:77378144 C>T maps to NM_016578.3 E1381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr11:77436695 A>G maps to NM_016578.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:77388021 G>A maps to NM_016578.3 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:11933602 G>A maps to NM_015659.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:11931871 G>A maps to NM_015659.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:11931649 C>T maps to NM_015659.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:43913093 G>A maps to NM_080860.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:6798759 C>T maps to NM_173565.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr7:6838056 A>G maps to NM_173565.3 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:6819347 G>T maps to NM_173565.3 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:6821073 G>A maps to NM_173565.3 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:159420831 G>T maps to NM_031924.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:159407450 G>A maps to NM_031924.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:159403717 G>T maps to NM_031924.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:159414905 G>A maps to NM_031924.4 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:116949322 C>T maps to NM_001010892.2 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:116943929 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:116938193 A>G maps to NM_001010892.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:46318263 C>T maps to NM_030785.3 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:46299174 C>T maps to NM_030785.3 E702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:43638601 C>T maps to NM_152732.4 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:43618168 G>A maps to NM_152732.4 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:38079991 C>T maps to NM_001038633.2 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:38080005 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:38079994 G>A maps to NM_001038633.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:108913335 G>A maps to NM_178565.4 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:127440393 C>T maps to ENST00000368317 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr6:127517127 G>A maps to ENST00000368317 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:127440408 C>A maps to ENST00000368317 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:57238575 C>T maps to NM_133368.1 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:57261309 G>A maps to NM_133368.1 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:57261294 T>C maps to NM_133368.1 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:57238575 C>T maps to NM_133368.1 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:157839923 G>T maps to NM_016625.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:122990177 G>A maps to NM_023012.5 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:16794652 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:100741174 G>A maps to NM_001130841.1 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:100741238 G>T maps to NM_001130841.1 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:23476312 G>A maps to NM_014433.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:23401822 C>T maps to NM_014433.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:23406297 G>T maps to NM_014433.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:62305417 G>A maps to ENST00000482936 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:62305429 G>A maps to ENST00000482936 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:62305307 G>T maps to ENST00000482936 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:62294234 C>T maps to ENST00000482936 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr20:62326166 C>T maps to ENST00000482936 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:62324553 G>A maps to ENST00000482936 Q970Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:62294234 C>T maps to ENST00000482936 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:41750030 G>T maps to NM_015138.4 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:41763430 C>T maps to NM_015138.4 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:41767950 C>A maps to NM_015138.4 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:74659787 C>T maps to NM_001015055.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:74656977 G>T maps to NM_001015055.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:64022543 G>A maps to NM_145307.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:64022543 G>A maps to NM_145307.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:64000948 G>A maps to NM_145307.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:64022543 G>A maps to NM_145307.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:101349301 G>A maps to NM_001134888.2 Y608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:101348569 G>A maps to NM_001134888.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:101349643 G>A maps to NM_001134888.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:101348665 G>A maps to NM_001134888.2 R820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:101348785 G>A maps to NM_001134888.2 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:101349907 G>A maps to NM_001134888.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:101348659 G>A maps to NM_001134888.2 F822F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:101347453 G>A maps to NM_001134888.2 V1224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:101348638 G>A maps to NM_001134888.2 I829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:101349703 G>T maps to NM_001134888.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:101348446 G>A maps to NM_001134888.2 I893I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:101349577 G>A maps to NM_001134888.2 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:101350108 G>A maps to NM_001134888.2 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr14:101349697 C>T maps to NM_001134888.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr14:60194063 C>T maps to NM_021136.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:60213101 G>T maps to NM_021136.2 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:60193694 G>A maps to NM_021136.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:60212573 T>C maps to NM_021136.2 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr14:60193991 C>T maps to NM_021136.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:60194386 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:60194111 G>A maps to NM_021136.2 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:60194162 G>A maps to NM_021136.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:45997943 G>A maps to NM_005619.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr19:45997525 C>A maps to NM_005619.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:63472368 G>A maps to ENST00000377819 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:63525731 G>A maps to NM_201430.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:63487585 G>T maps to ENST00000377819 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:63488436 T>C maps to ENST00000377819 V821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:63472321 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:55253095 C>T maps to NM_020532.4 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:55252494 C>A maps to NM_020532.4 E914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:55252929 C>A maps to NM_020532.4 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:55253155 A>C maps to NM_020532.4 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:107019896 C>A maps to NM_032730.4 G389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr17:1840680 A>G maps to NM_178568.2 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr17:1840572 G>A maps to NM_178568.2 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:1840632 G>A maps to NM_178568.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:186917620 G>A maps to NM_153708.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr3:186917638 C>T maps to NM_153708.2 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:186917488 C>T maps to NM_153708.2 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:187088743 G>A maps to NM_022147.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr18:67742585 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:67718778 C>A maps to NM_173630.3 E1731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:67801740 C>T maps to NM_173630.3 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:67806868 C>T maps to NM_173630.3 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr18:67806868 C>T maps to NM_173630.3 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr18:67684646 A>C maps to NM_173630.3 A2139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:67776919 C>T maps to NM_173630.3 T1239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:67742648 C>A maps to NM_173630.3 R1501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:67753847 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:67759946 A>G maps to NM_173630.3 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:179034584 C>T maps to NM_025158.3 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr5:179036468 C>T maps to NM_025158.3 C692C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:70164500 A>C maps to NM_017987.4 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:71655241 G>T maps to NM_001037442.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:71665916 C>T maps to NM_001037442.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr4:71659507 C>T maps to NM_001037442.2 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:71659517 C>T maps to NM_001037442.2 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:42392344 C>T maps to NM_001144825.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:87436835 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:87407140 C>T maps to NM_138290.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:87407140 C>T maps to NM_138290.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:87407140 C>T maps to NM_138290.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:87400010 G>A maps to NM_138290.2 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:36421170 G>T maps to NM_001754.4 S9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:36259145 A>C maps to NM_001754.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:92998376 G>A maps to NM_175634.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:93023319 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:25228663 C>T maps to NM_001031680.2 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:25228690 G>A maps to NM_001031680.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:25256137 G>A maps to NM_001031680.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:155291626 C>A maps to NM_001105203.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:155292034 G>A maps to NM_001105203.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:155291620 C>T maps to NM_001105203.1 H19H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:155295664 T>C maps to NM_001105203.1 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr9:35548530 C>T maps to NM_001135999.1 D671D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:35560482 C>T maps to NM_001135999.1 I1282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35560764 C>A maps to NM_001135999.1 A1376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:35547906 C>A maps to NM_001135999.1 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:35555066 C>T maps to NM_001135999.1 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:127819493 C>A maps to NM_003707.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:49513292 C>T maps to NM_006666.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:116910145 A>T maps to NM_015952.2 K138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:116914254 A>C maps to NM_015952.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:83905937 G>T maps to NM_033411.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:30380774 G>A maps to NM_016940.2 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr21:30380242 C>T maps to NM_016940.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:95712132 T>C maps to NM_015485.4 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr1:95710069 C>G maps to NM_015485.4 S130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:159567979 C>T maps to ENST00000440678 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:159572990 A>G maps to ENST00000440678 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr4:159569720 T>C maps to ENST00000440678 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:159566232 C>T maps to ENST00000440678 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:159573170 G>C maps to ENST00000440678 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:159566192 T>G maps to ENST00000440678 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:32356833 T>A maps to NM_130806.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:32371362 C>A maps to NM_130806.3 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:32332524 G>A maps to NM_130806.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:32365958 C>T maps to NM_130806.3 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:32366824 C>T maps to NM_130806.3 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:32367032 C>T maps to NM_130806.3 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr13:32365985 C>T maps to NM_130806.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:32366032 C>A maps to NM_130806.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:33937424 C>T maps to NM_016568.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:33938065 C>T maps to NM_016568.3 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr5:33938123 G>T maps to NM_016568.3 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:33937696 C>A maps to NM_016568.3 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:155911907 C>T maps to NM_181885.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:155912033 C>T maps to NM_181885.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:137328311 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:137321071 C>T maps to NM_002957.4 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr6:33162786 C>T maps to ENST00000374685 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:165406394 T>C maps to ENST00000367891 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:165397994 C>T maps to NM_006917.4 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:165380011 G>A maps to NM_006917.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:165398201 G>T maps to NM_006917.4 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:165406406 G>T maps to ENST00000367891 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:72427727 G>A maps to ENST00000477973 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:72495647 T>G maps to ENST00000477973 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:72495822 G>T maps to ENST00000477973 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:133896917 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:133907741 C>T maps to ENST00000296084 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:133941270 C>T maps to ENST00000296084 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:39002959 C>T maps to NM_000540.2 I3103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:38985196 C>A maps to NM_000540.2 G2160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:39023369 C>A maps to NM_000540.2 S3751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:38951218 G>A maps to NM_000540.2 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:39057624 C>T maps to NM_000540.2 A4504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:38959987 T>C maps to NM_000540.2 H1200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:38954146 C>T maps to NM_000540.2 Q888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:39005681 C>A maps to NM_000540.2 V3163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:38976331 C>T maps to NM_000540.2 R1679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:38959670 C>A maps to NM_000540.2 G1149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:38997131 G>T maps to NM_000540.2 E2880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:39025820 C>T maps to NM_000540.2 G3800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:39062861 G>T maps to NM_000540.2 L4650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:39003091 C>T maps to NM_000540.2 I3147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:38990275 C>T maps to NM_000540.2 G2343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:38931461 C>T maps to NM_000540.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:39034481 C>T maps to NM_000540.2 H3993H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:38991551 C>T maps to NM_000540.2 I2512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:39075641 C>T maps to NM_000540.2 I4902I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:38987588 G>T maps to NM_000540.2 E2296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:38933032 G>A maps to NM_000540.2 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:39062759 C>T maps to NM_000540.2 A4616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr19:38943578 C>T maps to NM_000540.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:38998417 G>A maps to NM_000540.2 Q2961Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr19:38939045 C>A maps to NM_000540.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr1:237893565 G>A maps to NM_001035.2 R3615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:237604719 C>T maps to NM_001035.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:237608720 C>T maps to NM_001035.2 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:237754196 G>A maps to NM_001035.2 V1355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:237778056 G>T maps to NM_001035.2 G1877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:237863699 C>T maps to NM_001035.2 A3100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:237954754 C>T maps to NM_001035.2 N4501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:237664179 C>T maps to NM_001035.2 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:237711797 C>T maps to NM_001035.2 Q992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:237791141 C>T maps to NM_001035.2 R2068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:237843757 C>T maps to NM_001035.2 V2966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:237875070 C>T maps to NM_001035.2 F3419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:237947137 C>A maps to NM_001035.2 V4042V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:237666765 G>A maps to NM_001035.2 T858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:237787144 C>T maps to NM_001035.2 F1999F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr1:237890493 G>T maps to NM_001035.2 L3611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:237949333 C>T maps to NM_001035.2 A4442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:237659840 T>C maps to NM_001035.2 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:237666612 A>G maps to NM_001035.2 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:237713897 C>T maps to NM_001035.2 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:237806661 T>C maps to NM_001035.2 I2419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:237843757 C>T maps to NM_001035.2 V2966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:237872857 G>A maps to NM_001035.2 S3407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:237957279 A>G maps to NM_001035.2 R4632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:237778052 G>A maps to NM_001035.2 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:237791125 T>C maps to NM_001035.2 I2062I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:237813371 G>T maps to NM_001035.2 E2570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:237664185 T>C maps to NM_001035.2 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:237532832 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:237754221 G>T maps to NM_001035.2 E1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:237780710 C>A maps to NM_001035.2 V1947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:237947911 C>T maps to NM_001035.2 S4300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:237949283 G>T maps to NM_001035.2 E4426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:237949337 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:237838057 G>A maps to NM_001035.2 T2914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:237758839 C>T maps to NM_001035.2 S1493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr1:237604645 G>T maps to NM_001035.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:237850790 G>A maps to NM_001035.2 R3018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:237948059 G>T maps to NM_001035.2 E4350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:237791200 G>A maps to NM_001035.2 L2087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:237729888 C>T maps to NM_001035.2 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:237791105 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:237802447 C>T maps to NM_001035.2 A2354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:237823298 G>A maps to NM_001035.2 W2741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:237798237 G>A maps to NM_001035.2 S2246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:237872857 G>A maps to NM_001035.2 S3407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:237947506 C>G maps to NM_001035.2 V4165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr1:237617759 A>C maps to NM_001035.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:237540623 G>T maps to NM_001035.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:237863555 T>C maps to NM_001035.2 S3052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:237880517 A>G maps to NM_001035.2 E3448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:237982394 C>T maps to NM_001035.2 I4831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:237693783 G>A maps to NM_001035.2 K960K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:237664158 C>T maps to NM_001035.2 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:237732585 G>T maps to NM_001035.2 E1189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:237777626 G>A maps to NM_001035.2 T1733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:237778119 C>T maps to NM_001035.2 L1898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:237819173 G>A maps to NM_001035.2 A2673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:237947308 C>T maps to NM_001035.2 A4099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:237659841 G>T maps to NM_001035.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:237982493 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:237754055 C>T maps to NM_001035.2 I1308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:33795848 C>A maps to NM_001036.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:34064309 G>A maps to NM_001036.3 T3002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:34130645 C>T maps to NM_001036.3 D4155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:34042193 C>T maps to NM_001036.3 V2738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:33873797 T>C maps to NM_001036.3 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:33936602 C>T maps to NM_001036.3 C1216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:34147052 C>T maps to NM_001036.3 I4649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr15:34153352 A>G maps to NM_001036.3 L4813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:33855048 G>A maps to NM_001036.3 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:33895539 C>A maps to NM_001036.3 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:33926899 C>T maps to NM_001036.3 Y1047Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:34015015 C>A maps to NM_001036.3 L2240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:34080593 C>T maps to NM_001036.3 F3255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:34102838 C>T maps to NM_001036.3 R3396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:33938586 G>A maps to NM_001036.3 P1267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:33945008 C>T maps to NM_001036.3 I1411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:33955007 T>C maps to NM_001036.3 S1759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:34130376 C>T maps to NM_001036.3 R4066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:33876638 C>A maps to NM_001036.3 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:33991958 C>T maps to NM_001036.3 R2102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:33876626 C>T maps to NM_001036.3 C535C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:34080593 C>T maps to NM_001036.3 F3255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:34118894 C>T maps to NM_001036.3 D3729D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:33795929 C>T maps to NM_001036.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:34040437 C>T maps to NM_001036.3 R2705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr15:33893706 C>A maps to NM_001036.3 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:34015063 C>T maps to NM_001036.3 L2256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:33831612 C>T maps to NM_001036.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:33835880 G>A maps to NM_001036.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:34049783 G>T maps to NM_001036.3 E2898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:34152814 C>T maps to NM_001036.3 F4773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:34023763 C>A maps to NM_001036.3 L2431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:34133072 C>T maps to NM_001036.3 S4342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:34134068 G>T maps to NM_001036.3 E4348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:34140490 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:34151795 C>T maps to NM_001036.3 Y4721Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr15:34040340 G>A maps to NM_001036.3 A2672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:33603278 G>A maps to NM_001036.3 E11E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:34080413 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:33895386 C>T maps to NM_001036.3 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr15:33855088 G>T maps to NM_001036.3 G342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:34040437 C>T maps to NM_001036.3 R2705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr15:33954713 C>T maps to NM_001036.3 L1661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:153346364 C>A maps to NM_005621.1 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:153587767 C>T maps to NM_020672.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:153391727 C>T maps to NM_176823.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:153333262 C>T maps to NM_002965.3 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:48022244 C>T maps to NM_006272.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:16672550 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:16669189 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:33321533 C>T maps to NM_022753.2 A374A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AX-A05Z-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:10335095 G>A maps to NM_004230.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:91616516 C>T maps to NM_005226.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:18288488 C>T maps to NM_199161.3 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:18269466 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:64811853 C>A maps to ENST00000301885 C289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:45751030 C>A maps to NM_014016.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr13:23912322 C>A maps to NM_014363.4 E1898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:23905089 C>A maps to NM_014363.4 E4309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:23910762 C>A maps to NM_014363.4 E2418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:23909140 C>T maps to NM_014363.4 K2958K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:23911921 A>C maps to NM_014363.4 S2031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:23906233 C>T maps to NM_014363.4 A3927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:23915332 C>T maps to NM_014363.4 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr13:23929961 G>A maps to NM_014363.4 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:23907159 C>A maps to NM_014363.4 E3619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:23913540 C>A maps to NM_014363.4 E1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:23913963 C>A maps to NM_014363.4 E1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:23914716 C>A maps to NM_014363.4 E1100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:23932557 C>A maps to NM_014363.4 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:23907075 C>A maps to NM_014363.4 E3647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:23929247 G>A maps to NM_014363.4 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:23929832 C>T maps to NM_014363.4 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:23911753 C>T maps to NM_014363.4 E2087E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:23930114 G>A maps to NM_014363.4 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr13:23909872 C>T maps to NM_014363.4 S2714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr13:23929565 A>G maps to NM_014363.4 C395C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr13:23939314 C>T maps to NM_014363.4 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:23905089 C>A maps to NM_014363.4 E4309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:23908581 C>A maps to NM_014363.4 E3145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:23914938 C>A maps to NM_014363.4 E1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:23906317 G>A maps to NM_014363.4 L3899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:23913742 C>T maps to NM_014363.4 E1424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:23907633 C>A maps to NM_014363.4 E3461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:23928796 C>A maps to NM_014363.4 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr13:23908276 A>G maps to NM_014363.4 N3246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:47658418 C>T maps to NM_005500.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:47700572 C>T maps to NM_005500.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:47634240 G>A maps to NM_005500.2 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:5657298 C>T maps to ENST00000433404 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:5626444 C>T maps to ENST00000433404 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:5654383 C>T maps to ENST00000433404 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:5654383 C>T maps to ENST00000433404 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:5612548 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:5604901 G>A maps to NM_014649.2 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:5598854 C>T maps to NM_014649.2 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:5595451 C>T maps to NM_014649.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:5616280 G>A maps to NM_014649.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:234250955 T>C maps to NM_000541.4 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:234247399 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:234243688 C>T maps to NM_000541.4 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:234243643 G>A maps to NM_000541.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:234247327 G>A maps to NM_000541.4 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:134988587 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:134991045 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:134994955 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134987433 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134994542 T>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:134990289 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:134992247 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:134995027 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:134989924 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:134988650 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:134983791 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:134993358 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:134994488 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:134994052 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0U9-01B-21D-A10M-09 chr23:134992696 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:134986702 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:134988293 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:134989170 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:134994053 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:134991796 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:134991805 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:134992289 G>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:134991926 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr16:51174488 C>T maps to ENST00000251020 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:51172901 G>A maps to ENST00000251020 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr16:51174791 G>A maps to ENST00000251020 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:51171055 G>A maps to ENST00000251020 F1314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:51172958 G>A maps to ENST00000251020 S1058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:51174551 T>C maps to ENST00000251020 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:51171082 G>A maps to ENST00000251020 N1305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:51174770 G>A maps to ENST00000251020 C454C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr16:51174287 G>T maps to ENST00000251020 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:21990863 G>A maps to NM_005407.1 R1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:21991974 T>C maps to NM_005407.1 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr14:21993141 G>A maps to NM_005407.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr14:21991632 G>A maps to NM_005407.1 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr14:21992766 G>T maps to NM_005407.1 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:21991701 G>A maps to NM_005407.1 N720N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr14:22004983 G>A maps to NM_005407.1 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:76752161 C>T maps to NM_171999.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:76753283 C>T maps to NM_171999.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:76753937 C>T maps to NM_171999.2 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:76757087 C>T maps to NM_171999.2 L1223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:76752161 C>T maps to NM_171999.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:76752161 C>T maps to NM_171999.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:76754951 T>G maps to NM_171999.2 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:76755281 C>T maps to NM_171999.2 G1097G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr20:50408580 C>T maps to NM_020436.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr20:50407890 C>T maps to NM_020436.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:50407920 G>A maps to NM_020436.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:50400989 A>G maps to NM_020436.3 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16G-01A-31D-A12J-09 chr20:50405675 C>A maps to NM_020436.3 R822R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr20:50407890 C>T maps to NM_020436.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:50406957 G>A maps to NM_020436.3 I688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:50408610 G>A maps to NM_020436.3 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:14199246 G>A maps to ENST00000269724 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:14200063 A>G maps to ENST00000269724 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:62607059 G>A maps to NM_080621.4 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:62608658 C>T maps to NM_080621.4 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:865623 C>T maps to ENST00000443100 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr8:119452146 G>T maps to NM_207506.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:130497110 G>A maps to ENST00000457563 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:130505719 C>T maps to ENST00000457563 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:55168924 A>G maps to NM_015589.4 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:39866446 C>T maps to NM_018028.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:39860694 A>G maps to NM_018028.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:39860601 A>G maps to NM_018028.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr19:39871712 G>A maps to NM_018028.2 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:147885588 C>A maps to NM_001030060.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:147885570 G>A maps to NM_001030060.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:169639019 C>T maps to NM_182610.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:169644784 G>A maps to NM_182610.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:76924435 G>A maps to ENST00000372690 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:76910712 C>T maps to ENST00000372690 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr10:76928310 G>A maps to ENST00000372690 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:76910811 C>T maps to ENST00000372690 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:92731609 G>T maps to NM_017654.3 S1267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:92731806 C>A maps to NM_017654.3 E1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:92733357 G>A maps to NM_017654.3 R685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:92731861 C>T maps to NM_017654.3 P1183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:92732491 G>A maps to NM_017654.3 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:92732790 C>A maps to NM_017654.3 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:92732940 G>A maps to NM_017654.3 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:92733820 A>G maps to NM_017654.3 H530H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:92732491 G>A maps to NM_017654.3 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:92735164 C>T maps to NM_017654.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:92733973 C>T maps to NM_017654.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:92732572 G>A maps to NM_017654.3 N946N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:92732788 T>C maps to NM_017654.3 E874E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr7:92731164 G>A maps to NM_017654.3 R1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr7:92763040 G>A maps to NM_152703.2 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:92762527 T>C maps to NM_152703.2 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:92763328 G>A maps to NM_152703.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:92763358 T>C maps to NM_152703.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:92764617 G>A maps to NM_152703.2 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr7:92761722 G>A maps to NM_152703.2 R1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr7:92763808 C>T maps to NM_152703.2 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:92762074 G>T maps to NM_152703.2 V1070V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:92761069 C>T maps to NM_152703.2 T1405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:92763219 G>A maps to NM_152703.2 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:35559207 G>A maps to NM_015474.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr20:35579998 A>G maps to NM_015474.3 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:35533796 C>T maps to NM_015474.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:35559210 C>A maps to NM_015474.3 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr22:44386232 C>A maps to NM_015380.4 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr22:44373839 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:15872854 G>A maps to ENST00000285670 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:128712740 G>A maps to NM_001145928.1 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:128699596 G>A maps to NM_001145928.1 R1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:128770601 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:128783764 T>C maps to NM_001145928.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:128699627 G>A maps to NM_001145928.1 N1068N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr2:128712713 C>T maps to NM_001145928.1 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:21715036 T>C maps to NM_005870.4 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:174295187 G>A maps to NM_003864.3 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:174294637 C>A maps to NM_003864.3 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:133956707 A>G maps to NM_016103.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:136577768 C>A maps to NM_007101.3 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr9:136584057 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:136582454 G>A maps to NM_007101.3 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:26711461 C>T maps to ENST00000379061 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:26711557 C>T maps to ENST00000379061 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:56151230 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:56189807 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U5-01A-11D-A10G-09 chr12:56188665 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:109778705 C>A maps to ENST00000369923 Y359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:39406317 G>A maps to NM_017827.3 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:65744522 G>A maps to NM_005146.4 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65733828 T>C maps to NM_005146.4 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:108929245 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr12:108941741 G>A maps to NM_014706.3 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:108931363 G>A maps to NM_014706.3 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:108924047 C>A maps to NM_014706.3 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:148835567 G>T maps to NM_015278.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr6:148865740 A>G maps to NM_015278.3 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:148854905 G>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:148865683 C>T maps to NM_015278.3 P1026P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr6:148865809 A>G maps to NM_015278.3 T1068T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:148869672 G>A maps to NM_015278.3 P1241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr6:148795285 C>T maps to NM_015278.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:148865585 G>T maps to NM_015278.3 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:128922504 G>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:128927085 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:128927706 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:128927021 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:128926580 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:128927023 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:128927717 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:128927025 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:128926542 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:100572977 T>C maps to NM_194292.1 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:23802061 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:23801841 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:23803447 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:23803527 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:23801479 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:23801976 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:23801954 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:18390844 G>A maps to ENST00000332610 H737H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:18391111 T>C maps to ENST00000332610 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:18458492 C>A maps to ENST00000332610 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:18391081 G>A maps to ENST00000332610 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:18427985 G>A maps to ENST00000332610 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:18393597 G>A maps to ENST00000332610 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:18390811 G>A maps to ENST00000332610 V748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:18436061 C>T maps to ENST00000332610 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:18436006 G>A maps to ENST00000332610 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:18438718 C>A maps to ENST00000332610 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:200136984 C>T maps to NM_001172509.1 E717E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:200245103 C>A maps to NM_001172509.1 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr2:200173512 G>A maps to NM_001172509.1 H570H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:200245103 C>A maps to NM_001172509.1 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:200137386 A>G maps to NM_001172509.1 H583H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:200233325 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:200136960 T>G maps to NM_001172509.1 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:84349969 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:84362814 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:84363392 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:84362714 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:84363933 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:84349939 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:84347535 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:84349143 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:66456123 G>A maps to NM_016038.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:66460317 G>A maps to NM_016038.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:50905769 C>T maps to ENST00000337034 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50902961 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:50903062 G>A maps to ENST00000337034 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:50893472 G>A maps to ENST00000337034 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50897720 C>T maps to ENST00000337034 T1273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50900236 C>T maps to ENST00000337034 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:50898710 G>A maps to ENST00000337034 D1101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:9853897 A>T maps to NM_030962.3 Y1175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:9817408 G>A maps to NM_030962.3 L1513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:9871707 G>A maps to NM_030962.3 R890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:9874254 G>A maps to NM_030962.3 R860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:9810726 T>G maps to NM_030962.3 R1621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr11:9874234 C>T maps to NM_030962.3 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:56047459 G>A maps to NM_001101401.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:123780597 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:123812287 C>A maps to NM_001167856.1 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:123821019 C>A maps to NM_001167856.1 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:123813289 G>A maps to NM_001167856.1 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:123780583 C>T maps to NM_001167856.1 P1351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:123801827 G>A maps to NM_001167856.1 R959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:123834928 C>T maps to NM_001167856.1 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:1149435 G>A maps to NM_014963.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:1111054 G>A maps to NM_014963.2 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:1122967 G>T maps to NM_014963.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:1122523 C>T maps to NM_014963.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:121175081 C>T maps to NM_001024956.2 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:50154137 G>A maps to NM_021228.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:50154320 C>T maps to NM_021228.2 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:127818261 G>T maps to NM_173690.4 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:127781107 G>A maps to NM_173690.4 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:127734009 C>A maps to NM_173690.4 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:75144524 G>A maps to NM_005697.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:75142987 G>A maps to NM_005697.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:75146957 C>T maps to NM_005697.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:155230378 C>T maps to NM_005698.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:155226201 G>T maps to NM_005698.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:155231471 G>T maps to NM_005698.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:155228623 G>T maps to NM_005698.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:155231471 G>T maps to NM_005698.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:75311305 G>A maps to ENST00000361900 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:28540442 G>A maps to NM_052923.1 R1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:28543524 T>C maps to NM_052923.1 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:28542516 C>T maps to NM_052923.1 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:28541333 G>A maps to NM_052923.1 R778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:28543485 C>T maps to NM_052923.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:28540700 C>A maps to NM_052923.1 E989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:28543485 C>T maps to NM_052923.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:47484456 C>T maps to NM_012235.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:47460158 G>A maps to NM_012235.2 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:47467093 G>A maps to NM_012235.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:47455768 G>A maps to NM_012235.2 S1165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:47462160 C>T maps to NM_012235.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:47456403 T>G maps to NM_012235.2 T1073T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:77046261 C>A maps to ENST00000324767 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:76763552 C>T maps to ENST00000324767 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:77064114 C>A maps to ENST00000324767 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:77067329 C>A maps to ENST00000324767 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:76995327 G>A maps to ENST00000324767 R755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:77176173 C>A maps to ENST00000303521 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:77021035 C>A maps to ENST00000324767 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:27516533 C>T maps to NM_016240.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:27516011 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:27514335 C>A maps to NM_016240.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:27737092 G>A maps to NM_173833.5 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:27779208 C>T maps to NM_173833.5 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:125298795 G>T maps to NM_005505.4 Y194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:246923507 A>G maps to NM_016002.2 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:246923513 C>T maps to NM_016002.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:246922347 T>G maps to NM_016002.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:102112121 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:102116291 C>T maps to NM_005063.4 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:102107822 C>T maps to NM_005063.4 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:102116381 C>T maps to NM_005063.4 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:83601921 C>T maps to NM_001037582.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:78171683 G>T maps to NM_144777.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:78177209 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:78165563 G>T maps to NM_144777.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:78183235 G>T maps to NM_144777.2 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:78191732 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:31164034 T>C maps to ENST00000311943 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:31169430 C>A maps to ENST00000311943 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:31107336 C>T maps to ENST00000311943 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:31169430 C>A maps to ENST00000311943 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:31107344 A>G maps to ENST00000311943 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:54179877 C>A maps to NM_152540.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:54231936 C>A maps to NM_152540.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:53751964 A>C maps to NM_152540.3 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr4:53787023 T>C maps to NM_152540.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:224463694 C>T maps to NM_003469.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:224463568 T>C maps to NM_003469.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:224463091 G>A maps to NM_003469.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:224462446 G>T maps to NM_003469.4 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:224463183 C>A maps to NM_003469.4 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:51991520 T>C maps to NM_013243.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:51980574 T>C maps to NM_013243.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:51980523 C>T maps to NM_013243.3 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:62189859 G>T maps to NM_003357.4 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:61960884 G>A maps to NM_006552.1 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:62010902 G>A maps to NM_006551.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:61977970 G>T maps to NM_002407.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:62040451 T>G maps to NM_002411.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:62038494 T>C maps to NM_002411.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:62038353 C>T maps to NM_002411.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:25701505 T>C maps to NM_006998.3 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:25661841 C>A maps to NM_006998.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:25689398 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:25670235 C>T maps to NM_006998.3 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:159614532 G>A maps to NM_001197113.1 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:12662514 C>T maps to NM_001112706.2 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:12662427 C>A maps to NM_001112706.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:130014222 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:129867196 C>T maps to NM_144643.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr4:129924978 G>A maps to NM_144643.2 L115L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A0LE-01A-11D-A127-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:239003068 C>T maps to NM_016510.4 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:239003068 C>T maps to NM_016510.4 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:41536327 A>G maps to NM_001031694.2 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:41494255 G>A maps to NM_001031694.2 H619H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:41493985 G>A maps to NM_001031694.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:41499700 A>G maps to NM_001031694.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:41494327 G>A maps to NM_001031694.2 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:17770060 C>A did not map to a codon.
Sequencing variant TCGA-AP-A05D-01A-11W-A027-09 chr23:17768091 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:17768265 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:17764184 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:17764147 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:17768047 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:17767568 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:17768305 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:17767534 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:17770068 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr23:18266003 T>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:18260682 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:18338510 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18264904 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:18278379 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:18338454 C>A did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:18342124 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:18343048 G>T did not map to a codon.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr23:18264813 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:18264782 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:18264943 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:18264742 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:18276277 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:18260654 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:18338496 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:18338511 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:108067946 G>A maps to NM_198081.3 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:108093500 G>A maps to NM_198081.3 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:38739270 C>A maps to NM_006514.2 E1814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr3:38833560 G>T maps to NM_006514.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:38797356 T>C maps to NM_006514.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:38830527 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr3:38835249 C>T maps to NM_006514.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:38752382 G>T maps to NM_006514.2 T1365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:38739880 G>A maps to NM_006514.2 I1610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:38739270 C>A maps to NM_006514.2 E1814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:38751007 A>G maps to NM_006514.2 V1414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:38739316 G>A maps to NM_006514.2 I1798I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:38739450 C>A maps to NM_006514.2 E1754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:38739538 G>A maps to NM_006514.2 N1724N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:38835284 C>A maps to NM_006514.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:38791624 A>G maps to NM_006514.2 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr3:38802217 G>A maps to NM_006514.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr3:38753912 G>A maps to NM_006514.2 G1276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:38739415 C>T maps to NM_006514.2 S1765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:38936385 C>A maps to ENST00000302328 G825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:38889081 C>T maps to ENST00000302328 S1493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:38927618 T>C maps to ENST00000302328 R982R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:38967000 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:38888901 C>T maps to ENST00000302328 W1553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:38904759 C>A maps to ENST00000302328 E1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:38913737 C>A maps to ENST00000302328 R1147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:38951637 C>T maps to ENST00000302328 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:38966904 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:38888790 G>T maps to ENST00000302328 I1590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr2:166904217 T>C maps to NM_001165963.1 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:166900387 G>A maps to NM_001165963.1 R612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:166848561 A>G maps to NM_001165963.1 C1741C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:166854637 G>T maps to NM_001165963.1 Y1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:166859104 G>A maps to NM_001165963.1 I1387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:166897776 C>T maps to NM_001165963.1 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:166850896 G>A maps to NM_001165963.1 F1537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:166850905 G>T maps to NM_001165963.1 V1534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:166912996 G>A maps to NM_001165963.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:166898844 T>C maps to NM_001165963.1 Q711Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:166900427 A>G maps to NM_001165963.1 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:166895979 C>A maps to NM_001165963.1 G848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:166892675 G>T maps to NM_001165963.1 S1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:166900451 G>A maps to NM_001165963.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:166900384 G>A maps to NM_001165963.1 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:166909377 C>T maps to NM_001165963.1 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:166911179 C>T maps to NM_001165963.1 W190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:166848843 T>C maps to NM_001165963.1 L1647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:166852582 G>T maps to NM_001165963.1 Y1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:166892665 G>A maps to NM_001165963.1 N1107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:35524608 C>T maps to NM_199037.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr19:35524446 G>A maps to NM_199037.3 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:35524419 T>C maps to NM_199037.3 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr2:166245649 C>T maps to NM_001040142.1 N1778N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:166210934 C>T maps to NM_001040142.1 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:166164356 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:166165181 C>A maps to NM_001040142.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:166201303 C>T maps to NM_001040142.1 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:166243299 C>A maps to NM_001040142.1 V1532V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:166165684 G>T maps to NM_001040143.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:166198864 T>G maps to NM_001040142.1 Y816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:166198877 G>T maps to NM_001040142.1 E821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:166201334 G>T maps to NM_001040142.1 E945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:166243359 C>A maps to NM_001040142.1 T1552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:166231199 T>C maps to NM_001040142.1 V1326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:166170494 C>A maps to NM_001040142.1 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:166187838 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:166243299 C>A maps to NM_001040142.1 V1532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:166170458 C>A maps to NM_001040142.1 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:166187924 G>A maps to NM_001040142.1 W745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:166210775 C>T maps to NM_001040142.1 N998N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:166229827 A>C maps to NM_001040142.1 R1315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:166164372 C>A maps to NM_001040142.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr2:166245667 A>G maps to NM_001040142.1 E1784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:166201219 C>T maps to NM_001040142.1 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:166245191 C>T maps to NM_001040142.1 R1626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:166245631 C>T maps to NM_001040142.1 I1772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:118047092 A>G maps to NM_004588.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:165947688 G>A maps to NM_006922.3 I1658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr2:165997295 G>T maps to NM_006922.3 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr2:165947742 C>G maps to NM_006922.3 G1640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:165953956 G>T maps to NM_006922.3 I1348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:165947049 T>C maps to NM_006922.3 R1871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:165947739 G>A maps to NM_006922.3 I1641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:165987767 G>A maps to NM_006922.3 R851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:165997337 C>T maps to NM_006922.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:165947004 G>T maps to NM_006922.3 V1886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:166012312 G>A maps to NM_006922.3 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:165947397 G>T maps to NM_006922.3 I1755I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:165946839 T>C maps to NM_006922.3 K1941K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:165969418 G>A maps to NM_006922.3 C1273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:166003415 G>A maps to NM_006922.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr2:165947766 T>C maps to NM_006922.3 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:165997321 G>A maps to NM_006922.3 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr2:165947295 G>A maps to NM_006922.3 D1789D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr17:62018997 G>A maps to NM_000334.4 S1548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr17:62026051 G>A maps to NM_000334.4 R1021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:62036660 G>A maps to NM_000334.4 N661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:62036708 G>A maps to NM_000334.4 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:62018601 G>T maps to NM_000334.4 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:62019156 G>T maps to NM_000334.4 I1495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:62042028 T>G maps to NM_000334.4 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:62034785 C>T maps to NM_000334.4 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:62050153 G>A maps to NM_000334.4 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr17:62020210 G>A maps to NM_000334.4 F1421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:62049140 G>A maps to NM_000334.4 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:62019252 G>A maps to NM_000334.4 R1463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:62019318 G>A maps to NM_000334.4 F1441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:62026015 G>A maps to NM_000334.4 F1033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:62036623 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:62036708 G>A maps to NM_000334.4 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:62034737 C>T maps to NM_000334.4 Q720Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:118007722 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:118011992 G>A maps to NM_174934.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:118007621 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:118015882 G>T maps to NM_174934.3 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:118007717 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:118007777 G>T maps to NM_174934.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:38671911 G>A maps to NM_001099404.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:38592489 G>A maps to NM_001099404.1 F1791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:38595794 G>A maps to NM_001099404.1 F1596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:38601751 G>A maps to NM_001099404.1 I1377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:38627421 G>A maps to NM_001099404.1 I849I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:38674543 G>T maps to NM_001099404.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:38616790 C>T maps to NM_001099404.1 A1221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:38640472 G>A maps to NM_001099404.1 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:38592426 C>T maps to NM_001099404.1 S1812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr3:38592636 G>A maps to NM_001099404.1 C1742C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:38640472 G>A maps to NM_001099404.1 F653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:38639285 G>A maps to NM_001099404.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:38663892 G>A maps to NM_001099404.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:38595794 G>A maps to NM_001099404.1 F1596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:38607992 G>T maps to NM_001099404.1 V1249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:38628934 G>A maps to NM_001099404.1 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr3:38592795 G>A maps to NM_001099404.1 D1689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr3:38595989 G>A maps to NM_001099404.1 D1531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr3:38646357 G>A maps to NM_001099404.1 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:38598015 G>T maps to NM_001099404.1 V1451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:38622576 C>A maps to NM_001099404.1 E1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:38655513 G>A maps to NM_001099404.1 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:38592882 G>A maps to NM_001099404.1 I1660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:38597182 G>A maps to NM_001099404.1 G1502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:38601708 C>A maps to NM_001099404.1 E1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:38627238 C>T maps to NM_001099404.1 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:38627211 G>A maps to NM_001099404.1 F919F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:38595794 G>A maps to NM_001099404.1 F1596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:167288881 T>C maps to NM_002976.2 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:167334104 T>C maps to NM_002976.2 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr2:167284450 A>T maps to NM_002976.2 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:167313403 A>G maps to NM_002976.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:167322293 G>A maps to NM_002976.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:167279780 G>A maps to NM_002976.2 F1005F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:167322356 G>A maps to NM_002976.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:167262092 G>A maps to NM_002976.2 I1682I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:167321979 T>G maps to NM_002976.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:167322356 G>A maps to NM_002976.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:167288921 G>C maps to NM_002976.2 S833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr2:167297986 G>T maps to NM_002976.2 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:167334151 C>A maps to NM_002976.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:167277770 C>A maps to NM_002976.2 E1022*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:52100279 C>A maps to NM_014191.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:52180591 C>A maps to NM_014191.2 Y1403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:52200654 C>T maps to NM_014191.2 F1795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:52200888 C>T maps to NM_014191.2 F1873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:52159700 C>T maps to NM_014191.2 R931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:52184183 C>T maps to NM_014191.2 F1474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:52200888 C>T maps to NM_014191.2 F1873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:52159700 C>T maps to NM_014191.2 R931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:52099238 C>T maps to NM_014191.2 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:52080886 A>G maps to NM_014191.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:52156454 C>A maps to NM_014191.2 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:52168094 C>T maps to NM_014191.2 F1256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:167141208 G>A maps to ENST00000303354 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:167160828 C>A maps to ENST00000303354 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:167055775 G>A maps to ENST00000303354 P1792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:167055907 G>T maps to ENST00000303354 S1748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:167085230 G>A maps to ENST00000303354 V1393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:167141178 G>A maps to ENST00000303354 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:167168242 T>C maps to ENST00000303354 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:167160828 C>A maps to ENST00000303354 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:167089933 G>T maps to ENST00000303354 Y1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:167085302 G>A maps to ENST00000303354 S1369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:167129145 A>T maps to ENST00000303354 I1039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:167143024 C>A maps to ENST00000303354 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:167160828 C>A maps to ENST00000303354 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:167163021 G>A maps to ENST00000303354 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:167160632 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:167168023 G>T maps to ENST00000303354 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:167056320 G>A maps to ENST00000303354 R1611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:167094708 G>T maps to ENST00000303354 I1233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:23382770 C>T maps to ENST00000307331 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:23392046 G>A maps to ENST00000307331 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr16:23366675 A>G maps to ENST00000307331 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:23364358 C>T maps to ENST00000307331 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:1223176 C>T maps to NM_001130413.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:23197723 C>T maps to NM_001039.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:23197804 C>T maps to NM_001039.3 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:23205490 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:23226489 C>T maps to NM_001039.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:23203722 C>T maps to NM_001039.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:23221150 C>T maps to NM_001039.3 N386N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:10596249 G>A maps to NM_004589.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:10596132 A>G maps to NM_004589.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:10595212 C>A maps to NM_004589.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr22:50962075 C>T maps to NM_001169111.1 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:141264772 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:53453726 G>T maps to NM_002979.4 G334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:53413741 C>T maps to NM_002979.4 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:53453713 G>A maps to NM_002979.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:53443985 G>T maps to NM_002979.4 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:53443985 G>T maps to NM_002979.4 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:53420454 T>C maps to NM_002979.4 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:53443985 G>T maps to NM_002979.4 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:53443888 T>C maps to NM_002979.4 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:55072980 A>G maps to NM_021626.2 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr17:55079508 T>C maps to NM_021626.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:144887347 G>A maps to NM_182706.3 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr8:144885672 G>A maps to NM_182706.3 N1161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr8:144895095 G>A maps to NM_182706.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:144874796 G>A maps to NM_182706.3 L1396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:29966079 G>A maps to NM_001145514.1 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr7:29966214 G>A maps to NM_001145514.1 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:29980429 C>A maps to NM_001145514.1 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:29983740 G>T maps to NM_001145514.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:30029820 C>T maps to NM_001145514.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:175292497 G>T maps to NM_024583.4 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:175263158 G>T maps to NM_024583.4 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:175287640 A>G maps to NM_024583.4 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:175287647 C>T maps to NM_024583.4 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:120252108 G>A maps to NM_002980.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr22:43715940 A>G did not map to a codon.
Alternatively spliced codon TCGA-A5-A0VP-01A-21D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:43610138 G>A maps to NM_173050.2 D670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:43715961 G>A maps to NM_173050.2 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:43735182 G>A maps to NM_173050.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:43606958 G>A maps to NM_173050.2 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:43658774 G>A maps to NM_173050.2 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:43610138 G>A maps to NM_173050.2 D670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:43606958 G>A maps to NM_173050.2 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr22:43687118 G>A maps to NM_173050.2 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr11:9111263 C>T maps to ENST00000457346 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:9100946 G>A maps to ENST00000457346 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:35209436 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:35209658 G>A maps to ENST00000394681 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:35207595 C>T maps to ENST00000394681 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:35213185 C>T maps to ENST00000394681 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr11:65298135 G>T maps to NM_020680.3 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65304187 G>T maps to NM_020680.3 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:65305781 C>T maps to NM_020680.3 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:65304123 C>A maps to NM_020680.3 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:65305742 G>A maps to NM_020680.3 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:100685391 C>T maps to NM_017988.4 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:100727970 G>T maps to NM_017988.4 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:100732874 G>A maps to NM_017988.4 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:100732460 A>G maps to NM_017988.4 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:100732688 C>A maps to NM_017988.4 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:100717364 C>T maps to NM_017988.4 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr12:100709472 T>C maps to NM_017988.4 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:100717325 A>G maps to NM_017988.4 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:169838172 C>T maps to NM_181093.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:76881239 C>A maps to NM_018115.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:76886946 T>C maps to NM_018115.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:76881296 C>A maps to NM_018115.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:97620597 C>A maps to NM_002998.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:97614719 G>A maps to NM_002998.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:97620651 T>C maps to NM_002998.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:31349581 C>T maps to NM_014654.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:31346192 G>T maps to NM_014654.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:31350003 G>A maps to NM_014654.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:1301045 G>A maps to NM_080489.4 Y5Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:139301842 G>A maps to NM_001039707.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr9:139298565 G>A maps to NM_001039707.1 N383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr9:139298624 G>A maps to NM_001039707.1 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:243581363 C>A maps to NM_006642.3 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:243504410 C>A maps to NM_006642.3 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:243493904 G>T maps to NM_006642.3 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:243471351 G>T maps to NM_006642.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:243493966 G>A maps to NM_006642.3 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:243493918 G>A maps to NM_006642.3 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:243456499 T>C maps to NM_006642.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:1163948 G>A maps to NM_016176.3 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr1:1153094 C>T maps to NM_016547.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr5:235381 G>A maps to NM_004168.2 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:226017 G>A maps to NM_004168.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:251210 C>T maps to NM_004168.2 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:233680 C>T maps to NM_004168.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:226017 G>A maps to NM_004168.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:225649 G>A maps to NM_004168.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr5:256474 C>A maps to NM_004168.2 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:161326470 C>A maps to NM_003001.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:161332311 G>A maps to NM_001035511.1 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:4116738 C>A maps to NM_152744.3 T1040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:4014108 C>T maps to NM_152744.3 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:4002353 C>T maps to NM_152744.3 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr7:4008910 C>T maps to NM_152744.3 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:4167088 G>A maps to NM_152744.3 V1300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:4008941 G>T maps to NM_152744.3 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:4152924 C>T maps to NM_152744.3 R1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:4277345 C>T maps to NM_152744.3 I2020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:4014012 G>A maps to NM_152744.3 K610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:4285305 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr7:4014108 C>T maps to NM_152744.3 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:4002439 T>C maps to NM_152744.3 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:4050718 G>A maps to NM_152744.3 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr7:4272965 G>A maps to NM_152744.3 R1969R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr7:4167034 C>T maps to NM_152744.3 N1282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:71420061 G>A maps to NM_001144952.1 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:71375650 G>A maps to NM_001144952.1 S1600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:71380056 G>A maps to NM_001144952.1 R1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:71391348 G>A maps to NM_001144952.1 N1179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:71391486 G>A maps to NM_001144952.1 G1133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:71375665 G>A maps to NM_001144952.1 Y1595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:71415386 G>A maps to NM_001144952.1 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:71418493 G>T maps to NM_001144952.1 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:71335061 G>A maps to NM_001144952.1 Y2061Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr17:71395348 G>A maps to NM_001144952.1 Y1017Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr17:71384113 G>A maps to NM_001144952.1 L1419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:71334929 G>A maps to NM_001144952.1 S2105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:71431697 G>A maps to NM_001144952.1 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:71361433 G>A maps to NM_001144952.1 G1756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr17:71434109 T>A maps to NM_001144952.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:71412022 G>A maps to NM_001144952.1 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:71380056 G>A maps to NM_001144952.1 R1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:192711273 G>A maps to NM_004657.5 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:192711285 G>A maps to NM_004657.5 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:57228615 G>A maps to NM_138969.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:57224746 G>T maps to NM_138969.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:57224829 G>A maps to NM_138969.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr12:57324170 G>A maps to NM_148897.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:113835049 G>A maps to NM_006843.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:113836339 G>T maps to NM_006843.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:113831739 A>G maps to NM_006843.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:113836589 G>A maps to NM_006843.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:113835049 G>A maps to NM_006843.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:113875851 C>T maps to NM_138432.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:113874657 G>T maps to NM_138432.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:85213985 C>T maps to NM_014300.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr18:56823018 C>T maps to NM_033280.2 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr3:10345798 T>A maps to ENST00000343726 K302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:10353684 G>T maps to ENST00000343726 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:10357051 G>T maps to ENST00000343726 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:10346827 G>A maps to ENST00000343726 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:75208057 G>A maps to NM_001039573.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:75209490 C>T maps to NM_001039573.2 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:75202394 C>T maps to NM_001039573.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr17:75208078 C>T maps to NM_001039573.2 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:75190772 C>T maps to NM_001039573.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:75186928 C>T maps to NM_001039573.2 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:30890139 G>A maps to NM_174977.3 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:30890139 G>A maps to NM_174977.3 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr22:30887873 G>A maps to NM_174977.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:30885863 C>A maps to NM_001161368.1 *361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:30886165 C>T maps to NM_174977.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr22:30890139 G>A maps to NM_174977.3 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:5046854 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:5057400 G>T maps to NM_014692.1 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:139357581 G>A maps to NM_014866.1 T1550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:139360537 C>T maps to NM_014866.1 P1393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:139339557 C>T maps to NM_014866.1 S2291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:139369733 C>T maps to NM_014866.1 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr9:139357401 G>A maps to NM_014866.1 A1610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:139353672 G>A maps to NM_014866.1 F1774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:139371121 C>A maps to NM_014866.1 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:139347908 C>A maps to NM_014866.1 E2044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:139353672 G>A maps to NM_014866.1 F1774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:139354290 C>T maps to NM_014866.1 P1703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:177917020 C>T maps to NM_033127.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:177927347 C>T maps to NM_033127.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr1:177930737 A>G maps to NM_033127.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:177921099 T>C maps to NM_033127.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:42594853 C>T maps to NM_032970.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:39560822 G>T maps to NM_006364.2 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:18522971 A>T maps to NM_001172745.1 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:18516316 G>A maps to NM_001172745.1 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:121658164 G>A maps to NM_007190.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:121685666 G>A maps to NM_007190.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:121691750 G>A maps to NM_007190.2 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:121677346 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr10:121662333 G>A maps to NM_007190.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:121662505 G>T maps to NM_007190.2 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:121658164 G>A maps to NM_007190.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr10:121662333 G>C maps to NM_007190.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:121658164 G>A maps to NM_007190.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:133997277 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:134028295 T>G maps to NM_021982.1 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr5:134015362 C>G maps to NM_021982.1 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:133997007 G>A maps to NM_021982.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr5:134002681 A>G maps to NM_021982.1 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:134015380 G>A maps to NM_021982.1 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:134029590 C>T maps to NM_021982.1 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr5:134029433 G>A maps to NM_021982.1 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:110412519 A>G maps to NM_006323.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:110394199 G>A maps to NM_006323.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:110433112 C>T maps to NM_006323.2 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr4:110437682 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr4:110402917 G>A maps to NM_006323.2 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:110434910 G>T maps to NM_006323.2 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr10:75523680 G>A maps to NM_198597.1 K389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:75526137 C>T maps to NM_198597.1 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:75530508 C>T maps to NM_198597.1 R1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr10:75520136 A>G maps to NM_198597.1 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:119652449 A>G maps to ENST00000419654 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:119754818 C>T maps to ENST00000379735 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr4:119666149 C>T maps to ENST00000379735 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:119754805 G>A maps to ENST00000379735 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:119660424 C>T maps to ENST00000379735 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:119649722 G>T maps to ENST00000379735 S985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:83793104 G>A maps to ENST00000505472 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:83788411 G>A maps to ENST00000505472 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr4:83763578 T>A maps to ENST00000505472 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:83793139 G>A maps to ENST00000505472 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:83796936 G>T maps to ENST00000505472 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:83788016 G>A maps to ENST00000505472 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:83787986 G>A maps to ENST00000505472 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:83778842 C>T maps to ENST00000505472 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:102257898 G>A maps to NM_015490.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:102269198 G>A maps to NM_015490.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr10:102267210 C>T maps to NM_015490.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:102249807 G>A maps to NM_015490.3 C974C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr10:102269201 G>A maps to NM_015490.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:12211255 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr10:12211360 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:12211295 A>G maps to NM_001142627.1 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr10:12209884 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:169694782 G>A maps to NM_003262.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:108218909 G>A maps to NM_007214.4 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:108197812 T>C maps to NM_007214.4 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:108215091 C>A maps to NM_007214.4 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:108197770 C>T maps to NM_007214.4 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:91940884 C>A maps to NM_024077.3 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:91949452 A>G maps to NM_024077.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:91940936 G>A maps to NM_024077.3 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr9:91973098 A>G maps to NM_024077.3 P818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:91940540 C>T maps to NM_024077.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:49320862 G>A maps to NM_001193489.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:49327821 C>T maps to NM_001193489.1 W79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:49284581 C>T maps to NM_001193489.1 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr15:49325228 T>C maps to NM_001193489.1 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr15:49293238 G>A maps to NM_001193489.1 Q695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr15:49329894 A>G maps to NM_001193489.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:49309756 A>C maps to NM_001193489.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:80282695 G>A maps to NM_003004.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr17:80280038 A>G maps to NM_003004.2 *249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:80282548 G>T maps to NM_003004.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:12984159 G>A maps to NM_001013437.1 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:81969178 G>A maps to NM_005065.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:81945991 G>A maps to NM_005065.4 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:81943521 G>A maps to NM_005065.4 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:81945988 G>A maps to NM_005065.4 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr14:81945991 G>A maps to NM_005065.4 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:81943521 G>A maps to NM_005065.4 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:81943521 G>A maps to NM_005065.4 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr14:81970623 G>A maps to NM_005065.4 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:81952723 G>A maps to NM_005065.4 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:13850182 G>A maps to NM_025229.1 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:13850237 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:13866046 G>A maps to NM_025229.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:13912372 T>C maps to NM_025229.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:13894443 G>T maps to NM_025229.1 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr20:13845827 G>A maps to NM_025229.1 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:13912270 G>T maps to NM_025229.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:25769162 G>A maps to NM_015187.3 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:25769162 G>A maps to NM_015187.3 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:25806174 C>A maps to NM_015187.3 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:25783980 G>A maps to NM_015187.3 Y780Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:25821486 C>A maps to NM_015187.3 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:169697036 C>T maps to NM_000450.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:169697036 C>T maps to NM_000450.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:151339309 T>C maps to ENST00000435071 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:151341587 G>A maps to ENST00000435071 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:169677597 A>G maps to NM_000655.4 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:169676498 C>T maps to NM_000655.4 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:169673844 A>G maps to NM_000655.4 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:50644928 T>C maps to NM_031454.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:169564065 G>T maps to NM_003005.3 C717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:169581522 A>C maps to NM_003005.3 L298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:169582824 G>A maps to NM_003005.3 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:109017290 C>A maps to ENST00000228463 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:109017753 C>T maps to ENST00000228463 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr12:109017666 C>T maps to ENST00000228463 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:109017099 C>T maps to ENST00000228463 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:109017305 C>A maps to ENST00000228463 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:83764139 G>A maps to NM_006080.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:83592543 G>A maps to NM_006080.2 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr7:83640535 T>C maps to NM_006080.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:83592583 C>T maps to NM_006080.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:50308388 G>A maps to NM_004636.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:50308849 T>C maps to NM_004636.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:50311358 C>T maps to NM_004636.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:80439942 C>T maps to NM_006379.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:84628892 G>A maps to NM_152754.2 Q733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:84644523 C>T maps to NM_152754.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:84628880 T>G maps to NM_152754.2 R737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:84647579 C>T maps to NM_152754.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:84727281 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:84628805 G>A maps to NM_152754.2 R762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:84644454 G>A maps to NM_152754.2 C541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr7:84694808 G>A maps to NM_152754.2 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:84636125 G>A maps to NM_152754.2 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:84628805 G>A maps to NM_152754.2 R762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:84629132 G>A maps to NM_152754.2 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:84697546 A>G maps to NM_152754.2 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:83026003 C>A maps to NM_012431.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:83026003 C>A maps to NM_012431.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:50211373 C>T maps to NM_004186.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:50211310 C>T maps to NM_004186.3 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:50214232 C>T maps to NM_004186.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:50211680 C>T maps to NM_004186.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:50220413 G>A maps to NM_004186.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:52475348 C>T maps to NM_020163.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:52476311 G>A maps to NM_020163.1 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr3:52474032 G>A maps to NM_020163.1 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:52469819 G>A maps to NM_020163.1 F716F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156146322 T>C maps to NM_022367.3 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:156144611 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:156132761 G>A maps to NM_022367.3 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:90768592 A>T maps to NM_198925.2 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:90770879 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:90771448 G>A maps to NM_198925.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr15:90767150 G>A maps to NM_198925.2 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:90771511 G>A maps to NM_198925.2 E717E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:90760698 C>T maps to NM_198925.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:97530524 G>A maps to NM_017789.4 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:97530614 G>A maps to NM_017789.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:97529977 G>A maps to NM_017789.4 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:97530835 G>T maps to NM_017789.4 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:97530781 G>T maps to NM_017789.4 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:91993699 G>A maps to NM_006378.3 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:91994233 C>T maps to NM_006378.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:92007425 C>T maps to NM_006378.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:92007425 C>T maps to NM_006378.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr9:91994305 C>T maps to NM_006378.3 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:92001347 G>T maps to NM_006378.3 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:74907084 C>T maps to NM_004263.3 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:74902958 C>T maps to NM_004263.3 C522C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr2:74884721 C>T maps to NM_004263.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:74902889 T>C maps to NM_004263.3 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:74902417 C>T maps to NM_004263.3 L427L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:102740946 G>T maps to NM_017893.2 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:9054250 G>T maps to NM_003966.2 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:9044505 G>A maps to NM_003966.2 Y1028Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:9337843 C>A maps to NM_003966.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr5:9227037 G>A maps to NM_003966.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:9136645 C>T maps to NM_003966.2 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:9052062 G>A maps to NM_003966.2 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:9066611 C>T maps to NM_003966.2 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:9119117 G>A maps to NM_003966.2 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:9122852 G>A maps to NM_003966.2 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:122641144 G>A maps to NM_001031702.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:122646784 G>A maps to NM_001031702.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:122642462 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:122629719 C>T maps to NM_001031702.2 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:115782911 C>T maps to ENST00000257414 V847V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:115783187 C>T maps to ENST00000257414 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:115815879 C>T maps to ENST00000257414 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:115818195 C>T maps to ENST00000257414 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:4550181 C>T maps to NM_032108.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:4558053 G>A maps to NM_032108.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:151109505 G>A maps to NM_001178061.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:151111186 A>G maps to NM_001178061.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:151108982 C>T maps to NM_001178061.1 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:151112164 G>A maps to NM_001178061.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr15:48063189 G>A maps to NM_153618.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:48062763 C>A maps to NM_153618.1 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:48062913 T>C maps to NM_153618.1 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:48060850 C>A maps to NM_153618.1 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:48057154 T>C maps to NM_153618.1 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:48058155 C>T maps to NM_153618.1 C506C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:48054439 C>T maps to NM_153618.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:48057118 A>G maps to NM_153618.1 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:48058064 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:48062818 C>T maps to NM_153618.1 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:48055252 C>A maps to NM_153618.1 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:48053202 G>T maps to NM_153618.1 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:48063852 C>T maps to NM_153618.1 Y1031Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:48062818 C>T maps to NM_153618.1 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:48052586 C>T maps to NM_153618.1 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:74708936 G>T maps to NM_003612.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:74709055 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr20:43836411 A>G maps to NM_003007.3 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:43836951 G>A maps to NM_003007.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:43850368 G>A maps to NM_003008.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:43851616 C>T maps to NM_003008.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:43850915 C>T maps to NM_003008.2 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:48477429 G>A maps to ENST00000004980 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:48442881 G>A maps to ENST00000004980 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:48468122 T>C maps to ENST00000004980 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:48477429 G>A maps to ENST00000004980 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:185330446 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:185316753 G>A maps to ENST00000427465 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr17:7467981 A>G maps to ENST00000321337 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr3:196612429 T>C maps to NM_152699.4 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:196627273 C>T maps to NM_152699.4 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:76312251 C>G maps to NM_015571.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:76405552 C>T maps to NM_015571.2 D703D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:76419318 C>T maps to NM_015571.2 V931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:76419277 G>T maps to NM_015571.2 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:101058936 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:101085528 C>A maps to NM_020654.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:101066773 A>G maps to NM_020654.3 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:72432104 C>T maps to NM_145204.3 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr15:72432393 G>T maps to NM_145204.3 G144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:72432335 C>T maps to NM_145204.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:87329183 G>A maps to NM_004261.3 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr10:13370372 G>A maps to NM_012247.4 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:13386833 T>C maps to NM_012247.4 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:13380770 G>A maps to NM_012247.4 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:13371763 G>A maps to NM_012247.4 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:26138246 C>T maps to NM_020451.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:26138246 C>T maps to NM_020451.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:26139206 C>T maps to NM_020451.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:26136284 C>T maps to NM_020451.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:26138360 C>A maps to NM_020451.2 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:42807136 C>A maps to NM_001093726.1 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:42807074 A>T maps to NM_001093726.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:42801325 T>G maps to NM_001093726.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:25128910 A>G maps to NM_016955.3 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr16:30393474 G>A maps to NM_052838.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:110310692 C>A maps to ENST00000356688 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:110350672 C>T maps to ENST00000356688 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:110310677 C>A maps to ENST00000356688 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr4:77936124 T>C maps to ENST00000510515 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr16:4828124 C>T maps to NM_144605.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:55872964 C>A maps to NM_207366.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:55874925 G>A maps to NM_207366.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:55873075 C>A maps to NM_207366.2 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:55910721 G>A maps to NM_207366.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:42383222 C>T maps to NM_145733.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:56599407 G>A maps to NM_004574.3 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:56599293 C>T maps to NM_080415.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:19707354 C>T maps to NM_002688.5 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr22:19709390 C>G maps to NM_002688.5 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:19709369 C>T maps to NM_002688.5 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr22:19709216 C>T maps to NM_002688.5 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:118809624 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:118763402 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:118786966 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118786947 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118786966 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:118784026 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:118771049 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:118797510 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118797492 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:118763285 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:118767330 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:118786882 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118786966 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:118763444 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:35922131 C>T maps to NM_001788.4 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:132097283 C>T maps to NM_001098811.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr17:75398441 C>A maps to NM_001113491.1 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:75494649 C>T maps to NM_001113491.1 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:75483611 C>T maps to NM_001113491.1 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:75488707 C>T maps to NM_001113491.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:75494649 C>T maps to NM_001113491.1 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:48284608 C>T maps to NM_003009.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:67890629 G>A maps to NM_001018067.1 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:18010267 C>T maps to NM_012139.2 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:18017454 C>T maps to NM_012139.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:17899773 C>T maps to NM_012139.2 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:18017454 C>T maps to NM_012139.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:42967167 G>A maps to NM_014509.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr22:42951001 G>A maps to NM_014509.3 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:122766248 G>A maps to NM_020755.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:122775305 A>C maps to NM_020755.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:122775053 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:31899624 C>A maps to NM_178865.4 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:43142612 C>T maps to NM_006811.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:44088415 G>T maps to ENST00000319327 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:79498728 G>T maps to NM_001174072.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:94750364 G>T maps to NM_001100607.1 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:94752573 C>T maps to NM_001100607.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:94964559 G>A maps to NM_173850.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:94964290 A>G maps to NM_173850.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:94956016 G>T maps to NM_173850.2 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:95088734 C>T maps to ENST00000393080 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr14:95081023 C>T maps to ENST00000393080 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:95030337 C>T maps to NM_006215.2 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:95034558 G>A maps to NM_006215.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr14:95035832 C>T maps to NM_006215.2 H395H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:95054271 C>T maps to NM_000624.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:95054286 C>T maps to NM_000624.4 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:95054133 C>T maps to NM_000624.4 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:94770826 G>T maps to NM_001756.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:94780382 G>T maps to NM_001756.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr14:94780754 C>T maps to NM_001756.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:105278298 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:105280635 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr23:105280473 G>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:105280539 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:105279309 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:105280745 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:105279209 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:105279330 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:105280932 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:105277493 C>T did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:105277620 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:94931103 G>T maps to NM_175739.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:94933678 C>T maps to NM_175739.3 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:61602400 T>C maps to NM_005024.1 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:61390294 G>T maps to NM_080475.2 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:61390485 G>A maps to NM_080475.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:61383307 T>C maps to NM_080475.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:61390599 G>A maps to NM_080475.2 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:61232676 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:61225623 G>T maps to ENST00000382768 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:61256937 G>T maps to NM_012397.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:61256909 G>A maps to NM_012397.3 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:61570236 G>T maps to NM_001143818.1 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr18:61562610 T>A maps to NM_001143818.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:61324079 G>A maps to NM_006919.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:61325785 G>A maps to NM_006919.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:61324562 G>A maps to NM_006919.2 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr18:61324079 G>A maps to NM_006919.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr18:61326647 C>T maps to NM_006919.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr18:61323249 A>G maps to NM_006919.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:61306939 G>T maps to NM_002974.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:61305069 G>A maps to NM_002974.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:61308225 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:61308146 G>A maps to NM_002974.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:61310451 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:61156656 G>A maps to NM_002639.4 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:2948923 C>A maps to ENST00000316782 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr6:2953313 C>T maps to ENST00000316782 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:2948899 C>A maps to ENST00000316782 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:61471493 G>A maps to NM_001040147.1 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:61465946 C>T maps to NM_001040147.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr18:61471760 A>T maps to NM_001040147.1 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:61654340 C>T maps to NM_198833.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:173873032 A>G maps to NM_000488.3 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:173878807 C>T maps to NM_000488.3 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:173881152 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:21134043 C>T maps to NM_000185.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:21134292 A>G maps to NM_000185.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr22:21134136 G>A maps to NM_000185.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:21134169 C>T maps to NM_000185.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:100771787 C>T maps to NM_000602.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:224849513 C>T maps to NM_001136530.1 W292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:224845061 G>T maps to NM_001136530.1 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:224866563 G>T maps to NM_001136530.1 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:224856583 G>A maps to NM_001136530.1 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr13:51936021 T>C maps to NM_001101320.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:51929177 G>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr13:51935953 T>C maps to NM_001101320.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:1673285 G>A maps to NM_002615.4 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:1675358 G>A maps to NM_002615.4 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:1648294 G>A maps to NM_000934.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:1657506 G>A maps to NM_000934.3 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:57367821 C>T maps to ENST00000403558 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:57373854 G>A maps to ENST00000403558 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:57374021 T>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr11:57373519 G>A maps to ENST00000403558 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:57381993 C>T maps to ENST00000403558 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:75277519 G>A maps to NM_001235.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:75277927 G>A maps to NM_001235.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr11:75282989 C>T maps to NM_001235.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:75280203 C>T maps to NM_001235.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr3:167512529 C>T maps to NM_005025.4 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:167159926 C>T maps to NM_006217.3 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:167183306 G>T maps to NM_006217.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:40929249 C>A maps to NM_013376.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:64863429 C>T maps to NM_014755.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:64863594 C>T maps to NM_014755.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:64863861 G>A maps to NM_014755.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr2:64863704 G>A maps to NM_014755.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:40947407 G>A maps to NM_203344.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:40947732 G>A maps to NM_203344.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:210415270 C>A maps to NM_019605.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:210415588 C>T maps to NM_019605.3 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:210415034 G>T maps to NM_019605.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:210415459 T>C maps to NM_019605.3 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:210415097 G>T maps to NM_019605.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:210414967 C>T maps to NM_019605.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:28599954 C>T maps to NM_031459.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:28607231 C>T maps to NM_031459.3 H454H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:94917634 C>A maps to NM_144665.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:94906472 T>C maps to NM_144665.2 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:94918514 C>A maps to NM_144665.2 G223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:94910995 C>T maps to NM_144665.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:180008404 G>A maps to NM_178123.4 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:42532310 C>T maps to NM_015559.2 D1002D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:42530862 G>T maps to NM_015559.2 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:42529988 C>T maps to NM_015559.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr18:42532628 G>A maps to NM_015559.2 K1108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:42533093 C>A maps to NM_015559.2 Y1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr18:42281509 C>A maps to NM_015559.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr18:42532385 C>T maps to NM_015559.2 D1027D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr18:42618513 G>A maps to NM_015559.2 V1355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:30976118 T>G maps to NM_014712.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:30977163 G>A maps to NM_014712.1 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:30977193 G>A maps to NM_014712.1 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr16:30995305 C>T maps to NM_014712.1 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:30976166 G>A maps to NM_014712.1 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:30977559 G>A maps to NM_014712.1 P786P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:47127804 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:47161745 C>T maps to NM_014159.6 W1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:47161693 C>A maps to NM_014159.6 E1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:47161945 C>A maps to NM_014159.6 E1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:47164576 C>A maps to NM_014159.6 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:47163574 C>A maps to NM_014159.6 E851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:47164010 C>T maps to NM_014159.6 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:47098427 T>C maps to NM_014159.6 V2282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:47061294 G>T maps to NM_014159.6 T2462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr3:47164289 A>G maps to NM_014159.6 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:47162717 T>G maps to NM_014159.6 G1136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr14:99932085 A>G maps to NM_032233.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:99865429 A>G maps to NM_032233.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:99865290 C>A maps to NM_032233.2 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:37431180 C>T maps to NM_017438.3 Q2Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:37429427 A>G maps to NM_017438.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:9516776 G>A maps to ENST00000407969 E1238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:9476085 G>A maps to ENST00000407969 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:9515080 A>G maps to ENST00000407969 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr3:9485041 G>A maps to ENST00000407969 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:9488936 C>A maps to ENST00000407969 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:9506238 C>A maps to ENST00000407969 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr3:9483909 C>A maps to ENST00000407969 S372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:58550477 C>T maps to NM_001160305.1 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:58552389 C>A maps to NM_001160305.1 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:58552788 C>T maps to NM_001160305.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:58550750 G>A maps to NM_001160305.1 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:58552707 C>T maps to NM_001160305.1 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:140444505 A>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:123889510 C>T maps to NM_020382.3 H246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:123892171 G>A maps to NM_020382.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:123875326 C>T maps to NM_020382.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr1:150917637 A>C maps to ENST00000368960 *398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr1:150923545 C>T maps to NM_001145415.1 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150936764 C>T maps to NM_001145415.1 Y1267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:150933438 C>A maps to NM_001145415.1 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:150935117 G>T maps to NM_001145415.1 G1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:150900432 C>A maps to NM_001145415.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:150936156 C>T maps to NM_001145415.1 G1203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:150915097 C>T maps to NM_001145415.1 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:150921903 C>T maps to NM_001145415.1 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:150923290 C>T maps to NM_001145415.1 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:150923194 G>A maps to NM_001145415.1 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:50050872 C>T maps to NM_031915.2 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:50050984 G>T maps to NM_031915.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:50062516 T>A maps to NM_031915.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:50050683 G>A maps to NM_031915.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:50050984 G>T maps to NM_031915.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:4358023 A>G maps to NM_006515.3 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr3:4358390 C>T maps to NM_006515.3 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:4355198 C>A maps to NM_006515.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:4358563 C>T maps to NM_006515.3 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:4358563 C>T maps to NM_006515.3 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:4358242 C>T maps to NM_006515.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:135205028 C>T maps to ENST00000372169 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:135150787 C>A maps to ENST00000372169 E2319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:135204701 C>T maps to ENST00000372169 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:135202085 C>T maps to ENST00000372169 S1633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:135204749 A>G maps to ENST00000372169 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:135150653 G>A maps to ENST00000372169 F2363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:135204044 T>C maps to ENST00000372169 S980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:135150653 G>A maps to ENST00000372169 F2363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:135202511 T>G maps to ENST00000372169 A1491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:135171321 C>A maps to ENST00000372169 E2015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:135202085 C>T maps to ENST00000372169 S1633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:135156868 C>T maps to ENST00000372169 P2213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:135203740 C>A maps to ENST00000372169 E1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:135211829 C>A maps to ENST00000372169 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:135204701 C>T maps to ENST00000372169 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:135205589 C>A maps to ENST00000372169 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:27286890 G>T maps to NM_178860.4 C532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr22:26706650 C>T maps to NM_021115.4 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:26688519 C>T maps to NM_021115.4 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr22:26693011 C>T maps to NM_021115.4 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr22:26747087 G>T maps to NM_021115.4 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:26693014 C>T maps to NM_021115.4 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:26702090 T>C maps to NM_021115.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:26706767 C>T maps to NM_021115.4 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:26707791 C>T maps to NM_021115.4 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:26761392 C>A maps to NM_021115.4 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr22:26688519 C>T maps to NM_021115.4 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:26736437 C>T maps to NM_021115.4 Y684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:29897009 G>A maps to NM_201575.2 D423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:29883758 G>A maps to NM_201575.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:29891293 G>A maps to NM_201575.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:29908167 A>G maps to NM_201575.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:30741086 G>A maps to NM_005877.4 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:30738243 G>A maps to NM_005877.4 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr22:30742336 C>T maps to NM_005877.4 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:38444392 G>A maps to NM_006802.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:38435064 G>A maps to NM_006802.2 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:198273202 G>T maps to NM_012433.2 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:198288677 C>A maps to NM_012433.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:198260868 C>T maps to NM_012433.2 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr2:198283298 A>G maps to NM_012433.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr2:198263269 G>A maps to NM_012433.2 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:198267394 G>A maps to NM_012433.2 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:24297060 G>A maps to NM_016047.3 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:65827009 C>T maps to NM_006842.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:65829167 C>T maps to NM_006842.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:70602199 T>C maps to NM_012426.4 Y989Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:70562789 G>T maps to NM_012426.4 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:149897809 C>T maps to NM_005850.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:32009186 C>T maps to NM_001007467.1 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:32010834 G>A maps to NM_001007467.1 A1019A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:32002313 C>T maps to NM_001007467.1 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:31985510 C>T maps to NM_001007467.1 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:32009142 C>T maps to NM_001007467.1 Q836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:52945097 G>A maps to NM_016329.3 C609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:52950217 C>T maps to NM_016329.3 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:7230653 C>T maps to NM_001018039.1 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:7214495 C>T maps to NM_001018039.1 R704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:7218020 A>G maps to NM_001018039.1 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:7409761 C>T maps to NM_001018039.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:7205749 G>A maps to NM_001018039.1 Y889Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr10:7218057 G>A maps to NM_001018039.1 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:7214510 G>A maps to NM_001018039.1 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr10:7290595 G>A maps to NM_001018039.1 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:7217976 G>A maps to NM_001018039.1 C653C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr10:7409698 C>T maps to NM_001018039.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:7290521 C>T maps to NM_001018039.1 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:27189930 G>A maps to NM_006142.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:27189996 C>G maps to NM_006142.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:35650116 T>C maps to NM_005066.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:35652825 G>A maps to NM_005066.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:35654847 G>A maps to NM_005066.2 D517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:35656460 C>A maps to NM_005066.2 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:35656994 C>A maps to NM_005066.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:35658440 T>C maps to NM_005066.2 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:41122987 C>A maps to NM_003012.4 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:154702868 G>A maps to NM_003013.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:154709591 G>A maps to NM_003013.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:37956178 G>A maps to ENST00000223214 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:166743675 G>A maps to NM_145169.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:81373613 C>T maps to NM_001093770.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:81317074 G>A maps to NM_001098668.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:81317180 G>A maps to NM_001098668.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr10:81319104 G>A maps to NM_001098668.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:81317047 C>A maps to NM_001098668.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:81317180 G>A maps to NM_001098668.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:85892740 C>T maps to NM_198843.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:85890543 G>A maps to NM_198843.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:22020106 G>T maps to NM_003018.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:22019361 G>A maps to NM_003018.3 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:81697823 G>A maps to NM_003019.4 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:174936068 G>T maps to NM_022754.5 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:104492638 A>C maps to NM_178858.4 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:104493351 C>T maps to NM_178858.4 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:102795328 T>C maps to NM_030971.3 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:120923698 G>A maps to NM_213649.1 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:73195599 C>T maps to NM_144579.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:48248024 C>T maps to NM_000023.2 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:52894952 C>T maps to NM_000232.4 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:52890194 G>T maps to NM_000232.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:52895947 G>A maps to NM_000232.4 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:94232652 A>G maps to NM_001099401.1 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:94228091 C>T maps to NM_001099401.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:94228088 C>T maps to NM_001099401.1 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:94232733 C>T maps to NM_001099401.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:23853607 C>T maps to NM_000231.2 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr13:23898583 C>T maps to NM_000231.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:23824854 C>T maps to NM_000231.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:23777863 G>T maps to NM_000231.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:13948041 G>T maps to NM_139167.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:67160158 G>A maps to ENST00000371039 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:67205068 C>T maps to ENST00000237247 R726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:67108545 C>A maps to ENST00000237247 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:67000050 G>T maps to ENST00000237247 G4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:67194968 G>T maps to ENST00000237247 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:67155970 C>A maps to ENST00000237247 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:134492178 G>A maps to NM_001143676.1 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:134492795 C>T maps to NM_001143676.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:134492313 C>T maps to NM_001143676.1 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:134498827 C>A maps to NM_001143677.1 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:42977653 C>T maps to NM_032237.3 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr20:42198071 G>A maps to NM_016276.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr20:42200716 C>T maps to NM_016276.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:8235408 G>A maps to NM_001080826.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:8185951 C>T maps to NM_001080826.1 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:8175768 G>T maps to NM_001080826.1 G1372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr8:8185831 G>A maps to NM_001080826.1 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:77474250 G>T maps to NM_024776.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:77471637 A>C maps to NM_024776.2 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:77425853 G>A maps to NM_024776.2 I1190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:67759559 C>T maps to NM_013257.3 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:67753269 C>A maps to NM_013257.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:108824390 C>A maps to NM_152621.5 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:108824427 C>T maps to NM_152621.5 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:20225462 C>T maps to NM_001012410.3 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:20216353 G>A maps to NM_001012410.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:20225489 G>T maps to NM_001012410.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:20216494 A>C maps to NM_001012410.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:20219760 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:201399719 T>C maps to NM_152524.5 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:201438119 C>T maps to NM_152524.5 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:201436856 C>A maps to NM_152524.5 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:201436083 G>T maps to NM_152524.5 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:201436757 C>T maps to NM_152524.5 D563D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr2:201448170 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:201436259 T>G maps to NM_152524.5 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:72619246 G>T maps to NM_003901.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:64153128 A>G maps to NM_030791.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:78184304 G>A maps to NM_000199.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:25272640 C>T maps to NM_001039948.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:25282586 G>A maps to NM_001039948.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:25313717 C>T maps to NM_001039948.2 R1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:25315898 C>A maps to NM_001039948.2 V1099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:25320204 C>T maps to NM_001039948.2 L1137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr22:25294030 C>T maps to NM_001039948.2 N760N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr22:25270412 C>T maps to NM_001039948.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:2265507 G>A maps to NM_014853.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr17:2270613 C>T maps to NM_014853.2 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:40804665 C>T maps to NM_015705.4 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:40804366 C>T maps to NM_015705.4 F572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr22:40803250 G>A maps to NM_015705.4 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:40798177 C>T maps to NM_015705.4 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:40803469 C>T maps to NM_015705.4 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:40805010 C>T maps to NM_015705.4 C659C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:2769039 G>A maps to NM_003021.3 Y9Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:64968090 C>T maps to NM_019072.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:64976371 T>G maps to NM_019072.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:28878068 G>A maps to NM_001145795.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:28883853 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:28880340 C>T maps to NM_001145795.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:28883580 C>T maps to NM_001145795.1 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr16:28880670 G>T maps to NM_001145795.1 G426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:111884555 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:111885614 C>T maps to NM_005475.2 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123505211 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:123499648 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:123480598 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:123504127 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:123504037 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123504135 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:123499660 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:162372546 G>A maps to NM_053282.4 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr1:156785878 G>A maps to NM_001161441.1 H14H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:6763740 C>A maps to NM_005490.2 G7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr19:6759614 G>A maps to NM_005490.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr9:130513580 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:130502054 G>A maps to NM_170600.2 H771H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr9:130501087 G>A maps to NM_170600.2 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:19190569 G>T maps to NM_022071.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:19231122 C>T maps to NM_022071.3 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:19218746 G>T maps to NM_022071.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:19218808 G>A maps to NM_022071.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:82331300 A>G maps to NM_207372.2 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:85663599 C>T maps to NM_198482.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:85662802 C>A maps to NM_198482.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr15:78390286 C>T maps to NM_001101404.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:78390769 C>T maps to NM_001101404.1 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:78393392 A>G maps to NM_001101404.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr21:40834318 G>T maps to NM_007341.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:80532662 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:80533857 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:80532587 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:80532663 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr23:80533838 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:80532568 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:80532485 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:26607562 C>T maps to ENST00000374243 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr22:38046678 G>A maps to NM_018957.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:2831586 C>G maps to NM_001145856.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr4:2831394 C>A maps to NM_001145856.1 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:235950999 C>T maps to NM_014521.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:235951299 C>T maps to NM_014521.2 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:235951029 C>A maps to NM_014521.2 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:235950306 C>T maps to NM_014521.2 H298H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:235951056 C>T maps to NM_014521.2 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:235950321 T>C maps to NM_014521.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:235950762 C>T maps to NM_014521.2 Y450Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:235949574 C>T maps to NM_014521.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:235949778 C>T maps to NM_014521.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:235950999 C>T maps to NM_014521.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:235950999 C>T maps to NM_014521.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:235951773 C>T maps to NM_014521.2 C787C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:235950762 C>T maps to NM_014521.2 Y450Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:15303664 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:15311246 C>T maps to NM_004844.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:15298549 G>T maps to NM_004844.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:249106374 C>T maps to NM_030645.1 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:249118949 A>G did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:249106302 G>A maps to NM_030645.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:152054263 G>A maps to NM_001009555.3 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:152069120 G>A maps to NM_001009555.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:152096154 C>A maps to NM_001009555.3 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:4365494 G>A maps to NM_003025.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:4366973 G>A maps to NM_003025.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:4361701 C>T maps to NM_003025.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:17795683 C>T maps to NM_003026.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:17795740 G>T maps to NM_003026.2 *353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:17791248 C>A maps to NM_003026.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:84287207 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:84241450 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:84286873 C>A maps to ENST00000434347 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:84286967 G>T maps to ENST00000434347 G333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:84237404 C>T maps to ENST00000434347 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:84241350 G>A maps to ENST00000434347 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr15:84245349 C>T maps to ENST00000434347 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:87188271 A>G maps to ENST00000482504 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:87185203 G>T maps to ENST00000482504 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:131772972 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:131772120 G>A maps to ENST00000372554 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:131771609 G>A maps to ENST00000372554 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:19702024 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:19764515 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:19554555 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19564077 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19610220 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:19713761 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:19606543 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:19554564 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:19560128 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:19560284 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:19613100 C>T did not map to a codon.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr23:19626154 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:19725010 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:19560228 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:19606856 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:19560254 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:105362709 C>T maps to ENST00000369774 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:105484062 G>A maps to ENST00000369774 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr10:105361746 C>T maps to ENST00000369774 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr10:105363273 T>C maps to ENST00000369774 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:171765882 G>A maps to NM_001017995.2 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:171766896 G>T maps to NM_001017995.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:171766620 C>T maps to NM_001017995.2 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:171765537 G>A maps to NM_001017995.2 A857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr4:170190012 G>A maps to NM_020870.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:170017782 C>A maps to NM_020870.3 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:170028268 C>A maps to NM_020870.3 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:145442059 C>T maps to NM_152550.3 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:145439780 C>T maps to NM_152550.3 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:145428703 C>T maps to NM_152550.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:145317745 G>A maps to NM_152550.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:110259139 C>T maps to NM_001099289.1 G847G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:109964257 C>T maps to NM_001099289.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:110259124 C>T maps to NM_001099289.1 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:110107251 C>T maps to NM_001099289.1 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:110107341 G>A maps to NM_001099289.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:8216219 C>T maps to NM_018986.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:8217961 C>T maps to NM_018986.3 H202H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:8217836 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:8220027 C>T maps to NM_018986.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:8237239 C>T maps to NM_018986.3 F1121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr4:8242549 C>T maps to NM_018986.3 D1293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:148386692 T>C maps to ENST00000502274 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:148388413 C>A maps to NM_024577.3 G1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:148407845 A>G maps to NM_024577.3 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:148407674 C>T maps to NM_024577.3 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr5:148384441 G>T maps to NM_024577.3 Y1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:51172438 C>T maps to ENST00000391814 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:51165263 G>A maps to ENST00000391814 R2156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:51220103 C>A maps to ENST00000391814 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:51175332 G>A maps to ENST00000391814 Y880Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:51192472 G>A maps to ENST00000391814 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:51165488 C>T maps to ENST00000391814 S2081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:51165335 G>A maps to ENST00000391814 I2132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:51215202 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr19:51165572 G>A maps to ENST00000391814 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:70319249 C>T maps to ENST00000338508 A1752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:70319005 C>A maps to ENST00000338508 E1834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:70333583 G>A maps to ENST00000338508 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:70507712 G>A maps to ENST00000338508 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:70331579 G>A maps to ENST00000338508 G1600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:70644608 G>A maps to ENST00000338508 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:70333709 C>T maps to ENST00000338508 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:70332332 G>A maps to ENST00000338508 T1349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:70858348 G>A maps to ENST00000338508 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr11:70336398 G>A maps to ENST00000338508 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:51143507 C>T maps to NM_001080420.1 D687D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:51115063 G>A maps to NM_001080420.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:51117212 C>T maps to NM_001080420.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr22:51113642 C>A maps to NM_001080420.1 Y77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:51153474 C>T maps to NM_001080420.1 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:51160274 A>C maps to NM_001080420.1 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:145157952 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr9:37974664 G>T maps to NM_003028.2 Y336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7535062 C>T maps to NM_001040.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:154936281 C>T maps to NM_001130040.1 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:154938527 G>T maps to NM_001130040.1 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:434852 C>T maps to NM_012435.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:438735 G>A maps to NM_012435.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:434831 G>A maps to NM_012435.2 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:91666952 G>A maps to NM_016848.5 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:91657042 C>A maps to NM_016848.5 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:91727525 C>A maps to NM_016848.5 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:91660705 C>A maps to NM_016848.5 G386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:91661836 G>A maps to NM_016848.5 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr9:91660724 A>G maps to NM_016848.5 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr15:49254759 C>A maps to NM_203349.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:49127129 C>A maps to NM_203349.3 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:49160042 G>A maps to NM_203349.3 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:49254675 C>T maps to NM_203349.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:49143402 C>A maps to NM_203349.3 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:46615712 C>T maps to NM_024745.4 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr16:46615862 A>T maps to NM_024745.4 C599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:46637894 C>A maps to NM_024745.4 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr15:45490990 C>T maps to ENST00000437903 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:155596250 G>A maps to NM_000193.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr13:26620839 G>A maps to NM_001007538.1 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr13:26621088 C>T maps to NM_001007538.1 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr13:26620847 G>A maps to NM_001007538.1 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:26620854 G>A maps to NM_001007538.1 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:48511223 G>A maps to NM_016479.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:41086499 C>T maps to NM_138392.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:41083340 C>T maps to NM_138392.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:41089540 C>T maps to NM_138392.3 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:18251701 G>A maps to NM_004169.3 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:18250896 C>T maps to NM_004169.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:57627876 G>A maps to NM_005412.5 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:57626615 C>T maps to NM_005412.5 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:112724415 G>A maps to NM_007373.3 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:112767342 G>T maps to NM_007373.3 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:112724137 G>T maps to NM_007373.3 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:112769581 G>T maps to NM_007373.3 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr10:112767398 C>T maps to NM_007373.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:591763 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:591831 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:595552 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:595371 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:591653 G>T did not map to a codon.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr3:157815965 G>A maps to NM_003030.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:157820597 G>A maps to NM_003030.4 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:157817735 A>C maps to NM_003030.4 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:157818084 G>A maps to NM_003030.4 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:157820577 G>A maps to NM_003030.4 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:3527406 C>T maps to NM_013276.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr17:3526785 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:146267367 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:146264361 G>A maps to ENST00000367503 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr6:146266635 G>A maps to ENST00000367503 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr6:146262962 C>T maps to ENST00000367503 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:146244836 G>A maps to ENST00000367503 R1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:146264652 C>A maps to ENST00000367503 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:146242463 G>A maps to ENST00000367503 R1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:72890311 C>A maps to NM_018130.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:132159326 G>T maps to NM_001172700.1 I647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:9900788 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr23:9912853 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:9907349 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:9862774 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:9863179 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:9905372 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:9912899 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:9863585 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:9914961 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:9912912 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:9859060 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:9866271 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:9862975 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:9907376 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:9900381 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:9905645 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:9863221 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:9863521 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:9912832 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:9863780 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:9900562 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:9900609 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:9912734 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:9914788 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:9905446 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:9841712 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr4:77661572 G>A maps to NM_020859.3 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:77661743 C>A maps to NM_020859.3 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr4:77691967 C>T maps to NM_020859.3 L1847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:77661800 C>T maps to NM_020859.3 F825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:77700113 G>T maps to NM_020859.3 V1925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:77660726 C>A maps to NM_020859.3 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:77675898 G>A maps to NM_020859.3 S1421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr4:77675758 C>T maps to NM_020859.3 R1375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr4:77677829 T>C maps to NM_020859.3 S1646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:77675763 G>A maps to NM_020859.3 Q1376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr4:77651989 G>A maps to NM_020859.3 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:77661689 C>T maps to NM_020859.3 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:50377832 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:50341280 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:50376548 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:50378545 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:50341444 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:50350949 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:50376238 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:50376735 C>A did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:50378302 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:50341506 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr23:50376991 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:50339688 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:50376275 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:50376841 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:50377307 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:50341323 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:50350730 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr23:50350499 A>G did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:50376424 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:50376869 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:50351085 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50351087 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50376328 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50377154 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50377846 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50378020 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:50438804 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:50381208 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:50351123 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:50351182 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:50376744 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:50350811 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:164733850 G>A maps to NM_001041.3 D1259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:164776848 G>A maps to NM_001041.3 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr3:164700075 G>A maps to NM_001041.3 N1790N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:164700135 T>C maps to NM_001041.3 G1770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:164785125 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:164727116 C>A maps to NM_001041.3 E1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:164700060 C>T maps to NM_001041.3 S1795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:164733742 G>T maps to NM_001041.3 I1295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr3:164704923 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:164758843 C>T maps to NM_001041.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:164783128 C>A maps to NM_001041.3 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:164773028 C>A maps to NM_001041.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:164748589 A>T maps to NM_001041.3 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:124509730 G>A maps to NM_170601.3 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:150460185 G>A maps to NM_005067.5 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:150460065 C>T maps to NM_005067.5 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:150480318 C>T maps to NM_005067.5 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr3:150480348 G>T maps to NM_005067.5 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr3:150460071 C>T maps to NM_005067.5 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:46357610 G>T maps to NM_198849.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:46357762 G>A maps to NM_198849.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:113321948 C>T maps to ENST00000393830 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:113286488 C>T maps to ENST00000393830 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:113321984 C>A maps to ENST00000393830 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr3:113327300 C>T maps to ENST00000393830 Y546Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:117052591 G>A maps to NM_001040455.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:117063356 G>A maps to NM_001040455.1 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr11:117066727 G>A maps to NM_001040455.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:407871 G>A maps to NM_021805.2 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:3686997 T>C maps to NM_023068.3 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:3675343 C>T maps to NM_023068.3 T970T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:3677314 G>A maps to NM_023068.3 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:3670696 C>T maps to NM_023068.3 A1602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr20:3677407 C>T maps to NM_023068.3 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:51918561 G>T maps to NM_033130.4 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:51919980 G>T maps to NM_033130.4 C215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:51919986 G>T maps to NM_033130.4 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:51917746 C>T maps to NM_033130.4 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:51918216 G>A maps to NM_033130.4 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:51920435 G>A maps to NM_033130.4 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr19:51919314 G>A maps to NM_033130.4 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr19:50463397 C>A maps to NM_052884.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:50463968 C>T maps to NM_052884.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:50455598 G>A maps to NM_052884.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:50461971 C>A maps to NM_052884.2 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr19:52001406 G>A maps to NM_053003.2 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:52001488 G>T maps to NM_053003.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:52003468 G>T maps to ENST00000441969 C22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:52004981 T>C maps to NM_053003.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:52149197 G>T maps to NM_001098612.1 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:52147277 G>A maps to NM_001098612.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:52132803 G>A maps to ENST00000222107 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:52133241 G>A maps to NM_003830.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:52131126 C>T maps to ENST00000222107 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr19:52133125 T>C maps to NM_003830.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:52130418 G>A maps to ENST00000222107 C455C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:52133128 T>G maps to NM_003830.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr19:52129334 T>A maps to ENST00000222107 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:52034450 G>A maps to NM_001245.5 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:52023365 A>G maps to NM_001245.5 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:52031430 A>G maps to NM_001245.5 C363C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:51648166 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:51960913 G>T maps to NM_014442.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:51958903 G>A maps to NM_014442.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:51961500 G>T maps to NM_014442.2 C47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:51958773 G>A maps to NM_014442.2 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:51955791 A>G maps to NM_014442.2 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:51957993 G>A maps to NM_014442.2 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:51960724 G>A maps to NM_014442.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:51630305 T>C maps to NM_014441.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:51630503 T>C maps to NM_014441.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr21:44838263 C>T maps to NM_173354.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr21:44836855 G>T maps to NM_173354.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:111574102 C>T maps to NM_015191.1 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:111575754 C>T maps to NM_015191.1 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:111594232 C>T maps to NM_015191.1 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:111582954 A>G maps to NM_015191.1 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:111571608 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:111594309 G>A maps to NM_015191.1 Q746Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:116718321 T>C maps to ENST00000445177 V1267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:116733034 C>T maps to ENST00000445177 E697E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr11:116728622 A>C maps to ENST00000445177 S1179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:116717159 G>A maps to ENST00000445177 S1347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:116719844 G>A maps to ENST00000445177 D1263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:116730252 C>T maps to ENST00000445177 E824E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr11:116968891 G>C maps to ENST00000445177 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:138362519 C>T maps to ENST00000509534 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr5:138282843 G>A maps to ENST00000509534 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:100838365 G>A maps to ENST00000262901 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:100911230 G>A maps to ENST00000262901 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:100896034 G>A maps to ENST00000262901 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:100841486 C>T maps to ENST00000262901 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr6:100838698 T>C maps to ENST00000262901 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:100895235 G>A maps to ENST00000262901 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr6:100896392 G>A maps to ENST00000262901 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:38095364 G>A maps to NM_005069.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:38072204 C>T maps to NM_005069.3 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:38095374 C>T maps to NM_005069.3 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:75684744 G>A maps to NM_001145357.1 R897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:75684841 G>A maps to NM_001145357.1 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:75673042 G>A maps to NM_001145357.1 R1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:75687178 G>A maps to NM_001145357.1 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:75684801 C>A maps to NM_001145357.1 G878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr15:75693184 G>A maps to NM_001145357.1 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr15:75684630 G>A maps to NM_001145357.1 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr15:75704003 C>T maps to NM_001145357.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr15:75673042 G>A maps to NM_001145357.1 R1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:16942358 T>C maps to NM_015260.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:16974594 C>T maps to NM_015260.1 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:16973371 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:16952772 G>A maps to NM_015260.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr19:16942394 C>T maps to NM_015260.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:65409719 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr11:65417454 C>T maps to NM_153253.29 D927D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:65418140 C>T maps to NM_153253.29 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:72117174 C>T maps to NM_015556.1 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:72128130 C>T maps to NM_015556.1 H734H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:72128058 C>T maps to NM_015556.1 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:72205751 T>C maps to NM_015556.1 A1763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:72128058 C>T maps to NM_015556.1 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:72205853 C>A maps to NM_015556.1 V1797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:72054862 G>T maps to NM_015556.1 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr14:72152327 C>T maps to NM_015556.1 D1118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:72117050 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:72196848 G>A maps to NM_015556.1 S1585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:72152255 T>C maps to NM_015556.1 N1094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:72055105 C>T maps to NM_015556.1 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:72152141 C>T maps to NM_015556.1 Y1056Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:232626676 T>C maps to NM_020808.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:232626723 C>A maps to NM_020808.3 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:232561500 A>G maps to NM_020808.3 S1488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:232601013 G>A maps to NM_020808.3 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:232650433 C>A maps to NM_020808.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr1:232581276 C>T maps to NM_020808.3 T1117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:232561506 C>T maps to NM_020808.3 T1486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:232596889 G>A maps to NM_020808.3 C946C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:232600770 C>A maps to NM_020808.3 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr1:232574912 G>A maps to NM_020808.3 S1324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:232581432 C>T maps to NM_020808.3 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:232600900 C>T maps to NM_020808.3 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr1:232619628 C>T maps to NM_020808.3 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:232626733 T>C maps to NM_020808.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:232650227 C>T maps to NM_020808.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:232601116 C>T maps to NM_020808.3 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:38633323 C>T maps to NM_015073.1 Y1169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:38572735 C>T maps to NM_015073.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:38573233 C>T maps to NM_015073.1 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:38600898 C>T maps to NM_015073.1 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:38610380 C>T maps to NM_015073.1 F909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:38597228 C>A maps to NM_015073.1 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:38655538 C>T maps to NM_015073.1 Q1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:38692532 C>T maps to NM_015073.1 N1672N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:38579376 C>T maps to NM_015073.1 F517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:1902122 C>T maps to ENST00000400068 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:1905410 G>A maps to ENST00000400068 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:1895790 C>T maps to ENST00000400068 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr20:1903211 C>T maps to ENST00000400068 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:1915388 G>T maps to ENST00000400068 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr20:1559158 G>A maps to NM_006065.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:1546800 T>C maps to NM_006065.3 *399W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr20:1546899 A>G maps to NM_006065.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:1551637 C>T maps to NM_006065.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr20:1471987 C>T maps to NM_001122962.1 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:1460543 A>T maps to NM_001122962.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:1457956 G>T maps to ENST00000381628 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:1629947 G>A maps to NM_018556.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:1615979 C>T maps to NM_018556.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:1616903 G>A maps to NM_018556.3 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:1616975 A>G maps to NM_018556.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:1630054 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:1629904 C>A maps to NM_018556.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:1616216 C>T maps to NM_018556.3 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:69672430 G>T maps to NM_012238.4 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:69672271 G>T maps to NM_012238.4 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:69669101 A>G maps to NM_012238.4 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:69676199 C>T maps to NM_012238.4 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:39370136 G>A maps to NM_012237.3 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:39374312 G>A maps to NM_012237.3 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:120741375 C>T maps to NM_012240.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:120750519 C>T maps to NM_012240.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:120750736 G>A maps to NM_012240.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:13595736 T>C maps to NM_012241.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:13588576 C>T maps to NM_012241.3 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr17:79872256 C>T maps to NM_016538.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:35650039 C>T maps to NM_014450.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:35650210 C>T maps to NM_014450.2 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr14:105221977 C>T maps to NM_006427.3 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:61115709 G>A maps to NM_005982.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:45236030 G>A maps to NM_016932.4 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:45233379 G>A maps to NM_016932.4 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr2:45235817 C>T maps to NM_016932.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:45233416 T>C maps to NM_016932.4 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:45233308 C>A maps to NM_016932.4 *292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:45236183 C>T maps to NM_016932.4 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:45169812 G>A maps to NM_005413.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:61190737 C>A maps to NM_017420.4 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr14:61186820 G>A maps to NM_017420.4 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:61180559 A>G maps to NM_017420.4 I637I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:46269106 G>A maps to NM_175875.4 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr19:46268938 T>C maps to NM_175875.4 E680E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr14:60976475 G>C maps to ENST00000381716 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr14:60976247 C>T maps to ENST00000381716 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:57196745 G>A maps to NM_182620.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:57189673 C>T maps to NM_182620.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:21734121 G>A maps to NM_145061.5 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:21746625 A>C maps to NM_145061.5 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr13:21742299 G>T maps to NM_145061.5 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:26729928 A>G maps to NM_003930.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:170110204 G>T maps to NM_005414.3 *685Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:170102356 A>G maps to NM_005414.3 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:170078545 G>T maps to NM_005414.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr3:170108990 A>G maps to NM_005414.3 Q613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr5:54635987 A>G maps to NM_015360.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:54603975 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:54674268 A>G maps to NM_015360.4 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:54640442 G>T maps to NM_015360.4 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:54618269 G>T maps to NM_015360.4 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:54649098 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:54718746 C>T maps to NM_015360.4 R1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:134072407 C>A maps to NM_006748.3 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr20:35242811 G>A maps to NM_032214.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:78318541 G>A maps to ENST00000389459 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr4:48385787 T>C maps to NM_020846.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:48422244 C>T maps to NM_020846.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:48422226 C>T maps to NM_020846.1 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:160589592 C>T maps to NM_003037.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:160604637 G>A maps to NM_003037.2 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:160461122 G>T maps to NM_001184714.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:160718188 C>T maps to NM_021181.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:160718302 C>T maps to NM_021181.3 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:159803055 A>C maps to NM_020125.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:159799776 G>A maps to NM_020125.2 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:159922265 G>A maps to NM_033438.3 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:159923132 G>T maps to NM_033438.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:159922142 C>T maps to NM_033438.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:1698019 G>A maps to ENST00000318386 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr13:103718242 G>A maps to NM_000452.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:103718398 G>A maps to NM_000452.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:103718443 G>A maps to NM_000452.2 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:103710650 G>A maps to NM_000452.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:153716639 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153716358 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153716395 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153716388 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:153716713 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:153716662 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:48490748 T>C maps to NM_152679.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr8:82606558 C>A maps to NM_001010893.2 G217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr8:82606129 G>A maps to NM_001010893.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:87744921 A>G maps to NM_197965.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr4:87770133 G>C maps to NM_197965.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:147431198 C>T maps to ENST00000507030 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:147247142 G>A maps to ENST00000507030 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr2:219249961 C>T maps to NM_000578.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:219254675 C>A maps to NM_000578.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:219252581 C>T maps to NM_000578.3 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:51390698 G>T maps to NM_001174125.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:48551501 C>A maps to NM_000338.2 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:48537079 C>T maps to NM_000338.2 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:48591408 G>A maps to NM_000338.2 E1011E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:48593535 G>T maps to NM_000338.2 E1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:48500104 G>A maps to NM_000338.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:48518751 C>T maps to NM_000338.2 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:48593526 C>T maps to NM_000338.2 R1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:48593570 C>A maps to NM_000338.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:48595009 C>T maps to NM_000338.2 I1076I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:48521428 C>T maps to NM_000338.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:127518624 G>A maps to NM_001046.2 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:127474290 G>T maps to NM_001046.2 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:127474323 C>T maps to NM_001046.2 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:127520112 G>T maps to NM_001046.2 E1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:127518628 G>T maps to NM_001046.2 E1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:127520156 A>G maps to NM_001046.2 R1133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:56936314 C>A maps to NM_000339.2 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr16:56899290 C>T maps to NM_000339.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:56914073 C>T maps to NM_000339.2 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:56901106 C>T maps to NM_000339.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:56920908 C>T maps to NM_000339.2 N694N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr16:56926061 C>T maps to NM_000339.2 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:56904128 C>T maps to NM_000339.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:56926067 C>T maps to NM_000339.2 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr16:56918060 C>G maps to NM_000339.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr16:67983737 G>A maps to NM_005072.4 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:67985133 C>T maps to NM_005072.4 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:67985801 G>A maps to NM_005072.4 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr16:67995579 C>G maps to NM_005072.4 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:44680390 C>T maps to NM_001134771.1 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:44665381 G>A maps to NM_001134771.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:44682326 G>A maps to NM_001134771.1 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:44681755 G>A maps to NM_001134771.1 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:44685095 G>A maps to NM_001134771.1 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:44685544 G>A maps to NM_001134771.1 E1063E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr20:44664474 C>T maps to NM_001134771.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr20:44674991 C>A maps to NM_001134771.1 C591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:44665417 G>A maps to NM_001134771.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr20:44673610 C>T maps to NM_001134771.1 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr20:44671939 C>A maps to NM_001134771.1 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr20:44680426 G>C maps to NM_001134771.1 G788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:34532927 A>G maps to NM_133647.1 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:34538064 G>A maps to NM_133647.1 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:34538064 G>A maps to NM_133647.1 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:34553177 G>T maps to NM_133647.1 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:34543217 G>A maps to NM_133647.1 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:34553132 G>T maps to NM_133647.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:1060509 C>T maps to NM_006598.2 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr5:1053520 G>A maps to NM_006598.2 Q1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:1074767 G>C maps to NM_006598.2 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:124802799 G>A maps to NM_001195483.1 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:124896593 C>T maps to NM_001195483.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:100459115 G>A maps to NM_020246.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:100452338 C>T maps to NM_020246.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr7:122768953 G>A maps to NM_022444.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:122839955 G>A maps to NM_022444.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:122787339 G>A maps to NM_022444.3 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:122774537 C>T maps to NM_022444.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:122809210 C>A maps to NM_022444.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:122757603 G>T maps to NM_022444.3 S524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:26820717 C>T maps to NM_001145975.1 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:26818768 C>T maps to NM_001145975.1 N308N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:26816242 C>T maps to NM_001145975.1 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:26817587 C>T maps to NM_001145975.1 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:26817353 C>T maps to NM_001145975.1 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:26820717 C>T maps to NM_001145975.1 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:45192103 C>T maps to NM_022829.5 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr7:135376065 G>A maps to NM_012450.2 N442N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:135368985 G>T maps to NM_012450.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr17:6594139 G>A maps to NM_177550.3 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:6616610 G>A maps to NM_177550.3 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:6599002 C>T maps to ENST00000381074 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr18:43311040 C>T maps to NM_001146037.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:43316498 G>A maps to NM_001146037.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr18:43307322 C>T maps to NM_001146037.1 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr18:43205787 C>T maps to NM_007163.3 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:43204724 G>A maps to NM_007163.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:43262477 C>A maps to NM_007163.3 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:43207073 G>A maps to NM_007163.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:43205688 C>T maps to NM_007163.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:43224099 C>T maps to NM_007163.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:43207094 C>T maps to NM_007163.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr18:43224063 C>T maps to NM_007163.3 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr13:99338467 T>C maps to NM_005073.3 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:99362007 G>A maps to NM_005073.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:99378399 G>A maps to NM_005073.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:99338473 G>A maps to NM_005073.3 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr13:99361824 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:60705441 G>A maps to NM_016582.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr11:60714275 G>T maps to NM_016582.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:129299465 G>A maps to ENST00000376744 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:129278781 G>A maps to ENST00000376744 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:129285462 C>T maps to ENST00000376744 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:113456589 C>A maps to NM_003051.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:113460300 G>A maps to NM_003051.3 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:113459959 G>A maps to NM_003051.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr1:113459863 G>A maps to NM_003051.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:111543324 G>T maps to NM_018593.4 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:111543272 T>C maps to NM_018593.4 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:111543348 G>T maps to NM_018593.4 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:111540096 C>A maps to NM_018593.4 C389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr6:111498810 G>A maps to NM_018593.4 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr17:6945387 T>A maps to NM_153357.1 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:91198923 A>C maps to NM_213606.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:91196036 G>A maps to NM_213606.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:91203555 C>T maps to NM_213606.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:91198854 G>A maps to NM_213606.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:91196036 G>A maps to NM_213606.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:91198649 C>A maps to NM_213606.3 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:91203588 G>A maps to NM_213606.3 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:91192942 C>A maps to NM_213606.3 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:91192859 C>T maps to NM_213606.3 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:230911370 G>A maps to NM_152527.4 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:230911250 G>A maps to NM_152527.4 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:73744369 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:73744254 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:73749146 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:73641703 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:73740841 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:73749104 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:73744532 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr23:73751372 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr23:73744293 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:73744202 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:73744451 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:73751176 G>A did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:73744294 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:73744266 C>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:73641339 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:73749176 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr23:73740832 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:80195518 G>T maps to NM_001042423.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr17:80194608 G>A maps to NM_001042423.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:73089832 C>T maps to ENST00000450736 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:73089931 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:66274372 G>T maps to NM_004694.4 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:66267274 G>A maps to NM_004694.4 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:66274254 G>T maps to NM_004694.4 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:66268801 G>A maps to NM_004694.4 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:66274338 G>T maps to NM_004694.4 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:60098689 C>T maps to NM_004731.3 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:60168460 C>T maps to NM_004731.3 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:60173361 G>T maps to NM_004731.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:60169009 C>T maps to NM_004731.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:60173309 T>C maps to NM_004731.3 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:60168774 T>G maps to NM_004731.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:60168517 G>T maps to NM_004731.3 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:61414116 C>A maps to NM_194298.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:61412568 A>C maps to NM_194298.2 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:61413679 C>T maps to NM_194298.2 W368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:25813343 G>T maps to NM_005074.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr6:25813441 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:25915984 G>A maps to NM_005835.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:25924039 C>T maps to NM_005835.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:25851049 G>A maps to NM_001098486.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:25855458 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:25862046 G>A maps to NM_001098486.1 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr6:25851094 G>A maps to NM_001098486.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:25851021 C>A maps to NM_001098486.1 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:25862046 G>A maps to NM_001098486.1 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:25845644 C>A maps to NM_001098486.1 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr6:25868564 T>C maps to NM_001098486.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:25769211 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr6:25773853 G>A maps to NM_005495.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:25771172 C>T maps to NM_005495.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:22384324 C>T maps to NM_020346.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr11:22399004 G>T maps to NM_020346.2 G490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:22363298 C>A maps to NM_020346.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:22382530 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:22398169 G>A maps to NM_020346.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:22364815 G>A maps to NM_020346.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:22396309 C>T maps to NM_020346.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:49937252 G>A maps to NM_020309.3 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:100813601 G>T maps to NM_139319.2 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:61597011 C>A maps to NM_022082.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:61588221 C>T maps to NM_022082.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:20008214 G>A maps to NM_001135691.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:20036651 G>A maps to NM_001135691.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:20005545 G>A maps to NM_001135691.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr8:20036740 G>A maps to NM_001135691.2 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:119029886 G>A maps to NM_003054.4 W451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr10:119003743 C>T maps to NM_003054.4 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr10:119013616 C>T maps to NM_003054.4 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:50818905 C>T maps to NM_003055.2 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr10:50820255 G>A maps to NM_003055.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:50819454 C>T maps to NM_003055.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:50819649 C>T maps to NM_003055.2 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:50819175 C>T maps to NM_003055.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr21:46951345 C>T maps to NM_194255.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr21:46951606 G>A maps to NM_194255.1 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr21:46951390 G>A maps to NM_194255.1 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:228563509 C>T maps to NM_025243.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:228566926 G>T maps to NM_025243.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr2:228564141 G>A maps to NM_025243.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:228563887 G>A maps to NM_025243.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:4567710 G>T maps to NM_004170.5 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:4573930 C>T maps to NM_004170.5 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:35339031 G>A maps to NM_004171.3 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:35308446 A>G maps to NM_004171.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:35287081 C>A maps to NM_004171.3 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr11:35323076 G>A maps to NM_004171.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:36629690 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:36671137 G>A maps to NM_004172.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:36608596 A>G maps to NM_004172.4 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:65243798 C>A maps to NM_003038.4 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr2:65245366 A>G maps to NM_003038.4 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:47278814 C>T maps to NM_005628.2 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr19:15079218 G>A maps to NM_005071.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:15083542 C>T maps to NM_005071.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:53558350 G>A maps to NM_006671.4 C302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:53569135 G>T maps to NM_006671.4 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:53580545 G>A maps to NM_006671.4 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:53558443 G>A maps to NM_006671.4 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:53555606 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:53553754 G>A maps to NM_006671.4 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:53556426 G>A maps to NM_006671.4 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:113417109 C>T maps to NM_005415.3 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:113417109 C>T maps to NM_005415.3 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:42294688 C>T maps to NM_006749.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr8:42287685 C>T maps to NM_006749.3 W535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr8:42294517 G>T maps to NM_006749.3 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:160557670 G>A maps to NM_003057.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:160579592 C>A maps to NM_003057.2 T548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:160564675 C>T maps to NM_003057.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:160555067 G>A maps to NM_003057.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:63069799 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:63067096 T>C maps to NM_001039752.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:64359372 G>A maps to NM_144585.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:38316633 C>T maps to NM_004256.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr3:38357967 G>A maps to NM_004803.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:38355331 C>T maps to NM_004803.3 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:38347756 G>A maps to NM_004803.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:38354585 C>A maps to NM_004803.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:116577888 G>A maps to NM_018420.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:116609273 C>A maps to NM_018420.2 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:110763906 C>T maps to NM_033125.2 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:110768129 C>T maps to NM_033125.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:110778003 C>T maps to NM_033125.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:23818556 G>T maps to NM_020372.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:23817803 G>A maps to NM_020372.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:23817480 G>A maps to NM_020372.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:2943414 C>T maps to NM_002555.5 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:2940621 C>T maps to NM_002555.5 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:160679513 G>A maps to NM_003058.3 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:160670366 G>A maps to NM_003058.3 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:160666544 T>C maps to NM_003058.3 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:160677662 G>A maps to NM_003058.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:160645759 G>A maps to NM_003058.3 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:160662569 G>T maps to NM_003058.3 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:160679618 G>A maps to NM_003058.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:160668275 G>A maps to NM_003058.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr6:160664700 G>T maps to NM_003058.3 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:160662518 C>T maps to NM_003058.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:160679513 G>A maps to NM_003058.3 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:160679774 C>T maps to NM_003058.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:160679603 G>A maps to NM_003058.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:64985149 C>T maps to ENST00000438990 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:65009496 G>T maps to ENST00000438990 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:65009545 G>T maps to ENST00000454680 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:64985098 C>T maps to ENST00000438990 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr6:3273420 C>T maps to ENST00000436008 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:3287186 G>A maps to ENST00000436008 C484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:62863493 G>A maps to NM_001136506.1 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:62948201 T>A maps to NM_199352.3 K334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:62996887 G>A maps to NM_199352.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:62948222 C>A maps to NM_199352.3 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:160829920 G>A maps to ENST00000392145 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:160829947 T>G maps to ENST00000392145 Y284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:160857810 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:160857810 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:131719913 G>A maps to ENST00000435065 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:131719862 C>T maps to ENST00000435065 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:131724708 C>T maps to ENST00000435065 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:131728296 C>T maps to ENST00000435065 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:62751802 G>A maps to NM_004790.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62744336 G>A maps to NM_004790.3 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:62749416 G>A maps to NM_004790.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:62747356 G>T maps to NM_004790.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:62751075 G>T maps to NM_004790.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:43266323 G>A maps to ENST00000372585 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:43267505 C>T maps to ENST00000372585 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:43269946 G>A maps to ENST00000372585 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr6:43267397 C>T maps to ENST00000372585 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62760729 T>C maps to ENST00000430500 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:62760912 G>A maps to ENST00000430500 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr11:62763613 C>A maps to ENST00000430500 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:63177325 C>T maps to NM_080866.2 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:138713748 G>A maps to NM_152685.3 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:138715466 G>A maps to NM_152685.3 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr5:138716568 C>T maps to NM_152685.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:138707859 G>A maps to NM_152685.3 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr5:138715928 G>A maps to NM_152685.3 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:4893567 C>T maps to NM_203327.1 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:4880331 C>T maps to NM_203327.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:4839968 G>A maps to NM_203327.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:220026819 T>C maps to NM_001144890.1 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:220029959 G>A maps to NM_001144890.1 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:65917329 G>A maps to NM_004727.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr15:65917239 C>T maps to NM_004727.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:65917242 C>A maps to NM_004727.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:65942931 C>T maps to NM_004727.2 H815H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:65917239 C>T maps to NM_004727.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr15:65943202 C>T maps to NM_004727.2 Q906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:19786708 G>A maps to NM_020344.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr9:19516273 G>A maps to NM_020344.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:19576982 G>A maps to NM_020344.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:19566166 C>A maps to NM_020689.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:19566166 C>A maps to NM_020689.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:19664949 C>A maps to NM_020689.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:19673951 C>T maps to NM_020689.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:19701771 C>T maps to NM_020689.3 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:19496165 C>T maps to NM_020689.3 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:19665994 C>T maps to NM_020689.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:92908446 C>T maps to NM_153646.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr14:92920289 C>T maps to NM_153646.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:48427079 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr15:48431164 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:48428984 C>T maps to NM_205850.2 C232C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:113759021 G>C maps to NM_024959.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:113754447 C>T maps to NM_024959.2 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr12:113737755 C>A maps to NM_024959.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:113770674 G>A maps to NM_024959.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:19164410 C>T maps to NM_005984.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:79683844 C>T maps to ENST00000331531 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr17:79682050 C>T maps to ENST00000331531 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:4842101 T>C maps to NM_003562.4 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:4841131 C>T maps to NM_003562.4 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:172701006 C>A maps to NM_003705.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr2:172650265 A>G maps to NM_003705.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:172701006 C>A maps to NM_003705.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:95822480 C>T maps to NM_001160210.1 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:95814245 A>G maps to NM_001160210.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:95864212 C>A maps to NM_001160210.1 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:95775966 G>A maps to NM_001160210.1 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:95818927 G>T maps to NM_001160210.1 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:129479165 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:129479166 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:129480574 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:129484644 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:129498658 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:129499573 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:129506884 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:129492616 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:129492698 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:129492669 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:41379385 C>T maps to NM_014252.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:41382628 G>A maps to NM_014252.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:70243298 G>A maps to NM_152707.2 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:18070789 C>T maps to NM_031481.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:140682844 C>T maps to NM_031947.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr11:792388 G>A maps to NM_001191061.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:6454713 G>A maps to NM_024103.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:6456475 C>T maps to NM_024103.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:6442024 G>A maps to NM_024103.2 Y456Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr1:108697691 T>C maps to NM_013386.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:108690936 A>C maps to NM_013386.3 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:130854247 A>G maps to ENST00000373066 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:130868666 C>T maps to ENST00000373069 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:130868108 C>T maps to ENST00000373069 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:130869720 T>C maps to ENST00000373069 *516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:130865957 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:130864660 C>T maps to ENST00000373069 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:46632562 C>T maps to NM_004277.3 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:46623608 C>T maps to NM_004277.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:46623613 C>A maps to NM_004277.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr6:46638861 G>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:101370941 A>G maps to NM_031212.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr10:101372303 C>A maps to NM_031212.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:98991779 C>A maps to NM_213611.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:98991725 G>A maps to NM_213611.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:98987751 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:98987809 T>C maps to NM_213611.2 H18H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:98991774 G>T maps to NM_213611.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:98989503 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:45973124 G>A maps to NM_001010875.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:45975288 C>T maps to NM_001010875.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:45976490 C>T maps to NM_001010875.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:128694557 G>A maps to NM_031291.2 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:128688231 C>T maps to NM_031291.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:104412707 G>T maps to NM_030780.3 C293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:104415460 T>C maps to NM_030780.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:9640107 G>A maps to NM_032315.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:9642444 C>A maps to NM_032315.2 Y284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr1:16064649 C>T maps to NM_207348.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:8194240 G>A maps to NM_201520.1 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:8194788 C>T maps to NM_201520.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr3:140695225 G>C maps to NM_001104647.1 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:23423724 A>G maps to NM_016612.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr8:23386589 C>T maps to NM_016612.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:186066327 C>T maps to NM_001151.3 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:186066072 C>T maps to NM_001151.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:186066381 C>T maps to NM_001151.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:87479241 G>A maps to NM_018843.3 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:87465580 G>A maps to NM_018843.3 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:87465580 G>T maps to NM_018843.3 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:6430076 G>A maps to NM_173637.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:6430163 G>A maps to NM_173637.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:6429827 G>A maps to NM_173637.3 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:6427452 G>A maps to NM_173637.3 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:6430025 G>A maps to NM_173637.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:19206959 G>A maps to NM_178526.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19216464 C>T maps to NM_178526.3 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:118586924 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:118586919 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118540512 T>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:118586979 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:118587015 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:118587003 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:118586876 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:118540639 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:65144084 C>T maps to NM_182556.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:110096915 C>T maps to NM_138773.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:110075035 G>A maps to NM_138773.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:110096915 C>T maps to NM_138773.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr5:110092443 G>A maps to NM_138773.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:118603726 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:118603828 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:1505635 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:1508473 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:1505571 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:1508592 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:1505533 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:1508277 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:1508151 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:1508568 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:1506217 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:1508155 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:1506262 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:985179 C>T maps to NM_213613.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr4:982725 G>A maps to NM_213613.2 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr4:983142 G>A maps to NM_213613.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr12:58016692 T>G maps to NM_133489.2 Y305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:58018740 C>T maps to NM_133489.2 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:58014820 C>T maps to NM_133489.2 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr17:78210847 G>A maps to NM_173626.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:149359912 C>T maps to NM_000112.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:149360494 G>T maps to NM_000112.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:149360932 G>T maps to NM_000112.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:149360122 G>T maps to NM_000112.3 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:149360151 G>A maps to NM_000112.3 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr5:149360445 C>T maps to NM_000112.3 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:107423292 G>A maps to NM_000111.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:107431669 C>T maps to NM_000111.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:107414594 C>A maps to NM_000111.2 G593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:107329497 G>A maps to NM_000441.1 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:107334849 T>C maps to NM_000441.1 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:107353046 G>T maps to NM_000441.1 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:107342474 C>T maps to NM_000441.1 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:103030919 G>A maps to ENST00000354356 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:103050846 G>T maps to ENST00000354356 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:103033455 G>A maps to ENST00000354356 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:103033464 G>A maps to ENST00000354356 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr7:103061835 A>G maps to ENST00000354356 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:103017300 T>C maps to ENST00000354356 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:103053515 G>C maps to ENST00000354356 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:48669453 G>A maps to NM_022911.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:48665453 G>A maps to NM_022911.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:48667107 C>T maps to NM_022911.2 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:48670932 G>A maps to NM_022911.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:92307852 C>T maps to NM_134266.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:92378848 G>A maps to NM_134266.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:92346558 C>T maps to NM_134266.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr8:92346617 G>A maps to NM_134266.1 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:35980078 G>A maps to NM_052961.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:35927289 C>A maps to NM_052961.3 G604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:35923074 C>A maps to NM_052961.3 G696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:35980126 G>A maps to NM_052961.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:35987432 G>A maps to NM_052961.3 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:35911687 C>A maps to NM_052961.3 E968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:35980078 G>A maps to NM_052961.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:205890891 G>A maps to NM_134325.2 G619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205889331 G>A maps to NM_134325.2 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:205892260 C>T maps to NM_134325.2 K574K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:205892556 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:205896679 A>G maps to NM_134325.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:205889322 G>T maps to NM_134325.2 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:205892741 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:205901026 G>A maps to NM_134325.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:17599835 G>A maps to NM_198580.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr19:17599707 T>C maps to NM_198580.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:17615411 C>T maps to NM_198580.1 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:17597548 G>A maps to NM_198580.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr19:17599716 C>T maps to NM_198580.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:50489760 T>C maps to NM_003645.3 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:50519276 C>A maps to NM_003645.3 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:50474950 C>T maps to NM_003645.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:153749126 G>T maps to ENST00000271857 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:153750797 G>A maps to ENST00000271857 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:153749111 C>A maps to ENST00000271857 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:131107688 C>T maps to NM_005094.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:131107688 C>T maps to NM_005094.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:59011971 G>T maps to NM_012254.2 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:59022949 G>A maps to NM_012254.2 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:59021364 C>T maps to NM_012254.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:128324428 A>C maps to NM_001017372.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:128359344 C>T maps to NM_001017372.1 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr5:128320958 G>A maps to NM_001017372.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:85438201 C>T maps to NM_004213.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:85433734 C>T maps to NM_004213.3 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr15:45560512 C>A maps to NM_004212.3 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:86914552 G>A maps to NM_022127.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:86900956 G>A maps to NM_022127.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:86928345 G>A maps to NM_022127.2 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr6:44198192 C>T maps to ENST00000313248 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:66130915 C>T maps to NM_001532.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:66131700 C>T maps to NM_001532.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr10:73082531 C>T maps to NM_018344.5 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:5330824 C>T maps to NM_153247.2 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:5336810 C>T maps to NM_153247.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr7:5336639 G>A maps to NM_153247.2 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:43396733 G>A maps to NM_006516.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:43408959 T>G maps to NM_006516.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:43395160 C>T maps to ENST00000415851 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:43395281 C>T maps to NM_006516.2 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:45354076 G>A maps to NM_030777.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:45355557 C>T maps to NM_030777.3 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:45354004 C>T maps to NM_030777.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr20:45354485 C>T maps to NM_030777.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:24226218 G>A maps to ENST00000407566 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:24226176 C>A maps to NM_030807.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:40158367 A>G maps to NM_052885.3 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:40224026 G>A maps to NM_052885.3 Y441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:7967025 C>T maps to NM_153449.2 E483E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:7982463 A>G maps to NM_153449.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:170720394 G>A maps to NM_000340.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr3:170723085 G>A maps to NM_000340.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:170716176 G>A maps to NM_000340.1 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:170716930 G>A maps to NM_000340.1 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:170723771 G>T maps to NM_000340.1 Y245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:8083102 T>G maps to NM_006931.2 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:8084032 G>T maps to NM_006931.2 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:8083211 C>T maps to NM_006931.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:8075620 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7189941 C>T maps to NM_001042.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr17:7187353 C>T maps to NM_001042.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7189842 G>A maps to NM_001042.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:7186901 C>A maps to NM_001042.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:9129574 G>A maps to NM_003039.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:9107747 C>T maps to NM_003039.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr1:9101840 C>A maps to NM_001135585.1 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:136338627 G>A maps to NM_017585.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:136343501 G>A maps to NM_017585.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:9064852 C>T maps to NM_207420.2 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:9083116 G>A maps to NM_207420.2 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:9064822 G>A maps to NM_207420.2 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:9079291 G>A maps to NM_207420.2 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:9070243 G>A maps to NM_207420.2 C358C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr9:130166033 C>T maps to NM_014580.3 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:130162256 C>T maps to NM_014580.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr9:130164872 C>T maps to NM_014580.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:9987319 C>A maps to NM_020041.2 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:9828134 T>C maps to NM_020041.2 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:211751597 G>A maps to NM_021194.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:220089024 G>A maps to NM_018713.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:26370918 G>A maps to NM_001004434.1 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:26365707 G>A maps to NM_001004434.1 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:27478209 G>A maps to NM_003459.4 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:45781229 G>A maps to NM_013309.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr15:45783052 G>A maps to NM_013309.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:68417561 C>A maps to NM_022902.2 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:68425299 A>G maps to NM_022902.2 G718G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:32445674 G>T maps to NM_001193513.1 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:32429694 T>G maps to NM_001193513.1 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:32445305 C>T maps to NM_001193513.1 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:101431455 A>C maps to NM_133496.4 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:101427402 G>T maps to NM_133496.4 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:118175668 G>A maps to NM_173851.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:118165285 G>A maps to NM_173851.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr4:42062224 C>T maps to NM_006345.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:116021038 C>T maps to NM_001859.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr20:37356450 C>T maps to NM_080552.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:155560318 C>A maps to NM_004733.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:155571029 C>A maps to NM_004733.3 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:155571462 G>A maps to NM_004733.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:155571117 C>A maps to NM_004733.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:176813303 C>T maps to NM_003052.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:176815165 G>A maps to NM_003052.4 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr5:176813526 C>T maps to NM_003052.4 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:176825049 G>A maps to NM_003052.4 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr4:25669568 T>C maps to NM_006424.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:25678340 G>A maps to NM_006424.2 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr4:25678014 C>T maps to NM_006424.2 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:25664151 C>T maps to NM_006424.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:88210994 A>G maps to NM_006416.4 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48762366 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48762376 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48762203 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48768815 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48760707 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48762242 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:48763748 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:48762539 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48762044 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:48767196 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:48762122 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:48761925 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr23:48767195 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:48762203 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48762567 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr23:48767111 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:100459209 G>T maps to ENST00000370153 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr5:139947772 C>T maps to ENST00000432254 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:47782484 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:47783577 G>A maps to ENST00000415270 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:47780309 G>A maps to ENST00000415270 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:8430201 G>A maps to NM_001142540.1 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:8417703 A>G maps to NM_001142540.1 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:8428131 A>C maps to ENST00000426876 *219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:8420990 G>A maps to NM_001142540.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:45832510 C>A maps to NM_018389.4 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:45832495 C>T maps to NM_018389.4 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:44986385 C>T maps to NM_173179.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:67486114 G>A maps to NM_015139.2 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:99113453 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:137245812 C>T maps to NM_001008783.1 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:137245551 G>A maps to NM_001008783.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:16664576 G>A maps to NM_024881.4 Y382Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:1666200 T>C maps to NM_182838.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:1602955 G>T maps to NM_001110781.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:69145848 C>A maps to NM_018656.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr22:31042819 C>T maps to NM_001001479.2 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:118588240 C>T maps to NM_001029858.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:118588246 C>T maps to NM_001029858.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:118588240 C>T maps to NM_001029858.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:107673747 T>C maps to NM_017515.4 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr11:107663445 G>A maps to NM_017515.4 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:234444918 T>A maps to NM_173508.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:234041361 C>T maps to NM_173508.2 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr1:234452370 C>T maps to NM_173508.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr14:58030885 T>C maps to NM_001080455.1 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr14:58030930 C>A maps to NM_001080455.1 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr14:58038641 C>A maps to NM_001080455.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:114476740 G>A maps to NM_025181.2 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:114476740 G>A maps to NM_025181.2 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:114493387 T>C maps to NM_025181.2 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:114480712 G>A maps to NM_025181.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr5:150844715 C>T maps to NM_078483.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:150853328 A>G maps to NM_078483.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A186-01A-11D-A12J-09 chr5:150838427 G>A maps to NM_078483.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr5:150838427 G>A maps to NM_078483.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr5:150859003 G>A maps to NM_078483.2 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr5:150838427 G>A maps to NM_078483.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:150701676 G>T maps to NM_181776.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:150714887 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:150726916 A>C maps to NM_181776.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:150722446 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:150666866 C>T maps to NM_001145017.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:92918855 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:92895892 A>C maps to NM_152313.2 L339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:92881797 C>A maps to NM_152313.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:92881894 C>T maps to NM_152313.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:92896013 C>A maps to NM_152313.2 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:92895933 T>C maps to NM_152313.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:92918855 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:92918912 C>T maps to NM_152313.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:92881963 G>A maps to NM_152313.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:43954911 T>C maps to NM_018964.3 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr21:43963620 C>T maps to NM_018964.3 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr21:43974218 G>A maps to NM_018964.3 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:43963650 C>T maps to NM_018964.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:43982237 T>C maps to NM_018964.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr11:124953753 C>T maps to NM_198277.2 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:124955352 C>T maps to NM_198277.2 D437D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:124949581 C>A maps to NM_198277.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:124958021 G>T maps to NM_001145290.1 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:140080090 C>A maps to NM_207113.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:140051901 G>A maps to NM_207113.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:140045747 G>A maps to NM_207113.1 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:118898459 C>T maps to NM_001164278.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:118900040 G>T maps to NM_001164278.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:118899956 C>T maps to NM_001164278.1 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:46582764 G>A maps to NM_030674.3 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr12:46622973 G>A maps to NM_030674.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:79234131 G>A maps to NM_001037984.1 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:79225167 C>T maps to NM_138570.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:79225269 C>T maps to NM_138570.2 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:79219976 G>A maps to NM_001037984.1 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:79220054 G>A maps to NM_001037984.1 G887G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:79249909 G>A maps to NM_001037984.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr17:79225389 C>T maps to NM_001037984.1 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:165768193 A>G maps to ENST00000409662 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:46758953 C>A maps to NM_018976.4 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr12:46758904 G>A maps to NM_018976.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:50252886 C>A maps to NM_006841.4 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:50252086 C>T maps to NM_006841.4 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:47170708 G>T maps to NM_018018.4 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:47168956 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:47182373 A>G maps to NM_018018.4 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48325237 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48319448 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:48320423 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:48324702 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:48325415 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48319406 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:48325461 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:48326171 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:48320423 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48324663 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48325237 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48319045 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48325446 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48325450 G>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:48319116 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:48325239 C>T did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:48319078 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:61451459 G>A maps to NM_001172702.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:58706133 G>A maps to NM_018231.1 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:84050237 G>A maps to NM_001080442.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:84043403 G>T maps to NM_001080442.1 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:54922369 G>A maps to NM_173514.2 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:54929697 G>A maps to NM_173514.2 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:153933211 C>A maps to NM_014437.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:196544801 T>C maps to NM_001127257.1 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:196578266 G>A maps to NM_001127257.1 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:196581656 G>T maps to NM_001127257.1 G665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:196545452 G>A maps to NM_001127257.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:196545578 T>C maps to NM_001127257.1 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:196545419 T>C maps to NM_001127257.1 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:196548547 G>A maps to NM_001127257.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:70645394 A>G maps to NM_001159770.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:70845926 A>C maps to NM_001159770.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:18250572 G>T maps to NM_001145195.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:18242118 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:18242288 A>G maps to NM_001145195.1 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:18250730 G>A maps to NM_001145195.1 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:18276495 G>A maps to NM_001145195.1 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:47436904 C>T maps to NM_001128225.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:22273295 C>T maps to NM_001135153.1 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:22273406 T>C maps to NM_001135153.1 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:22262486 C>A maps to NM_001135153.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr8:22273680 C>T maps to NM_001135153.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:22265924 C>T maps to NM_001135153.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:22269694 C>T maps to NM_001135153.1 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:56626471 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:56625330 C>T maps to NM_001135195.1 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:33689576 G>A maps to NM_012319.3 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:33706378 C>A maps to NM_012319.3 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:33703613 A>G maps to NM_012319.3 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:33694321 G>T maps to NM_012319.3 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:33696636 G>A maps to NM_012319.3 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr18:33696635 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:33696636 G>A maps to NM_012319.3 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr18:33689609 A>G maps to NM_012319.3 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr18:33706652 T>A maps to NM_012319.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr18:33706235 A>G maps to NM_012319.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:33169601 G>A maps to NM_006979.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:33169342 A>G maps to NM_006979.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:103189056 G>A maps to NM_001135146.1 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:103189134 G>A maps to NM_001135146.1 H314H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:103226244 G>A maps to NM_001135146.1 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:103225593 T>C maps to NM_001135146.1 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:69925108 C>T maps to NM_018375.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:69922546 A>G maps to NM_018375.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr14:69866097 C>T maps to NM_018375.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:69908876 C>T maps to NM_018375.3 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:44528146 G>A maps to NM_000341.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:44513287 G>T maps to NM_000341.3 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:44531344 A>G maps to NM_000341.3 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:62649446 T>C maps to NM_001012661.1 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr2:190426774 T>C maps to NM_014585.5 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:190426888 T>C maps to NM_014585.5 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:205779377 G>A maps to NM_173854.4 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr12:105239708 A>G maps to NM_032148.3 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:105322200 G>A maps to NM_032148.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:125775346 G>A maps to NM_001008487.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:125734400 G>T maps to NM_001008485.1 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:125775266 G>A maps to NM_001008487.1 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr3:125775245 G>A maps to NM_001008487.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:125745307 G>A maps to NM_001008485.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:125725306 G>A maps to NM_001008485.1 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:125775343 G>A maps to NM_001008487.1 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:57263538 G>A maps to NM_003627.5 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:1494632 C>T maps to ENST00000382147 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:1494644 C>T maps to ENST00000382147 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr17:1519899 G>A maps to ENST00000382147 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr11:57177466 G>T maps to ENST00000428603 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:57188507 C>T maps to ENST00000428603 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:57193519 G>T maps to ENST00000428603 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:108118628 G>T maps to NM_080546.3 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:108123524 G>T maps to NM_080546.3 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr9:108118591 C>T maps to NM_080546.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr9:108136922 C>A maps to NM_080546.3 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:108118628 G>T maps to NM_080546.3 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:10746124 C>T maps to NM_020428.3 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:10747255 G>A maps to NM_020428.3 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:10745668 T>C maps to NM_020428.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:10753092 T>C maps to NM_020428.3 Y660Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr1:95330434 C>T maps to NM_001114106.1 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:95303288 C>T maps to NM_001114106.1 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:95358064 G>T maps to NM_001114106.1 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:31833837 G>A maps to NM_025257.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:31833542 C>T maps to NM_025257.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:31832432 G>T maps to NM_025257.2 C669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:75684293 G>A maps to NM_152697.4 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:75684964 C>A maps to NM_152697.4 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr1:75683548 A>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:75684296 G>A maps to NM_152697.4 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:8390479 G>A maps to ENST00000377479 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:8384574 G>A maps to ENST00000377479 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:33947399 C>T maps to NM_016180.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:33982503 G>A maps to NM_016180.3 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:205628522 G>A maps to NM_033102.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:205632051 C>T maps to NM_033102.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205628361 C>T maps to NM_033102.2 *554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205628565 C>T maps to NM_033102.2 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205632051 C>T maps to NM_033102.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:205632075 G>A maps to NM_033102.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:142222391 G>A maps to NM_001080431.1 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:142228457 G>A maps to NM_001080431.1 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:142229884 G>A maps to NM_001080431.1 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:142227279 C>T maps to NM_001080431.1 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr8:142221642 G>A maps to NM_001080431.1 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr8:142229917 G>A maps to NM_001080431.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:26731649 C>T maps to ENST00000440501 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:26727660 T>C maps to ENST00000440501 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:26729339 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:115648777 G>T maps to NM_033051.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:115648855 G>A maps to NM_033051.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:29286850 G>A maps to NM_001135919.1 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05D-01A-11W-A027-09 chr13:29287612 T>C maps to NM_001135919.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:29287374 G>A maps to NM_001135919.1 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:29287603 A>G maps to NM_001135919.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:29287107 G>A maps to NM_001135919.1 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:29275093 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:29287395 C>A maps to NM_001135919.1 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:19458544 C>T maps to ENST00000395585 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:19618494 G>A maps to NM_152908.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:42331903 G>A maps to NM_000342.3 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:42335837 G>A maps to NM_000342.3 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:42332628 G>T maps to NM_000342.3 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr17:42335140 C>T maps to NM_000342.3 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:42328915 G>T maps to NM_000342.3 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:162711557 C>T maps to NM_001178015.1 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:162805660 C>T maps to NM_001178015.1 R757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:162735687 G>A maps to NM_001178015.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:162820722 C>T maps to NM_001178015.1 R981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:3215508 G>A maps to NM_001174090.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:3211204 A>C maps to NM_001174090.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:3214921 C>T maps to NM_001174090.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:3211615 G>A maps to NM_001174090.1 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr20:3209829 G>A maps to NM_001174090.1 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:27887981 C>T maps to NM_018158.2 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:27907902 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27891720 G>T maps to NM_018158.2 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27892159 C>A maps to NM_018158.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:27888112 G>A maps to NM_018158.2 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:150761713 C>T maps to NM_003040.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:150767964 C>T maps to NM_003040.3 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr7:150767427 C>T maps to NM_003040.3 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:150767375 C>T maps to NM_003040.3 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:220501535 G>A maps to NM_201574.2 E852E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:220493884 C>T maps to NM_201574.2 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:220501535 G>A maps to NM_201574.2 E852E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:220505608 C>A maps to NM_201574.2 P1209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:72423598 A>G maps to NM_001098484.2 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:72222722 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:72319250 G>A maps to NM_001098484.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:72306475 T>A maps to NM_001098484.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr4:72205183 C>T maps to NM_001098484.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr4:72316140 G>A maps to NM_001098484.2 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:74483026 C>T maps to NM_021196.3 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:74480225 G>A maps to NM_021196.3 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:74474250 G>A maps to NM_021196.3 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:74479457 G>A maps to NM_021196.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:74483008 G>A maps to NM_021196.3 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:74475490 G>A maps to NM_021196.3 F592F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:74452119 G>A maps to NM_021196.3 I1047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:27444628 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:27473160 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:27427459 C>A maps to ENST00000454389 E1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:27477887 C>A maps to ENST00000454389 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:27463207 G>T maps to ENST00000454389 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:27477998 G>A maps to ENST00000454389 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:27460062 C>A maps to ENST00000454389 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:27436170 T>G maps to ENST00000454389 A985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:27444712 G>A maps to ENST00000454389 Y746Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:51899624 C>T maps to NM_001039960.1 D1060D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr12:51888847 C>T maps to NM_001039960.1 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:51868950 C>T maps to NM_001039960.1 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51834554 G>T maps to NM_001039960.1 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51865242 G>T maps to NM_001039960.1 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr12:51853748 C>T maps to NM_001039960.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:139745812 A>G maps to ENST00000507527 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:139741648 G>A maps to ENST00000507527 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr5:139743773 T>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:139743766 C>T maps to ENST00000507527 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:139750747 G>A maps to ENST00000507527 Q856Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr22:32498160 C>T maps to NM_000343.3 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:24922829 C>A maps to NM_052944.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:24920279 C>T maps to NM_052944.2 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:24909401 T>C maps to NM_052944.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:26725355 G>A maps to NM_178498.3 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:26694951 C>T maps to NM_178498.3 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:31497549 C>A maps to ENST00000431354 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:31500559 C>T maps to ENST00000431354 C522C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:31497051 G>A maps to ENST00000431354 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:31500021 G>A maps to ENST00000431354 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:35467808 A>G maps to NM_006933.4 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr22:32626979 C>T maps to NM_014227.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:32644728 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:32614659 G>A maps to NM_014227.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:32627030 G>A maps to NM_014227.2 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:17988624 G>A maps to NM_000453.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr19:17991702 C>T maps to NM_000453.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:27423901 G>T maps to NM_021095.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:27424302 C>T maps to NM_021095.2 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27423972 G>A maps to NM_021095.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr2:27430464 G>A maps to NM_021095.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:108626704 C>T maps to NM_021815.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:108618399 C>T maps to NM_021815.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:108627215 C>T maps to NM_021815.2 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:108627310 A>G maps to NM_021815.2 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:101560272 T>G maps to NM_145913.3 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr12:101581286 G>C maps to NM_145913.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:101581247 G>A maps to NM_145913.3 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:101595993 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:101560317 C>A maps to NM_145913.3 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:48713022 G>A maps to NM_001135181.1 W643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:11061918 C>T maps to NM_003042.3 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:11071022 C>A maps to NM_003042.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:11059532 C>T maps to NM_003042.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:11072885 C>A maps to NM_003042.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:11060306 C>T maps to NM_003042.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:10970991 C>T maps to NM_014229.1 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:10916758 C>A maps to NM_014229.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:10953794 G>A maps to NM_014229.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:10858057 G>A maps to NM_014229.1 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:10974898 C>T maps to NM_014229.1 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:319209 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:305935 C>T maps to NM_003044.3 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr12:307154 C>T maps to NM_003044.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:335628 G>C maps to NM_016615.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:369114 C>T maps to NM_016615.3 W35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:336795 G>A maps to NM_016615.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:115572200 T>G did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:115582836 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:115585493 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:115584286 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:115569036 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:115588808 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:115573860 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:115586188 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:115588927 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:115590031 C>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:115588908 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:85279214 A>C maps to NM_182767.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:85255517 G>A maps to NM_182767.4 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:49814669 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:49797168 G>A maps to NM_014037.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:49813759 G>A maps to NM_014037.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:110734701 C>T maps to NM_001010898.2 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr1:110740768 G>A maps to NM_001010898.2 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:110737277 C>T maps to NM_001010898.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:1244740 G>A maps to NM_182632.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:1240714 C>T maps to NM_182632.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:1216893 T>C maps to ENST00000515652 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:1213642 G>A maps to NM_001003841.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:1216671 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:1216839 G>A maps to ENST00000515652 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:1214102 C>T maps to NM_001003841.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:1201863 G>A maps to NM_001003841.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:1222000 C>T maps to NM_001003841.2 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:55705811 C>T maps to NM_001172502.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:55725861 C>T maps to NM_001043.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:45814047 G>A maps to NM_020208.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:45801514 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:45812899 G>T maps to NM_020208.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:45823692 G>T maps to NM_020208.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:45817360 C>T maps to NM_020208.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr5:1411432 G>T maps to NM_001044.4 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:1401089 G>A maps to NM_001044.4 Y593Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:1411360 G>A maps to NM_001044.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:1416304 G>A maps to NM_001044.4 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:1409231 G>T maps to NM_001044.4 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:1416265 G>A maps to NM_001044.4 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr5:1411426 C>T maps to NM_001044.4 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr5:1406361 G>A maps to NM_001044.4 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:28530327 C>T maps to ENST00000394821 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:28545856 C>A maps to ENST00000394821 G188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:28536191 C>A maps to ENST00000394821 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:28549089 G>A maps to ENST00000394821 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:20628551 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:20652324 G>T maps to NM_004211.3 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:20668387 A>C maps to NM_004211.3 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:20628622 G>A maps to NM_004211.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:20636355 G>T maps to NM_004211.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:20660081 C>T maps to NM_004211.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:20668480 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:20636345 T>C maps to NM_004211.3 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:14487240 G>A maps to NM_001134367.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr5:149582168 C>T maps to NM_014228.3 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:149576315 C>A maps to NM_014228.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:149576300 C>T maps to NM_014228.3 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:149582237 C>T maps to NM_014228.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:149584132 C>T maps to NM_014228.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16O-01A-11D-A12J-09 chr5:149576809 C>T maps to NM_014228.3 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152957458 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152957588 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152960207 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:152959969 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152957438 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:152960032 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:152959561 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:152958594 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:152959566 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:152959494 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152956835 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152958462 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:44467175 G>A maps to NM_201649.2 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:44468261 G>A maps to NM_201649.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr13:30091887 G>T maps to NM_003045.4 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:30088670 G>A maps to NM_003045.4 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:30107105 T>C maps to NM_003045.4 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:33702397 G>A maps to NM_019849.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:33706778 G>A maps to NM_019849.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:139106301 C>T maps to ENST00000280612 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:139101829 G>A maps to ENST00000280612 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:87226839 G>A maps to NM_138817.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr8:87226683 T>C maps to NM_138817.2 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr8:87242197 C>A maps to NM_138817.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:170201209 G>A maps to NM_020949.2 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr3:170198390 C>T maps to NM_020949.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr3:170201116 G>A maps to NM_020949.2 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:17409357 C>A maps to NM_001164771.1 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:17400904 C>T maps to NM_001164771.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:17409357 C>A maps to NM_001164771.1 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:17417899 G>A maps to NM_001164771.1 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:70149842 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70149629 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70146727 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70145724 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70149681 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70149797 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:70148476 A>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:70147823 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70148305 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70148012 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr23:70145998 C>G did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:70149603 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:87872372 G>A maps to NM_003486.5 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:87868146 G>A maps to NM_003486.5 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr16:87873424 C>T maps to NM_003486.5 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:68308817 C>A maps to NM_003983.4 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:68308964 C>T maps to NM_003983.4 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:68330534 C>T maps to NM_003983.4 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:68321724 C>T maps to NM_003983.4 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:23600735 G>A maps to NM_012244.2 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:23600756 G>A maps to NM_012244.2 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr19:33353427 G>A maps to NM_014270.4 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:33353094 G>A maps to NM_014270.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:33333093 C>A maps to NM_014270.4 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:33349410 G>A maps to NM_014270.4 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:40655917 A>C maps to NM_021097.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2HF-01A-11D-A17D-09 chr2:40366692 C>T maps to NM_021097.2 W798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr2:40366799 G>A maps to NM_021097.2 D762D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:40366763 G>A maps to NM_021097.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:40655629 G>A maps to NM_021097.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:40657092 C>A maps to NM_021097.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:40366565 G>A maps to NM_021097.2 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:47935352 G>A maps to ENST00000391903 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr19:47941144 G>A maps to NM_015063.2 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:47969195 G>A maps to NM_015063.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:47935430 G>T maps to NM_015063.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:70634341 G>A maps to NM_183002.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr14:70634328 G>A maps to NM_183002.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:70633369 C>T maps to NM_183002.1 K590K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:70527550 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:70634016 C>A maps to NM_183002.1 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:27426971 G>A maps to NM_003047.3 D758D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:27480516 G>A maps to NM_003047.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:27440745 G>A maps to NM_003047.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:27429000 G>A maps to NM_003047.3 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:27440592 C>T maps to NM_003047.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:27440439 G>A maps to NM_003047.3 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:111927030 T>C maps to NM_183061.1 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:111985095 T>G maps to NM_183061.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:111918262 C>A maps to NM_183061.1 E810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:111921243 G>T maps to NM_183061.1 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:111887813 G>T maps to NM_183061.1 I1049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:111923109 G>T maps to NM_183061.1 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:111983101 C>A maps to NM_183061.1 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:111898392 G>A maps to NM_183061.1 C968C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:111873860 C>A maps to NM_183061.1 E1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:111983117 A>G maps to NM_183061.1 H317H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:111923166 T>C maps to NM_183061.1 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:173474431 G>A maps to NM_178527.3 I1088I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:173490466 G>T maps to NM_178527.3 I904I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:173569288 G>A maps to NM_178527.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:173503632 G>T maps to NM_178527.3 S655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:173504993 C>A maps to NM_178527.3 E584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:173499099 G>A maps to NM_178527.3 Q753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr1:173569253 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:103318922 G>T maps to NM_003048.3 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:103300695 T>C maps to NM_003048.3 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:103274413 G>A maps to NM_003048.3 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:103324875 G>A maps to NM_003048.3 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:103299875 C>T maps to NM_003048.3 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:476788 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:485319 G>A maps to NM_004174.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr5:485313 C>T maps to NM_004174.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:476771 G>A maps to NM_004174.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr5:475113 G>A maps to NM_004174.2 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:482707 G>A maps to NM_004174.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:488463 G>A maps to NM_004174.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr16:2087919 C>T maps to ENST00000191922 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:103090379 G>A maps to NM_001011552.3 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:103119908 C>A maps to NM_001011552.3 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr2:103141487 G>T maps to NM_001011552.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:103141592 C>T maps to NM_001011552.3 H643H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:103090235 C>T maps to NM_001011552.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr2:103095610 C>T maps to NM_001011552.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:67291336 C>T maps to NM_004594.2 H475H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:67286709 C>T maps to NM_004594.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:67289047 C>T maps to NM_004594.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:67290488 C>T maps to NM_004594.2 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:135126618 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135095152 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135095158 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135092701 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:135067915 T>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:135067765 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:135095204 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:135126672 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr23:135106588 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:135098894 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:135067941 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:135095128 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:135126643 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:135095553 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:135104755 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:135106622 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:135084304 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:46508158 T>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:46466503 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:46466435 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:46513158 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:46529126 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:46539180 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:46472725 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:46466613 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:46522039 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:46466491 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:46502766 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:46495073 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:46502762 C>T did not map to a codon.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr23:46502751 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:46495060 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:46502729 G>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr20:48439604 C>T maps to ENST00000417961 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:48503377 C>T maps to ENST00000417961 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr20:48491320 C>T maps to ENST00000417961 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:48456126 G>A maps to ENST00000417961 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:143297447 C>T maps to NM_173653.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:143100949 G>A maps to NM_173653.3 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:143371134 C>T maps to NM_173653.3 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:142987785 C>T maps to NM_173653.3 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:143214263 C>T maps to NM_173653.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:143271275 G>T maps to NM_173653.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:21472352 G>A maps to ENST00000390670 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:21453368 G>A maps to NM_134431.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:21467606 A>G maps to NM_134431.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:21453288 G>T maps to NM_134431.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:21446941 G>A maps to NM_134431.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:21353562 G>A maps to NM_006446.4 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr12:21051409 C>T maps to NM_019844.2 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:21015789 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:21011427 G>A maps to NM_019844.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:21028324 C>A maps to NM_019844.2 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:21011427 G>A maps to NM_019844.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:21032373 C>A maps to NM_019844.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:21011427 G>A maps to NM_019844.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:21011427 G>A maps to NM_019844.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:21011427 G>A maps to NM_019844.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr12:20876186 C>T maps to NM_017435.4 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:20876111 C>T maps to NM_017435.4 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:20905356 G>A maps to NM_017435.4 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:133663937 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:133661501 G>A maps to NM_005630.2 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:74876953 C>T maps to NM_007256.4 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:74875146 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:74914418 C>T maps to NM_007256.4 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:92706124 C>T maps to NM_013272.3 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:92690281 C>T maps to NM_013272.3 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr15:92638147 C>T maps to NM_013272.3 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:92647677 C>T maps to NM_013272.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:92638180 C>A maps to NM_013272.3 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:92706355 C>T maps to NM_013272.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:92706022 C>T maps to NM_013272.3 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:61299852 C>A maps to NM_016354.3 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr20:61299243 G>A maps to NM_016354.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:61296285 C>G maps to NM_016354.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr20:61299213 C>T maps to NM_016354.3 C530C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:101627073 C>A maps to NM_180991.4 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:101575092 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:101606510 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:101597619 T>C maps to NM_180991.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:101572569 C>A maps to NM_180991.4 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:101631960 C>T maps to NM_180991.4 K2K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:101631806 C>A maps to NM_180991.4 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:70585330 C>A maps to NM_030958.2 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr8:70744341 G>A maps to NM_030958.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:70744673 A>G maps to NM_030958.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:101755693 G>A maps to NM_173488.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:101834422 C>T maps to NM_173488.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:101816049 C>T maps to NM_173488.3 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:101834188 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:101834310 C>A maps to NM_173488.3 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:101724490 C>A maps to NM_173488.3 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:101834422 C>T maps to NM_173488.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:33689902 G>T maps to NM_152270.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:33680776 G>A maps to NM_152270.3 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr17:33680665 C>T maps to NM_152270.3 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:33679518 A>C maps to NM_152270.3 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:33690003 C>A maps to NM_152270.3 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr17:33679566 G>A maps to NM_152270.3 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:33679521 A>G maps to NM_152270.3 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:33690214 G>A maps to NM_152270.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:33690379 G>A maps to NM_152270.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:33749311 C>A maps to NM_018042.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:33749389 C>A maps to NM_018042.3 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:33738799 G>A maps to NM_018042.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:33749311 C>A maps to NM_018042.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:33802205 T>C maps to ENST00000361112 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:33806415 C>T maps to ENST00000361112 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:33806438 C>A maps to ENST00000361112 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:33771970 G>A maps to NM_144682.5 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr17:33591577 C>T maps to NM_144975.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:33591266 G>T maps to NM_144975.3 G402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:33592465 C>A maps to NM_144975.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:33588005 T>C maps to NM_144975.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr17:33586416 T>A maps to NM_144975.3 C236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:41486065 C>T maps to NM_144990.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:41481810 G>A maps to NM_144990.3 H397H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:98764556 C>T maps to NM_003061.2 G1201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr10:98761033 C>T maps to NM_003061.2 T1480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:98807747 C>A maps to NM_003061.2 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:98808793 C>T maps to NM_003061.2 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr10:98819266 G>A maps to NM_003061.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:98760928 C>T maps to NM_003061.2 G1515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:98790533 G>A maps to NM_003061.2 D854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:98763897 G>A maps to NM_003061.2 G1264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:98763957 C>T maps to NM_003061.2 G1244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr10:98808781 G>A maps to NM_003061.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:20619269 C>T maps to ENST00000273739 R1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:20550743 C>T maps to ENST00000273739 R832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr4:20530585 C>T maps to ENST00000273739 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:20619079 C>T maps to ENST00000273739 C1398C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:20255462 C>T maps to ENST00000273739 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:20620523 G>A maps to ENST00000273739 P1507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:20512754 T>C maps to ENST00000273739 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:20620394 C>A maps to ENST00000273739 I1464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr5:168671718 G>A maps to NM_003062.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:168149966 G>T maps to NM_003062.2 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:168199839 G>A maps to NM_003062.2 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr5:168093590 C>A maps to NM_003062.2 G1480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:168199873 G>A maps to NM_003062.2 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:168123363 G>A maps to NM_003062.2 C1005C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:168678417 G>A maps to NM_003062.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:84454670 C>T maps to NM_052910.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:84455408 G>A maps to NM_052910.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:84454313 G>A maps to NM_052910.1 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr13:84454930 G>A maps to NM_052910.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:84455171 C>T maps to NM_052910.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:84454271 G>A maps to NM_052910.1 N457N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:84454670 C>T maps to NM_052910.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:84453629 G>T maps to NM_052910.1 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:144904870 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:144906316 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:144905447 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:144905882 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:144903964 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:144905974 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:144903950 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:144904090 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:144905392 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:144905718 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:144905218 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:144904883 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:144904701 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:144906464 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:144904921 A>G did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:144905468 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:144904046 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:144904621 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:144904644 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:144904851 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:144905023 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:144905829 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:144904134 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:144905740 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr23:144904102 G>A did not map to a codon.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr23:144904564 A>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:144906069 A>G did not map to a codon.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr23:144904062 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:144904042 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:144906204 G>A did not map to a codon.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr23:144904948 G>T did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:144905358 C>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:164906983 A>C maps to NM_014926.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr3:164906857 A>G maps to NM_014926.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:164905987 G>A maps to NM_014926.2 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr3:164906155 T>G maps to NM_014926.2 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:164908164 C>A maps to NM_014926.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:142716717 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:142717980 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:142716680 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:142716710 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:142718064 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:142718388 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:142716850 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:142718718 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:142716748 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:142717953 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:142718335 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:142718592 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:142716774 T>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:142718706 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:142718726 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:142718731 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:142717036 A>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:142718421 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:142718834 A>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:142717555 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:142717224 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:142718219 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:142716504 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:142717344 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:142718893 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:142718684 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:142718106 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:142718917 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:142716413 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:142717775 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:142718716 A>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:88329124 C>T maps to NM_015567.1 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:88329517 C>A maps to NM_015567.1 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:88329436 C>T maps to NM_015567.1 F598F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:88328828 C>T maps to NM_015567.1 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:88329001 C>T maps to NM_015567.1 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr13:88329880 C>T maps to NM_015567.1 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:88328905 C>T maps to NM_015567.1 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr13:88329697 C>T maps to NM_015567.1 F685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr13:88329607 C>A maps to NM_015567.1 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:86368382 G>T maps to NM_032229.2 S754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:86368432 G>A maps to NM_032229.2 Y737Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:86368522 A>G maps to NM_032229.2 N707N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:86369410 C>T maps to NM_032229.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr13:86368864 C>T maps to NM_032229.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:105763001 C>A maps to NM_014720.2 S689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:105780260 G>T maps to NM_014720.2 E1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:105761240 G>T maps to NM_014720.2 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:105762313 G>T maps to NM_014720.2 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:57857369 G>A maps to ENST00000428312 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr3:57857374 C>G maps to ENST00000428312 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:57850366 A>G maps to ENST00000428312 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:57847783 G>T maps to ENST00000428312 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr3:57893692 G>A maps to ENST00000428312 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:57893680 C>T maps to ENST00000428312 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:12427105 G>T maps to NM_006553.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:12429375 G>T maps to NM_006553.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:59186127 C>A maps to NM_024755.2 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:59205828 C>A maps to NM_024755.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:59186050 C>T maps to NM_024755.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:59175969 G>A maps to NM_024755.2 R951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:59186050 C>T maps to NM_024755.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:59182631 G>A maps to NM_024755.2 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr15:59180618 A>G maps to NM_024755.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:59185178 C>T maps to NM_024755.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:59186050 C>T maps to NM_024755.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr15:59185114 G>A maps to NM_024755.2 R627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:159842174 G>A maps to NM_006425.4 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr5:159842138 C>A maps to NM_006425.4 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:146435833 C>T maps to NM_001003688.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr4:146463740 G>A maps to NM_001003688.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:146461007 C>T maps to NM_001003688.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:45371762 T>G maps to NM_001003652.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:45394804 G>A maps to NM_001003652.2 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr18:45394804 G>T maps to NM_001003652.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:67477140 G>A maps to NM_005902.3 Q316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:67430384 G>A maps to NM_001145103.1 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:67430399 C>T maps to NM_001145103.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:67462910 G>A maps to NM_005902.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:48573436 G>A maps to NM_005359.5 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:135508328 C>T maps to NM_001001419.1 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:135489806 G>T maps to NM_001001419.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr18:46448257 A>G maps to NM_005904.3 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:46448092 C>T maps to NM_005904.3 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr18:46448209 C>T maps to NM_005904.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr18:46448065 G>T maps to NM_005904.3 C319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:37453490 G>T maps to NM_001127217.2 C112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:37453430 G>A maps to NM_001127217.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:37441422 C>T maps to NM_001127217.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:37447041 A>T maps to NM_001127217.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:37453525 G>A maps to NM_001127217.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:51640589 T>C maps to NM_001031628.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:71508407 G>T maps to NM_001044305.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr6:71377782 C>T maps to NM_001044305.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:40875447 C>T maps to NM_022733.2 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:40878690 G>T maps to NM_022733.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:40875447 C>T maps to NM_022733.2 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:40872451 C>T maps to NM_022733.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:128649939 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:128657269 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:128657198 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:128640104 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:128599548 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:128632026 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:128641997 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:128650349 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:128602774 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:128621064 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:128599651 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:128624132 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:128645922 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:128602857 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:128631867 A>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:128605188 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:128631827 C>A did not map to a codon.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr23:128624132 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:128582406 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:128602793 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:128627039 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:128638768 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:128649931 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:128605270 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:128657345 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:128633743 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:128599530 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:128621064 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:128642054 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr23:128649875 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:128652421 T>G did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:128599659 G>T did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:128602762 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr9:2054608 C>T maps to NM_003070.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:2186133 G>A maps to NM_003070.3 K1500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:2182211 C>T maps to NM_003070.3 N1477N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr19:11106977 G>T maps to NM_001128849.1 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:11123647 G>A maps to NM_001128849.1 V766V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:11118597 G>A maps to NM_001128849.1 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:11132465 G>A maps to NM_001128849.1 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:11123671 C>T maps to NM_001128849.1 N774N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr19:11105673 C>G maps to NM_001128849.1 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:144471239 C>T maps to NM_003601.2 R1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:144469178 T>C maps to NM_003601.2 C957C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:144464779 C>T maps to NM_003601.2 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:144467182 G>T maps to NM_003601.2 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:95147396 C>A maps to NM_001128429.1 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:95201892 C>T maps to NM_001128429.1 R859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:95173974 C>T maps to NM_001128429.1 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:95199796 C>T maps to NM_001128429.1 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:217279816 T>C maps to NM_014140.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:217285187 C>T maps to NM_014140.3 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:217279792 C>A maps to NM_014140.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:217285158 C>T maps to NM_014140.3 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G3-01A-11W-A062-09 chr22:24175800 G>A maps to NM_003073.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:24134005 C>T maps to NM_003073.3 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:24135749 C>T maps to NM_003073.3 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:24135836 G>A maps to NM_003073.3 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:47663795 G>A maps to NM_003074.3 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr3:47734758 A>G maps to NM_003074.3 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:47676807 C>A maps to NM_003074.3 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:47718129 G>A maps to NM_003074.3 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr3:47651715 C>T maps to NM_003074.3 Q961Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:56558156 G>A maps to NM_003075.3 A1166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56561849 T>C maps to NM_003075.3 R917R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:56574844 C>A maps to NM_003075.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:56558432 C>T maps to NM_003075.3 A1074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:56568538 G>T maps to NM_003075.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:56558357 A>G maps to NM_003075.3 F1099F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:50484056 C>T maps to NM_003076.4 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:50492747 G>T maps to NM_003076.4 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:61914829 C>T maps to NM_001098426.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr17:61911350 G>A maps to NM_001098426.1 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:150936820 C>T maps to NM_003078.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:150937527 G>A maps to NM_003078.3 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:150939620 G>A maps to NM_003078.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:38785066 A>G maps to NM_003079.4 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:38792251 G>A maps to NM_003079.4 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:53430549 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53432885 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53448964 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53407560 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53409290 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53421746 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:53439000 G>A did not map to a codon.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr23:53440263 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:53407602 C>T did not map to a codon.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr23:53432008 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53426534 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53440218 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:53432044 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr23:53407566 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:53432579 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53440244 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr23:53449448 T>C did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:53442058 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53432431 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:53438950 C>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:53432425 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:45795180 C>A maps to NM_148674.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:45779457 A>C maps to NM_148674.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:45792367 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr22:45755815 C>A maps to NM_148674.3 E911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:45779372 G>A maps to NM_148674.3 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:45795180 C>A maps to NM_148674.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:106861964 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:106878522 C>T maps to NM_001042550.1 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:106885511 T>C maps to NM_001042550.1 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:112361579 C>T maps to NM_005445.3 R944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:112337616 C>T maps to NM_005445.3 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:112350294 T>G maps to NM_005445.3 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:112361729 C>T maps to NM_005445.3 R967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:112337616 C>T maps to NM_005445.3 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:112360247 C>T maps to NM_005445.3 R827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:160151483 C>T maps to NM_005496.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:160141585 A>G maps to NM_005496.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:160150249 C>T maps to NM_005496.3 A1159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:160135596 C>A maps to NM_005496.3 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:160151483 C>T maps to NM_005496.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:160151483 C>T maps to NM_005496.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:160151483 C>T maps to NM_005496.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:160150822 A>G maps to NM_005496.3 P1180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:160151483 C>T maps to NM_005496.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:160143905 A>G maps to NM_005496.3 E841E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:72892280 C>T maps to NM_015110.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:72913084 C>T maps to NM_015110.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:72965053 C>T maps to NM_015110.3 R972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr9:72895704 C>T maps to NM_015110.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:72893537 C>T maps to NM_015110.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr9:72929750 A>T maps to NM_015110.3 K558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr9:72967219 C>T maps to NM_015110.3 R1093R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:17884559 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:17884431 C>A maps to ENST00000381272 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:17877660 A>G maps to ENST00000381272 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr2:17876519 T>C maps to ENST00000381272 E885E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:17896305 C>A maps to ENST00000381272 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:17906571 A>G maps to ENST00000381272 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:17898376 G>A maps to ENST00000381272 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:17860142 C>A maps to ENST00000381272 E991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:17898413 A>G maps to ENST00000381272 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:2705753 C>T maps to NM_015295.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:2762167 A>G maps to NM_015295.2 P1500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:2784501 C>T maps to NM_015295.2 R1868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:2726448 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:152857215 T>C maps to NM_030663.2 H106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:152857137 C>T maps to NM_030663.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:18167651 C>T maps to NM_148886.1 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr17:18166551 G>A maps to NM_148886.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:18167891 G>A maps to NM_148886.1 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:39910259 G>T maps to NM_019008.4 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr22:39910027 C>G maps to NM_019008.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:18220533 G>A maps to NM_144775.2 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:18220735 G>T maps to NM_144775.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:18220941 C>T maps to NM_144775.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:18220545 C>A maps to NM_144775.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr17:18219249 C>T maps to NM_144775.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:91948224 G>A maps to ENST00000417249 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:91948213 A>C maps to ENST00000417249 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:91929136 C>A maps to ENST00000417249 G639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:55792168 G>T maps to NM_001122964.1 I648I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:55805440 G>A maps to NM_001122964.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:55825806 G>A maps to NM_001122964.1 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:55825647 G>T maps to NM_001122964.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr2:55805478 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:18858848 G>A maps to ENST00000389467 H1974H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:18861669 A>G maps to ENST00000389467 S1724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:18893660 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:18847333 G>A maps to ENST00000389467 R2660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:18883507 C>T maps to ENST00000389467 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:18844476 C>T maps to ENST00000389467 S2859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:18849401 C>T maps to ENST00000389467 Q2449Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:18903638 C>T maps to ENST00000389467 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:18823109 C>T maps to ENST00000389467 P3628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YV-01A-11D-A10M-09 chr16:18866017 G>A maps to ENST00000389467 P1481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:18861567 G>A maps to ENST00000389467 N1758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:18851085 C>T maps to ENST00000389467 P2293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:18828692 G>A maps to ENST00000389467 R3333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:18859301 C>A maps to ENST00000389467 E1893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr16:18844442 G>A maps to ENST00000389467 R2871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156230265 C>T maps to NM_015327.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:156228858 G>A maps to NM_015327.2 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr1:156220437 G>A maps to NM_015327.2 H997H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156236413 G>A maps to NM_015327.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156237312 G>T maps to NM_015327.2 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156244414 G>A maps to NM_015327.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:156221192 C>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:156238079 C>A did not map to a codon.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr1:156222848 C>T maps to NM_015327.2 E841E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:2203007 G>A maps to NM_017575.4 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr17:1989032 G>A maps to NM_017575.4 R1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:2203926 C>T maps to NM_017575.4 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:183520222 C>A maps to ENST00000367537 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:183486802 G>T maps to ENST00000444547 *74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:183511477 A>G maps to ENST00000367537 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:183519029 G>A maps to ENST00000367537 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:183506285 G>A maps to ENST00000367537 W433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:183514351 C>T maps to ENST00000367537 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:183498024 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:112063321 C>T maps to NM_005871.3 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:128845458 C>T maps to NM_005631.4 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:128850206 T>A maps to NM_005631.4 C490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:128845144 C>T maps to NM_005631.4 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:128852034 C>T maps to NM_005631.4 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:128849217 C>T maps to NM_005631.4 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:128850359 G>A maps to NM_005631.4 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:70420219 G>T maps to NM_001034852.1 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:70489919 G>A maps to NM_001034852.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:70442475 G>A maps to NM_001034852.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr6:169053813 C>T maps to NM_022138.2 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:168944303 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr20:4162836 G>A maps to ENST00000443211 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr20:4162827 C>T maps to ENST00000443211 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr20:4163400 C>T maps to ENST00000443211 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:6415527 G>A maps to NM_000543.4 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:6415704 G>A maps to NM_000543.4 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:6414605 C>T maps to NM_000543.4 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:6412711 C>A maps to NM_000543.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:6414845 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr6:109764975 T>C maps to NM_003080.2 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:68397677 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:68405670 G>A maps to NM_018667.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:130910181 G>T maps to NM_017951.4 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:130911291 G>A maps to NM_017951.4 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr2:130910889 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:123130408 C>A maps to NM_006714.3 Y406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:28285039 G>A maps to NM_014474.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:28285039 G>A maps to NM_014474.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:28284994 G>A maps to NM_014474.2 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:21755698 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:21755705 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:21772397 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr23:22025267 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:21995199 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:22010812 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:22003329 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:21990626 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:22002475 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr23:22003306 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:22010809 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:21990678 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:21990654 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:21995181 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:21985430 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:31484687 C>T maps to ENST00000454496 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:31491377 G>A maps to ENST00000454496 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:31493041 G>A maps to ENST00000454496 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:31487397 C>T maps to ENST00000454496 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:4495708 C>A maps to NM_001114974.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:4498568 G>A maps to NM_001114974.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:33073752 C>T maps to NM_018225.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:54576130 C>A maps to NM_014311.1 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:98645366 C>T maps to NM_020429.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr7:98649896 G>A maps to NM_020429.2 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr7:98658235 G>A maps to NM_020429.2 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:98655065 G>A maps to NM_020429.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr7:98633219 G>A maps to NM_020429.2 F669F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:98648572 G>A maps to NM_020429.2 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:62552002 C>T maps to NM_022739.3 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:62594510 C>T maps to NM_022739.3 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:62551110 A>G maps to NM_022739.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:62582247 T>C maps to NM_022739.3 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:62543721 C>T maps to NM_022739.3 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:62589639 C>T maps to NM_022739.3 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:88367406 C>T maps to NM_198274.3 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:88407888 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:88387578 G>A maps to NM_198274.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:214504324 C>T maps to NM_020197.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:214492307 C>T maps to NM_020197.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:214505379 G>A maps to NM_020197.2 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:214505385 C>T maps to NM_020197.2 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:246093212 A>G maps to NM_001167740.1 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:246091307 G>A maps to NM_001167740.1 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:246078829 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:246091335 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:1703412 G>T maps to NM_052928.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:73453016 G>A maps to NM_006062.2 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:49832689 G>A maps to NM_003068.3 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:49832539 G>A maps to NM_003068.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:49831490 G>A maps to NM_003068.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr8:49831458 T>C maps to NM_003068.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:10280020 C>T maps to NM_130811.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:10279978 C>T maps to NM_130811.1 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:21237843 C>T maps to NM_004782.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:21242112 C>T maps to NM_004782.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr22:21242112 C>T maps to NM_004782.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:227935805 G>A maps to NM_053052.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:227935544 C>T maps to NM_053052.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:227935737 C>T maps to NM_053052.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:84302257 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:84302216 C>T maps to NM_014841.2 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:84375169 C>T maps to NM_014841.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:84371275 C>A maps to NM_014841.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr14:62229195 C>T maps to NM_003082.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr14:62235383 C>T maps to NM_003082.3 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:62245591 G>A maps to NM_003082.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:7986378 C>A maps to NM_003083.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:15447167 C>T maps to NM_001039697.1 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:15453182 C>A maps to NM_001039697.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:139290215 C>A maps to NM_003086.2 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:139289776 C>T maps to NM_003086.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr9:139283015 G>A maps to NM_003086.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr9:139287147 G>A maps to NM_003086.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:121786662 C>T maps to ENST00000379533 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:121780325 C>T maps to ENST00000379533 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:121799255 G>T maps to ENST00000379533 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:121739486 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:121787134 C>T maps to ENST00000379533 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr5:121761102 A>G maps to ENST00000379533 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:121787058 T>C maps to ENST00000379533 D886D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:121759421 G>A maps to ENST00000379533 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:176048217 G>T maps to NM_003085.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:127727075 C>A maps to NM_014390.2 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:127342561 C>A maps to NM_014390.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:127731926 C>T maps to NM_014390.2 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:127326665 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:127341309 G>A maps to NM_014390.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:127631004 G>T maps to NM_014390.2 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:241979570 C>T maps to NM_001080437.1 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:241991275 C>T maps to NM_001080437.1 I617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:242004356 C>T maps to NM_001080437.1 G899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:242021764 C>T maps to NM_001080437.1 G1369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:242002211 C>T maps to NM_001080437.1 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:242008376 G>A maps to NM_001080437.1 G1082G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:242011246 C>T maps to NM_001080437.1 S1257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:47009067 G>A maps to NM_007241.2 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:47009025 G>A maps to NM_007241.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:38003479 C>A maps to NM_024700.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:38005963 C>T maps to NM_024700.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:1285596 C>T maps to ENST00000381876 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:1276948 A>G maps to ENST00000381876 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:1277824 C>T maps to ENST00000381876 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr20:1281226 G>A maps to ENST00000381876 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:43344703 A>G maps to NM_017719.4 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:96942656 C>T maps to NM_014014.3 A2053A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:96944649 G>A maps to NM_014014.3 I1740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:96944079 G>A maps to NM_014014.3 S1835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:96958733 G>T maps to NM_014014.3 I712I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:96947556 G>A maps to NM_014014.3 I1673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:96952139 C>T maps to NM_014014.3 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:96959241 C>T maps to NM_014014.3 E616E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:96964572 C>A maps to NM_014014.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:96949562 C>T maps to NM_014014.3 E1524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:96967375 G>A maps to NM_014014.3 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:96943589 C>T maps to NM_014014.3 Q1903Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:96951046 G>A maps to NM_014014.3 N1345N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:96944016 C>T maps to NM_014014.3 E1856E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:123950368 C>T maps to NM_180699.2 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:123950704 C>T maps to NM_180699.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:31762265 A>G maps to ENST00000446633 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:7594381 G>A maps to NM_152551.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49601735 C>T maps to NM_003089.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:49601735 C>T maps to NM_003089.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:2446431 C>T maps to ENST00000339610 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:16712827 T>C maps to NM_198220.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:16721613 G>A maps to NM_198220.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr6:34735774 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:34735745 G>A maps to ENST00000374017 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:24953653 T>C maps to NM_004175.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:70515288 A>G maps to NM_003096.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:25220557 T>C maps to NM_022805.2 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:25223412 G>A maps to NM_022805.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr20:32000461 C>T maps to NM_003098.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:121706095 G>A maps to NM_021021.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr8:51362261 C>G maps to NM_018967.2 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr8:51442735 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:1093904 A>G maps to NM_018968.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:1161316 G>A maps to NM_018968.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:1271141 G>A maps to NM_018968.3 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:75902272 G>A maps to ENST00000371091 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:75913311 G>T maps to ENST00000371091 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:25207303 G>T maps to NM_022804.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr14:78205306 A>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:78221345 G>A maps to NM_012245.2 Y44Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr15:64418414 C>T maps to NM_003099.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:64418351 G>A maps to NM_003099.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:26404213 C>T maps to ENST00000446848 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:26404213 C>T maps to ENST00000446848 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70281748 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70288023 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70280889 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:70280888 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70281729 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:70282703 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:70288020 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:17836500 G>A maps to ENST00000417048 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:17838723 G>A maps to ENST00000417048 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:17915405 C>A maps to ENST00000417048 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:17855900 G>A maps to ENST00000417048 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:86239918 C>A maps to NM_153816.3 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:86239985 G>A maps to NM_153816.3 H606H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr6:86257067 C>T maps to NM_153816.3 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:86238021 T>C maps to NM_153816.3 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:86275105 C>A maps to NM_153816.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:82727615 C>A maps to NM_152836.2 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:27599478 C>T maps to NM_014748.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27599558 C>T maps to NM_014748.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:53814963 G>A maps to NM_052870.2 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:53814852 C>T maps to NM_052870.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:53814534 C>T maps to NM_052870.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr5:53814690 G>A maps to NM_052870.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:53814981 C>T maps to NM_052870.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:53815476 A>G maps to NM_052870.2 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:130785042 G>A maps to NM_014758.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:130784394 C>T maps to NM_014758.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:130785480 G>T maps to NM_014758.2 Y118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:130784750 G>A maps to NM_014758.2 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:130785117 G>A maps to NM_014758.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:130784838 G>A maps to NM_014758.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:130773265 C>T maps to NM_014758.2 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:130784459 C>A maps to NM_014758.2 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:122165292 C>T maps to NM_003100.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:122137620 G>T maps to NM_003100.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:50707907 G>A maps to NM_182854.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:50707973 G>T maps to NM_182854.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:44469922 G>T maps to NM_033421.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr20:44469297 C>T maps to NM_033421.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:122335639 C>T maps to ENST00000395451 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:186241933 C>T maps to NM_031953.2 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:186260645 C>A maps to NM_031953.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:186263164 C>A maps to NM_031953.2 Y530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:186283083 C>T maps to NM_031953.2 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:186244738 G>T maps to NM_031953.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:151655870 G>T maps to ENST00000458013 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:151633284 C>T maps to ENST00000458013 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr1:151665937 C>T maps to ENST00000458013 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:12155432 G>A maps to NM_001080530.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:108544221 C>A maps to NM_003795.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:108544179 G>A maps to NM_003795.4 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:115579983 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:115580095 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:115598543 C>T maps to NM_001012994.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr8:101589288 C>T maps to NM_152628.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:101642560 C>T maps to NM_152628.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:101625265 G>A maps to NM_152628.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:101625285 G>T maps to NM_152628.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:101612574 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:65616953 C>A maps to NM_152760.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:65617946 C>A maps to NM_152760.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:75942573 C>T maps to NM_153271.1 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:75942679 G>T maps to NM_153271.1 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr15:75942561 C>T maps to NM_153271.1 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:125170261 C>A maps to NM_003794.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:125208286 C>T maps to NM_003794.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:125176127 A>G maps to NM_003794.2 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:125199090 A>G maps to NM_003794.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr20:17933344 G>A maps to NM_152227.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr20:17932179 C>T maps to NM_152227.1 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:17930825 G>A maps to NM_152227.1 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:17933320 G>T maps to NM_152227.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:35045035 G>A maps to NM_152233.2 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:35072588 A>G maps to NM_152233.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr14:35036978 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:35050778 G>A maps to NM_152233.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:35050778 G>A maps to NM_152233.2 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:99164436 C>T maps to NM_015976.4 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:99156708 C>T maps to NM_015976.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:2296538 G>A maps to NM_013321.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr7:2309274 C>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr7:2297104 C>T maps to NM_013321.2 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr7:2317821 C>G maps to NM_013321.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:158330948 C>T maps to NM_016224.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:158359774 G>A maps to NM_016224.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:179311289 C>T maps to NM_003101.4 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:179320491 G>A maps to NM_003101.4 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:179322775 G>T maps to NM_003101.4 *551Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:53498973 C>A maps to NM_003578.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr12:53509368 G>A maps to NM_003578.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:53512197 C>A maps to NM_003578.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr12:93968496 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76354762 C>T maps to NM_003955.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:55510862 C>T maps to NM_199421.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:55510976 C>T maps to NM_199421.1 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:55510976 C>A maps to NM_199421.1 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:55510290 C>T maps to NM_199421.1 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:46985849 G>T maps to NM_144949.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:46986072 C>A maps to NM_144949.2 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:46986775 C>T maps to NM_144949.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr2:46986361 T>C maps to NM_144949.2 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:160113600 C>T maps to ENST00000452684 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr9:138585553 G>A maps to NM_001101677.1 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:138585660 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:36766001 C>A maps to ENST00000511166 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:36743179 C>T maps to ENST00000511166 W500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:36764165 C>T maps to ENST00000511166 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr13:36743176 C>T maps to ENST00000511166 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:36765929 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:602429 C>T maps to NM_005632.2 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr16:601517 G>A maps to NM_005632.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:603374 C>T maps to NM_005632.2 N1040N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:34922130 G>A maps to NM_138927.1 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:34948854 T>C maps to ENST00000436227 T1445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:34941293 G>A maps to NM_138927.1 Q2262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:34931534 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:34922544 G>A maps to NM_138927.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr21:34926069 A>G maps to NM_138927.1 E1511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr21:34922664 G>A maps to NM_138927.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr21:34923048 C>T maps to NM_138927.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:34921780 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:34931534 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:34923522 G>A maps to NM_138927.1 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:34921987 G>T maps to NM_138927.1 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:97170405 G>T maps to NM_001034954.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:97082508 G>A maps to ENST00000371227 S1185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:97096777 G>A maps to NM_001034954.1 R1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:97144008 G>T maps to NM_001034954.1 S465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:186544277 G>A maps to ENST00000355634 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:186545457 C>T maps to ENST00000355634 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:186578640 T>C maps to ENST00000355634 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:186533062 T>C maps to ENST00000355634 R1085R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:186567881 C>T maps to ENST00000355634 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:186583270 G>A maps to ENST00000355634 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr4:186544808 G>A maps to ENST00000355634 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr4:186544809 C>T maps to ENST00000355634 E687E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr4:186544263 G>A maps to ENST00000355634 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:186560087 C>T maps to NM_001145671.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr4:186536017 G>A maps to ENST00000355634 N1050N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:22429891 C>T maps to NM_005775.4 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr8:22428454 C>T maps to NM_005775.4 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:22424369 G>A maps to NM_005775.4 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:108459025 C>T maps to NM_001013031.1 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:108357160 G>A maps to NM_001013031.1 F1071F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:108388984 G>A maps to NM_001013031.1 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:108389107 G>A maps to NM_001013031.1 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:108339146 G>A maps to NM_001013031.1 F1117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:108437080 G>A maps to NM_001013031.1 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:108521350 G>A maps to NM_001013031.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:108923724 A>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:108366986 G>T maps to NM_001013031.1 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:108389032 G>A maps to NM_001013031.1 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:108489808 A>G maps to NM_001013031.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:108447996 G>A maps to NM_001013031.1 Q505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:7668921 G>A maps to NM_020777.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:7668882 C>A maps to NM_020777.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:7736056 C>T maps to NM_020777.2 I1089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:7668892 C>T maps to NM_020777.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:7677877 C>T maps to NM_020777.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:7668906 C>T maps to NM_020777.2 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr4:7716019 G>A maps to NM_020777.2 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:7668892 C>T maps to NM_020777.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr4:7533274 G>A maps to NM_020777.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:7640107 C>T maps to NM_020777.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:7728626 C>T maps to NM_020777.2 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr4:7731321 C>T maps to NM_020777.2 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:106737164 A>T maps to NM_014978.1 K290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:106918699 C>T maps to NM_014978.1 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:107005407 G>T maps to NM_014978.1 E993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:106849589 G>A maps to NM_014978.1 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:106960987 C>A maps to NM_014978.1 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:106916994 C>T maps to NM_014978.1 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:106907445 G>A maps to NM_014978.1 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:45364615 C>T maps to NM_003104.5 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:45360377 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:45353313 C>T maps to NM_003104.5 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr15:45357498 C>T maps to NM_003104.5 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:121491774 G>A maps to NM_003105.5 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:121490577 C>T maps to NM_003105.5 S1947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr11:121391559 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:121425921 G>A maps to NM_003105.5 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:121460004 C>T maps to NM_003105.5 F1328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:121340813 G>A maps to NM_003105.5 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:121491772 T>C maps to NM_003105.5 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:121498378 G>A maps to NM_003105.5 T2160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr11:121489587 C>T maps to NM_003105.5 Q1904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:109859530 G>A maps to NM_002959.4 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:109856992 G>A maps to NM_002959.4 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:109910070 T>C maps to NM_002959.4 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:39251268 C>A maps to NM_005633.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:39222288 G>A maps to NM_005633.3 S1107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:50611953 A>G maps to NM_006939.2 N867N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:50649318 G>A maps to NM_006939.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:50655255 G>A maps to NM_006939.2 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:50600911 C>A maps to NM_006939.2 E1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:50655255 G>A maps to NM_006939.2 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:50655255 G>T maps to NM_006939.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:50596706 G>T maps to NM_006939.2 I1117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:41835938 G>A maps to NM_025237.2 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:41835932 C>T maps to NM_025237.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:16502229 G>A maps to ENST00000396652 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:16502526 G>A maps to ENST00000396652 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:38373928 G>A maps to NM_006941.3 H214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:5834010 G>A maps to NM_003108.3 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:5833143 G>A maps to NM_003108.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:204086746 C>A maps to ENST00000367206 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr1:204091085 G>A maps to ENST00000367206 G289G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:181430258 C>T maps to NM_003106.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr3:181430801 C>T maps to NM_003106.2 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:95364027 G>A maps to NM_007084.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:139586540 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:139587160 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:139586639 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:139586874 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:139587063 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:139586801 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:139586644 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:139586880 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:139586568 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:139587021 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:157078327 C>T maps to NM_178424.1 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr5:157065491 G>A maps to NM_178424.1 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:157065356 T>G maps to NM_178424.1 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:157078270 C>T maps to NM_178424.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr5:157078219 G>A maps to NM_178424.1 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr6:21595041 C>T maps to NM_003107.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:23687260 G>A maps to NM_006940.4 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:23687401 G>A maps to NM_006940.4 I681I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:23893905 G>A maps to NM_006940.4 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:16007855 G>A maps to NM_001145819.1 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:16010672 G>A maps to NM_001145819.1 R625R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr8:10583715 G>A maps to ENST00000354846 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:10583418 G>A maps to ENST00000354846 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:10584030 G>A maps to ENST00000354846 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:10583478 G>A maps to ENST00000354846 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:70119855 C>T maps to NM_000346.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:53800402 T>C maps to NM_138473.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:53776702 C>T maps to NM_138473.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:53776174 T>C maps to NM_138473.2 V148V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A5-A0VP-01A-21D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:231307661 G>T maps to NM_001080391.1 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:231309041 T>A maps to NM_001080391.1 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:231313822 C>T maps to NM_001080391.1 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:231331016 G>A maps to NM_001080391.1 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:231326019 C>A maps to NM_001080391.1 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:231328804 G>T maps to NM_001080391.1 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:231406035 G>A maps to NM_001080391.1 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:231404055 C>A maps to NM_001080391.1 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:231379956 G>T maps to NM_003113.3 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:231077551 G>A maps to NM_080424.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:231037654 G>A maps to NM_080424.2 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:231079814 T>G maps to NM_080424.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:231176180 T>C maps to NM_007237.4 C792C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:231175566 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:231174667 C>T maps to NM_007237.4 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr2:231176282 C>T maps to NM_007237.4 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:231106122 C>A maps to NM_007237.4 C137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:231118052 C>A maps to NM_007237.4 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:231118043 T>C maps to NM_007237.4 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:231157364 C>A maps to NM_007237.4 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:231106119 A>G maps to NM_007237.4 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr2:231235668 A>G maps to NM_138402.4 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:231265668 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:231223779 A>G maps to NM_138402.4 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:45994391 C>T maps to NM_003110.5 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:45993880 A>G maps to NM_003110.5 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:46002460 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:174820237 G>A maps to NM_003111.4 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:174774769 C>A maps to NM_003111.4 G749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:174820641 C>A maps to NM_003111.4 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:174820867 A>G maps to NM_003111.4 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:21469067 G>A maps to NM_003112.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:21516700 G>A maps to NM_003112.3 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:45925777 G>A maps to NM_199262.2 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:53722253 G>A maps to NM_001173467.1 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:20825306 G>T maps to NM_182700.4 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TG-01A-32D-A10B-09 chr11:124545165 G>A maps to NM_017425.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:88769169 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:88767408 C>T maps to NM_030960.2 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:88767343 G>T maps to NM_030960.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:88763686 G>T maps to NM_030960.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr6:88763709 C>T maps to NM_030960.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:31323984 G>A maps to NM_173847.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:31324750 C>T maps to NM_173847.3 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:31323984 G>A maps to NM_173847.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:101243441 C>T maps to NM_003114.3 N638N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:101252863 G>A maps to NM_003114.3 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:214794787 G>A maps to NM_024532.3 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:214878728 G>A maps to NM_024532.3 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:215274981 C>T maps to NM_024532.3 H613H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:215275024 C>T maps to NM_024532.3 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:214204920 G>T maps to NM_024532.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr2:215274984 C>T maps to NM_024532.3 D614D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:118629541 G>A maps to NM_206996.2 H483H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:118537133 G>A maps to NM_206996.2 V1691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:118634278 G>A maps to NM_206996.2 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:118523989 G>A maps to NM_206996.2 S1969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:118548165 G>T maps to NM_206996.2 C1549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:118644465 A>G maps to NM_206996.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:118539231 T>C maps to NM_206996.2 E1637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:118640367 G>T maps to NM_206996.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:34205457 G>A maps to NM_003116.1 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:34207517 G>T maps to NM_003116.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:26905498 C>T maps to NM_006461.3 A1082A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr17:26919199 G>A maps to NM_006461.3 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:26913440 A>G did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr17:26911668 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:26913460 C>T maps to NM_006461.3 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:22676870 C>T maps to ENST00000376603 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:22634700 G>A maps to ENST00000376603 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:22657521 G>A maps to ENST00000376603 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:22676870 C>T maps to ENST00000376603 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:22699983 C>T maps to ENST00000376603 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:4863145 G>A maps to NM_004890.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:4863370 G>A maps to NM_004890.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr9:35811199 G>C maps to NM_001039592.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:35810550 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:35810882 G>A maps to NM_001039592.1 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:49091650 T>C maps to ENST00000376407 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:49097575 G>A maps to ENST00000376407 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:49072811 G>T maps to ENST00000376407 S684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:49062335 G>A maps to ENST00000376407 I1013I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:49071179 G>A maps to ENST00000376407 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:49057278 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:49059917 G>T maps to ENST00000376407 I1069I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:49079094 G>A maps to ENST00000376407 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr17:49067943 T>C maps to ENST00000376407 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:123594386 G>T maps to NM_001174046.1 E255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:123599536 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:123595074 G>T maps to NM_001174046.1 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:123594427 G>A maps to NM_001174046.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:123594055 T>C maps to NM_001174046.1 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16B-01A-11D-A12J-09 chr7:123599918 G>T maps to NM_001174046.1 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr7:123594427 G>A maps to NM_001174046.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:140786495 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:140786522 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:140785774 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:140785701 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:144337273 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:144337306 A>T did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr23:144337284 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:144329129 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:144337198 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:142795276 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:142795593 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:142803718 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:142795280 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:142795302 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr23:142795244 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:142795235 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:142795366 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:142795341 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:142596892 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:142596729 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:142596826 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:142596729 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:142605154 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:142596810 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:142596879 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:142596719 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:52825632 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:151052740 C>A maps to NM_003118.2 G53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:151049282 G>A maps to NM_003118.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:88415090 G>A maps to NM_004684.4 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:88415318 A>G maps to NM_004684.4 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:32379498 C>T maps to NM_014946.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:32379498 C>T maps to NM_014946.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:32379558 T>G maps to NM_014946.3 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:32353547 C>T maps to NM_014946.3 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:85018716 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:85011432 C>T maps to ENST00000263717 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:84991730 G>A maps to ENST00000263717 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:24797831 G>T maps to ENST00000424834 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:24825944 C>T maps to ENST00000424834 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:24863183 G>A maps to ENST00000424834 A942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:24798554 G>A maps to ENST00000424834 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:24876763 G>A maps to ENST00000424834 P1266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr13:24871622 C>T maps to ENST00000424834 C1148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:172642041 G>A maps to NM_031955.5 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:172834945 G>A maps to NM_031955.5 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:172835473 G>A maps to NM_031955.5 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:217915436 G>A maps to NM_138796.2 K172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:217822287 G>T maps to NM_138796.2 G45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:217975156 C>A maps to NM_138796.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:52926625 C>A maps to NM_145263.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:133711951 G>T maps to NM_174927.1 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:48523205 G>A maps to NM_006038.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:48626462 C>A maps to NM_022827.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:48629350 C>T maps to NM_022827.2 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr17:48632645 C>T maps to NM_022827.2 C737C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr17:48629482 C>T maps to NM_022827.2 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:3352217 G>A maps to NM_001170695.1 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:3343617 C>T maps to NM_001170695.1 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:3346479 G>T maps to NM_001170695.1 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:3352261 C>A maps to NM_001170695.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:3352394 A>G maps to NM_001170695.1 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:177114185 G>A maps to NM_144644.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:177109386 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:177113985 G>A maps to NM_144644.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:177109360 C>A maps to NM_144644.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:123949345 C>A maps to NM_145207.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:123949433 C>T maps to NM_145207.2 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:124177290 C>T maps to NM_145207.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:123868468 C>T maps to NM_145207.2 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:123855811 G>T maps to NM_145207.2 G356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:123949474 G>A maps to NM_145207.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:45702631 C>T maps to NM_024063.2 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:48825412 G>A maps to NM_019073.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:48877137 G>A maps to NM_019073.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:48825412 G>A maps to NM_019073.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:48865184 G>A maps to NM_019073.2 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:88883169 T>G maps to NM_018418.4 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr14:88895756 C>T maps to NM_018418.4 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:88862512 C>T maps to NM_018418.4 C68C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:88892856 G>A maps to NM_018418.4 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:88892856 G>A maps to NM_018418.4 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:94999692 G>A maps to NM_031952.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:145094969 G>A maps to NM_198572.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:44344770 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:44336177 G>T maps to NM_145026.3 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:49888573 C>T maps to NM_023071.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:49883289 G>T maps to NM_023071.3 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:201337624 C>T maps to ENST00000409151 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:201284139 C>T maps to ENST00000409151 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:201337658 C>T maps to ENST00000409151 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:201334701 C>T maps to ENST00000409151 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:201281124 G>T maps to ENST00000409151 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:169745735 G>A maps to NM_020675.3 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:177249432 C>T maps to NM_021928.3 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:177245362 G>A maps to NM_021928.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:34511902 G>A maps to NM_012391.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:64940483 C>T maps to NM_001008778.1 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:64938872 C>T maps to NM_001008778.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44040761 C>T maps to NM_175064.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr7:99917597 C>T maps to NM_001004351.4 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:99909547 G>A maps to NM_001004351.4 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:99917322 G>A maps to NM_001004351.4 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:75131063 G>A maps to NM_001099435.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A186-01A-11D-A12J-09 chr20:3760357 G>A maps to NM_015417.4 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:3759530 A>T maps to ENST00000312411 L162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:35704716 C>T maps to NM_024867.3 N820N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:35740059 G>T maps to NM_024867.3 E1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:35771835 A>G maps to NM_024867.3 K1309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:35763731 G>A maps to NM_024867.3 E1243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr5:35763776 G>A maps to NM_024867.3 Q1258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:35694415 T>C maps to NM_024867.3 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:35806966 A>G maps to NM_024867.3 T1723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:35807288 C>A maps to NM_024867.3 V1771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:35793301 C>T maps to NM_024867.3 F1532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:220344862 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr2:220326652 C>G maps to NM_005876.4 Y830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:220309646 G>A maps to NM_005876.4 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:220354241 G>A maps to NM_005876.4 S2834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:220332070 C>T maps to NM_005876.4 F1019F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:220326643 C>T maps to NM_005876.4 D827D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:220342096 C>T maps to NM_005876.4 G1553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr2:220338271 C>T maps to NM_005876.4 I1398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:220333958 G>A maps to NM_005876.4 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:220354241 G>T maps to NM_005876.4 S2834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:220309805 G>A maps to NM_005876.4 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr2:220353301 G>A maps to NM_005876.4 A2647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr2:220353827 C>T maps to NM_005876.4 N2734N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:220342135 C>A maps to NM_005876.4 V1566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:220354611 C>T maps to NM_005876.4 R2958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:220355271 G>A maps to NM_005876.4 R3021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:220348808 C>A maps to NM_005876.4 P2208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:7323813 C>A maps to NM_199339.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7323789 C>T maps to NM_199339.2 V29V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A0JY-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:16200651 G>T maps to ENST00000438066 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:16247444 C>A maps to NM_015001.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:16261485 C>A maps to NM_015001.2 L2917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:16255365 C>T maps to NM_015001.2 C877C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:16262661 C>T maps to NM_015001.2 G3309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:16264443 C>T maps to NM_015001.2 I3549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:16265283 C>T maps to NM_015001.2 T3592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:16256919 C>A maps to NM_015001.2 A1395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:16256830 C>T maps to NM_015001.2 R1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:16257321 T>A maps to NM_015001.2 R1529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:16261485 C>A maps to NM_015001.2 L2917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:16247420 T>C maps to NM_015001.2 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:16256223 C>T maps to NM_015001.2 I1163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:16256787 T>C maps to NM_015001.2 F1351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:16258975 C>T maps to NM_015001.2 R2081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:16235855 C>T maps to NM_015001.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:16259974 G>T maps to NM_015001.2 E2414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:16260687 G>A maps to NM_015001.2 V2651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:16202924 G>A maps to NM_015001.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:16257459 C>A maps to NM_015001.2 S1575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:16245425 T>C maps to NM_015001.2 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:16254700 G>T maps to NM_015001.2 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:16256080 C>T maps to NM_015001.2 L1116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:16242707 C>T maps to NM_015001.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:16202786 C>T maps to NM_015001.2 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:16256083 C>T maps to NM_015001.2 Q1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:16261434 G>A maps to NM_015001.2 S2900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:16262685 G>A maps to NM_015001.2 P3317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:16247459 C>T maps to NM_015001.2 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:69238448 C>T maps to NM_145658.3 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:69238760 C>T maps to NM_145658.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:44890928 G>A maps to NM_025137.3 D1264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:44858194 G>A maps to NM_025137.3 R2286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:44878048 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:44900761 C>A maps to NM_025137.3 V1111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:44856863 A>G maps to NM_025137.3 V2344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:44890502 C>A maps to NM_025137.3 E1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:44876399 G>T maps to NM_025137.3 I1826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:44890523 C>A maps to NM_025137.3 E1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:44914927 A>G maps to NM_025137.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:44921530 A>G maps to NM_025137.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:44865793 G>A maps to NM_025137.3 L2052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:44903067 A>C maps to NM_025137.3 T1087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:44861697 C>T maps to NM_025137.3 R2161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:44951501 C>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:44921006 A>G maps to NM_025137.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr15:44865010 C>T maps to NM_025137.3 K2071K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr15:44925825 C>A maps to NM_025137.3 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:36905643 T>C maps to NM_001142294.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:36886575 C>A maps to NM_001142294.1 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:36903575 C>A maps to NM_001142294.1 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:36886530 C>A maps to NM_001142294.1 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:65256044 G>A maps to NM_016630.3 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr15:65266977 A>G maps to NM_016630.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:89597110 T>G maps to NM_003119.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:89598391 G>A maps to NM_003119.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr16:89590263 C>T maps to ENST00000312632 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:89597173 C>T maps to NM_003119.2 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr16:89598337 C>T maps to NM_003119.2 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr17:74382183 T>C maps to NM_182965.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:49132504 A>C maps to NM_020126.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr19:49132783 C>T maps to NM_020126.3 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:228881963 G>A maps to NM_001142644.1 I1202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr2:228884687 T>C maps to NM_001142644.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:228996761 C>T maps to NM_001142644.1 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:228883859 G>T maps to NM_001142644.1 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr2:228881456 C>T maps to NM_001142644.1 P1371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:228846564 G>A maps to NM_001142644.1 V1657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:228881963 G>A maps to NM_001142644.1 I1202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:228884339 A>T maps to NM_001142644.1 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:228881234 G>T maps to NM_001142644.1 P1445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:228881783 G>T maps to NM_001142644.1 G1262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:228881882 T>C maps to NM_001142644.1 R1229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:228882998 G>A maps to NM_001142644.1 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr2:228884563 G>A maps to NM_001142644.1 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:228886634 G>A maps to NM_001142644.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr12:101880173 G>A maps to ENST00000299272 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:101880155 C>T maps to ENST00000299272 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr12:101871355 G>A maps to ENST00000299272 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:101880173 G>A maps to ENST00000299272 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:101873447 T>C maps to ENST00000299272 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:91077581 C>T maps to NM_006717.2 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:91083521 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:57162349 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:57162431 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:57162650 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:57146848 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr23:57146313 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:57146944 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:57146626 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:57146309 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:57146609 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:57146745 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:57020733 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:57021323 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:57020623 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:57021233 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:57021267 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:62570168 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:62570622 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:62570360 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:62570023 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:147661692 G>T maps to NM_001040129.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:147504369 A>G maps to NM_001127698.1 K903K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:147492434 C>T maps to NM_001127698.1 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:147498546 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:147504331 C>T maps to NM_001127698.1 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:147473984 A>G maps to NM_001127698.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr5:147491434 C>A maps to NM_001127698.1 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:147443687 C>T maps to ENST00000398459 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:147478851 G>T maps to NM_001127698.1 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:147486664 T>C maps to NM_001127698.1 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:147475438 G>T maps to NM_001127698.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:147503467 C>T maps to NM_001127698.1 R871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:147478851 G>T maps to NM_001127698.1 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:147499933 G>T maps to NM_001127698.1 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:44171498 G>A maps to ENST00000396669 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr15:41137174 C>A maps to NM_181642.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:41145999 C>T maps to NM_181642.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:38782600 C>T maps to NM_021102.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:38782501 C>T maps to NM_021102.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:12512497 G>A maps to NM_001128626.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr18:12506550 A>G maps to NM_001128626.1 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:12506636 G>A maps to NM_001128626.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:89927194 C>T maps to NM_032451.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:89936661 G>A maps to NM_032451.1 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:89911745 C>T maps to NM_032451.1 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:89922624 C>T maps to NM_032451.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:89936090 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:89922084 A>G maps to NM_032451.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:89916974 C>T maps to NM_032451.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:89936613 G>A maps to NM_032451.1 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:29675528 C>A maps to NM_003123.3 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:29675429 C>A maps to NM_003123.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:28993317 C>T maps to NM_032038.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:28993224 T>C maps to NM_032038.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:4440215 G>A maps to NM_001124758.1 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:4435863 G>T maps to NM_001124758.1 G274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:4436346 G>A maps to NM_001124758.1 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr17:4350206 C>T maps to NM_182538.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr20:55909834 C>T maps to ENST00000371258 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:32279674 C>T maps to NM_144569.4 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:32262244 G>A maps to NM_144569.4 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:32280067 G>A maps to NM_144569.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:32258344 C>T maps to NM_144569.4 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:32256605 G>T maps to NM_144569.4 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:32256689 C>T maps to NM_144569.4 P1055P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:32256722 C>T maps to NM_144569.4 E1044E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:32263861 C>T maps to NM_144569.4 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:136448204 C>T maps to NM_004598.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:136448204 C>T maps to NM_004598.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:136448204 C>T maps to NM_004598.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:73822855 G>A maps to NM_014767.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:73847942 G>A maps to NM_014767.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:167675728 A>G maps to NM_016950.2 N290N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AX-A05Z-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:167983649 G>A maps to NM_016950.2 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:14101476 C>T maps to NM_006108.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:14096906 A>G maps to NM_006108.2 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:14157105 C>T maps to NM_006108.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:14278225 G>T maps to NM_006108.2 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:14284424 C>T maps to NM_006108.2 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:14277323 C>T maps to NM_006108.2 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:14284294 G>A maps to NM_006108.2 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:14276271 T>C maps to NM_006108.2 Y362Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr4:1164358 C>T maps to NM_012445.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:47684730 G>A maps to NM_003563.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr17:47699331 G>T maps to NM_003563.3 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr17:47696739 G>A maps to NM_003563.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:139310140 C>T maps to NM_001001664.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:139322306 C>T maps to NM_001001664.2 C289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:88902823 G>A maps to NM_001040058.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:88903927 C>T maps to NM_001040058.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:234959456 G>A maps to NM_006944.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:121206270 G>T maps to NM_139015.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:73118534 C>T maps to NM_003124.4 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr2:65540826 C>T maps to NM_181784.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:153066116 T>C maps to NM_001024209.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:153066119 G>A maps to NM_001024209.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:153122607 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:124322690 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:80911237 G>A maps to NM_005842.2 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:80911692 G>A maps to NM_005842.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:80911300 G>A maps to NM_005842.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:155003608 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:155004299 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:155003804 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:155003934 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:155003613 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:155004348 G>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:155004199 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:141694466 G>A maps to NM_030964.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:56863220 C>T maps to NM_207344.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr11:55655738 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:55653245 G>A maps to NM_032681.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:9416306 G>A maps to NM_025106.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:9416591 T>C maps to NM_025106.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr16:1828577 C>T maps to NM_080861.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:140785549 C>T maps to NM_080862.1 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:158582744 G>A maps to NM_003126.2 G2332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:158585175 G>A maps to NM_003126.2 I2206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:158614186 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:158624466 G>A maps to NM_003126.2 A990A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:158626362 G>A maps to NM_003126.2 N963N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:158656283 G>A maps to NM_003126.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:158626431 C>T maps to NM_003126.2 K940K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:158655005 G>T maps to NM_003126.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:158626362 G>A maps to NM_003126.2 N963N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr1:158614069 G>A maps to NM_003126.2 D1437D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:158607880 C>A maps to NM_003126.2 E1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:158587839 G>A maps to NM_003126.2 Y2179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr1:158650375 G>A maps to NM_003126.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr1:158627400 G>A maps to NM_003126.2 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:158644361 C>A maps to NM_003126.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:158589073 A>G maps to NM_003126.2 F2156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:158636152 G>A maps to NM_003126.2 R725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:158582696 T>C maps to NM_003126.2 S2348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:158622337 A>G maps to NM_003126.2 I1098I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:131329151 C>T maps to NM_001130438.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:131346610 C>T maps to NM_001130438.2 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:131388166 C>T maps to NM_001130438.2 H2063H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:131394970 A>G maps to NM_001130438.2 A2378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr9:131374063 C>T maps to NM_001130438.2 I1615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:131371404 C>T maps to NM_001130438.2 R1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:131388788 T>G maps to NM_001130438.2 A2133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:131395092 C>T maps to NM_001130438.2 G2389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:131394743 G>T maps to NM_001130438.2 E2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:131394964 C>T maps to NM_001130438.2 F2376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:131394743 G>T maps to NM_001130438.2 E2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:131336951 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:131395573 C>T maps to NM_001130438.2 F2465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr9:131331070 A>G maps to NM_001130438.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:131339175 C>T maps to NM_001130438.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:131388735 G>T maps to NM_001130438.2 E2116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:131339202 C>A maps to NM_001130438.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr14:65216398 G>A maps to ENST00000389723 S2268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:65266643 G>A maps to ENST00000389723 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:65216398 G>A maps to ENST00000389723 S2268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr14:65253878 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:65241860 G>T maps to ENST00000389723 I1612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr14:65241938 G>A maps to ENST00000389723 D1586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:65252518 C>A maps to ENST00000389723 G1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:65262276 G>A maps to ENST00000389723 Y478Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr14:65250970 G>T maps to ENST00000389723 I1336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:65246547 G>A maps to ENST00000389723 I1460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:65250970 G>A maps to ENST00000389723 I1336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:65246624 G>A maps to ENST00000389723 R1435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:54852044 C>T maps to NM_003128.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:54851939 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:54853250 G>A maps to NM_003128.2 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:54856406 G>A maps to NM_003128.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:54874273 C>T maps to NM_003128.2 Q1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:54895654 C>T maps to NM_003128.2 D2348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:54857112 C>T maps to NM_003128.2 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:54893177 C>T maps to NM_003128.2 C2262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:54849513 T>C maps to NM_003128.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:54880969 C>T maps to NM_003128.2 I1934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:54859794 C>T maps to NM_003128.2 D1219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:54858079 G>T maps to NM_003128.2 E966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:54851976 G>T maps to NM_003128.2 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:54853118 C>T maps to NM_003128.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:54870247 G>A maps to NM_003128.2 W1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:54858039 G>A maps to NM_003128.2 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:54880861 C>T maps to NM_003128.2 D1898D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:54891624 C>T maps to NM_003128.2 N2152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr11:66469056 G>A maps to NM_006946.2 H938H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:66475757 G>A maps to NM_006946.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:66468400 G>A maps to NM_006946.2 R1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr11:66454625 G>A maps to NM_006946.2 N2245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr11:66453434 G>A maps to NM_006946.2 P2360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:66483312 C>T maps to NM_006946.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:41008081 G>A maps to NM_020971.2 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr19:41066291 G>A maps to NM_020971.2 G1966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:41063299 C>T maps to NM_020971.2 L1887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:41003491 G>A maps to NM_020971.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:41029417 C>T maps to NM_020971.2 D1243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:41038578 G>A maps to NM_020971.2 T1332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:41009849 C>A maps to NM_020971.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:42158670 C>T maps to ENST00000320955 A2167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:42159243 C>A maps to ENST00000320955 R2131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:42145090 C>T maps to ENST00000320955 R3426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:42144454 C>T maps to ENST00000320955 S3503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr15:42156153 A>G maps to ENST00000320955 P2329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr15:42143985 G>A maps to ENST00000320955 G3549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:42162754 G>A maps to ENST00000320955 T1817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:42153935 T>C maps to ENST00000320955 L2578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:94842337 G>A maps to NM_006415.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:94843210 C>A maps to NM_006415.2 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:78063720 G>A maps to NM_004863.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:78063662 C>A maps to NM_004863.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:13074168 G>A maps to NM_018327.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:13098263 C>T maps to NM_018327.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:13029624 C>A maps to NM_018327.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:13134719 C>T maps to NM_018327.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:18636511 G>A maps to NM_194285.2 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:18631436 G>A maps to NM_194285.2 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:18655791 C>A maps to NM_194285.2 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr11:18636575 G>T maps to NM_194285.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:79616144 C>T maps to NM_032567.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:79616256 G>T maps to NM_032567.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:79616471 G>A maps to NM_032567.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:79616256 G>T maps to NM_032567.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:79616364 G>T maps to NM_032567.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:79617153 G>T maps to NM_032567.3 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:126021538 G>A maps to NM_003129.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:126021289 T>C maps to NM_003129.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:45965848 G>A maps to NM_021199.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:45983188 A>C maps to NM_021199.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:45965848 G>A maps to NM_021199.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:45965989 C>A maps to NM_021199.2 Y215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr15:45968396 G>A maps to NM_021199.2 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:179250981 C>T maps to NM_003900.4 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:179263653 G>A maps to ENST00000510187 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:179250037 C>T maps to NM_003900.4 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:139930727 T>C maps to NM_001035235.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:45773944 G>A maps to NM_018079.4 A600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:45807062 C>T maps to NM_018079.4 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:45829067 C>A maps to NM_018079.4 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:36022369 G>A maps to ENST00000373558 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr20:36026156 G>A maps to ENST00000373558 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:30734431 G>A maps to NM_006662.2 T1347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:30718970 C>T maps to NM_006662.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:30718592 C>T maps to NM_006662.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:30747579 A>G maps to NM_006662.2 E2263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:30749557 C>T maps to NM_006662.2 Q2733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:30749490 G>A maps to NM_006662.2 S2710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:30735778 G>A maps to NM_006662.2 T1678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:30718619 C>T maps to NM_006662.2 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:30721281 C>T maps to NM_006662.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:30747905 A>G maps to NM_006662.2 S2323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:30749578 C>T maps to NM_006662.2 Q2740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:30749602 C>T maps to NM_006662.2 R2748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:30749221 G>T maps to NM_006662.2 E2621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:36707615 G>A maps to NM_025248.2 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:36708268 G>A maps to NM_025248.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:36719125 G>T maps to NM_025248.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:76028100 C>T maps to NM_080744.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:76028046 C>T maps to NM_080744.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:6656236 T>C maps to NM_001047.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr5:6656218 G>A maps to NM_001047.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:31805777 C>T maps to NM_000348.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr22:42263156 C>T maps to NM_004599.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr22:42269983 C>A maps to NM_004599.2 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr22:42271661 C>A maps to NM_004599.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:42263057 G>A maps to NM_004599.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:42264699 C>T maps to NM_004599.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:42271430 C>T maps to NM_004599.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:64509593 C>T maps to NM_020762.2 C715C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:64238652 T>C maps to NM_020762.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr12:64474112 A>G maps to NM_020762.2 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:64410785 T>A maps to NM_020762.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:64456833 C>T maps to NM_020762.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:64456869 G>A maps to NM_020762.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr12:64519842 C>T maps to NM_020762.2 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:64377782 C>T maps to NM_020762.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:64491087 C>G maps to NM_020762.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr12:64456755 G>A maps to NM_020762.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr12:64536343 G>A maps to NM_020762.2 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:64491124 G>T maps to NM_020762.2 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:64480776 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:64505574 C>T maps to NM_020762.2 D651D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:206557430 G>A maps to ENST00000414359 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:206566939 C>T maps to ENST00000414359 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:9106265 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:9032273 C>T maps to NM_014850.2 S936S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:9034621 G>A maps to NM_014850.2 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:4292026 G>A maps to NM_001098814.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:4245758 C>T maps to ENST00000330063 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr1:11118892 G>A maps to NM_003132.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:11115063 G>A maps to NM_003132.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:11118931 G>A maps to NM_003132.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr20:62173615 G>A maps to NM_080823.2 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:62172311 C>A maps to NM_080823.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:112203165 G>T maps to NM_003135.1 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:35468784 G>T maps to NM_003136.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:35468844 G>T maps to NM_003136.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr17:74068539 G>A maps to NM_014230.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:74046559 G>A maps to NM_014230.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:74037044 C>T maps to NM_014230.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:57368026 A>G maps to NM_006947.3 *672W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:57349351 G>A maps to NM_006947.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr4:57356748 T>C maps to NM_006947.3 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr6:35825085 G>T maps to ENST00000361690 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:35803245 C>T maps to ENST00000361690 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:35854588 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:104783647 C>A maps to ENST00000336613 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:104783683 C>A maps to ENST00000336613 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:104909272 C>T maps to NM_182691.1 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:153050904 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153049626 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153050590 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153046984 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153047600 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:153046622 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr23:153046584 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr23:153046984 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr11:126135713 C>T maps to NM_003139.3 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:126135870 A>G maps to NM_003139.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:126134094 A>G maps to NM_003139.3 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:133534431 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:133534543 C>A maps to NM_021203.3 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:38033506 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:38031170 G>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:38037562 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:38013776 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:38031188 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:38019360 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:38009056 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:38037571 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:38009076 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:38019352 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:38016185 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:38020191 C>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:38019346 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr23:38016243 G>C did not map to a codon.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr23:38009093 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:99919935 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:99905859 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:99917313 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:99920590 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:99920259 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:99922393 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:99917298 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:99917313 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:99919924 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:99921795 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:99905836 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:99922276 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:99921755 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr23:99917285 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:2222204 C>T maps to NM_021947.1 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr16:2816108 G>A maps to NM_016333.3 P1860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:2815890 C>T maps to NM_016333.3 R1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:2819123 C>A maps to NM_016333.3 S2620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:2814312 G>T maps to NM_016333.3 E1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:2812430 G>A maps to NM_016333.3 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:2812625 A>G maps to NM_016333.3 R699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:2811843 G>T maps to NM_016333.3 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:2812947 A>T maps to NM_016333.3 K807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr16:2818849 T>C maps to ENST00000382300 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr16:2808539 T>C maps to NM_016333.3 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:2814653 G>A maps to NM_016333.3 S1375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:119554805 C>T maps to NM_194286.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:119554805 C>T maps to NM_194286.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:119554805 C>T maps to NM_194286.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:119591400 C>T maps to NM_194286.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:100484720 C>T maps to NM_015908.5 Y625Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:100482659 C>T maps to NM_015908.5 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:100485932 G>A maps to NM_015908.5 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:100479844 G>A maps to NM_015908.5 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:100479342 G>A maps to NM_015908.5 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:60749618 C>A maps to NM_198935.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:60735016 C>T maps to NM_198935.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:60749651 G>A maps to NM_198935.1 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr20:60736529 G>A maps to NM_198935.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr20:60738544 G>A maps to NM_198935.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:170667780 G>A maps to NM_003142.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:170663403 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:170663555 G>T maps to NM_003142.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:141445295 G>A maps to NM_003143.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:141443406 C>T maps to NM_003143.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr5:80736413 T>C maps to ENST00000380182 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:80770323 G>A maps to ENST00000380182 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:54722843 G>A maps to NM_145716.2 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:54870274 C>T maps to NM_145716.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:54707866 T>C maps to NM_145716.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:18542221 C>T maps to NM_032627.3 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:182780191 C>T maps to NM_001130445.1 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:182774684 G>A maps to NM_001130445.1 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:182781106 C>T maps to NM_001130445.1 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr2:182780934 G>A maps to NM_001130445.1 R856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr2:182767194 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:182774684 G>A maps to NM_001130445.1 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:109181868 C>T maps to NM_018984.3 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:109192888 G>A maps to NM_018984.3 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:109210914 G>A maps to NM_018984.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:109210926 G>A maps to NM_018984.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr12:109186538 G>A maps to NM_018984.3 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:109198846 G>A maps to NM_018984.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:109200123 G>A maps to NM_018984.3 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:109198846 G>A maps to NM_018984.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:109192888 G>A maps to NM_018984.3 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:109246429 G>A maps to NM_018984.3 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:109194557 C>T maps to NM_018984.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:27963753 G>T maps to NM_033389.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:28011620 C>A maps to NM_033389.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:27993932 G>T maps to NM_033389.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:27963456 G>A maps to NM_033389.2 C570C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:27959365 G>T maps to NM_033389.2 S922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:27958421 C>A maps to NM_033389.2 E1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:27959879 C>A maps to NM_033389.2 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:27959879 C>A maps to NM_033389.2 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:67074412 C>T maps to NM_017857.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:67076906 C>T maps to NM_017857.3 N367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:26383984 C>T maps to NM_005086.4 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr7:149477453 C>T maps to NM_198455.2 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:149515810 G>A maps to NM_198455.2 W3908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:149477953 C>T maps to NM_198455.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:149485526 C>T maps to NM_198455.2 G1312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:149492669 C>T maps to NM_198455.2 S2151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:149523272 C>T maps to NM_198455.2 R4792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:149477453 C>T maps to NM_198455.2 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:149485989 C>T maps to NM_198455.2 G1404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:149505656 C>G maps to NM_198455.2 G3014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:149475924 C>T maps to NM_198455.2 V297V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A0JY-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr7:149519671 C>T maps to NM_198455.2 R4392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:149515560 G>A maps to NM_198455.2 T3876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:149477935 C>T maps to NM_198455.2 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:149506510 G>A maps to NM_198455.2 Q3098Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:149516591 C>T maps to NM_198455.2 R4003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:149490532 G>A maps to NM_198455.2 P2004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:155988152 T>C maps to ENST00000368312 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:156261031 G>T maps to ENST00000467789 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:153061979 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153061902 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153061904 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153061890 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153063085 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr23:153062921 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153063204 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:57094913 G>A maps to NM_003146.2 G619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:57095242 C>A maps to NM_003146.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:57099260 G>A maps to NM_003146.2 H368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:57100434 C>A maps to NM_003146.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65338156 C>A maps to NM_006396.1 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:187386905 C>A maps to NM_001048.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:38679679 C>A maps to NM_001049.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:38679199 C>T maps to NM_001049.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:38679007 G>A maps to NM_001049.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr14:38678629 C>A maps to NM_001049.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:37603479 C>T maps to NM_001051.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:23016359 G>A maps to NM_001052.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr20:23016482 G>A maps to NM_001052.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr20:23016947 C>T maps to NM_001052.2 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:23016479 C>T maps to NM_001052.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr20:23016632 G>A maps to NM_001052.2 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17T-01A-11D-A12J-09 chr20:23016947 C>T maps to NM_001052.2 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:1129692 G>A maps to NM_001053.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:1129539 C>T maps to NM_001053.3 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:1477514 G>A maps to NM_014188.2 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr23:48123283 A>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48125760 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48117268 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48118065 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48118017 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48123352 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr1:85113136 T>C maps to NM_001166417.1 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:85128047 C>A maps to NM_001166417.1 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr1:85113145 A>G maps to NM_001166417.1 N605N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:85116178 C>T maps to NM_001166417.1 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:85121642 G>A maps to NM_001166417.1 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48214134 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48209518 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48206932 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48207017 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:48206939 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:48207020 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48209545 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48211594 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:48214092 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:48213483 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:48213515 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:48213476 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:48244866 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48244007 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48244832 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48244866 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48244828 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48244870 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:48244871 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48244007 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48270228 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48270301 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr23:48269477 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48269438 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48270214 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48270258 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48270301 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48053629 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48054565 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48047096 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48049670 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:48049699 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:48049627 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48054518 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr23:48054724 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48054750 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48054270 T>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:48051743 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:52682007 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:52674554 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:52674522 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:52679435 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:52674497 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:52681986 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:52682010 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:41226869 G>A maps to NM_003932.3 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:130066581 C>T maps to NM_021978.3 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:130068905 C>T maps to NM_021978.3 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:130068266 C>T maps to NM_021978.3 C508C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr11:130059642 C>T maps to NM_021978.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:130058477 G>T maps to NM_021978.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr11:130060577 C>T maps to NM_021978.3 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:53045803 G>A maps to NM_014682.2 H786H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:53071633 G>A maps to NM_014682.2 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr8:134474159 G>A maps to NM_173344.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:134477151 C>T maps to NM_173344.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:134474201 G>A maps to NM_173344.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr8:134478219 C>A maps to NM_173344.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:134474201 G>T maps to NM_173344.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:44290451 G>T maps to NM_174963.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:44395805 C>A maps to NM_174963.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:44365341 C>T maps to NM_174963.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:44365284 C>T maps to NM_174963.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:44201995 A>G maps to NM_174963.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:44257775 C>A maps to NM_174963.2 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:44360120 C>T maps to NM_174963.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:44303914 C>T maps to NM_174963.2 Y147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:126278288 C>T maps to ENST00000356132 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:86067398 G>A maps to NM_003896.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:86067398 G>A maps to NM_003896.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:98503842 G>A maps to ENST00000493584 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:8728768 G>A maps to NM_005418.3 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:8717081 G>A maps to NM_005418.3 R1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:8719084 G>A maps to NM_005418.3 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:8751750 G>A maps to NM_005418.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:8752476 G>A maps to NM_005418.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:8747643 C>A maps to NM_005418.3 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr11:8734138 G>A maps to NM_005418.3 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:186760556 C>T maps to NM_003032.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:107459644 C>T maps to NM_001142351.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:107460132 G>A maps to NM_001142351.1 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:107449026 A>G maps to NM_001142351.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:107460244 G>A maps to NM_001142351.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:107460349 G>T maps to NM_001142351.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:74621456 C>T maps to NM_018414.3 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:74621489 G>T maps to NM_018414.3 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:74625114 G>A maps to NM_018414.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:77093211 C>T maps to NM_152996.2 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:130676979 C>T maps to NM_175039.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:77528734 C>A maps to NM_030965.1 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:77528701 T>A maps to NM_030965.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr1:77510061 G>A maps to NM_030965.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr9:130658568 G>A maps to NM_013443.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:130658537 C>A maps to NM_013443.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr9:130653118 C>T maps to NM_013443.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr9:130653015 G>A maps to NM_013443.3 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr9:130653187 T>C maps to NM_013443.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr7:116776207 C>T maps to ENST00000323984 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:116810957 G>T maps to ENST00000323984 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:113124718 C>A maps to NM_017744.4 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:22486965 C>T maps to NM_003034.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:93007437 C>A maps to NM_006011.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:92981711 C>T maps to NM_006011.3 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr15:92988004 C>T maps to NM_006011.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr15:93007611 G>A maps to NM_006011.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:55024395 T>C maps to NM_015879.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:55024557 C>T maps to NM_015879.2 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:55024660 C>T maps to NM_015879.2 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:100147585 G>A maps to NM_005668.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:100238589 C>A maps to NM_005668.4 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:100147552 A>G maps to NM_005668.4 *360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr5:100231462 G>C maps to NM_005668.4 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:44284627 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:44260331 G>A maps to NM_013305.4 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:44260331 G>A maps to NM_013305.4 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:44261938 C>A maps to NM_013305.4 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:44260322 C>T maps to NM_013305.4 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:44260331 G>A maps to NM_013305.4 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:44272210 G>A maps to NM_013305.4 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:17363044 G>A maps to NM_001004470.1 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:17369026 G>A maps to NM_001004470.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:17362927 A>G maps to NM_001004470.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:17363212 G>A maps to NM_001004470.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52551928 C>T maps to NM_015136.2 C1557C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52555007 C>T maps to NM_015136.2 G1965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr3:52551979 C>T maps to NM_015136.2 T1574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:52554677 G>A maps to NM_015136.2 G1890G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:52548229 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:52554926 G>A maps to NM_015136.2 R1938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:52537021 C>T maps to NM_015136.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:52550556 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:104030994 C>T maps to NM_017564.9 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:104033908 C>T maps to NM_017564.9 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:104131548 C>T maps to NM_017564.9 F1896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:104049328 C>T maps to NM_017564.9 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:104049238 C>A maps to NM_017564.9 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:104134517 C>T maps to NM_017564.9 F1955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:104111612 C>T maps to NM_017564.9 C1559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:104056695 C>T maps to NM_017564.9 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:104123925 C>A maps to NM_017564.9 I1705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:104142891 C>T maps to NM_017564.9 N2132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:104142891 C>T maps to NM_017564.9 N2132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:104025439 C>A maps to NM_017564.9 Y184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:104134517 C>T maps to NM_017564.9 F1955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:104118760 C>T maps to NM_017564.9 G1564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:36527722 C>T maps to NM_003149.1 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:36526506 C>A maps to NM_003149.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:37368631 G>A maps to NM_198993.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:37373144 G>T maps to NM_198993.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:37373087 G>T maps to NM_198993.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:37371255 G>A maps to NM_198993.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:57642899 G>A maps to NM_145064.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:57637900 C>T maps to NM_145064.1 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:57642488 G>A maps to NM_145064.1 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:57637999 G>A maps to NM_145064.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:136076580 G>A maps to NM_005862.2 R1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:136087947 A>G did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:136141654 T>C maps to NM_005862.2 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:136088109 G>T maps to NM_005862.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:136076580 G>A maps to NM_005862.2 R1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:123176468 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:123215310 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr23:123197001 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:123229295 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:123227988 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:123184040 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:123197704 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:123176489 G>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:123202492 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:123215293 G>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:123179150 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:123179132 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:123224530 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123159734 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123164903 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123176488 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123181244 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123189993 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:123229235 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:123185061 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:123217337 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr23:123195680 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:123227871 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:123215301 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123224465 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:123196777 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:123191726 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:123210306 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:123184040 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:123205072 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:123181310 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:123189993 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:123210229 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:123176488 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:123200072 C>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:123171401 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr7:99802987 C>A maps to NM_012447.2 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr7:99797902 G>T maps to NM_012447.2 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11M-01A-11D-A122-09 chr7:99802380 C>T maps to NM_012447.2 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:99798390 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:17737214 G>T maps to NM_003473.2 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:17746458 G>A maps to NM_003473.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:152977231 T>C maps to NM_005843.4 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:152980449 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:74071967 C>T maps to NM_213622.1 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr2:74074752 A>G maps to NM_213622.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:68472018 G>T maps to NM_012108.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:68441173 G>A maps to NM_012108.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:68472018 G>T maps to NM_012108.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:68441173 G>A maps to NM_012108.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:68424541 G>A maps to NM_012108.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:68472074 A>C maps to NM_012108.2 *296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:4325249 A>G maps to ENST00000314714 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:4325441 G>A maps to ENST00000314714 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr19:4327199 G>A maps to ENST00000314714 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:4327184 G>A maps to ENST00000314714 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:4328706 G>A maps to ENST00000314714 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:38003854 C>T maps to NM_000349.2 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:38003604 C>A maps to NM_000349.2 G176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:38005845 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:72466766 A>C maps to NM_006645.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr11:72466073 C>T maps to NM_006645.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr11:72492048 C>A maps to NM_006645.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr11:72470294 G>A maps to NM_006645.2 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr11:72466010 G>T maps to NM_006645.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr11:72469677 C>T maps to NM_006645.2 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:33680956 G>A maps to NM_178007.2 Y1046Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:33680938 G>A maps to NM_178007.2 G1052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:33701544 C>T maps to NM_178007.2 E621E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr13:33700334 G>A maps to NM_178007.2 Y647Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:33703313 G>A maps to NM_178007.2 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr13:33704320 G>A maps to NM_178007.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:33741736 A>G maps to NM_178007.2 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:33703172 T>C maps to NM_178007.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:37817121 G>A maps to NM_006804.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:110843043 G>A maps to NM_139164.1 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:110836753 C>A maps to NM_139164.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:110837722 C>T maps to NM_139164.1 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:110835762 G>A maps to NM_139164.1 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:81605710 G>A maps to NM_181900.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:81610811 C>T maps to NM_181900.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:81605605 G>A maps to NM_181900.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:81610811 C>T maps to NM_181900.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:96852976 A>G maps to NM_020151.3 C302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:96859009 G>A maps to NM_020151.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr23:67937781 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:67867768 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:67939241 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:67940186 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:67938343 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:67932828 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:67942414 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:67937818 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr23:67941536 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:67941537 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:67944176 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:67943668 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:191841712 C>A maps to NM_007315.3 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:191854351 G>T maps to NM_007315.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:191859863 G>A maps to NM_007315.3 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:191847240 G>A maps to NM_007315.3 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:191851597 C>T maps to NM_007315.3 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr17:40485755 G>A maps to NM_139276.2 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:40469240 G>A maps to NM_139276.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr17:40489798 C>T maps to NM_139276.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:40476864 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:40475321 G>T maps to NM_139276.2 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:40498634 C>T maps to NM_139276.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:40498609 G>A maps to NM_139276.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:191922752 A>G maps to NM_003151.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:191905835 C>T maps to NM_003151.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:191922751 G>A maps to NM_003151.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:192011430 A>G maps to NM_003151.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:40453291 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:40457693 C>T maps to NM_003152.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:40370266 G>A maps to NM_012448.3 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:57490407 G>A maps to NM_003153.4 Q831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:70866590 C>T maps to NM_003154.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:70865522 C>T maps to NM_003154.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:47739726 G>A maps to NM_017453.2 R290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:74526112 C>A maps to NM_001164380.1 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr5:172750286 C>T maps to NM_003714.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:172752951 G>A maps to NM_003714.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:172750223 G>A maps to NM_003714.2 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:89789176 C>T maps to ENST00000433102 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:89793933 G>C maps to ENST00000433102 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:89866208 T>C maps to NM_001040666.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:89854537 C>T maps to NM_152999.3 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:120005430 C>T maps to NM_182915.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:120020643 C>T maps to NM_182915.2 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:120005310 C>T maps to NM_182915.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:120005391 G>A maps to NM_182915.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr2:120003398 G>A maps to NM_182915.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:87912377 C>A maps to NM_024636.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:87911987 G>A maps to NM_024636.2 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:87913515 A>G maps to NM_024636.2 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:87910240 G>A maps to NM_024636.2 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr17:44076872 T>C maps to NM_001007532.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:47746207 G>T maps to NM_001048166.1 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:47735311 T>C maps to NM_001048166.1 V870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:47767904 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:47746065 C>T maps to NM_001048166.1 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:47759167 G>A maps to NM_001048166.1 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:47716837 T>C maps to NM_001048166.1 K1279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:3877592 G>A maps to NM_003156.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:4104507 G>A maps to NM_003156.3 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:4112724 G>A maps to NM_003156.3 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:27004725 G>A maps to ENST00000382009 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:27019549 G>A maps to ENST00000382009 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:27000969 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:27010572 G>T maps to ENST00000382009 G575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr11:63962066 C>T maps to ENST00000358794 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:63961949 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:63964813 C>T maps to ENST00000358794 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr11:63964828 G>A maps to ENST00000358794 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:171479986 C>T maps to NM_005990.3 E904E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr5:171491816 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:171481611 C>T maps to NM_005990.3 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:171509485 C>T maps to NM_005990.3 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:220471827 G>A maps to NM_052902.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr2:220472844 G>A maps to NM_052902.2 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:220470332 T>C maps to NM_052902.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:220473919 C>A maps to NM_052902.2 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr2:220479852 G>A maps to NM_052902.2 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:220111953 G>A maps to ENST00000409260 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:220113470 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:220115037 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:220111501 C>T maps to ENST00000409260 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:43647872 C>A maps to NM_004760.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr7:43635502 G>A maps to NM_004760.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr7:43664330 G>T maps to NM_004760.2 G379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:43663331 C>A maps to NM_004760.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:197002221 G>A maps to NM_004226.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:197002221 G>A maps to NM_004226.3 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:31938987 G>T did not map to a codon.
Alternatively spliced codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:99115964 C>T maps to NM_003576.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:99127563 C>A maps to NM_003576.3 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:99134568 T>A maps to NM_003576.3 K106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:99718795 C>A maps to ENST00000354930 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:23768847 G>T maps to NM_031414.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:23775302 G>A maps to NM_031414.3 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:23793933 G>A maps to NM_031414.3 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:23768847 G>T maps to NM_031414.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:23830456 G>A maps to NM_031414.3 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:23826128 C>T maps to NM_031414.3 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:146658881 G>T maps to NM_001112724.1 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:5448454 C>A maps to NM_018401.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:5448488 C>T maps to NM_018401.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:5053598 G>A maps to NM_018401.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:134038820 A>T maps to NM_173575.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:8494809 G>C maps to NM_030906.2 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:8457621 C>A maps to NM_030906.2 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:219563959 C>T maps to NM_015690.3 C1231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:219559355 G>T maps to NM_015690.3 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:219559336 T>C maps to NM_015690.3 H830H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:36465576 G>A maps to NM_007271.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:36483171 G>A maps to NM_007271.2 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:168986254 C>A maps to NM_013233.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:168997200 G>A maps to NM_013233.2 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr2:168931651 G>A maps to NM_013233.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:43607200 G>A maps to NM_006282.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr20:43615853 C>T maps to NM_006282.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:43610566 C>T maps to NM_006282.2 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:36820008 G>A maps to ENST00000373130 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:36807400 G>T maps to ENST00000373130 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:36821016 G>A maps to ENST00000373130 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:36821016 G>A maps to ENST00000373130 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:26230229 C>A maps to NM_203399.1 E30*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BS-A0UF-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:80553701 C>T maps to NM_007029.3 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:62275609 G>A maps to NM_015894.2 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:27099986 C>T maps to NM_030795.2 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr15:74277003 A>G maps to NM_004809.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:74277024 G>A maps to NM_004809.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:35101168 G>A maps to NM_013442.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:35100957 G>A maps to NM_013442.1 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:39541048 C>T maps to NM_145286.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr13:39541003 G>A maps to NM_145286.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:39541003 G>A maps to NM_145286.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:39542667 A>G maps to NM_145286.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:48822375 G>T maps to NM_001198595.1 E715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:48807792 C>G maps to NM_172311.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:48809499 G>A maps to NM_172311.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:48897063 G>A maps to NM_172311.2 E1098E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:48807846 G>A maps to NM_172311.2 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:48808551 T>C maps to NM_172311.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:48869590 G>T maps to NM_172311.2 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:48896992 G>T maps to NM_172311.2 E1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:48848322 T>C maps to NM_172311.2 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:48808113 C>T maps to NM_172311.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:48872173 C>A maps to NM_172311.2 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:81744049 G>A maps to NM_033104.2 Y535Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr14:81864720 C>T maps to NM_033104.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:70652419 C>T maps to NM_001130161.2 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:70645762 A>C maps to NM_001130161.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr4:184932194 T>A maps to NM_020225.1 L735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:184930788 C>T maps to NM_020225.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:184932240 G>T maps to NM_020225.1 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:184932060 C>T maps to NM_020225.1 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:184930779 A>C maps to NM_020225.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:184930788 C>T maps to NM_020225.1 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr4:184932384 C>T maps to NM_020225.1 D798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:184931233 G>T maps to NM_020225.1 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:184932015 C>T maps to NM_020225.1 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr4:184931823 C>G maps to NM_020225.1 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LV-01A-11W-A062-09 chr15:74474712 G>A maps to ENST00000449139 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:74487705 C>T maps to ENST00000449139 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr15:74483227 G>A maps to ENST00000449139 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr15:74487741 C>T maps to ENST00000449139 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr15:74481531 G>A maps to ENST00000449139 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:61781012 G>T maps to NM_001003787.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:61781921 G>A maps to NM_001003787.2 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:202323505 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:202323583 C>A maps to NM_018571.5 Y30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:16055878 C>T maps to ENST00000025399 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:16052952 A>T maps to ENST00000025399 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:16050926 T>C maps to ENST00000025399 Y263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:16048317 G>T maps to ENST00000025399 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:16047035 T>C maps to ENST00000025399 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:125922742 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:125932244 C>T maps to NM_018387.4 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:125932298 C>T maps to NM_018387.4 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:125920293 C>A maps to NM_018387.4 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:43906623 C>T maps to NM_153700.2 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:43910165 C>A maps to NM_153700.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:43991977 C>T maps to ENST00000381686 Q1742Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr15:43893086 G>A maps to NM_153700.2 I1609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:43992302 C>A maps to ENST00000381686 G1663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:43893653 G>A maps to NM_153700.2 I1547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:43902547 G>A maps to NM_153700.2 R1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:43902547 G>A maps to NM_153700.2 R1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:44002885 G>A maps to ENST00000381686 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:43900288 G>A maps to NM_153700.2 R1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:43997075 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr15:43999751 C>T maps to ENST00000381686 L1228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:37082372 C>A maps to NM_003162.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr2:37076643 A>C maps to NM_003162.2 Y766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr2:37193438 C>T maps to NM_003162.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:31405830 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:31404446 C>A maps to NM_001083893.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:47230774 G>A maps to NM_001039877.1 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:7175394 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr23:7268183 C>G did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:7268150 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:7267971 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:7177681 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:7268055 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:7177479 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:7268041 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:7252142 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:7177468 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:7267974 C>T did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:125478177 C>T maps to NM_152713.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:125478125 C>T maps to NM_152713.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:125474138 G>T maps to NM_152713.3 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:31663635 C>T maps to NM_178862.1 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:31656645 T>G maps to NM_178862.1 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:31667620 T>C did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:732232 G>A maps to NM_005861.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:13255588 G>A maps to NM_003765.1 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:28120101 G>T maps to ENST00000373939 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:57246220 G>A maps to NM_001001433.1 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:57251331 C>T maps to NM_001001433.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr9:102713457 A>G maps to NM_017919.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:4436529 G>A maps to NM_016930.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:4426918 C>A maps to NM_016930.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:4436547 C>T maps to NM_016930.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:73118577 C>T maps to NM_004603.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:31008347 T>C maps to NM_052874.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:131283132 G>A maps to NM_194356.1 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr12:131286010 G>A maps to NM_194356.1 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:31046354 A>G maps to NM_004604.3 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:180959175 G>A maps to NM_005819.4 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr6:132793422 G>A maps to NM_003569.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:9408430 C>T maps to NM_004853.2 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:9460797 G>A maps to NM_004853.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:130416073 G>A maps to NM_003165.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr9:130425488 T>A maps to NM_003165.3 Y145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:130439013 C>T maps to NM_003165.3 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:7712248 C>T maps to ENST00000441779 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:7709502 C>T maps to ENST00000441779 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr19:7712320 C>T maps to ENST00000441779 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:7712248 C>T maps to ENST00000441779 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:7707168 G>A maps to ENST00000441779 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:7703903 G>A did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr19:7707117 G>C maps to ENST00000441779 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:109340783 G>A maps to NM_007269.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr1:109340813 T>C maps to NM_007269.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr1:109294877 G>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:109337465 C>T maps to NM_007269.2 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:109325118 A>G maps to NM_007269.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:109337486 T>C maps to NM_007269.2 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:53155489 C>T maps to NM_178509.5 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:147684753 G>A maps to NM_001127715.1 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:147588218 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:147581798 C>T maps to NM_001127715.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr6:147646169 A>G maps to NM_001127715.1 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr6:147525814 C>T maps to NM_001127715.1 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:121126129 C>A maps to NM_014980.2 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:121137341 C>T maps to NM_014980.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:121100155 C>A maps to NM_014980.2 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:121097678 C>T maps to NM_014980.2 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:120957826 C>A maps to NM_014980.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:121097678 C>T maps to NM_014980.2 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:121100197 A>G maps to NM_014980.2 K826K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:121137908 C>T maps to NM_014980.2 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:120760594 A>G maps to NM_014980.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:10782234 G>A maps to NM_018423.2 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:10783731 G>A maps to NM_018423.2 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:53235563 G>T maps to NM_145251.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:75643071 G>A maps to NM_016086.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:48542765 C>A maps to NM_003850.2 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:84658703 G>A maps to NM_003849.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:84658735 C>A maps to NM_003849.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:67451239 G>A maps to NM_003848.3 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:67568691 G>A maps to NM_003848.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:151598688 C>T maps to NM_033050.4 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:151599143 C>T maps to NM_033050.4 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:104359301 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:104389893 C>T maps to NM_016169.3 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:104359283 C>T maps to NM_016169.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:53241026 G>A maps to NM_001130912.1 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:70488406 T>G maps to NM_001128206.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:70501204 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:70540441 G>A maps to NM_001128206.1 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr8:70533367 C>A maps to NM_001128206.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:70517112 C>T maps to NM_001128206.1 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:46331379 G>A maps to NM_001161841.1 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr20:46331357 T>A maps to NM_001161841.1 K158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:46294678 G>A maps to NM_001161841.1 N608N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:46301014 G>A maps to NM_001161841.1 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr20:46288474 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:28620134 G>A maps to NM_177529.1 Y14Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:70599907 C>T maps to NM_014465.3 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr4:70620786 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:108869810 C>T maps to NM_001008743.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:108863670 C>T maps to NM_001008743.1 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:109002778 G>A maps to NM_006588.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:109002691 G>A maps to NM_006588.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:70721028 G>A maps to NM_005420.2 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:70707714 G>T maps to NM_005420.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:48389454 G>A maps to NM_003167.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:48382321 G>A maps to NM_003167.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:48382310 A>G maps to NM_003167.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:49094987 C>T maps to NM_177973.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:49096069 G>A maps to NM_177973.1 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:44234873 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:44225066 C>T maps to NM_014351.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:44234776 C>A maps to NM_014351.3 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:44234776 C>A maps to NM_014351.3 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:37398607 G>A maps to NM_001032377.1 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:37410582 G>A maps to NM_001032377.1 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:4459713 A>G maps to NM_182760.3 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr3:4494607 A>G maps to NM_182760.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr7:56136277 G>T maps to ENST00000395437 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:203075459 C>A maps to ENST00000409368 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:46229000 G>A maps to ENST00000411651 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:889235 G>A maps to ENST00000456758 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:891105 C>T maps to ENST00000456758 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:892546 C>T maps to ENST00000456758 D526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:878593 C>T maps to ENST00000456758 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:908996 C>T maps to ENST00000456758 Y853Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr7:899940 C>T maps to ENST00000456758 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr7:909143 C>T maps to ENST00000456758 F902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:883205 T>A maps to NM_001171945.1 L257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:883200 A>T maps to NM_001171945.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:909008 C>T maps to ENST00000456758 C857C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:39132274 G>A maps to ENST00000405018 H738H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr22:39132346 C>A maps to ENST00000405018 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:39134985 G>A maps to ENST00000405018 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:39137525 G>A maps to ENST00000405018 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:39148626 G>A maps to ENST00000405018 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:39137513 G>A maps to ENST00000405018 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:48026964 G>A maps to NM_152782.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:48056935 C>A maps to NM_152782.3 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:48046872 G>A maps to NM_152782.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:48033953 C>T maps to NM_152782.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:31592110 G>A maps to NM_080675.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:31590714 G>A maps to NM_080675.3 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:31573550 G>A maps to NM_080675.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr20:31592101 G>A maps to NM_080675.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:56397577 C>T maps to NM_001032387.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:56398735 C>T maps to NM_001032387.1 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:21840161 G>T maps to NM_007192.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:21820957 G>A maps to NM_007192.3 Y1006Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:21837507 G>A maps to NM_007192.3 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:44921049 A>G maps to NM_181356.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:39965174 C>T maps to NM_003169.3 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:39955586 G>A maps to NM_003169.3 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:39960838 C>T maps to NM_003169.3 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:39964629 C>T maps to NM_003169.3 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:39955601 G>T maps to NM_003169.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr19:39965168 G>A maps to NM_003169.3 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr19:39964916 C>T maps to NM_003169.3 Q899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:39944153 C>T maps to NM_003169.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:27016528 C>T maps to NM_003170.3 R1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:27001322 C>T maps to NM_003170.3 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:27011945 A>G maps to NM_003170.3 R818R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:27011677 C>T maps to NM_003170.3 D768D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:27027979 C>T maps to NM_003170.3 Q1610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27878391 C>T maps to NM_014860.1 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr2:27880454 G>T maps to NM_014860.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:70967667 C>T maps to NM_003171.3 H632H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:70949112 C>A maps to NM_003171.3 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr10:70947404 G>A maps to NM_003171.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr10:70946298 C>T maps to NM_003171.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:136220671 G>A maps to NM_003172.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:136200594 G>A maps to NM_006753.4 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:114905775 C>T maps to NM_022486.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:114820860 G>A maps to NM_022486.3 Y652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:24583359 C>T maps to NM_019601.3 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:24579112 C>A maps to NM_019601.3 C55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:24579516 C>T maps to NM_019601.3 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:24582228 G>A maps to NM_019601.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:24579073 T>C maps to NM_019601.3 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr22:24581637 C>T maps to NM_019601.3 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:95840224 C>A maps to NM_145006.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:95841836 A>G maps to NM_145006.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:223402692 G>A maps to NM_017982.3 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:223402554 G>T maps to NM_017982.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:223396738 G>A maps to NM_017982.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:223402608 G>A maps to NM_017982.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:223438059 G>A maps to NM_017982.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:223396738 G>A maps to NM_017982.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:223402692 G>A maps to NM_017982.3 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:223438008 G>T maps to NM_017982.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:33255582 G>A maps to NM_015551.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:33194725 C>T maps to NM_015551.1 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:33195511 T>A maps to NM_015551.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:33194395 G>A maps to NM_015551.1 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48557293 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48557431 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48558486 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48558588 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48565967 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48565904 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr23:48557341 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48564690 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:48559021 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:48564708 C>T did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:48558763 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:14939269 T>C maps to NM_001193424.1 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:14943175 C>T maps to NM_001193424.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:67925465 G>A maps to NM_017635.3 R783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr11:67939115 C>T maps to NM_017635.3 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr11:67925553 G>A maps to NM_017635.3 N753N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:67926402 G>A maps to NM_017635.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:55853312 C>T maps to NM_032701.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:55853333 A>G maps to NM_032701.3 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:55857621 C>T maps to NM_032701.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:30293213 T>C maps to NM_015355.2 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:30315352 C>T maps to NM_015355.2 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:30315376 G>A maps to NM_015355.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:30293189 G>A maps to NM_015355.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr17:30300204 T>C maps to NM_015355.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:30293189 G>A maps to NM_015355.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:149878199 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:149881105 C>T maps to NM_014849.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:149884935 C>A maps to NM_014849.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:149879697 G>A maps to NM_014849.3 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:149884792 G>A maps to NM_014849.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:149885385 C>A maps to NM_014849.3 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr15:91769693 G>A maps to NM_014848.4 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:91810873 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:91824955 A>G did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr15:91795122 C>T maps to NM_014848.4 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:91811725 G>T maps to NM_014848.4 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr15:91795209 C>T maps to NM_014848.4 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:75428096 C>T maps to NM_014979.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:75505674 C>T maps to NM_014979.1 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:75427751 C>T maps to NM_014979.1 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:75505593 C>A maps to NM_014979.1 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:75581080 C>T maps to NM_014979.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr9:113242016 G>A maps to ENST00000374463 H795H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:113168735 G>A maps to ENST00000374463 A3051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:113212499 G>A maps to ENST00000374463 N1314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:113163181 G>T maps to ENST00000374463 T3261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:113312261 G>A maps to ENST00000374463 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:113217960 G>A maps to ENST00000374463 I1232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr9:113208196 G>A maps to ENST00000374463 D1461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:113168735 G>A maps to ENST00000374463 A3051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:113168972 G>A maps to ENST00000374463 G2972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:113219608 G>A maps to ENST00000374463 N1200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:113243564 G>A maps to ENST00000374463 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:113198674 G>A maps to ENST00000374463 V1586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:113208196 G>A maps to ENST00000374463 D1461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:113170607 A>C maps to ENST00000374463 P2427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:113205822 A>G maps to ENST00000374463 G1547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr9:113275326 G>A maps to ENST00000374463 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:113170289 G>A maps to ENST00000374463 L2533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:113166750 G>T maps to ENST00000374463 I3177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:113213625 C>A maps to ENST00000374463 G1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:113171165 G>A maps to ENST00000374463 V2241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:113192571 G>A maps to ENST00000374463 L1841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:113213581 C>A maps to ENST00000374463 V1296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:113276234 G>T maps to ENST00000374463 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:113141792 G>T maps to ENST00000374463 I3417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:113251993 G>A maps to ENST00000374463 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:113197635 T>C maps to ENST00000374463 S1594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:29782171 G>A maps to NM_021738.2 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:29782315 G>A maps to NM_021738.2 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:29812665 T>A maps to NM_021738.2 R959R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:29776109 G>A maps to NM_021738.2 N1489N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:29813567 C>A maps to NM_021738.2 E807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:29812748 G>A maps to NM_021738.2 Q932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:29812766 G>A maps to NM_021738.2 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:29839761 C>T maps to NM_021738.2 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr10:29769616 G>A maps to NM_021738.2 H1742H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:29788176 G>A maps to NM_021738.2 R1178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr10:29812497 C>T maps to NM_021738.2 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:22848788 A>G maps to NM_148893.1 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:109334568 C>A maps to NM_018711.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:109316478 G>T maps to NM_018711.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:109328022 G>A maps to NM_018711.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:138281257 T>A maps to NM_001139456.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr7:138305859 G>A maps to NM_001139456.1 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:138341225 C>T maps to NM_001139456.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:138341225 C>T maps to NM_001139456.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:9715817 G>A maps to NM_015055.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:9754163 G>A maps to NM_015055.2 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A052-01A-11W-A027-09 chr23:16754329 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:16761952 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:16778478 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:16773164 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:16759852 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:16775341 G>C did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:16759880 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:110587863 C>T maps to NM_001099744.1 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:110587578 C>T maps to NM_001099744.1 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:110587400 C>A maps to NM_001099744.1 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:110587800 G>A maps to NM_001099744.1 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:135371686 G>T maps to NM_001143764.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr10:135369360 G>A maps to NM_001143764.1 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:135372811 G>A maps to NM_001143764.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr19:39694672 G>A maps to NM_001080468.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:115453071 G>T maps to NM_003176.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:115430245 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:115420823 G>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:115527449 T>C maps to NM_003176.2 F888F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:115453041 G>T maps to NM_003176.2 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:115468946 G>T maps to NM_003176.2 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:115438112 G>T maps to NM_003176.2 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:115489880 C>T maps to NM_003176.2 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:115419395 G>T maps to NM_003176.2 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:115428860 C>A maps to NM_003176.2 S374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:115401166 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:115456634 G>T maps to NM_003176.2 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:58489268 A>T maps to NM_014258.2 C224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:58457057 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:58467461 T>C maps to NM_014258.2 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:58468614 C>A maps to NM_014258.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:58439412 C>A maps to NM_014258.2 E1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:58452477 C>A maps to NM_014258.2 E1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:58467091 C>A maps to NM_014258.2 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:58495518 G>A maps to NM_014258.2 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:58450337 C>A maps to NM_014258.2 E1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:58455427 C>T maps to NM_014258.2 P957P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:58455432 C>A maps to NM_014258.2 E956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:58482445 C>A maps to NM_014258.2 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:58467059 C>T maps to NM_014258.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:58467059 C>T maps to NM_014258.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr20:58450512 G>A maps to NM_014258.2 I1054I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:10913098 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:10924804 A>C maps to NM_001040274.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:10907890 G>T maps to NM_001040274.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr6:10961743 G>A maps to NM_001040274.2 G789G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:102127363 C>A maps to ENST00000449403 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:15222242 C>A maps to NM_033025.4 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr19:15223272 C>T maps to NM_033025.4 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr19:15224596 C>T maps to NM_033025.4 H677H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:15224524 C>T maps to NM_033025.4 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:15224485 A>G maps to NM_033025.4 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:85656163 T>G maps to NM_032184.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:85647933 C>T maps to NM_032184.1 Q797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:85648385 C>A maps to NM_032184.1 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:85666049 A>G maps to NM_032184.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:93624610 C>T maps to NM_003177.5 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:93636535 G>A maps to NM_003177.5 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:46357675 G>T maps to NM_004819.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:46352129 G>A maps to NM_004819.2 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:46326689 G>T maps to NM_004819.2 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:46326056 G>A maps to NM_004819.2 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47435576 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47466426 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47435759 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47435984 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47464775 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47466584 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47464396 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:47434604 G>A did not map to a codon.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr23:47435549 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47464450 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47479088 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:47435611 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr23:47435800 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47466426 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47434111 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:47435994 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:47464423 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:47432302 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:12203615 C>T maps to NM_133625.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:12211363 T>C maps to NM_133625.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:12182195 C>A maps to NM_133625.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:33260970 G>A maps to NM_003490.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:32929823 G>A maps to NM_003490.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:33376683 C>T maps to NM_003490.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr22:33376683 C>T maps to NM_003490.3 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:33161086 C>T maps to NM_030786.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:33160798 C>T maps to NM_030786.2 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:86350231 C>A maps to NM_006372.4 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:152510440 A>G maps to NM_182961.2 I7749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:152688315 C>A maps to ENST00000454018 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R6-01A-11D-A10B-09 chr6:152510495 A>T maps to NM_182961.2 L7731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:152640108 C>T maps to NM_182961.2 T5426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:152647642 G>A maps to NM_182961.2 S5027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:152806029 G>A maps to NM_182961.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:152832713 C>A maps to NM_033071.2 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:152589255 T>C maps to NM_182961.2 S6250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:152602995 C>T maps to NM_182961.2 A6109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:152671316 A>G maps to NM_182961.2 L3963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:152720814 G>A maps to NM_182961.2 A2391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:152749437 A>C maps to NM_182961.2 V1626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:152826486 G>A maps to NM_182961.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:152557411 G>A maps to NM_182961.2 Y6742Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:152673434 C>T maps to NM_182961.2 E3769E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr6:152546853 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:152443750 G>A maps to NM_182961.2 R8738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:152651529 G>A maps to NM_182961.2 R4764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:152671401 G>A maps to NM_182961.2 V3934V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:152737802 G>A maps to NM_182961.2 A1923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:152737871 G>A maps to NM_182961.2 N1900N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:152823872 A>G maps to NM_182961.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:152605162 G>A maps to NM_182961.2 R6053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:152716682 A>G maps to NM_182961.2 V2560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:152763362 G>T maps to NM_182961.2 I1285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:152680544 C>A maps to NM_182961.2 E3450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:152697631 G>A maps to NM_182961.2 R3070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:152737762 G>A maps to NM_182961.2 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:152673398 G>A maps to NM_182961.2 G3781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:152728223 G>A maps to NM_182961.2 C2216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:152757142 G>A maps to NM_182961.2 L1415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:152637962 G>T maps to ENST00000413186 I5579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr6:152708235 G>A maps to NM_182961.2 Q2820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:152646230 G>T maps to NM_182961.2 G5215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:152651998 G>A maps to NM_182961.2 N4607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:152652364 T>C maps to NM_182961.2 L4485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:152706913 G>A maps to NM_182961.2 V2849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:152826375 G>A maps to NM_182961.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:152826378 G>A maps to NM_182961.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr6:152466676 G>A maps to NM_033071.2 P8259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:152565760 C>A maps to NM_182961.2 E6535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:152577881 G>T maps to NM_182961.2 R6331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:152637962 G>T maps to ENST00000413186 I5579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:152683408 G>A maps to NM_182961.2 R3399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:152716700 T>C maps to NM_182961.2 K2554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:152730207 G>A maps to NM_182961.2 L2179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:152642908 C>A maps to NM_182961.2 E5344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:152501300 G>T maps to NM_182961.2 L7810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:152765626 A>G maps to NM_182961.2 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:152577786 G>A maps to NM_182961.2 F6362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:152642423 T>C maps to NM_182961.2 E5395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:152765700 G>A maps to NM_182961.2 L1228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:152642450 T>C maps to NM_182961.2 L5386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:64540713 G>T maps to NM_182914.2 E3576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:64560170 C>T maps to NM_182914.2 D4027D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:64565526 C>T maps to NM_182914.2 S4123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:64589027 T>C maps to NM_182914.2 N4435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:64619361 A>G maps to NM_182914.2 A5240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:64679608 C>T maps to NM_182914.2 S6314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:64679608 C>T maps to NM_182914.2 S6314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:64457657 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:64483261 T>C maps to NM_182914.2 N1600N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:64496719 T>C maps to NM_182914.2 S2274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:64520062 C>T maps to NM_182914.2 L3144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:64604611 C>T maps to NM_182914.2 I4918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:64683008 C>T maps to NM_182914.2 S6482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:64687168 C>A maps to NM_182914.2 A6625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:64691225 C>T maps to NM_182914.2 D6810D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr14:64469640 G>A maps to NM_182914.2 A1330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:64519706 G>T maps to NM_182914.2 E3026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:64545240 G>T maps to NM_182914.2 E3694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:64519654 T>C maps to NM_182914.2 I3008I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:64545312 G>T maps to NM_182914.2 E3718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:64542722 C>T maps to NM_182914.2 R3643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr14:64519072 A>G maps to NM_182914.2 Q2814Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:64522933 G>A maps to NM_182914.2 K3339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr14:64630229 C>G maps to NM_182914.2 G5470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:64593449 G>C maps to NM_182914.2 L4614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr14:64593491 G>A maps to NM_182914.2 L4628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr14:64483195 A>G maps to NM_182914.2 E1578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr14:64467318 G>T maps to NM_182914.2 E1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:64483234 A>G maps to NM_182914.2 V1591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:64556369 G>T maps to NM_182914.2 E3917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:64519762 A>G maps to NM_182914.2 E3044E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:64483208 G>T maps to NM_182914.2 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:64518295 G>A maps to NM_182914.2 T2555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr14:64450592 C>T maps to NM_182914.2 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:64434459 G>T maps to NM_182914.2 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:64596827 C>T maps to NM_182914.2 F4734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:33406194 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:33411043 C>T maps to NM_006772.2 R905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:33405524 C>A maps to NM_006772.2 Y281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr6:33415703 C>T maps to NM_006772.2 D1293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr22:39770532 C>T maps to NM_004711.4 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:76167589 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:76167914 C>A maps to NM_004710.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr17:76167604 C>T maps to NM_004710.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:48878933 G>A maps to NM_012451.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:48869119 C>A maps to NM_012451.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr19:48878930 G>A maps to NM_012451.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:48876796 C>A maps to NM_012451.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:34029205 G>A maps to NM_003895.3 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:34004077 C>A maps to NM_003895.3 E1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:34029205 G>A maps to NM_003895.3 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:34038342 G>A maps to NM_003895.3 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr21:34038273 T>C maps to NM_003895.3 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr21:34003858 G>A maps to NM_003895.3 R1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr21:34003781 G>A maps to NM_003895.3 N1454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:158454681 C>A maps to NM_003898.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr6:158507956 C>T maps to NM_003898.3 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:158483058 G>A maps to NM_003898.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:158492639 A>G maps to NM_003898.3 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:158497777 C>T maps to NM_003898.3 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr6:158497758 C>T maps to NM_003898.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:158454696 C>T maps to NM_003898.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:158487584 C>T maps to NM_003898.3 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:158497731 C>T maps to NM_003898.3 Y789Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:99670295 G>A maps to ENST00000336292 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:99673109 C>A maps to ENST00000336292 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:99653920 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:99670983 C>T maps to ENST00000336292 Q806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr15:99670835 C>T maps to ENST00000336292 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:99670952 A>G maps to ENST00000336292 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:99666962 G>A maps to ENST00000336292 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr15:99673229 T>C maps to ENST00000336292 N1554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:99670079 G>A maps to ENST00000336292 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:99671319 G>T maps to ENST00000336292 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:99671340 G>T maps to ENST00000336292 E925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:99672617 G>A maps to ENST00000336292 V1350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:99673116 G>T maps to ENST00000336292 E1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:150027890 C>A maps to NM_001166209.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:150028061 G>A maps to NM_001166209.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:150029477 C>T maps to NM_001166209.1 G791G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:150029009 G>A maps to NM_001166209.1 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:150028139 G>C maps to NM_001166209.1 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:150029288 C>T maps to NM_001166209.1 Y728Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:150029009 G>A maps to NM_001166209.1 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:119951231 A>G maps to NM_133477.2 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:119947884 C>T maps to NM_133477.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:119951912 C>T maps to NM_133477.2 Y661Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:119952569 G>A maps to NM_133477.2 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:119978644 C>A maps to NM_133477.2 Y1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:119951717 G>T maps to NM_133477.2 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:119952398 C>T maps to NM_133477.2 N823N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:119951837 T>C maps to NM_133477.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:119978971 G>A maps to NM_133477.2 R1223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:75407360 G>T maps to NM_001114133.1 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:75407663 G>T maps to NM_001114133.1 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr10:75407267 C>T maps to NM_001114133.1 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:75407957 C>T maps to NM_001114133.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:75407135 A>G maps to NM_001114133.1 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:75413975 G>A maps to NM_001114133.1 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr10:75413401 G>A maps to NM_001114133.1 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:75412938 C>A maps to NM_001114133.1 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:75413401 G>A maps to NM_001114133.1 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:75408401 G>A maps to NM_001114133.1 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:63542290 C>T maps to NM_001130003.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:35937658 C>T maps to NM_007247.4 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:35880751 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr17:35913778 T>G maps to NM_007247.4 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:35913589 G>A maps to NM_007247.4 Y745Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:49049761 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:49049906 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:49049895 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:49054267 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:49049760 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:49048049 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:49047956 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:49054103 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:49047972 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:49050733 G>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:49049854 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:105738264 G>A maps to NM_006754.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:110018264 T>C maps to NM_001040709.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:110019433 T>C maps to NM_001040709.1 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:110019439 G>A maps to NM_001040709.1 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:43995676 T>C maps to NM_033542.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr12:79693186 C>T maps to NM_005639.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:79747319 C>T maps to NM_005639.2 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:79685838 G>T maps to NM_005639.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr12:79842832 C>T maps to NM_005639.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:33532801 G>A maps to NM_198992.3 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:33579170 G>A maps to NM_198992.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:33560107 G>T maps to NM_198992.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:33560166 C>A maps to NM_198992.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:33579238 C>A maps to NM_198992.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:33560205 G>A maps to NM_198992.3 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:155850987 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:155851193 C>A maps to NM_152280.4 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:155851154 C>T maps to NM_152280.4 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:66811215 T>C maps to NM_001177880.1 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:66816092 C>T maps to NM_001177880.1 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:66807538 C>T maps to NM_001177880.1 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:66811212 C>T maps to NM_001177880.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:45265683 C>T maps to NM_020826.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:210334309 G>T maps to NM_001146261.1 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:210334371 G>A maps to NM_001146261.1 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:210334182 C>A maps to NM_001146261.1 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:210273661 T>C maps to NM_001146261.1 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:210329067 C>A maps to NM_001146261.1 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:210329118 C>A maps to NM_001146261.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:210273707 G>T maps to NM_001146261.1 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:210329226 C>T maps to NM_001146261.1 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr10:46968620 C>T maps to NM_031912.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr10:46968704 G>A maps to NM_031912.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:46962095 G>C maps to NM_031912.3 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:46967503 G>A maps to NM_031912.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr14:62550927 G>A maps to NM_031914.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr14:62541898 C>T maps to NM_031914.2 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:62547550 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr14:62547847 C>A maps to NM_031914.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:62541922 T>C maps to NM_031914.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:19184822 C>T maps to NM_016524.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr16:19195207 C>T maps to NM_016524.2 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:19234453 C>T maps to NM_016524.2 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr16:19194991 A>G maps to NM_016524.2 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:19184853 G>T maps to NM_016524.2 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:19191859 G>A maps to NM_016524.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:202572240 G>A maps to NM_177402.4 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:202574774 G>A maps to NM_177402.4 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr1:202574720 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:51136039 G>A maps to NM_001160329.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:51133283 C>T maps to NM_001160329.1 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:51128669 G>A maps to NM_001160329.1 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:51136014 G>A maps to NM_001160329.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:40854297 G>T maps to NM_020783.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:40853690 C>A maps to NM_020783.3 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:55687420 C>T maps to NM_003180.2 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:114682235 C>T maps to ENST00000447981 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:114640438 G>A maps to ENST00000369545 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:114641716 G>A maps to ENST00000369545 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:61290681 C>T maps to NM_004200.2 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:61295621 C>T maps to NM_004200.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:1857514 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr11:1858595 G>T maps to NM_138567.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:7334913 C>A maps to NM_175733.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:27676742 C>T maps to ENST00000485269 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:27680285 G>A maps to NM_001193308.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:85435680 C>A maps to ENST00000359152 E1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:85406360 C>A maps to ENST00000359152 V1740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:85420462 T>C maps to ENST00000359152 E1483E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:85436350 C>T maps to ENST00000359152 T907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:85437199 G>T maps to ENST00000359152 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:85437426 C>A maps to ENST00000359152 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:85435302 C>A maps to ENST00000359152 E1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:85437426 C>A maps to ENST00000359152 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:85435680 C>A maps to ENST00000359152 E1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:85429856 C>A maps to ENST00000359152 E1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:85435878 C>A maps to ENST00000359152 E1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:85437049 G>T maps to ENST00000359152 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:85422206 C>T maps to ENST00000359152 P1439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr6:159084344 C>G maps to ENST00000297239 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:159185626 C>T maps to ENST00000297239 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:99942228 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:99946189 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:99942165 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:99943431 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:99956274 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:99946197 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:99936233 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:99956564 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:99957104 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:99934360 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:99943339 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:99956659 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:99931105 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:99956978 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:99945152 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:99946119 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:99945596 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:37953663 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:37948762 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:37931346 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:37955395 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:37985946 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:37961615 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:37979658 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:37981396 A>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:37984740 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:37893200 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:37969663 G>A did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:37913532 G>A did not map to a codon.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr23:37948726 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:166579328 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:166578154 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:166581058 C>T maps to NM_003181.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:132967061 G>A maps to NM_138327.1 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:132966641 G>A maps to NM_138327.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:132966458 A>G maps to NM_138327.1 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:132938299 C>A maps to NM_001033080.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:132891981 C>T maps to NM_175067.1 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr6:132891738 G>A maps to NM_175067.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:132874646 G>A maps to NM_053278.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:132859635 C>T maps to NM_175057.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:132859928 C>A maps to NM_175057.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:132860432 G>A maps to NM_175057.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr6:132859715 C>T maps to NM_175057.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:39813852 C>T maps to NM_006116.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:39824032 A>G maps to NM_006116.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:39817885 G>A maps to NM_006116.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:39811624 C>T maps to NM_006116.2 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:39826208 C>T maps to NM_006116.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:149719194 C>T maps to NM_015093.4 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr6:149699330 G>T maps to NM_015093.4 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:149700404 C>T maps to NM_015093.4 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr6:149700166 C>T maps to NM_015093.4 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:30872752 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:30872925 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:30873224 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:30852203 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:30852232 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:30861147 G>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:30872891 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:30849644 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:30873359 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:30871016 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:30849647 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:30873102 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:30872308 G>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:30872917 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:30864691 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:30877656 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:30870991 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:30872555 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr23:30873212 T>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZV-01A-11D-A10M-09 chr23:30870925 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:30872636 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:30849574 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:30873651 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:30873351 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:97364150 C>A maps to NM_003182.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:57406441 C>T maps to ENST00000423009 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:38677968 C>T maps to ENST00000379931 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:38677638 G>T maps to ENST00000379931 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:38677205 C>T maps to ENST00000379931 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:38677638 G>T maps to ENST00000379931 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:123842359 G>A maps to NM_206862.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:123971091 C>A maps to NM_206862.2 S2384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:123843317 G>T maps to NM_206862.2 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:123972883 T>C maps to ENST00000368999 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:123842456 G>T maps to NM_206862.2 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:123843307 T>C maps to NM_206862.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:123987351 G>A maps to NM_206862.2 G2575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:123843389 G>T maps to NM_206862.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:123844855 G>A maps to NM_206862.2 K947K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:123846898 A>G maps to NM_206862.2 P1628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:123781450 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:123985888 C>T maps to NM_206862.2 D2539D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:123842395 G>A maps to NM_206862.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr10:123809993 C>T maps to NM_206862.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:1746486 G>A maps to NM_006342.1 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:1729773 G>A maps to NM_006342.1 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:75278511 G>T maps to NM_001058.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:75425859 C>T maps to NM_001058.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:75276591 C>T maps to NM_001058.3 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:75425988 C>T maps to NM_001058.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:75347736 C>A maps to NM_001058.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:75425859 C>T maps to NM_001058.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:71175863 G>A maps to NM_001057.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:71166958 G>A maps to NM_001057.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:71164770 G>A maps to NM_001057.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:71175860 G>T maps to NM_001057.2 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr10:71174807 G>A maps to NM_001057.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:104640685 G>A maps to NM_001059.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:104511012 G>T maps to NM_001059.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:104512660 G>A maps to NM_001059.2 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr4:104640577 G>A maps to NM_001059.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr4:104640322 G>A maps to NM_001059.2 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:104511146 G>A maps to NM_001059.2 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:104640772 G>A maps to NM_001059.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr4:104579525 G>A maps to NM_001059.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:104579485 C>T maps to NM_001059.2 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:59042030 C>T maps to NM_002353.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:35831230 T>G maps to NM_001166105.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:35836996 G>A maps to NM_001166105.1 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:35787057 C>T maps to NM_001166105.1 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:7055934 C>T maps to NM_152293.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr4:7056280 C>T maps to NM_152293.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:7056093 T>C maps to NM_152293.2 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr3:9831638 G>T maps to NM_006354.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:9825749 A>G maps to NM_006354.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:70613298 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:70598177 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:70608221 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70602466 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70608209 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70621533 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70679439 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70597629 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70603863 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70608625 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70618453 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:70608188 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70587941 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70598835 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70601670 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70608636 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70617242 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70618464 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:70613214 G>C did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:70683820 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:70612538 A>G did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:70607238 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:70608189 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:70617186 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:70595075 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:70602460 A>G did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:70607121 C>G did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:70596999 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70587423 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70602466 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70618510 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70621537 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70680588 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70598195 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70613304 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70617186 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:70617240 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70601697 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70607172 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70618465 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:70608188 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70596821 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70608169 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70678091 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr23:70603919 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:70587975 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:70617233 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70598277 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70602987 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70608640 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70618497 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70603854 T>G did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr23:70602841 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:70586287 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:70608188 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:70603869 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:70595061 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:70612781 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:70612489 G>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:70608189 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:70614067 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:70612821 A>C did not map to a codon.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr23:70617203 C>T did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:70617290 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:34847765 G>A maps to NM_005643.2 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:28931895 T>C maps to NM_005644.3 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr1:109607312 A>C maps to NM_005645.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:34147190 G>T maps to NM_139215.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:34169375 G>T maps to NM_139215.1 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:34163187 G>A maps to NM_139215.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:222761886 C>A maps to NM_005681.2 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:222761824 T>G maps to NM_005681.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:222757511 G>T maps to NM_005681.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr2:10045014 A>T maps to NM_005680.2 K279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:10053328 A>T maps to NM_005680.2 K408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:10053378 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:10045001 C>T maps to NM_005680.2 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:9994459 T>C maps to NM_005680.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:84216893 G>A maps to NM_005679.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:84216897 C>T maps to NM_005679.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:84213293 G>A maps to NM_005679.2 C621C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:93471478 C>T maps to NM_024116.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:32632904 C>T maps to NM_153809.2 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:32630653 C>A maps to NM_153809.2 E1642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:32631964 G>A maps to NM_153809.2 R1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:32632799 G>T maps to NM_153809.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:32633999 C>T maps to NM_153809.2 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr9:32631848 C>T maps to NM_153809.2 R1243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr9:32632025 G>A maps to NM_153809.2 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:32634992 C>T maps to NM_153809.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:32634584 C>T maps to NM_153809.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:32632208 A>G maps to NM_153809.2 I1123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr9:32630588 A>C maps to NM_153809.2 S1663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:120809948 A>G maps to NM_003184.3 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:120797487 G>T maps to NM_003184.3 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr8:120801941 C>T maps to NM_003184.3 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr10:8007249 A>T maps to NM_031923.2 K593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:8055696 C>T maps to NM_031923.2 R858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:7866348 G>T maps to NM_031923.2 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:8006792 G>A maps to NM_031923.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:7866477 G>T maps to NM_031923.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr10:8006477 G>A maps to NM_031923.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:60585191 C>T maps to NM_003185.3 Q557Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr20:60584155 C>T maps to NM_003185.3 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:60574071 C>T maps to NM_003185.3 E960E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:60582646 C>A maps to NM_003185.3 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr20:60587963 C>T maps to NM_003185.3 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:23847568 G>A maps to ENST00000418698 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr18:23895276 T>G maps to ENST00000418698 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr10:105139710 C>T maps to NM_006951.3 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:105143014 G>T maps to NM_006951.3 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:229730559 C>T maps to NM_014409.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:229738364 G>A maps to NM_014409.3 N183N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:229745901 T>C maps to NM_014409.3 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:229738424 G>A maps to NM_014409.3 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:99709745 G>A maps to ENST00000472509 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:99711493 G>A maps to ENST00000472509 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr7:99709598 C>A maps to ENST00000472509 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:62550278 G>A maps to NM_006473.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:140698981 G>A maps to NM_005642.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr5:140698693 G>A maps to NM_005642.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:100531501 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100547928 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100547798 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:100547927 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100547861 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100534007 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:100531364 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:100542467 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100530220 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100538441 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100537353 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100541606 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:42025130 G>A maps to NM_138572.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr6:42025184 C>T maps to NM_138572.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:77387182 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77393508 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:77387182 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:77393560 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:77394371 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:77388875 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:77392458 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:77393325 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:77394387 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr23:77392446 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:77393483 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:77394363 T>G did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:77393463 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:159457335 G>T maps to NM_054114.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:159457058 G>A maps to NM_054114.3 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:159459224 G>T maps to NM_054114.3 C273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:159461819 G>T maps to NM_054114.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:159456954 G>A maps to NM_054114.3 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:159457839 G>A maps to NM_054114.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:117074093 C>T maps to NM_003186.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:117073782 C>T maps to NM_003186.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:159890242 C>T maps to ENST00000368096 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:111732429 G>A maps to ENST00000494932 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:111732266 C>T maps to NM_001008272.1 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:108425082 T>A maps to NM_005421.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:160087102 G>A maps to NM_033394.2 P1722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:160085345 G>T maps to NM_033394.2 E1364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:160055562 A>G maps to NM_033394.2 T1081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:160005674 G>A maps to NM_033394.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:61345220 G>A maps to ENST00000389520 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:61498754 C>T maps to ENST00000389520 S1814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr17:61498667 C>T maps to ENST00000389520 S1785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:61432185 C>T maps to ENST00000389520 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:61466048 C>T maps to ENST00000389520 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:61466953 C>T maps to ENST00000434668 R960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:162091905 C>T maps to NM_004180.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:162087941 G>A maps to NM_004180.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:162091939 G>T maps to NM_004180.2 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:162088034 G>A maps to NM_004180.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:27844610 C>A maps to NM_020791.2 C615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:27849521 G>A maps to NM_020791.2 Q711Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:27844578 C>T maps to NM_020791.2 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:27857430 G>T maps to NM_020791.2 E719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:27857637 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:27837898 T>C maps to NM_020791.2 N531N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:27837989 C>T maps to NM_020791.2 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:29997695 G>A maps to NM_016151.2 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:29997827 A>G maps to NM_016151.2 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:29998322 G>A maps to NM_016151.2 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr16:30002220 G>A maps to NM_004783.2 Q854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr12:118677077 C>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:118671521 C>T maps to NM_016281.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:32816895 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:32818212 G>A maps to NM_000593.5 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:32818158 C>A maps to NM_000593.5 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:6566593 G>A maps to NM_018009.4 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:16188158 G>A maps to NM_153365.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:16188158 G>A maps to NM_153365.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:16215510 C>T maps to NM_153365.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:234556491 G>A maps to NM_005646.3 R1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:234582721 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:234569284 C>T maps to NM_005646.3 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:234608512 G>A maps to NM_005646.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:234565232 C>A maps to NM_005646.3 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:53898556 G>T maps to NM_134323.1 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53895876 G>A maps to NM_134323.1 K44K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:53898556 G>T maps to NM_134323.1 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:11080583 C>T maps to NM_007375.3 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr5:33457508 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:33461806 G>A maps to ENST00000455217 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150460482 T>C maps to NM_025150.3 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:150470082 G>A maps to NM_025150.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:150479528 G>T maps to NM_025150.3 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:150461541 C>T maps to NM_025150.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr1:150477197 C>T maps to NM_025150.3 C603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:102249049 C>T maps to NM_152334.2 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:102197200 G>A maps to NM_152334.2 D728D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr15:102224403 T>C maps to NM_152334.2 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr15:102263310 G>A maps to NM_152334.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:6639529 C>T maps to NM_138697.3 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:6639590 G>T maps to NM_138697.3 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:6634989 C>T maps to NM_138697.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:6634809 C>T maps to NM_138697.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:19166749 G>A maps to NM_152232.2 Y621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:19166950 C>T maps to NM_152232.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:19175954 C>T maps to NM_152232.2 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr1:19166926 A>G maps to NM_152232.2 H562H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:19181303 G>A maps to NM_152232.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:19181132 G>A maps to NM_152232.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:19180814 A>G maps to NM_152232.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:19166155 C>T maps to NM_152232.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:1268407 G>A maps to NM_152228.1 W461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:1267134 C>T maps to NM_152228.1 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:9629748 C>T maps to NM_019599.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr12:11061486 G>C maps to NM_023920.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:11061546 A>T maps to NM_023920.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:11061776 G>A maps to NM_023920.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:122635481 G>A maps to NM_016945.2 C69C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:11174831 G>A maps to NM_176888.1 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:141464165 G>T maps to NM_016943.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr12:11286213 C>T maps to NM_001097643.1 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:11183403 C>T maps to NM_176885.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:141672667 G>A maps to NM_176817.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:141673348 C>T maps to NM_176817.4 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:141478599 C>T maps to NM_016944.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:141478494 C>T maps to NM_016944.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:142919521 C>A maps to NM_176882.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:142919329 C>T maps to NM_176882.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:143175633 C>T maps to NM_176883.2 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:143175849 G>A maps to NM_176883.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:143175436 G>T maps to NM_176883.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:143175294 G>A maps to NM_176883.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:11339098 C>A maps to NM_181429.1 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:11338744 T>A maps to NM_181429.1 K267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr12:11244522 G>T maps to ENST00000422992 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:11214443 A>G maps to ENST00000422992 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:141490185 C>T maps to NM_018980.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:141490922 C>A maps to NM_018980.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:141490217 C>T maps to NM_018980.2 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:141490820 G>A maps to NM_018980.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:11139300 G>T maps to NM_176890.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:11138637 G>A maps to NM_176890.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:10954290 T>C maps to NM_023919.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:10954569 G>T maps to NM_023919.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:10954917 G>T maps to NM_023919.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:10954809 G>T maps to NM_023919.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr12:10958910 T>C maps to NM_023918.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:10959363 G>A maps to NM_023918.1 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:10959360 T>G maps to NM_023918.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:10962187 C>A maps to NM_023917.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:10962536 G>T maps to NM_023917.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:13398142 C>A maps to NM_017714.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr20:13398142 C>T maps to NM_017714.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr20:13567971 A>G maps to NM_017714.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:13514674 A>G maps to NM_017714.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:71602172 C>T maps to NM_000353.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:125528184 G>A maps to NM_032026.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:125528139 C>A maps to NM_032026.3 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr8:125520904 C>T maps to NM_032026.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr3:10312101 C>T maps to NM_014760.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:212969860 C>A maps to NM_001146171.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:3568056 C>T maps to NM_014604.2 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:153648052 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153640544 C>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:153648415 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153640474 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153641609 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:153648447 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:153641664 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:153648063 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:38091652 T>A maps to NM_015173.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:38117332 C>T maps to NM_015173.2 R854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:30369864 C>A maps to NM_015527.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:30376893 G>A maps to NM_015527.3 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:67174443 C>A maps to NM_198517.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr10:96234436 C>T maps to NM_015188.1 R370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:131550663 G>A maps to NM_018201.3 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:131565686 C>T maps to NM_018201.3 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr9:131568286 C>T maps to NM_018201.3 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:131565681 G>T maps to NM_018201.3 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:131566238 C>T maps to NM_018201.3 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:6925664 G>A maps to NM_001113361.1 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr4:6998130 C>T maps to NM_001113361.1 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr4:6925394 C>T maps to NM_001113361.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:7012483 G>A maps to NM_001113361.1 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr12:72288564 C>T maps to NM_022771.4 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:72278769 G>T maps to NM_022771.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:72255231 G>T maps to NM_001146214.1 G4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr17:77987189 G>A maps to NM_019020.2 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:77918742 C>T maps to NM_019020.2 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr17:77983987 G>A maps to NM_019020.2 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr4:26638863 T>A maps to NM_018317.2 L109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr4:26741510 T>C maps to NM_018317.2 H381H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:26668016 A>G maps to NM_018317.2 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:26622233 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:100961854 G>A maps to NM_018421.3 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:100995758 A>G maps to NM_018421.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr9:100965683 C>T maps to NM_018421.3 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr9:100971187 G>A maps to NM_018421.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:419397 A>G maps to ENST00000246077 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr20:428589 G>A maps to ENST00000246077 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:47193392 G>A maps to NM_014346.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr22:47189508 C>T maps to NM_014346.2 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:100002484 A>G maps to ENST00000394144 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:100037953 G>T maps to ENST00000394144 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:100039795 G>T maps to ENST00000394144 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:100016876 T>C maps to ENST00000394144 N329N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:2548379 C>T maps to ENST00000434757 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr16:2546985 G>A maps to ENST00000434757 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:2546823 C>T maps to ENST00000434757 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:48417410 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48418549 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48418598 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48403373 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48418568 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48419065 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48419184 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:48418448 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr23:48417655 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:48417698 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48417561 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48418261 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:48417608 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:48418480 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48417729 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48419293 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:18541184 G>A maps to NM_001039397.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:28890280 G>A maps to NM_015594.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:78317678 C>T maps to NM_144572.1 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr15:78317660 C>T maps to NM_144572.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:75900463 C>T maps to ENST00000431480 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:75886877 C>T maps to ENST00000431480 Q793Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:75900508 C>T maps to ENST00000431480 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:75923321 G>T maps to ENST00000431480 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:75861064 C>A maps to ENST00000431480 E1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:75898520 G>A maps to ENST00000431480 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:75880451 C>A maps to ENST00000431480 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:75898520 G>A maps to ENST00000431480 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:75936236 C>T maps to ENST00000431480 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:75884107 G>A maps to ENST00000431480 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:75900456 G>A maps to ENST00000431480 R637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:75898520 G>A maps to ENST00000431480 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:75876394 C>T maps to ENST00000431480 A966A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:76055662 C>A maps to ENST00000431480 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:75873507 G>A maps to ENST00000431480 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr13:75936665 A>G maps to ENST00000431480 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:75884107 G>A maps to ENST00000431480 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:75900508 C>A maps to ENST00000431480 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:75936575 G>A maps to ENST00000431480 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:17550097 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr3:17425425 G>A maps to NM_001134381.1 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:17444703 G>A maps to NM_001134381.1 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:17446396 T>C maps to NM_001134381.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:17279907 G>A maps to NM_001134381.1 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:17333464 G>A maps to NM_001134381.1 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:13316874 G>A maps to NM_016495.4 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:101624731 C>A maps to NM_001102426.1 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:101624654 G>A maps to NM_001102426.1 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:101638190 C>A maps to NM_001102426.1 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:101624477 C>T maps to NM_001102426.1 A1076A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:101624531 C>T maps to NM_001102426.1 S1058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr2:101650137 G>A maps to NM_001102426.1 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:101670714 G>A maps to NM_001102426.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:106083360 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:106046160 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:106065235 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:106083995 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:106046128 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:106091524 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:106109162 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:106109244 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:106091521 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:106069410 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:106083338 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:106093484 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:106097481 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:106069273 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:106082589 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:106096815 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:106116863 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:106070527 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:106065411 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:106083349 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:106096753 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:106070527 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:106096753 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:106083299 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:106083902 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:106117096 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:141578883 G>A maps to NM_015130.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:141590793 C>T maps to NM_015130.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:141600117 T>A maps to NM_015130.2 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:141578277 G>T maps to NM_015130.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr4:141543675 G>A maps to NM_015130.2 D1158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:141600930 C>A maps to NM_015130.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr4:141578310 G>A maps to NM_015130.2 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:141600906 G>A maps to NM_015130.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:179297288 C>T maps to NM_198868.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:179299969 G>A maps to NM_198868.2 A779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:179292280 C>T maps to NM_198868.2 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:179292318 G>A maps to NM_198868.2 R1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:179302026 G>A maps to NM_198868.2 I687I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A186-01A-11D-A12J-09 chr5:179294721 C>T maps to ENST00000444477 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr5:179290627 G>T maps to NM_198868.2 T1191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:186276277 G>A maps to NM_001134415.1 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:186272841 A>C maps to NM_001134415.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:80890602 G>A maps to NM_005993.4 T1061T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:80863885 G>T maps to NM_005993.4 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:80828140 C>A maps to NM_005993.4 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:80726396 G>A maps to NM_005993.4 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr17:80887018 G>A maps to NM_005993.4 Q908Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:80888411 C>A maps to NM_005993.4 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:80895186 G>T maps to NM_005993.4 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:235600761 C>A maps to NM_003193.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:235577846 A>G maps to NM_003193.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:120929157 C>T maps to NM_152715.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:120957708 C>A maps to NM_152715.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:107169418 G>T maps to NM_001163436.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:107163688 G>A maps to NM_001163436.1 R370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:107183308 T>C maps to NM_001163436.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr4:107154173 T>A maps to NM_001163436.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:64868036 C>T maps to NM_013254.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:64889477 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:64895145 C>T maps to NM_013254.3 N725N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:45776130 C>A maps to NM_014726.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:45785840 C>A maps to NM_014726.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:45785771 G>A maps to NM_014726.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr17:45777025 C>T maps to NM_014726.2 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr17:45777036 G>A maps to NM_014726.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:9656078 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:9660238 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:9661248 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:9679794 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:9621666 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:9621684 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr23:9683000 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:9656301 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:9656070 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:9661421 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:9656229 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:9656241 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:9682940 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:9659625 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:9656196 T>G did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:9659748 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:9660258 C>T did not map to a codon.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr23:9683030 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:176767840 G>A maps to NM_024665.4 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:176756100 C>T maps to NM_024665.4 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:176767840 G>T maps to NM_024665.4 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:176769435 T>G maps to NM_024665.4 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:176752058 C>A maps to NM_024665.4 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:72987776 G>A maps to NM_012453.2 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:72987671 G>A maps to NM_012453.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:2024809 C>T maps to NM_006453.2 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr16:2025587 G>A maps to NM_006453.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:134303711 T>C maps to NM_004865.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:55890971 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:55903621 C>A maps to NM_199047.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr14:55903276 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:162273316 G>A maps to NM_006593.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:124495565 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:124493083 G>A maps to NM_032811.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr7:45143023 G>A maps to ENST00000404564 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:45143706 G>T maps to ENST00000404564 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:67399303 C>T maps to NM_005995.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:119456802 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:85457772 C>T maps to NM_001080508.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:85446834 G>T maps to NM_001080508.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:85457661 G>A maps to NM_001080508.1 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:85446782 G>A maps to NM_001080508.1 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:85466460 G>A maps to NM_001080508.1 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:168260559 C>A maps to NM_005149.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:59485434 C>T maps to NM_005994.3 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:59485479 C>T maps to NM_005994.3 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr7:35280610 C>T maps to NM_001077653.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:45821607 C>T maps to NM_013351.1 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr17:45820026 C>T maps to NM_013351.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:79278610 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:79278691 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:79278683 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:79286168 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:79286499 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:79281114 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:79277783 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:79282758 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:79282782 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:79286241 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:79286168 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:79281213 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:79282776 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:79286447 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:79286195 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:79286362 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:79286545 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:79278693 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:79282753 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:115114127 C>T maps to NM_016569.3 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:114836449 C>T maps to NM_000192.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:114793905 C>A maps to NM_000192.3 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:114841625 C>T maps to NM_000192.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:114841625 C>T maps to NM_000192.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:114841664 C>T maps to NM_000192.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:114832699 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:30098116 C>A maps to NM_004608.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:30102200 C>T maps to NM_004608.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:139653237 C>T maps to NM_001166253.1 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:139657496 G>T maps to NM_001166253.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:139653192 C>T maps to NM_001166253.1 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:92251540 G>A maps to NM_001128596.1 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:92253905 T>C maps to NM_001128596.1 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:92280103 C>A maps to NM_001128596.1 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:92265402 A>G maps to NM_001128596.1 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr14:92258815 C>T maps to NM_001128596.1 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:54891682 C>A maps to NM_006756.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr20:62701930 G>A maps to NM_003195.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr20:62694736 G>A maps to NM_003195.4 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:102885050 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102884931 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102885149 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:102885125 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:101382183 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:101382464 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101381918 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:102864314 G>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:102864095 A>G did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:102841600 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102842177 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:102841693 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:102842074 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:102842153 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102528911 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102529415 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:102529444 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:102528887 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:101396125 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101396011 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr23:101396020 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:102586469 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:102586608 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:102586414 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:102586469 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:102586482 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102508567 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:102508856 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:102508565 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:13680883 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:13681147 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13680767 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:13680991 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:13680892 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:13681115 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:13681614 A>C did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:13681453 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:2822077 G>A maps to NM_207013.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:24080871 A>G maps to NM_003198.2 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:24078294 C>T maps to NM_003198.2 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:24077451 G>A maps to NM_003198.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr1:24078895 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:44561533 G>T maps to NM_016427.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:44560804 C>T maps to NM_016427.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:44561553 C>A maps to NM_016427.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr18:44560087 C>T maps to NM_016427.2 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:44559943 G>A maps to NM_016427.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:44560609 G>A maps to NM_016427.2 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:145862160 C>T maps to NM_006706.3 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:145836765 T>C maps to NM_006706.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:145843356 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:145887489 C>T maps to NM_006706.3 R989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:145890186 G>A maps to NM_006706.3 T1093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr5:145862251 C>T maps to NM_006706.3 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:145883446 C>T maps to NM_006706.3 R870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:133107523 G>T maps to NM_174937.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:133058636 G>T maps to NM_174937.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr10:133058657 G>A maps to NM_174937.3 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:57565422 C>A maps to NM_207036.1 A647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:57544624 C>T maps to NM_207036.1 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:57526289 A>G maps to NM_207036.1 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:42607885 A>G maps to NM_005650.1 G1142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr22:42610372 C>T maps to NM_005650.1 Q313Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr22:42608371 C>T maps to NM_005650.1 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr22:42610261 A>T maps to NM_005650.1 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr22:42609148 G>A maps to NM_005650.1 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:134210780 C>T maps to NM_003206.3 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:27373202 G>A maps to NM_175769.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:27375563 G>A maps to NM_175769.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:89952326 C>T maps to NM_014972.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:89960262 C>T maps to NM_014972.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr16:89977618 C>T maps to NM_014972.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:1615286 G>A maps to NM_003200.2 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:1625650 C>T maps to NM_003200.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:1611809 G>A maps to NM_003200.2 R621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:1621855 G>A maps to NM_003200.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:53017618 G>A maps to ENST00000398339 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:52896230 G>A maps to ENST00000398339 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr18:53018186 A>C maps to ENST00000398339 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:53302957 C>T maps to ENST00000398339 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:53252520 A>G maps to ENST00000398339 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:53017618 G>A maps to ENST00000398339 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:53017618 G>A maps to ENST00000398339 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:53017618 G>A maps to ENST00000398339 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:53131362 C>A maps to ENST00000398339 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:52927189 T>C maps to ENST00000398339 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:133480539 G>A maps to ENST00000395029 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:85529608 T>G maps to NM_031283.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:85529725 C>T maps to NM_031283.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr10:114901025 G>A maps to NM_030756.4 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:114910864 C>T maps to NM_030756.4 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:114912129 C>T maps to NM_030756.4 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:61488918 G>A maps to NM_006602.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:152079923 G>A maps to NM_007113.2 V1923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:152080820 G>A maps to NM_007113.2 D1624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:152081480 G>A maps to NM_007113.2 R1404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:152083792 G>A maps to NM_007113.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:152081138 G>A maps to NM_007113.2 L1518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr1:152081441 G>A maps to NM_007113.2 R1417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:152080301 G>A maps to NM_007113.2 F1797F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:152080096 G>A maps to NM_007113.2 Q1866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:152081141 G>A maps to NM_007113.2 F1517F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:152059926 G>T maps to NM_001008536.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:152057628 G>T maps to NM_001008536.1 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:152059683 G>A maps to NM_001008536.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:152059077 A>T maps to NM_001008536.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:67815372 G>A maps to NM_006019.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:67811328 C>T maps to NM_006019.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:67816586 G>A maps to NM_006019.3 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr11:67812507 G>A maps to NM_006019.3 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:67811375 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:59633910 C>T maps to NM_001062.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr11:59631479 G>A maps to NM_001062.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:59623525 G>T maps to NM_001062.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr22:31010333 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr22:31011585 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:149754972 C>T maps to ENST00000451292 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:149754674 C>T maps to ENST00000451292 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:149751627 T>A maps to ENST00000451292 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr6:160200259 T>C maps to NM_030752.2 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:160206481 C>A maps to NM_030752.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:160201533 T>G maps to NM_030752.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:160201094 C>T maps to NM_030752.2 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:167787871 G>A maps to NM_004610.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:167787929 G>T maps to NM_004610.3 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:167794572 G>A maps to ENST00000476779 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:167590525 T>G maps to NM_001145121.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:35096877 G>A maps to NM_001093728.1 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:35089948 G>A maps to NM_001093728.1 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:35096849 C>A maps to NM_001093728.1 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:33083145 C>T maps to NM_001145541.1 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:33078708 C>T maps to NM_001145541.1 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:106717315 C>T maps to NM_152772.1 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:106729808 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:106734602 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:106729448 G>T maps to NM_152772.1 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr12:106708134 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:106715428 C>T maps to NM_152772.1 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:106740245 C>T maps to NM_152772.1 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:44255514 G>T maps to NM_182539.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:44255388 G>A maps to NM_182539.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:44254078 G>A maps to NM_182539.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:44250241 G>A maps to NM_182539.3 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr6:44253874 G>A maps to NM_182539.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:170144352 T>C maps to NM_174910.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:170143246 C>A maps to NM_174910.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:67220431 C>T maps to NM_152665.2 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:111085594 G>A maps to NM_001082538.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr12:111085687 G>A maps to NM_001082538.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:124171405 G>A maps to NM_024809.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:124175195 G>A maps to NM_024809.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:124189109 G>A maps to NM_024809.3 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:124155822 G>A maps to NM_024809.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:124175195 G>A maps to NM_024809.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:97423949 C>T maps to ENST00000371217 W584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:97440279 C>T maps to ENST00000371217 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:104376598 G>A maps to NM_003211.4 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:104380858 C>T maps to NM_003211.4 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:104380732 C>T maps to NM_003211.4 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:46620614 C>A maps to NM_003212.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:156825187 C>T maps to NM_005651.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:90450937 T>C maps to NM_018319.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr14:90499490 C>T maps to NM_018319.3 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:115971781 G>A maps to NM_198795.1 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:115973330 C>T maps to NM_198795.1 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:115987002 G>A maps to NM_198795.1 V1116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:115963184 C>T maps to NM_198795.1 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:115973240 C>A maps to NM_198795.1 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:115970721 C>T maps to NM_198795.1 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr10:115961250 C>T maps to NM_198795.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:115964630 G>T maps to NM_198795.1 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:115981147 G>T maps to NM_198795.1 E935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:115962019 C>A maps to NM_198795.1 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:154480957 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:154516525 G>A maps to NM_001098475.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:154480958 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:154516585 G>A maps to NM_001098475.1 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr13:61102732 A>G maps to NM_001146070.1 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr13:61102777 G>A maps to NM_001146070.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr13:61102847 A>T maps to NM_001146070.1 K497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr13:61102729 T>C maps to NM_001146070.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr1:179621301 A>G maps to ENST00000444136 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:179631285 T>C maps to ENST00000444136 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:179562607 A>G maps to ENST00000444136 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:179632481 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:179659876 C>T maps to ENST00000444136 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:179609045 C>A maps to ENST00000444136 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:179632590 C>T maps to ENST00000444136 Q872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:46657578 C>T maps to NM_001010870.2 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:46659431 G>A maps to NM_001010870.2 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:46660193 C>T maps to NM_001010870.2 S1443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:46657746 G>T maps to NM_001010870.2 E628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr6:46661433 C>T maps to NM_001010870.2 Q1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr6:46659899 C>T maps to NM_001010870.2 P1345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:46657583 C>T maps to NM_001010870.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:46660907 T>A maps to NM_001010870.2 I1681I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:46659035 A>G maps to NM_001010870.2 K1057K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:46656966 C>T maps to NM_001010870.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:46661337 G>T maps to NM_001010870.2 E1825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:46659149 T>G maps to NM_001010870.2 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:46659050 C>A maps to NM_001010870.2 V1062V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:100232904 G>A maps to NM_014290.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:100234692 C>T maps to NM_014290.2 Y620Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:100222962 A>C maps to NM_014290.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:100245567 C>T maps to NM_014290.2 S950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:100234641 C>A maps to NM_014290.2 I603I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:100204090 G>A maps to NM_014290.2 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:100243216 T>C maps to NM_014290.2 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr9:100235778 C>T maps to NM_014290.2 D650D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:104493206 C>A maps to NM_153046.2 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:104481163 C>T maps to NM_153046.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:104508479 G>A maps to NM_153046.2 E1310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:151752565 G>A maps to NM_001083965.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:151749033 C>A maps to NM_001083965.1 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:151747184 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:12901313 C>T maps to NM_021961.5 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:49844673 G>T maps to NM_003598.1 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:49845784 G>A maps to NM_003598.1 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:35442859 G>A maps to ENST00000357281 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:3129821 C>T maps to NM_003213.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:3128292 C>T maps to NM_003213.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:3147237 C>A maps to NM_003213.3 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:3131077 C>T maps to NM_003213.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:3131140 C>T maps to NM_003213.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr12:3147204 C>T maps to NM_003213.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:3104141 C>T maps to NM_003213.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:48169837 C>A maps to NM_003215.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:97852981 G>T maps to ENST00000379795 C915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:97861232 G>A maps to ENST00000379795 C620C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:97852981 G>T maps to ENST00000379795 C915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:97857396 C>T maps to ENST00000379795 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:97861253 G>A maps to ENST00000379795 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr7:97857396 C>T maps to ENST00000379795 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:97873996 C>T maps to ENST00000379795 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:97870550 C>T maps to ENST00000379795 W221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr7:97870557 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:102873694 T>C maps to NM_014844.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:102891492 G>A maps to NM_014844.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:102901085 C>T maps to NM_014844.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr14:102904459 G>A maps to NM_014844.3 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:102901143 C>T maps to NM_014844.3 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr14:102894612 C>T maps to NM_014844.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:102843278 T>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:102918872 G>A maps to NM_014844.3 A1183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:14673363 G>T maps to ENST00000436007 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:65147266 G>T maps to NM_001010874.4 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr11:121060495 G>T maps to NM_005422.2 G2092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:120998617 C>T maps to NM_005422.2 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:120976543 G>A maps to NM_005422.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:121031010 C>A maps to NM_005422.2 C1619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr11:121023728 C>T maps to NM_005422.2 N1415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:121008208 C>T maps to NM_005422.2 P1007P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:121008697 C>T maps to NM_005422.2 I1170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:121032948 C>T maps to NM_005422.2 Y1714Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:121023683 C>T maps to NM_005422.2 H1400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:121032804 C>T maps to NM_005422.2 N1666N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:121028716 C>T maps to NM_005422.2 G1491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:121028719 C>T maps to NM_005422.2 G1492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr11:121028593 C>T maps to NM_005422.2 R1450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr11:121008358 C>T maps to NM_005422.2 C1057C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:120980042 C>T maps to NM_005422.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr11:121028791 C>T maps to NM_005422.2 I1516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:120983833 C>A maps to NM_005422.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:121030896 C>T maps to NM_005422.2 I1581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:121028740 C>T maps to NM_005422.2 D1499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:120989265 C>T maps to NM_005422.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:114059254 C>T maps to NM_058222.1 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:114061877 C>T maps to NM_058222.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:182369053 G>A maps to NM_172000.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:41790097 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr22:41783394 C>T maps to ENST00000417325 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:27169568 G>A maps to NM_000459.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:27206597 C>T maps to NM_000459.3 Q795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:27197311 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:27158094 C>T maps to NM_000459.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr9:27169601 G>A maps to NM_000459.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:27209156 G>T maps to NM_000459.3 E872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:27192536 G>T maps to NM_000459.3 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:27209161 G>T maps to NM_000459.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:27157859 G>A maps to NM_000459.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:27158094 C>T maps to NM_000459.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:27228254 A>G maps to NM_000459.3 S1084S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:6718549 G>T maps to NM_053285.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr17:6718540 C>T maps to NM_053285.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:6718498 G>T maps to NM_053285.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr1:36553095 G>T maps to NM_014466.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:15212015 C>T maps to NM_031898.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:15215596 C>T maps to NM_031898.2 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:15207372 G>T maps to NM_031898.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:15215746 G>A maps to NM_031898.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:15231347 G>A maps to NM_031898.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:95540701 C>T maps to NM_144705.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:95539793 C>T maps to NM_144705.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:95539333 C>A maps to NM_144705.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr2:95540688 C>G maps to NM_144705.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:95542384 C>T maps to NM_144705.2 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr16:10769917 C>T maps to NM_144674.1 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:10788643 C>T maps to NM_144674.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:10775896 C>T maps to NM_144674.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr16:10788616 G>T maps to NM_144674.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:1544359 C>A maps to NM_016111.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:1551688 G>T maps to NM_016111.3 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr16:1544375 C>T maps to NM_016111.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:53454216 G>A maps to NM_170754.2 E882E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:53453518 G>A maps to NM_170754.2 A698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:53452203 G>A maps to NM_170754.2 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:53456879 C>T maps to NM_170754.2 S1277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr12:53453101 C>T maps to NM_170754.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:53452834 C>T maps to NM_170754.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:53457539 C>T maps to NM_170754.2 F1368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:53452495 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GM-01A-11W-A062-09 chr14:20846341 C>T maps to NM_007110.4 G1854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:20846233 C>T maps to NM_007110.4 A1890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:20854287 A>G maps to NM_007110.4 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:20874522 C>A maps to NM_007110.4 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:20863769 C>T maps to NM_007110.4 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr14:20853238 C>T maps to NM_007110.4 V1004V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:20863738 T>G maps to NM_007110.4 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr14:20846194 T>C maps to NM_007110.4 G1903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:20836631 G>A maps to NM_007110.4 D2616D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:20863769 C>T maps to NM_007110.4 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:20863769 C>T maps to NM_007110.4 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr14:20841477 G>A maps to NM_007110.4 T2255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:69390812 A>T maps to NM_005652.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:69395373 C>T maps to NM_005652.3 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:75690212 G>T maps to NM_018975.3 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr5:1282722 C>T maps to NM_198253.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:1264628 G>A maps to NM_198253.2 D911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:1264628 G>A maps to NM_198253.2 D911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr5:1272326 C>T maps to NM_198253.2 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:1264589 G>A maps to NM_198253.2 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:1272353 G>A maps to NM_198253.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:1294067 C>T maps to NM_198253.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:115891998 C>T maps to NM_015641.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:115889244 G>A maps to NM_015641.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:117479766 G>A maps to ENST00000392545 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:35609436 C>T maps to NM_006285.2 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:35608986 C>T maps to NM_006285.2 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:45811114 G>T maps to NM_007170.2 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr1:45810619 C>T maps to NM_007170.2 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:70406316 C>T maps to NM_030625.2 F1277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:70332413 C>T maps to NM_030625.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:70404826 G>T maps to NM_030625.2 E781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:70406352 G>T maps to NM_030625.2 T1289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr10:70333858 A>G maps to NM_030625.2 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:70451438 A>G maps to NM_030625.2 E2093E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:70333933 G>A maps to NM_030625.2 K613K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:106156397 A>G maps to ENST00000513237 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:106156728 C>T maps to ENST00000513237 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr4:106157435 T>C maps to ENST00000513237 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:106156730 A>G maps to ENST00000513237 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:106158143 C>T maps to ENST00000513237 S1036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:106155339 G>T maps to ENST00000513237 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr4:106162493 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:106155473 C>T maps to ENST00000513237 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:106196631 G>A maps to ENST00000513237 P1676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:106193806 C>A maps to ENST00000513237 V1444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:106197204 C>A maps to ENST00000513237 V1867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr4:106196433 T>C maps to ENST00000513237 Y1610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:106193806 C>T maps to ENST00000513237 V1444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:106157489 C>T maps to ENST00000513237 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:74273835 G>A maps to ENST00000409262 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:74327610 C>T maps to ENST00000409262 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:74274033 G>A maps to ENST00000409262 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:103082548 C>A maps to NM_017746.3 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:103092329 C>A maps to NM_017746.3 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr9:103072634 A>G maps to NM_017746.3 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr9:103090122 G>A maps to NM_017746.3 R583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:103082672 C>T maps to NM_017746.3 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr9:103109289 C>T maps to NM_017746.3 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:103108518 T>G maps to NM_017746.3 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:43920135 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:43922158 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:69964063 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70072968 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69902669 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:69945139 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70099864 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr23:69945132 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:69773238 G>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69748971 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:69830376 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69826812 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69849511 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69871301 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:69871345 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70073120 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69748985 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69773205 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:69960619 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:70127617 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:70080714 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:70099951 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:69945179 G>A did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:69902637 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GE-01A-11W-A062-09 chr23:104464338 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:104463856 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:104464815 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr23:104464319 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:104463926 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:104464718 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:104463684 G>A did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:107224929 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:107225249 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:107224434 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107225270 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107225308 C>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:107225308 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:107224632 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr17:56676845 G>A maps to ENST00000240361 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:56690781 T>G maps to ENST00000240361 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:56729260 C>T maps to ENST00000240361 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:56665300 C>T maps to ENST00000240361 R892R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:56642287 C>A maps to ENST00000240361 E1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:56679260 G>A maps to ENST00000240361 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr17:56694952 C>T maps to ENST00000240361 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:56634380 C>T maps to ENST00000240361 L1495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:56676431 G>A maps to ENST00000240361 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:56649391 C>A maps to ENST00000240361 E1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr17:56676692 C>T maps to ENST00000240361 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:56649279 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr8:30695219 C>T maps to NM_031271.3 L2477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:30700595 A>G maps to NM_031271.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:30704352 G>A maps to NM_031271.3 N727N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:30700761 G>T maps to NM_031271.3 A1924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:30701193 G>T maps to NM_031271.3 Y1780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:30703724 G>A maps to NM_031271.3 R937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:30694817 G>A maps to NM_031271.3 Y2611Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:30701726 C>A maps to NM_031271.3 E1603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:30700872 G>T maps to NM_031271.3 I1887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr8:30703275 T>C maps to NM_031271.3 L1086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr8:30704676 G>A maps to NM_031271.3 H619H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:30706316 A>G maps to NM_031271.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr17:62290263 C>T maps to NM_018469.3 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:62265638 C>T maps to NM_018469.3 K778K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:62238176 C>A maps to NM_018469.3 E937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:62248511 G>A maps to NM_018469.3 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:62272407 C>T maps to NM_018469.3 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr17:62290758 A>G maps to NM_018469.3 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:71219098 T>C maps to NM_144582.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:51733495 A>G maps to NM_015926.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:56657868 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:56657818 C>T maps to NM_198524.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:56686947 T>C maps to NM_198524.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr15:56681592 T>C maps to NM_198524.1 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:133478169 C>A maps to NM_001063.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:133495891 G>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr3:133467343 T>C maps to NM_001063.3 H44H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:133473406 C>T maps to NM_001063.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr3:133472443 C>T maps to NM_001063.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr10:60145388 C>T maps to NM_003201.1 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:60148512 G>A maps to NM_003201.1 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:10402839 C>T maps to ENST00000379613 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:10410256 C>T maps to ENST00000379613 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:50807984 C>T maps to ENST00000263046 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:50810957 C>T maps to ENST00000263046 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr6:50810966 G>A maps to ENST00000263046 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:50810936 C>T maps to ENST00000263046 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr6:50791172 G>A maps to ENST00000263046 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:55208569 C>T maps to NM_003222.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:55208487 G>A maps to NM_003222.3 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr20:55211801 G>A maps to NM_003222.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:55208589 C>T maps to NM_003222.3 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:55212805 G>T maps to NM_003222.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr6:50681797 C>T maps to NM_172238.3 H10H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:50683082 G>A maps to NM_172238.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:36060126 C>T maps to NM_178548.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:4310141 C>T maps to NM_003223.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:246711867 C>T maps to NM_022366.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr1:246729289 G>A maps to NM_022366.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:51512416 C>T maps to NM_005653.4 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51493438 G>A maps to NM_005653.4 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:51497497 G>A maps to NM_005653.4 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:51501075 T>C maps to NM_005653.4 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:51497986 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:121997138 G>A maps to NM_014553.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:122004482 G>A maps to NM_014553.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr2:122007161 G>A maps to NM_014553.2 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr2:121989413 C>A maps to NM_014553.2 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:114292157 C>T maps to NM_007111.4 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:114277537 G>A maps to NM_007111.4 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:114240087 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:114288275 C>A maps to NM_007111.4 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:114285985 G>T maps to NM_007111.4 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:114290378 C>T maps to NM_007111.4 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:141671838 A>G maps to NM_001178139.1 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:132351800 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:132351307 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:132352095 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:132351977 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:132352179 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:132351296 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:132351445 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:132352253 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:132351527 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:132351502 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:132351157 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:132351104 C>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:132352202 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:48896768 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48887740 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48891262 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48891019 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:48895835 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:48896668 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48891049 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48888961 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48891005 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:41655673 C>T maps to ENST00000343317 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr6:41652341 G>A maps to ENST00000343317 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:115596741 C>A maps to NM_012252.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:115582008 C>A maps to NM_012252.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:43783436 G>T maps to NM_003225.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:43732379 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:100432649 C>T maps to NM_001007565.2 Q41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:100432652 C>T maps to NM_001007565.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:26892855 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:26895165 G>A maps to NM_012143.2 Y411Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:26888020 C>T maps to NM_012143.2 W824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:188343498 C>T maps to NM_001032281.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:188368392 C>A maps to NM_006287.4 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:54611530 C>T maps to NM_013342.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:54618637 C>T maps to NM_013342.3 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:54618049 G>A maps to NM_013342.3 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:100225386 A>G maps to NM_003227.3 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:100238758 C>T maps to NM_003227.3 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:195778839 G>A maps to NM_001128148.1 D752D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:195800925 T>C maps to NM_001128148.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:195787074 C>T maps to NM_001128148.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:195789787 G>A maps to NM_001128148.1 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr8:133899032 T>C maps to NM_003235.4 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:133981784 G>A maps to NM_003235.4 V1982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:133941363 C>T maps to NM_003235.4 F1581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:134042142 G>T maps to NM_003235.4 G2372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:134108592 C>A maps to NM_003235.4 L2516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:133898756 A>G maps to NM_003235.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:133941366 C>T maps to NM_003235.4 D1582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:134145712 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr8:133906148 C>T maps to NM_003235.4 Y992Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:133923647 C>A maps to NM_003235.4 S1343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:133978815 G>T maps to NM_003235.4 E1854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:134145834 C>T maps to NM_003235.4 R2707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:133978942 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:134108556 C>T maps to NM_003235.4 V2504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:133980199 C>T maps to NM_003235.4 L1950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr8:134125685 C>T maps to NM_003235.4 G2531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:133881991 C>T maps to NM_003235.4 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:133953755 C>T maps to NM_003235.4 C1734C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:95243133 G>A maps to NM_014305.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:95246142 G>T maps to NM_014305.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:41850715 G>A maps to NM_000660.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:41848114 G>T maps to NM_000660.4 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:218607764 T>C maps to NM_001135599.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:218520252 C>T maps to NM_001135599.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:218614661 A>G maps to NM_001135599.2 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:76446912 G>A maps to NM_003239.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr14:76446960 G>T maps to NM_003239.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:135385183 G>A maps to NM_000358.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:135398899 G>A maps to NM_000358.2 E679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:135396584 T>C maps to NM_000358.2 N622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:101894905 C>A maps to NM_004612.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:101894794 G>A maps to NM_004612.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:101894983 C>T maps to NM_004612.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:101910041 C>T maps to NM_004612.2 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr9:101891137 G>A maps to NM_004612.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:30686365 C>A maps to NM_001024847.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:30713601 G>T maps to NM_001024847.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr3:30729912 G>A maps to NM_001024847.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:30713623 T>C maps to NM_001024847.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:30691812 G>A maps to NM_001024847.2 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:92181939 G>A maps to NM_003243.4 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:92181885 G>A maps to NM_003243.4 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:92182178 C>T maps to NM_003243.4 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:92177832 C>T maps to NM_003243.4 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:92149340 G>A maps to NM_003243.4 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:92200487 G>T maps to NM_003243.4 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:105924215 A>T maps to NM_004257.4 C181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:105889459 A>G maps to NM_004257.4 Y608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:105897080 G>A maps to NM_004257.4 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:105912956 G>A maps to NM_004257.4 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:105897131 C>G maps to NM_004257.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:105890144 G>A maps to NM_004257.4 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:105892094 G>A maps to NM_004257.4 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:3457580 G>A maps to NM_170695.2 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr18:3451994 C>T maps to NM_170695.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:35219734 G>A maps to NM_021809.6 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr20:35219566 G>A maps to NM_021809.6 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:89177146 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:89177329 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:89177570 C>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:89177194 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:89177282 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:89177397 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:89177720 G>A did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:89177503 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:89177300 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:89177194 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:24727594 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:24729893 G>T maps to NM_000359.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:24724454 T>C maps to NM_000359.2 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr14:24731012 G>A maps to NM_000359.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:36767991 G>A maps to NM_004613.2 Y388Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:36766731 G>A maps to NM_004613.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:36758680 G>A maps to NM_004613.2 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:36767874 G>A maps to NM_004613.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:36767964 G>T maps to NM_004613.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr20:2290953 C>T maps to NM_003245.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:2291016 T>G maps to NM_003245.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:2293647 C>T maps to NM_003245.3 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:2308829 C>T maps to NM_003245.3 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:2315786 G>A maps to NM_003245.3 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:2293647 C>T maps to NM_003245.3 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:44943134 G>A maps to NM_003241.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:44948450 C>A maps to NM_003241.3 C362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:44951828 C>T maps to NM_003241.3 D525D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:44935129 C>T maps to NM_003241.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:43552322 G>A maps to NM_201631.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr15:43545071 G>A maps to NM_201631.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr20:2375999 G>C maps to NM_198994.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:2397926 C>T maps to NM_198994.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr20:2380982 C>T maps to NM_198994.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr20:2375960 C>T maps to NM_198994.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:43574123 A>G maps to NM_052955.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:85553824 C>A maps to ENST00000409015 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:85553824 C>A maps to ENST00000409015 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr8:56723559 T>A maps to NM_024831.6 L755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:56723455 C>T maps to NM_024831.6 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:56711750 G>A maps to NM_024831.6 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:56699353 T>C maps to NM_024831.6 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr8:56723455 C>T maps to NM_024831.6 I720I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:56717539 C>T maps to NM_024831.6 D696D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:2186478 G>A maps to NM_199292.2 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:57565010 C>T maps to NM_198976.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr20:57568580 G>A maps to NM_198976.1 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:57564969 C>T maps to NM_198976.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:57566976 G>A maps to NM_198976.1 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:43519310 C>T maps to ENST00000330266 T1624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:43776469 A>G maps to ENST00000330266 I996I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:43520074 G>T maps to ENST00000330266 A1573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:43514104 G>A maps to ENST00000330266 V1703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr2:43520116 T>C maps to ENST00000330266 S1559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:43520308 G>T maps to ENST00000330266 I1495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr2:43547621 A>G maps to ENST00000330266 T1468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:42693241 G>A maps to NM_018105.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr16:67876889 C>T maps to NM_020457.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:76452234 C>T maps to NM_144721.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:36530434 C>T maps to NM_152658.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:83827661 C>T maps to NM_024672.4 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:83828980 C>T maps to NM_024672.4 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:83838841 T>C maps to NM_024672.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:83838831 A>G maps to NM_024672.4 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr20:23028479 G>A maps to NM_000361.2 C554C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr20:23028509 G>A maps to NM_000361.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr20:23029301 G>A maps to NM_000361.2 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:39874865 C>T maps to NM_003246.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:39885688 C>T maps to NM_003246.2 Y1029Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:39874805 G>A maps to NM_003246.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr15:39880844 C>T maps to NM_003246.2 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr15:39881286 G>A maps to NM_003246.2 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr15:39881530 C>T maps to NM_003246.2 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:39879644 C>T maps to NM_003246.2 C406C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:39881172 C>T maps to NM_003246.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:39874865 C>T maps to NM_003246.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr15:39886398 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr6:169632152 G>A maps to NM_003247.2 C691C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:169628244 G>A maps to NM_003247.2 D797D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:169622309 C>T maps to NM_003247.2 T1085T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:169632164 G>A maps to NM_003247.2 D687D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:169639736 A>G maps to NM_003247.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr6:169648853 C>T maps to NM_003247.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:169641907 G>T maps to NM_003247.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:169620331 C>A maps to NM_003247.2 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr6:169632140 C>T maps to NM_003247.2 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:155168317 G>A maps to NM_007112.3 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:155166925 G>A maps to NM_007112.3 R860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:155167412 G>T maps to NM_007112.3 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:155168003 G>A maps to NM_007112.3 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:79366160 C>A maps to NM_003248.4 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:79369115 C>T maps to NM_003248.4 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:79373935 C>T maps to NM_003248.4 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:79335931 C>T maps to NM_003248.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr5:79355622 A>G maps to NM_003248.4 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:151867529 T>C maps to NM_053055.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:151823622 C>A maps to NM_182578.3 G124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:151820271 A>C maps to NM_182578.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:151824844 C>A maps to NM_182578.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:128221984 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:128176235 A>G maps to NM_001164685.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr6:128150750 A>G maps to NM_001164685.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:128040908 T>C maps to NM_001164685.1 K645K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:128031161 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:128150890 C>A maps to NM_001164685.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:128135073 G>A maps to NM_001164685.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:25313574 C>T maps to NM_024838.4 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:25314188 A>G maps to NM_024838.4 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:25313396 T>C maps to NM_024838.4 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:25312580 G>A maps to NM_024838.4 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr10:25313606 C>T maps to NM_024838.4 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:25312196 G>A maps to NM_024838.4 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:88478332 G>A maps to NM_018271.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:88474906 A>G maps to NM_018271.3 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:88478458 G>A maps to NM_018271.3 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:88474233 C>T maps to NM_018271.3 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr18:216590 T>C maps to NM_005131.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:214667 G>A maps to NM_005131.2 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:214787 A>G maps to NM_005131.2 C604C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr18:216485 C>T maps to NM_005131.2 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:122774406 T>C did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:122801076 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:122801065 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:122747904 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:122755242 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:122769938 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:122805547 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:122829894 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:122846750 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:122754800 T>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:122757099 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:122772815 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:122755400 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:122754769 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:122747502 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:122755260 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:122820527 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:122866844 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:122765551 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:122866863 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:122759782 T>C did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:122747261 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:122756958 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:122765612 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:122766756 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:122820467 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:122799587 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:122753329 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:122755355 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:122802017 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:122758036 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:122759916 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:122778707 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:122866864 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:122756976 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr23:122760502 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr23:122866805 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:122778701 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:122837348 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:122747526 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:122765607 A>G did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:122760482 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:122820443 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:122846744 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:122866867 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:122747997 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:122758450 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:122758464 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:122779198 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:175392018 G>T maps to NM_032361.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:175387052 G>T maps to NM_032361.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:29916089 G>A maps to NM_003678.4 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:29925218 A>C maps to NM_003678.4 L286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr22:29907221 G>A maps to NM_003678.4 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:29927940 C>T maps to NM_003678.4 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:29945093 G>A maps to NM_003678.4 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:3077603 C>T maps to NM_024339.3 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:2796122 C>T maps to NM_003249.3 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:2794855 C>T maps to NM_003249.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:2807527 C>G maps to NM_003249.3 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:2794855 C>T maps to NM_003249.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:2810360 G>A maps to NM_003249.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:184090714 A>C maps to NM_000460.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:184090546 C>A maps to NM_000460.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38244583 C>T maps to NM_003250.5 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:38233854 C>T maps to NM_003250.5 G72G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr1:36754756 T>G maps to NM_005119.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:36752569 C>T maps to NM_005119.3 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:36762297 C>T maps to NM_005119.3 R744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:36752490 G>A maps to NM_005119.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:36762368 G>A maps to NM_005119.3 Q767Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:24185132 T>C maps to NM_001128177.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:24231724 G>A maps to NM_001128177.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:24164383 G>A maps to NM_001128177.1 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr3:24206734 G>A maps to ENST00000280696 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:24164383 G>A maps to NM_001128177.1 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:24231769 G>A maps to NM_001128177.1 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr3:24231703 C>T maps to NM_001128177.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:52952841 G>T maps to NM_018676.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:52952006 G>A maps to NM_018676.3 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:52951752 G>A maps to NM_018676.3 Y784Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:72020942 A>G maps to NM_024817.2 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:72030269 G>A maps to NM_024817.2 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:71952942 G>A maps to NM_024817.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:71952960 G>A maps to NM_024817.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:11514153 G>T maps to ENST00000423059 R687R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:11675992 G>A maps to ENST00000423059 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr7:11509563 C>T maps to ENST00000423059 K770K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:11446670 G>T maps to ENST00000423059 R1310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr7:11676148 G>A maps to ENST00000423059 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:11501635 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:11418730 C>A maps to ENST00000423059 R1589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:11501651 C>T maps to ENST00000423059 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:11676109 C>T maps to ENST00000423059 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:11485859 T>C maps to ENST00000423059 Q964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:11446978 A>C maps to ENST00000423059 S1290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:137852565 G>A maps to ENST00000272643 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:138434153 C>T maps to ENST00000272643 Y1603Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:137917795 G>T maps to ENST00000272643 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:137917849 C>A maps to ENST00000272643 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:138425348 C>T maps to ENST00000272643 R1556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:137928429 G>T maps to ENST00000272643 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:138169354 G>T maps to ENST00000272643 E958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:137814621 G>T maps to ENST00000272643 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:138400059 C>T maps to ENST00000272643 R1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:138413144 A>G maps to ENST00000272643 A1343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:138163336 G>A maps to ENST00000272643 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:24026148 A>G maps to NM_024328.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr14:24028254 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:20748275 C>A maps to ENST00000431224 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:20750267 T>C maps to ENST00000431224 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:20748261 T>C maps to ENST00000431224 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:20749050 C>A maps to ENST00000431224 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:20750320 C>A maps to ENST00000431224 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:39963964 G>T maps to NM_025264.4 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:39997095 G>T maps to NM_025264.4 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:39996894 T>C maps to NM_025264.4 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:9413064 G>T maps to NM_015453.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:9426218 A>G maps to NM_015453.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:134118766 A>G maps to NM_199298.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:134121167 C>T maps to NM_199298.1 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr2:70444096 A>T maps to NM_022173.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:121337030 C>T maps to NM_001033925.1 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:121338346 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:121336537 T>G maps to ENST00000369092 *266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:121336584 G>A maps to ENST00000369092 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:121339476 G>A maps to NM_001033925.1 G156G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D1-A17Q-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr21:32526570 G>A maps to NM_003253.2 Y1055Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr21:32595760 G>A maps to NM_003253.2 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr21:32639165 G>A maps to NM_003253.2 H41H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:32513670 C>T maps to NM_003253.2 A1209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:32525452 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:32575328 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr21:32598203 C>T maps to NM_003253.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:32624091 C>T maps to NM_003253.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:32598194 C>T maps to NM_003253.2 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr21:32519249 G>A maps to NM_003253.2 C1146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr21:32575276 C>A maps to NM_003253.2 E814*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BG-A187-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:32624385 T>C maps to NM_003253.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr21:32502548 G>A maps to NM_003253.2 R1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:155572087 G>A maps to ENST00000456144 T1360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:155503405 G>A maps to ENST00000456144 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr6:155500211 C>T maps to ENST00000456144 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:155575143 G>A maps to ENST00000456144 T1450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:155574086 G>A maps to ENST00000456144 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:155577855 C>T maps to ENST00000456144 S1598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:155485640 G>A maps to ENST00000456144 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:155504464 C>T maps to ENST00000456144 S965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:155574086 G>A maps to ENST00000456144 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:155497987 C>T maps to ENST00000456144 D800D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:155575143 G>A maps to ENST00000456144 T1450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr6:155451421 C>A maps to ENST00000456144 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:155485574 G>A maps to ENST00000456144 E685E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:155574086 G>A maps to ENST00000456144 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr6:155485664 C>T maps to ENST00000456144 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr6:155577786 C>A maps to ENST00000456144 P1575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:4817882 C>T maps to NM_182919.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr19:4817186 G>A maps to NM_182919.2 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:4817252 G>T maps to NM_182919.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:4817924 G>T maps to NM_182919.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:4816573 G>A maps to NM_182919.2 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:43785164 C>T maps to NM_005424.2 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:43775180 G>A maps to NM_005424.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:43777991 G>A maps to NM_005424.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:43777408 G>A maps to NM_005424.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr1:43779578 G>T maps to NM_005424.2 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:43775102 C>T maps to NM_005424.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr1:43774786 C>T maps to NM_005424.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:43775102 C>T maps to NM_005424.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:43775102 C>T maps to NM_005424.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:113199268 C>A maps to NM_052864.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:134785248 G>T maps to NM_001099221.1 C127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:90034220 C>T maps to NM_145715.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr11:65124580 C>T maps to NM_145719.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:65123308 C>T maps to NM_145719.2 H10H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:65123971 G>A maps to NM_145719.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:153691165 G>A maps to NM_145720.2 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:153691000 C>A maps to NM_145720.2 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:153690842 G>T maps to NM_145720.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:153692075 G>A maps to NM_145720.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr4:153691273 C>A maps to NM_145720.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:149374430 A>C maps to NM_030953.2 L494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:149375386 G>T maps to NM_030953.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr16:3349600 G>A maps to NM_033208.3 C338C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr16:3350354 C>T maps to NM_033208.3 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:3350314 G>A maps to NM_033208.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:3350145 G>A maps to NM_033208.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr16:3349102 C>T maps to NM_033208.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:114014579 C>T maps to ENST00000481065 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:156349122 C>T maps to NM_138379.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:156381482 C>A maps to NM_138379.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr5:156349115 G>A maps to NM_138379.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:56826188 A>G maps to NM_003920.3 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:56826247 G>A maps to NM_003920.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:56817596 G>T maps to NM_003920.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:56811535 C>T maps to NM_003920.3 K1197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:56824035 C>T maps to NM_003920.3 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:56817452 C>A maps to NM_003920.3 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:57297605 G>A maps to NM_012456.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48752377 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48754112 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48754132 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:48751500 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:902016 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:8006004 C>T maps to NM_006351.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:7992101 G>A maps to NM_006351.3 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:8002997 C>A maps to NM_006351.3 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:8002911 G>A maps to NM_006351.3 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:8002914 T>C maps to NM_006351.3 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:7998858 G>A maps to NM_006351.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:39979212 C>T maps to NM_001001563.1 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100603561 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr23:100601555 C>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:111957366 T>C maps to NM_012459.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47444914 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:47442934 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:47444663 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:47444622 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr17:76853711 G>A maps to NM_003255.4 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:76851838 G>A maps to NM_003255.4 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr17:76851760 G>A maps to NM_003255.4 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:76851838 G>A maps to NM_003255.4 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr22:33254031 G>A maps to NM_000362.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:33253241 C>T maps to NM_000362.4 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr22:33255313 C>T maps to NM_000362.4 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:12198386 C>T maps to NM_003256.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:54245350 G>A maps to NM_014464.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:54219384 G>T maps to NM_014464.3 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K7-01A-11W-A10C-09 chr6:54173503 C>T maps to NM_014464.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr6:54214693 C>T maps to NM_014464.3 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:24710453 A>G maps to NM_001099274.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:24710322 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:24709014 A>G maps to NM_001099274.1 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:24711188 C>T maps to NM_001099274.1 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:156396355 A>G maps to NM_015508.4 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:66633691 C>A maps to NM_017858.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:66641442 G>A maps to NM_017858.2 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:168169271 A>G maps to NM_152902.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:126160800 G>A maps to NM_148910.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:43470038 G>A maps to NM_001146016.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr15:30065520 G>A maps to NM_003257.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:30010867 G>A maps to NM_003257.3 Q1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:30011998 C>T maps to NM_003257.3 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:29997786 G>A maps to NM_003257.3 I1671I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:30054557 C>A maps to NM_003257.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:71863034 G>A maps to NM_004817.3 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:71867732 C>T maps to NM_004817.3 I1108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:71831253 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:71867816 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:71869250 C>T maps to NM_004817.3 Y1178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:71840305 G>T maps to NM_004817.3 G347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:71855005 C>T maps to NM_004817.3 R837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:71827471 C>T maps to NM_004817.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:71789297 C>T maps to NM_004817.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:3733785 C>T maps to NM_014428.1 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3743952 G>A maps to NM_014428.1 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:3736243 C>T maps to NM_014428.1 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr19:3743958 G>A maps to NM_014428.1 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr19:3728709 C>T maps to NM_014428.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr19:3736177 G>A maps to NM_014428.1 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:76170992 C>T maps to NM_003258.4 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:66582906 C>A maps to ENST00000299697 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:66545927 G>T maps to ENST00000299697 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:53259822 G>A maps to ENST00000423516 I615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:53269000 G>A maps to ENST00000423516 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:153556271 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153555944 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr23:153557962 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153524306 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153549115 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr23:153533706 C>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:153553700 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:153524337 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:153543542 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:153539320 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:153556198 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:153539310 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:153533756 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:164393511 C>A maps to NM_032136.4 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:164393962 G>T maps to NM_032136.4 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:164394409 G>T maps to NM_032136.4 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:164394543 G>A maps to NM_032136.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr4:164394295 C>T maps to NM_032136.4 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:27051659 G>A maps to NM_138463.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr9:84202634 G>A maps to NM_005077.3 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:84200567 G>T maps to NM_005077.3 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:84230907 C>A maps to NM_005077.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr9:84202673 C>A maps to NM_005077.3 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:84199126 C>A maps to NM_005077.3 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:84230907 C>A maps to NM_005077.3 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:3005536 G>A maps to NM_003260.4 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:3002501 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:3006492 G>A maps to NM_003260.4 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr15:70351091 G>A maps to NM_005078.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:70366928 C>T maps to NM_005078.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:70349823 G>A maps to NM_005078.2 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:70368485 C>T maps to NM_005078.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr15:70347576 G>A maps to NM_005078.2 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr15:70344791 C>T maps to NM_005078.2 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:82242326 G>A maps to ENST00000376537 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:82335193 C>T maps to ENST00000376537 N640N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:82337457 C>T maps to ENST00000376537 D725D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:82319750 C>T maps to ENST00000376537 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:82322052 A>T maps to ENST00000376537 K318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:82324603 G>T maps to ENST00000376537 G476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:82324560 C>T maps to ENST00000376537 H461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:82321802 G>T maps to ENST00000376537 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:82339957 G>T maps to ENST00000376537 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:82337463 C>T maps to ENST00000376537 Y727Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr9:82323670 T>C maps to ENST00000376537 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr9:82323613 C>A maps to ENST00000376537 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr9:82334974 C>T maps to ENST00000376537 Y567Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:2994929 C>T maps to NM_001143986.1 D549D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:171906620 G>A maps to ENST00000360843 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:171911591 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:171939298 C>A maps to ENST00000360843 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:60685475 C>T maps to ENST00000326270 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:60678134 C>A maps to ENST00000326270 Y580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:60601664 G>A maps to ENST00000326270 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:60683574 C>A maps to ENST00000326270 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:60637439 C>T maps to ENST00000326270 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:166996042 C>A maps to ENST00000507499 C757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:166976415 T>C maps to ENST00000507499 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:166999139 C>A maps to ENST00000507499 C823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:166999134 G>T maps to ENST00000507499 E822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:167012354 G>T maps to ENST00000507499 E863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr4:166795121 C>T maps to ENST00000507499 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:167012312 G>T maps to ENST00000507499 E849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:98155109 G>A maps to NM_012465.3 D520D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:98138841 G>A maps to NM_012465.3 D734D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:98146740 G>A maps to NM_012465.3 Y607Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:98133428 G>A maps to NM_012465.3 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:98188386 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:98146749 G>A maps to NM_012465.3 D604D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:98155127 G>A maps to NM_012465.3 H514H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:35721733 G>A maps to NM_006289.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35708403 G>T maps to NM_006289.3 A1468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35720092 G>T maps to NM_006289.3 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35724323 C>T maps to NM_006289.3 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr9:35706497 A>G maps to NM_006289.3 I1713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr9:35703882 G>A maps to NM_006289.3 N2082N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:62989988 C>A maps to NM_015059.2 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:63132748 C>T maps to NM_015059.2 A2523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:63058557 C>T maps to NM_015059.2 I1711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:63111768 C>T maps to NM_015059.2 R2276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:63125776 C>T maps to NM_015059.2 A2359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:63125737 C>A maps to NM_015059.2 I2346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:63008649 C>T maps to NM_015059.2 R919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:63111779 C>T maps to NM_015059.2 G2279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:63000912 C>T maps to NM_015059.2 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:63000912 C>T maps to NM_015059.2 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:63112736 A>G maps to NM_015059.2 L2310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr15:63084880 C>T maps to NM_015059.2 H1926H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:63045973 T>G maps to NM_015059.2 A1445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:63084958 C>T maps to NM_015059.2 I1952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:62942307 G>A maps to NM_015059.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:38799486 G>T maps to NM_003263.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:38775960 G>T maps to NM_030956.3 C417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:38776254 G>T maps to NM_030956.3 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:38774897 G>A maps to NM_030956.3 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:38775003 A>C maps to NM_030956.3 Y736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:38775803 C>A maps to NM_030956.3 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:154625499 G>T maps to NM_003264.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:154626023 G>C maps to NM_003264.3 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:154625597 G>A maps to NM_003264.3 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:154625225 A>G maps to NM_003264.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr4:187004555 C>T maps to NM_003265.2 N572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:187005910 C>T maps to NM_003265.2 R867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:187005014 T>C maps to NM_003265.2 F725F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:120475722 G>A maps to NM_138554.3 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:120475854 C>T maps to NM_138554.3 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr9:120475395 C>T maps to NM_138554.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:120475110 T>C maps to NM_138554.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:120475078 G>T maps to NM_138554.3 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:120475264 G>T maps to NM_138554.3 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:120475411 G>T maps to NM_138554.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:120475165 G>T maps to NM_138554.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:120475189 G>T maps to NM_138554.3 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:223283949 G>T maps to NM_003268.5 G808G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr1:223284894 G>T maps to NM_003268.5 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:38830587 C>T maps to NM_006068.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:38829615 G>A maps to NM_006068.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:38829479 C>A maps to NM_006068.3 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:38829729 A>C maps to NM_006068.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr4:38830078 G>T maps to NM_006068.3 S339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:12904753 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:12905852 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12904311 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12906104 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr23:12906682 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:12904320 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:12905567 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:12905970 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:12906097 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:12903908 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:12904018 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:12904868 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr23:12903908 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:12904320 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:12906389 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:12904695 C>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:12906270 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:12904830 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:12905208 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:12906408 C>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:12906582 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:12904182 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:12937666 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:12938141 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:12938452 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:12937793 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:12939356 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12937513 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12937762 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:12939862 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:12938852 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:12937522 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:12938992 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:12938453 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr23:12937828 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:12939564 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:12939224 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:12937647 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:12938182 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:12928543 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:12937920 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:12937926 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:12939988 T>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:12938464 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr3:52256365 G>A maps to ENST00000494383 Q809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:102893930 G>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:102893974 G>A maps to NM_005521.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:62190630 T>C maps to ENST00000371180 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:38851085 G>A maps to NM_031940.3 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr15:102182729 G>C maps to NM_078474.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:149040144 G>T maps to NM_138786.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:196053825 G>A maps to NM_138461.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:196050846 C>T maps to NM_138461.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:228243813 T>C maps to NM_024795.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:228243843 G>A maps to NM_024795.3 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:228243972 G>A maps to NM_024795.3 C4C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:4685922 C>T maps to NM_003963.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:4685826 C>T maps to NM_003963.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:4685934 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:4685922 C>T maps to NM_003963.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:83788337 G>A maps to NM_023003.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:19381140 G>A maps to ENST00000431465 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:64883422 C>T maps to NM_003273.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VV-01A-21D-A122-09 chr11:64881059 C>T maps to NM_003273.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:27128567 G>T maps to NM_016551.2 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:27132786 C>T maps to NM_016551.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:27133579 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:105360962 C>T maps to NM_030788.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:105361100 C>A maps to NM_030788.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr13:100153988 C>T maps to NM_004800.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:100196131 G>T maps to NM_004800.1 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:100169876 G>T maps to NM_004800.1 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:100191807 C>T maps to NM_004800.1 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:100196131 G>T maps to NM_004800.1 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr13:100193881 G>A maps to NM_004800.1 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:100206575 C>T maps to NM_004800.1 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:98287918 C>T maps to NM_020123.3 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:98287855 C>T maps to NM_020123.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:30745676 C>T maps to NM_014742.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:30730876 C>T maps to NM_014742.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:219143251 G>T maps to NM_022152.4 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:75435880 T>G maps to NM_138691.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:75404157 C>A maps to NM_138691.2 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:75309556 G>T maps to NM_138691.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:75431093 C>T maps to NM_138691.2 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:2572972 C>A maps to NM_080751.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:2582850 C>A maps to NM_080751.2 C439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:2593856 G>A maps to NM_080751.2 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:2591072 C>T maps to NM_080751.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr20:2539270 G>T maps to NM_080751.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:2604934 C>T maps to NM_080751.2 Y733Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:2597813 C>T maps to NM_080751.2 N679N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:2591237 C>T maps to NM_080751.2 H529H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:2552834 G>T maps to NM_080751.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:81625388 C>A maps to ENST00000454937 E895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:81633819 G>A maps to ENST00000454937 N585N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr15:81625493 G>A maps to ENST00000454937 R860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:81630993 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:81651764 A>G maps to ENST00000454937 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:81666409 G>T maps to ENST00000454937 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:81625493 G>A maps to ENST00000454937 R860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr15:81625551 C>T maps to ENST00000454937 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr15:81624960 G>A maps to ENST00000454937 F1037F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:81637210 C>A maps to ENST00000454937 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:81644067 C>T maps to ENST00000454937 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:54675766 C>T maps to NM_001145303.1 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr19:54666488 G>A maps to NM_001145303.1 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr19:54675820 C>T maps to NM_001145303.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:19451881 A>G maps to NM_001105248.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:19488818 C>A maps to NM_001105248.1 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:19451953 C>T maps to NM_001105248.1 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:19509267 G>T maps to NM_001105248.1 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:19503513 G>A maps to NM_001105248.1 K930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:19468325 G>T maps to NM_024780.4 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:76120197 C>T maps to NM_007267.6 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:19020668 C>T maps to NM_024847.3 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:19047039 G>A maps to NM_024847.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:19056742 C>T maps to NM_024847.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr16:19058552 C>A maps to NM_024847.3 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr3:129547007 G>A maps to NM_001017395.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:129373846 G>A maps to NM_001017395.3 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:205238991 C>T maps to NM_014858.3 C554C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:205241233 C>T maps to NM_014858.3 H704H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:205238499 C>T maps to NM_014858.3 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:205210655 C>A maps to NM_014858.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:205241026 G>A maps to NM_014858.3 E635E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:205241215 C>T maps to NM_014858.3 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:205241128 G>A maps to NM_014858.3 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:94965345 C>T maps to NM_020698.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:165721402 G>A maps to NM_019026.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:40713881 C>T maps to NM_001008740.3 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:114149956 C>T maps to NM_017905.4 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr13:114149929 C>T maps to NM_017905.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:114164578 G>A maps to NM_017905.4 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:114152665 G>T maps to NM_017905.4 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:114157837 G>T maps to NM_017905.4 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:20067309 G>A maps to NM_181719.4 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr1:20107209 C>T maps to NM_181719.4 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:20073668 G>A maps to NM_181719.4 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:38235575 G>T maps to NM_152453.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:38229563 G>A maps to NM_152453.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr16:68961562 C>T maps to NM_024562.1 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:68894336 C>A maps to NM_024562.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr16:68894117 G>A maps to NM_024562.1 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:68936243 G>T maps to NM_024562.1 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr16:68943226 G>A maps to NM_024562.1 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:10945960 G>A maps to NM_006858.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:75602546 G>A maps to NM_006827.5 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:124071421 A>T maps to NM_006815.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:124071335 G>T maps to NM_006815.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr7:44620697 G>A maps to NM_182547.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:93645688 G>T maps to NM_016040.4 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:93645609 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:77810127 G>A maps to NM_213601.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr14:77808155 C>T maps to NM_213601.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:192922424 G>A maps to NM_016192.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:53798371 C>T maps to NM_001099640.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:42091871 G>A maps to NM_032376.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:42089472 G>A maps to NM_032376.2 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:72832786 C>T maps to NM_017728.3 F484F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:72791202 C>T maps to NM_017728.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:72832144 C>T maps to NM_017728.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:41369771 C>T maps to NM_145041.1 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:12270055 T>C maps to NM_018374.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:12269342 C>T maps to NM_018374.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:48358168 C>A maps to NM_001143842.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr17:8079526 G>A maps to NM_032354.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:8077884 G>A maps to NM_032354.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:133114803 G>T maps to NM_001136469.1 G568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:133099121 C>T maps to NM_001136469.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:133099643 C>T maps to NM_001136469.1 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:60689492 C>T maps to NM_024092.2 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:60687344 T>C maps to NM_024092.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr17:21101963 C>T maps to NM_003876.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:52877754 G>A maps to ENST00000504329 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:52878928 G>A maps to ENST00000504329 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:112374573 T>C maps to NM_001193531.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr12:112369574 C>T maps to NM_001193531.1 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:44238574 G>T maps to NM_032256.1 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:44770475 C>A maps to NM_032256.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:44781911 C>T maps to NM_032256.1 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:44537327 A>T maps to NM_032256.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr12:122181539 G>A maps to NM_001080825.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:122186261 G>A maps to NM_001080825.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:102272683 G>A maps to NM_052932.2 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:43738575 C>T maps to NM_144626.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:85342820 G>T maps to NM_018480.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:4242175 A>G maps to ENST00000382753 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:1719964 C>T maps to NM_001127266.1 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:98460979 C>T maps to NM_001134450.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:98461021 G>A maps to NM_001134450.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:98413865 T>G maps to NM_015348.1 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:98422096 G>A maps to NM_015348.1 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:98419240 T>A maps to NM_015348.1 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:98429101 C>T maps to NM_015348.1 E576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:98504583 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr2:98375418 C>T maps to NM_015348.1 S1768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:98378622 G>A maps to NM_015348.1 N1588N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:98409379 G>A maps to NM_015348.1 R1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:98543923 C>A maps to NM_015348.1 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:98430748 C>T maps to NM_015348.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:98413337 G>T maps to NM_015348.1 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:98431765 C>T maps to NM_015348.1 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:98413913 T>C maps to NM_015348.1 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:98375489 G>A maps to NM_015348.1 R1745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:60703355 G>A maps to NM_017870.3 W684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:60695120 C>T maps to NM_017870.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:125834586 G>T maps to NM_052907.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:126139040 G>T maps to NM_052907.2 E1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:126138775 C>T maps to NM_052907.2 C919C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:125834064 G>A maps to NM_052907.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:126138875 G>T maps to NM_052907.2 E953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr12:125834403 G>A maps to NM_052907.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:126138736 C>T maps to NM_052907.2 C906C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr12:129566528 G>A maps to NM_133448.2 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr12:130184851 G>A maps to NM_133448.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:129822312 C>A maps to NM_133448.2 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:129558524 G>A maps to NM_133448.2 I1065I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:129559214 C>T maps to NM_133448.2 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:130184914 G>A maps to NM_133448.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CA-01A-21D-A122-09 chr12:130184851 G>A maps to NM_133448.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:129559340 G>T maps to NM_133448.2 I793I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:32964707 G>A maps to NM_207313.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:32961901 G>A maps to NM_207313.1 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:32953314 C>T maps to NM_207313.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:32959769 A>C maps to NM_207313.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:32959865 G>A maps to NM_207313.1 E452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:32959781 C>T maps to NM_207313.1 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:32964530 C>T maps to NM_207313.1 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:32959784 C>T maps to NM_207313.1 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr17:32962027 G>T maps to NM_207313.1 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:100863099 G>T maps to NM_032021.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:87024513 A>G maps to NM_022918.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:87020587 C>T maps to NM_022918.3 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr11:120201040 C>A maps to NM_001198670.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:61131867 C>A maps to NM_016464.4 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr11:61135510 A>G maps to ENST00000451389 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:142983088 G>A maps to NM_153345.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:142983852 C>T maps to NM_153345.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:48845965 G>A maps to NM_018273.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:159134019 T>C maps to ENST00000509278 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:159158769 T>C maps to NM_018342.4 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:42819143 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:42821974 C>T maps to ENST00000406159 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:42818841 C>T maps to ENST00000406159 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:42818847 T>C maps to ENST00000406159 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr19:36037641 C>T maps to NM_032635.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:36036825 T>A maps to NM_032635.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:52546668 T>G maps to NM_014051.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:10751369 C>T maps to NM_030969.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:10755513 G>A maps to ENST00000475942 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:85828165 G>A maps to NM_001031738.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr2:85826689 G>A maps to NM_001031738.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:55828313 C>T maps to NM_001085488.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:55831430 G>A maps to NM_001085488.1 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:122681517 T>C maps to NM_152399.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:122682792 C>A maps to NM_152399.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:21181816 C>A maps to ENST00000451578 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:21190855 C>T maps to ENST00000451578 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19230786 G>A maps to NM_017814.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19232371 C>A maps to NM_017814.1 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:87536730 A>G maps to NM_153354.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:135308199 C>T maps to NM_030923.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr23:109247076 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:109310615 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:109414696 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:109416478 G>A did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:109247173 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:109352369 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:109416525 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:56290757 A>G maps to NM_018475.3 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:82360897 G>T maps to NM_174909.4 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:109635643 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:216964916 C>T maps to NM_138390.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr2:216964916 C>T maps to NM_138390.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:62729640 A>G maps to NM_198276.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr16:75481527 G>T maps to NM_145254.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:72419637 C>T maps to NM_173490.6 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:72419331 C>T maps to NM_173490.6 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr5:72419442 G>A maps to NM_173490.6 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:138860462 G>A maps to NM_198282.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr5:138860414 T>C maps to NM_198282.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:72469591 C>T maps to NM_153217.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:945495 G>A maps to NM_032326.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:949224 C>T maps to NM_032326.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:947066 C>T maps to NM_032326.2 H184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr4:949245 C>G maps to NM_032326.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:951743 C>T maps to NM_032326.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:941902 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:150499322 G>T maps to NM_018487.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:150499361 C>T maps to NM_018487.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:39931276 C>T maps to NM_152390.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr2:39931239 G>A maps to NM_152390.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:39944195 G>A maps to NM_152390.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:39934243 C>T maps to NM_152390.2 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr14:105061516 C>T maps to NM_207379.1 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:62556622 C>T maps to NM_199337.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:104229790 C>T maps to NM_024789.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:159046768 C>T maps to NM_020823.1 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:159046206 G>A maps to NM_020823.1 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:159006375 C>T maps to NM_020823.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:103379069 G>T maps to NM_144632.3 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:149700725 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:149700262 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:149700177 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:1590605 G>A maps to NM_001097620.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:148690440 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:148693024 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:148685708 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:148690421 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:153247675 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153247539 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:153248130 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153247596 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:153248165 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:72091247 G>T maps to NM_018279.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:55889375 C>T maps to NM_139172.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:55889417 G>A maps to NM_139172.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:166024248 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:57454667 A>T maps to NM_001130963.1 Y347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr12:57472498 C>T maps to NM_001130963.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr12:57464672 G>A maps to NM_001130963.1 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:57464565 T>C maps to NM_001130963.1 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:220412328 C>T maps to NM_001005209.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:26686379 C>T maps to ENST00000457710 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:26687821 C>T maps to ENST00000457710 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:74345692 T>C maps to NM_013390.2 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:74319524 G>A maps to NM_013390.2 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:74349721 C>A maps to NM_013390.2 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr9:74360367 C>T maps to NM_013390.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:74365097 A>G maps to NM_013390.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr9:74313083 C>T maps to NM_013390.2 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr6:130762334 C>T maps to NM_052913.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:130762055 C>A maps to NM_052913.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:130762227 C>T maps to NM_052913.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:130762883 G>A maps to NM_052913.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:130762227 C>T maps to NM_052913.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:29447737 C>T maps to NM_001003682.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:9661203 G>T maps to NM_001130924.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:9670756 G>A maps to NM_001130924.2 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:72700067 C>A maps to NM_001080462.1 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:72691085 G>A maps to NM_001080462.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:72700112 C>A maps to NM_001080462.1 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:72691085 G>A maps to NM_001080462.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:1604999 C>T maps to NM_024600.4 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:11453733 G>A maps to NM_198536.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr3:190167525 G>A maps to NM_207316.1 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:67262735 G>A maps to NM_014187.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:129832633 A>G maps to NM_032842.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:25331326 G>T maps to ENST00000423535 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:25334188 A>C maps to ENST00000423535 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr7:138487708 C>A maps to ENST00000422794 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27259585 C>A maps to NM_017727.4 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27259971 C>T maps to NM_017727.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:27261982 C>T maps to NM_017727.4 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:32784342 C>A maps to NM_212558.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr9:32784471 C>A maps to NM_212558.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:32784795 C>T maps to NM_212558.2 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:37186605 G>A maps to NM_145316.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:124971135 C>T maps to NM_001080546.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:27657273 C>T maps to NM_032125.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:62558181 T>C maps to NM_001080501.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62558183 G>A maps to NM_001080501.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:123754009 G>A maps to NM_001013743.1 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:123755958 C>T maps to NM_001013743.1 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:67940316 G>A maps to NM_182526.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:67940502 G>A maps to NM_182526.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:75579318 G>A maps to NM_001077416.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:63188696 C>A maps to NM_178505.6 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:15682894 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:15677191 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:15677153 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr23:15663110 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:15657807 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:15657848 G>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:15646144 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:102967232 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:102968916 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr23:102968605 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr23:102967276 C>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:102968808 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:102968902 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:102968862 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:41945831 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:41945831 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:41945776 A>C maps to NM_018126.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:100349852 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:100349672 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:100349846 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:16797206 G>A maps to NM_024074.1 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:16791301 C>T maps to NM_024074.1 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:119153647 G>A maps to NM_018266.1 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:119155678 C>T maps to NM_018266.1 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:119171323 C>T maps to NM_018266.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:32542857 C>T maps to NM_018056.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:12778261 C>T did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr3:12778131 C>A maps to ENST00000431022 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:9316855 C>T maps to NM_015012.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr11:9310034 G>C maps to NM_015012.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:44906623 C>T maps to NM_144638.1 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:14183231 C>T maps to NM_024334.2 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:100287722 G>T maps to ENST00000403410 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:100277366 G>A maps to ENST00000403410 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:34657465 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:34648531 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:34648450 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:54266434 C>A maps to NM_018087.4 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:64174839 G>T maps to NM_014254.1 G71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:64202553 C>A maps to NM_014254.1 C338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr12:64202604 C>T maps to NM_014254.1 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:64202557 C>T maps to NM_014254.1 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:64199179 G>T maps to NM_014254.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:34837667 G>A maps to NM_006134.5 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr1:15541756 C>T maps to NM_018022.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr1:15545971 G>A maps to NM_018022.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:45120572 G>A maps to NM_024587.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:45120359 G>C maps to NM_024587.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:25785169 C>A maps to NM_018202.4 S314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:25783314 C>T maps to NM_018202.4 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:25812188 C>T maps to NM_018202.4 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:25824863 C>T maps to NM_018202.4 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:25810696 G>A maps to NM_018202.4 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:54509072 G>A maps to ENST00000371338 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:54506478 C>T maps to ENST00000371338 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:54511385 G>A maps to ENST00000371338 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:43473498 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:226054321 A>C maps to NM_014698.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:226050265 C>T maps to NM_014698.2 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:226059725 C>A maps to NM_014698.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:226055696 G>A maps to NM_014698.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:44122436 C>T maps to NM_018426.1 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:44107239 C>T maps to NM_018426.1 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:44121464 C>T maps to NM_018426.1 Y665Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:44122446 C>T maps to NM_018426.1 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:77715180 G>A maps to NM_020431.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:77686360 G>C maps to NM_020431.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:77714767 G>A maps to NM_020431.2 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:77712996 G>A maps to NM_020431.2 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:77709311 C>T maps to NM_020431.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr8:91637994 A>G maps to NM_001008495.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr8:29931530 G>A maps to NM_016127.4 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:29921412 C>T maps to NM_016127.4 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:94815887 C>T maps to NM_153704.5 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:94792910 G>T maps to NM_153704.5 G269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:94811922 T>G maps to NM_153704.5 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:94822104 C>A maps to NM_153704.5 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:94815887 C>T maps to NM_153704.5 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr8:94767234 T>G maps to NM_153704.5 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:94797484 T>C maps to NM_153704.5 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:94822104 C>A maps to NM_153704.5 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:94815879 C>T maps to NM_153704.5 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:94822104 C>A maps to NM_153704.5 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:94784852 T>C maps to NM_153704.5 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:56675381 C>T maps to ENST00000434581 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr8:56652774 C>T maps to ENST00000434581 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:56675269 G>T maps to ENST00000434581 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:46158901 A>G maps to NM_016486.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr8:133764098 G>A maps to ENST00000395406 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:133734362 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:45430512 G>A maps to NM_001123376.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr10:45430155 G>A maps to NM_001123376.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr8:109796607 C>T maps to NM_153015.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156256136 C>T maps to NM_032323.2 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:156255106 C>T maps to NM_032323.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:205053343 C>A maps to NM_203376.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:18722736 C>T maps to NM_153347.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:18723507 C>T maps to NM_153347.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:18722736 C>T maps to NM_153347.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr11:18723398 C>A maps to NM_153347.1 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr19:55738884 G>A maps to NM_173804.4 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:55740103 G>A maps to NM_173804.4 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr15:42536311 T>C maps to ENST00000389834 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:112856194 C>T maps to NM_032824.2 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:112873710 G>A maps to NM_032824.2 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:112834806 C>A maps to NM_032824.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:112858197 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7758397 G>A maps to NM_203411.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:48658295 C>A maps to NM_001008269.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:425224 G>A maps to NM_021259.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:35853530 C>A maps to NM_001042590.1 C371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:35852876 C>T maps to NM_001042590.1 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr9:35846997 C>T maps to ENST00000360192 C640C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:35846585 C>T maps to ENST00000360192 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr9:35842566 C>T maps to ENST00000360192 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:35852876 C>T maps to NM_001042590.1 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:35853759 C>T maps to NM_001042590.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:136389837 G>A maps to NM_001080483.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:136384130 G>A maps to NM_001080483.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:201120887 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:48356635 G>T maps to NM_153229.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:48356167 C>T maps to NM_153229.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:48356590 A>G maps to NM_153229.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7259772 C>T maps to NM_198154.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:31263369 G>A maps to NM_015544.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:31260260 C>T maps to NM_015544.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:38991256 G>A maps to NM_001195386.1 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:38990929 A>C maps to NM_001195386.1 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:69097036 C>T maps to NM_007114.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:69101174 C>T maps to NM_007114.2 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:69087782 C>A maps to NM_007114.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:69097077 C>A maps to NM_007114.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:69097300 C>T maps to NM_007114.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:69097036 C>T maps to NM_007114.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:69077055 C>A maps to NM_007114.2 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:69077067 C>A maps to NM_007114.2 E914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:46750730 G>A maps to NM_147196.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr3:46751114 A>T maps to NM_147196.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:46747383 C>T maps to NM_147196.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:46750670 C>T maps to NM_147196.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:28651987 G>A maps to NM_206832.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:28656383 G>T maps to NM_206832.1 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:4292742 C>T maps to NM_144615.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:4298058 G>A maps to NM_144615.2 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154736574 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:154736728 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:154721239 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:154743711 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:154743770 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:154754196 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:154741389 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:100328233 G>A maps to NM_003275.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:52186102 C>T maps to NM_014547.4 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:151144789 A>C maps to NM_013353.2 Y147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:151146915 T>C maps to NM_013353.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:151143488 G>A maps to NM_013353.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:98927477 G>A maps to NM_003276.2 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:98927087 G>A maps to NM_003276.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:98927499 G>T maps to NM_003276.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:98927087 G>A maps to NM_003276.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:98909671 G>A maps to NM_003276.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:98927570 G>A maps to NM_003276.2 Q512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:98926913 G>A maps to NM_003276.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:33135102 C>T maps to NM_001039770.2 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:68784808 G>T maps to NM_182606.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:68777059 T>C maps to NM_182606.3 *422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:68810271 G>A maps to NM_182606.3 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:69097078 G>T maps to NM_182502.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:69094474 T>C maps to NM_182502.3 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:68691451 G>A maps to NM_004262.2 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:68719812 C>T maps to NM_004262.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr4:68699022 G>A maps to NM_004262.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:68703916 C>A maps to NM_004262.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:69344586 C>T maps to NM_014058.3 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:68939703 A>T maps to NM_207407.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:68930601 C>A maps to NM_207407.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:68964698 T>C maps to NM_207407.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:68930433 G>A maps to NM_207407.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:68956302 C>A maps to NM_207407.2 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr12:51237682 C>T maps to NM_182559.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:51237736 C>T maps to NM_182559.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:117774353 G>A maps to ENST00000445164 Q564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:117789226 T>C maps to ENST00000413475 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:19732164 A>C maps to NM_002772.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:19737494 T>C maps to NM_002772.2 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr21:19770563 G>A maps to NM_002772.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr21:19687505 G>A maps to NM_002772.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:42845313 G>A maps to NM_001135099.1 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:42840453 C>A maps to NM_001135099.1 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:42870116 C>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr21:42866412 G>T maps to NM_001135099.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:43809146 G>A maps to ENST00000380399 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:43809146 G>A maps to ENST00000380399 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:117985919 C>T maps to NM_019894.3 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:117985628 G>A maps to NM_019894.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:117985925 G>A maps to NM_019894.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr11:113561587 G>T maps to NM_030770.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr11:113567608 T>C maps to NM_030770.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:113570821 G>T maps to NM_030770.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:37499388 C>T maps to ENST00000381792 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:37499384 C>A maps to ENST00000381792 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:37466962 C>T maps to ENST00000381792 E555E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:111800033 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:111768741 C>A maps to ENST00000443106 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:111780670 C>A maps to ENST00000443106 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr3:111799850 C>T maps to ENST00000443106 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:111766736 C>T maps to ENST00000443106 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:111793212 T>A maps to ENST00000443106 C567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:111797643 G>A maps to ENST00000443106 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:2405417 C>T maps to NM_182973.1 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:2408368 G>A maps to NM_182973.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:2413783 G>A maps to NM_182973.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:103219127 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr12:29911683 G>A maps to NM_001193451.1 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:29757193 G>A maps to NM_001193451.1 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr12:29667534 T>C maps to NM_001193451.1 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:83359508 C>T maps to NM_152588.1 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:83250986 G>A maps to NM_152588.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:88588831 G>A maps to NM_181783.3 K717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:101287432 G>A maps to NM_032813.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:101308637 C>A maps to NM_032813.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:101287373 G>A maps to NM_032813.2 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:101257340 G>T maps to NM_032813.2 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr13:101288808 G>A maps to NM_032813.2 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:150779404 C>T maps to NM_031434.3 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:42266575 C>T maps to NM_001076674.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:42267964 C>T maps to NM_001076674.1 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr14:51713890 G>A maps to NM_030755.4 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:51710663 G>A maps to NM_030755.4 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:51712151 G>A maps to ENST00000267434 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:66348216 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:66364515 C>A maps to NM_019022.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr18:66350219 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:66369003 G>A maps to NM_019022.3 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:7963134 G>A maps to NM_021156.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr20:7963107 C>T maps to NM_021156.2 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:117783543 G>A maps to NM_002160.2 G2166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:117844985 G>T maps to NM_002160.2 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr9:117848845 T>C maps to NM_002160.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:117808755 G>A maps to NM_002160.2 Y1686Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:117808956 G>A maps to NM_002160.2 A1619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:117852955 G>A maps to NM_002160.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr9:117846668 T>A maps to NM_002160.2 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr9:117786398 G>T maps to NM_002160.2 Y2116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:117838849 G>A maps to NM_002160.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:117849292 G>A maps to NM_002160.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:117849420 G>A maps to NM_002160.2 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:117808755 G>A maps to NM_002160.2 Y1686Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:117844174 G>A maps to NM_002160.2 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:26667446 T>G maps to NM_021137.4 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr17:26668261 G>T did not map to a codon.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr14:103596436 C>T maps to NM_006291.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:138199661 C>T maps to NM_006290.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:152230103 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:118728895 G>A maps to NM_014350.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr5:118728550 G>A maps to NM_014350.2 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:151131505 C>T maps to NM_024575.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:51350091 C>A maps to NM_207381.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:51350080 A>C maps to NM_207381.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:22885942 C>A maps to NM_003842.4 G217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:22886047 C>A maps to NM_003842.4 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:22886000 C>T maps to NM_003842.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:22886063 G>A maps to NM_003842.4 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr8:22926261 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:22879977 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr8:22960621 C>G maps to ENST00000356864 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:22960684 C>T maps to ENST00000356864 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:23001971 C>T maps to NM_003840.3 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr18:60036508 T>C maps to NM_003839.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:119936821 G>A maps to NM_002546.3 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:119945383 G>A maps to NM_002546.3 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:16842950 C>T maps to NM_012452.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:16855847 C>T maps to NM_012452.2 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:16852133 C>T maps to NM_012452.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:2489851 C>T maps to NM_003820.2 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:2489214 G>A maps to NM_003820.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:2493135 C>A maps to NM_003820.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:12061682 G>A maps to NM_001192.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:12060076 G>A maps to NM_001192.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:12059198 G>A maps to NM_001192.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:24190166 C>T maps to NM_018647.2 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:24234544 C>T maps to NM_018647.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:6443011 G>A maps to NM_001065.3 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:6443281 C>T maps to NM_001065.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:6442259 C>A maps to NM_001065.3 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:12252976 G>A maps to NM_001066.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:47251872 C>T maps to NM_014452.3 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:47253797 G>A maps to NM_014452.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:47254283 C>T maps to NM_014452.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:47251902 C>T maps to NM_014452.3 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:47253782 C>T maps to NM_014452.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:6521727 G>A maps to ENST00000355862 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:6522377 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:12157257 C>T maps to NM_001243.3 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:12198312 G>T maps to NM_001243.3 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:12175703 C>A maps to NM_001243.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:12157167 G>A maps to NM_001243.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:7993312 C>T maps to NM_001561.5 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:7998817 A>G maps to NM_001561.5 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:7993306 C>T maps to NM_001561.5 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:7998364 A>G maps to NM_001561.5 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:172232742 C>A maps to ENST00000382750 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:43180745 C>T maps to NM_003701.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:43180975 G>A maps to NM_003701.3 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:43174928 G>A maps to NM_003701.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:108922686 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:108955897 C>T maps to NM_006573.3 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:6667133 C>T maps to NM_003807.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:6665167 G>A maps to NM_003807.3 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:6664983 G>A maps to NM_003807.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:117552766 C>A maps to NM_005118.2 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V7-01A-21D-A122-09 chr9:117552979 G>A maps to NM_005118.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:173155701 C>A maps to NM_003326.3 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:173155915 A>G maps to NM_003326.3 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:173156004 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr9:117666366 C>T maps to NM_001244.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr3:170789080 A>G maps to NM_015028.2 I1160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:170797340 A>C maps to NM_015028.2 V1138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:170884947 C>T maps to NM_015028.2 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:170819341 G>T maps to NM_015028.2 Y829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:170828614 C>T maps to NM_015028.2 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:170843940 C>A did not map to a codon.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr3:170800135 G>A maps to NM_015028.2 R1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:170819400 C>A maps to NM_015028.2 E810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:170828505 G>A maps to NM_015028.2 R761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:170801979 G>A maps to NM_015028.2 R1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:170825888 C>A maps to NM_015028.2 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:170784371 C>T maps to NM_015028.2 T1284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:170784491 G>A maps to NM_015028.2 V1244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:170811696 C>T maps to NM_015028.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:170819284 G>A maps to NM_015028.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:170819391 C>A maps to NM_015028.2 E813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:2744127 C>T maps to NM_024309.3 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:122063003 G>T maps to ENST00000509841 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:122071347 C>T maps to ENST00000509841 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr4:122071335 G>A maps to ENST00000509841 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr17:7290404 G>A maps to NM_003985.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7286910 G>A maps to NM_003985.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:195593782 G>A maps to NM_001010938.1 G1077G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:195594351 G>T maps to NM_001010938.1 S1002S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr8:9634227 C>T maps to NM_003747.2 A1322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:9537497 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:9437893 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:9588455 G>A maps to NM_003747.2 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr8:9567463 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr8:9627720 G>A maps to NM_003747.2 P1282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:9622297 C>T maps to NM_003747.2 R1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr8:9622272 C>T maps to NM_003747.2 G1140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:57068455 C>T maps to NM_033396.2 S1677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr11:57088121 C>T maps to NM_033396.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:57076137 C>T maps to NM_033396.2 A1349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr11:57077913 G>A maps to NM_033396.2 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:57080391 G>A maps to NM_033396.2 Y590Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:57081066 G>A maps to NM_033396.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:93608153 C>T maps to NM_025235.3 S791S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr10:93572873 C>T maps to NM_025235.3 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:93609299 C>T maps to NM_025235.3 F881F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:93602107 C>T maps to NM_025235.3 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:93601082 G>T maps to NM_025235.3 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:93608177 C>A maps to NM_025235.3 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:99854050 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:99854664 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:99852513 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:99854570 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:99852616 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:175063270 C>T maps to NM_022093.1 H490H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:175049315 C>T maps to NM_022093.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:175113676 G>A maps to NM_022093.1 K1250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:175067561 C>T maps to NM_022093.1 Y650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:175052884 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:175086258 G>A maps to NM_022093.1 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:175066637 T>C maps to NM_022093.1 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:175086171 G>T maps to NM_022093.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr1:175067711 C>T maps to NM_022093.1 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:175097223 C>T maps to NM_022093.1 G1034G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr1:175067522 G>A maps to NM_022093.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:175063310 G>T maps to NM_022093.1 G504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:175086249 G>A maps to NM_022093.1 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr1:175049326 C>T maps to NM_022093.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:52486233 G>A maps to NM_003280.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:44452766 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:201380577 G>A maps to ENST00000367312 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:201379467 C>T maps to ENST00000367312 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:1862281 C>T maps to ENST00000381906 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:55666123 G>T maps to ENST00000344887 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:74929221 C>T maps to NM_001112808.2 N804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:74905289 C>T maps to NM_001112808.2 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:74716372 C>T maps to NM_001112808.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:74808842 C>T maps to NM_001112808.2 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:55653227 G>A maps to NM_003283.4 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:55644306 G>A maps to NM_003283.4 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:201337308 G>A maps to ENST00000421663 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:201337338 C>T maps to ENST00000421663 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:201342369 C>A maps to ENST00000421663 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:201336907 C>A maps to ENST00000421663 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:1953740 C>T maps to ENST00000397301 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:1955024 G>T maps to ENST00000397301 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:1955882 G>A maps to ENST00000397301 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:1955003 C>T maps to ENST00000397301 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:1955858 C>T maps to ENST00000397301 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:1959703 C>T maps to ENST00000397301 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:1953740 C>T maps to ENST00000397301 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:72151604 A>G maps to NM_002270.3 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:72192301 T>C maps to NM_002270.3 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:72171522 C>T maps to NM_002270.3 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:72171522 C>T maps to NM_002270.3 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:12826517 G>A maps to NM_001136196.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:12825663 G>T maps to NM_001136196.1 C287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:12814609 C>T maps to NM_001136196.1 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MO-01A-11W-A062-09 chr19:12822155 G>A maps to NM_001136196.1 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr19:12812634 G>A maps to NM_001136196.1 N814N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:128630165 C>T maps to ENST00000471166 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:128619051 C>T maps to ENST00000471166 Q716Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:128597313 G>A maps to ENST00000471166 R957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:175348868 G>A maps to NM_003285.2 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:175293512 G>A maps to NM_003285.2 Y1312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:175348849 G>A maps to NM_003285.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:175365737 G>A maps to NM_003285.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:175299321 G>A maps to NM_003285.2 R1227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:175365848 G>T maps to NM_003285.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:175335158 G>A maps to NM_003285.2 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:175362989 C>A maps to NM_003285.2 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:175365746 G>A maps to NM_003285.2 Y391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:175372558 G>A maps to NM_003285.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:175331826 G>A maps to NM_003285.2 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr1:175365860 C>T maps to NM_003285.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:175362945 G>A maps to NM_003285.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:5364834 C>T maps to NM_001080495.2 P2064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr7:5352658 G>T maps to NM_001080495.2 S2621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:5410585 G>A maps to NM_001080495.2 C1213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:5360231 G>A maps to NM_001080495.2 R2189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:5434071 T>C maps to NM_001080495.2 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:5434155 C>T maps to NM_001080495.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:5347799 C>T maps to NM_001080495.2 A2948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:5410350 C>A maps to NM_001080495.2 E1292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:24801345 C>A maps to NM_014494.2 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:24801528 G>A maps to NM_014494.2 W522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:24829956 C>A maps to NM_014494.2 A1672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:24802414 C>T maps to NM_014494.2 Q818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:24815559 C>T maps to NM_014494.2 R1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr16:24835004 G>A maps to NM_014494.2 P1922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:24834196 C>T maps to NM_014494.2 I1792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr16:24801150 T>C maps to NM_014494.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:24741604 G>T maps to NM_014494.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:24826565 G>T maps to NM_014494.2 G1591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:24802005 C>T maps to NM_014494.2 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr16:24800898 A>G maps to NM_014494.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:24815564 G>A maps to NM_014494.2 T1254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr22:40719130 A>G maps to ENST00000454349 P1810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:40642024 G>A maps to ENST00000454349 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:40661667 G>A maps to ENST00000454349 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:40666284 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:40719091 C>T maps to ENST00000454349 S1797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:40662994 C>T maps to ENST00000454349 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:40676078 C>T maps to ENST00000454349 R1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:40662603 C>T maps to ENST00000454349 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:40676078 C>T maps to ENST00000454349 R1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr22:40706950 A>G maps to ENST00000454349 P1477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr22:40661482 C>T maps to ENST00000454349 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr22:40711299 T>C maps to ENST00000454349 D1578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr22:40677280 C>T maps to ENST00000454349 F1204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr22:40696539 C>T maps to ENST00000454349 Q1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:76079171 C>T maps to NM_001142640.1 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:76047221 C>T maps to NM_001142640.1 I693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76047221 C>T maps to NM_001142640.1 I693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76082992 C>T maps to NM_001142640.1 A1204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76089761 C>T maps to NM_001142640.1 D1405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:76060929 C>T maps to NM_001142640.1 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:76089761 C>T maps to NM_001142640.1 D1405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:76093835 G>T maps to NM_001142640.1 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr17:76082938 G>A maps to NM_001142640.1 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:76083091 G>A maps to NM_001142640.1 S1237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:218712758 C>T maps to NM_022648.4 Q702Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr2:218677118 C>T maps to NM_022648.4 L1564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:218699835 C>T maps to NM_022648.4 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:218682692 C>T maps to NM_022648.4 T1350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:218682755 C>T maps to NM_022648.4 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:218762619 G>A maps to NM_022648.4 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr7:47408787 G>A maps to NM_022748.11 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:47408007 C>T maps to NM_022748.11 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:47341802 C>T maps to NM_022748.11 A1175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:47341789 C>A maps to NM_022748.11 E1180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:47408142 C>T maps to NM_022748.11 E700E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:47342587 G>A maps to NM_022748.11 P1139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr7:47474966 C>T maps to NM_022748.11 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:47408604 G>A maps to NM_022748.11 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:38644925 A>G maps to NM_032865.5 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr17:38640754 C>T maps to NM_032865.5 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:38635981 G>A maps to NM_032865.5 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:38638393 G>A maps to NM_032865.5 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr6:32052396 G>A maps to ENST00000375244 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr6:32020477 G>A maps to ENST00000375244 R3028R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:32015688 G>A maps to ENST00000375244 F3382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:32023805 G>A maps to ENST00000375244 F2763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:32024438 G>A maps to ENST00000375244 D2689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:32039944 G>A maps to ENST00000375244 F1604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:32017161 G>A maps to ENST00000375244 G3214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:32041666 G>A maps to ENST00000375244 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:32015688 G>A maps to ENST00000375244 F3382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr6:32049262 C>T maps to ENST00000375244 A1308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:32037982 G>A maps to ENST00000375244 A1733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:32046816 G>A maps to ENST00000375244 G1456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:32063394 G>A maps to ENST00000375244 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:32015688 G>A maps to ENST00000375244 F3382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:32020525 G>A maps to ENST00000375244 P3012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr6:32049415 C>T maps to ENST00000375244 E1257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:32037501 G>T maps to ENST00000375244 S1805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:32038078 G>A maps to ENST00000375244 F1701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:32010041 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:32021414 G>A maps to ENST00000375244 L2847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:32023742 G>A maps to ENST00000375244 G2784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:32023679 G>A maps to ENST00000375244 Y2805Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr6:32065663 C>T maps to ENST00000375244 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr6:32064810 G>A maps to ENST00000375244 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:41832989 G>A maps to NM_016272.3 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:45809115 C>T maps to NM_025077.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:1309892 G>A maps to ENST00000382211 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:1311513 G>T maps to ENST00000382211 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:35743314 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:35717987 C>T maps to ENST00000451197 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:53037969 C>T maps to NM_005486.2 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:53026967 G>A maps to NM_005486.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:53014507 C>T maps to NM_005486.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:17797055 G>A maps to NM_001082968.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:17786069 C>T maps to NM_001082968.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:17788063 G>A maps to NM_001082968.1 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr17:17772709 G>A maps to NM_001082968.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:17766125 G>T maps to NM_001082968.1 S374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:45404514 C>T maps to NM_006114.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:100096718 C>A maps to NM_014820.3 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:100100547 C>T maps to NM_014820.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr20:39744080 T>C did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr20:39746809 G>A maps to NM_003286.2 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr20:39745019 G>T maps to NM_003286.2 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:144392281 G>A maps to NM_052963.1 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:144391630 C>A maps to NM_052963.1 G596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:144407664 G>A maps to NM_052963.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr8:144392278 C>T maps to NM_052963.1 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:144407636 C>A maps to NM_052963.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:38552630 A>G maps to ENST00000357601 A1244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:38556216 C>A maps to ENST00000357601 E1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38556810 G>A maps to ENST00000357601 I959I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:38564256 C>A maps to ENST00000357601 G524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:38546356 T>G maps to ENST00000357601 R1480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:38548930 C>T maps to ENST00000357601 K1326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:38569538 G>A maps to ENST00000357601 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr17:38562674 G>A maps to ENST00000357601 F674F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:38555365 C>A maps to ENST00000357601 E1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr3:25639914 T>A maps to ENST00000264331 S1588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:25662277 C>T maps to ENST00000264331 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:25656716 C>T maps to ENST00000264331 A1190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:25677594 T>C maps to ENST00000264331 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:25686789 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr17:18210228 G>A maps to NM_004618.3 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:18205933 G>A maps to NM_004618.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:18205231 C>T maps to NM_004618.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr17:18211732 A>T maps to NM_004618.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:18181142 A>G maps to NM_004618.3 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:22314079 G>A maps to NM_003935.3 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:22314099 G>A maps to NM_003935.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:22328813 G>A maps to NM_003935.3 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:22312957 G>A maps to NM_003935.3 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:22312957 G>A maps to NM_003935.3 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:22312957 G>A maps to NM_003935.3 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:22312957 G>A maps to NM_003935.3 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:133371474 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:133356908 G>A maps to NM_007027.3 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:133327423 G>A maps to NM_007027.3 N1460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:133331327 G>A maps to NM_007027.3 R1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr3:133342955 C>T maps to NM_007027.3 R956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:32542872 A>G maps to NM_005802.4 C550C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr9:32543127 G>A maps to NM_005802.4 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:32543045 C>A maps to NM_005802.4 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:32542290 A>G maps to NM_005802.4 F744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr9:32542662 C>T maps to NM_005802.4 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr9:32541987 G>A maps to NM_005802.4 D845D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:179851906 C>T maps to ENST00000398836 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:179851895 C>T maps to ENST00000398836 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr1:179887335 C>T maps to ENST00000398836 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:179886639 C>T maps to ENST00000398836 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:179887055 A>G maps to ENST00000398836 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:179819994 G>A maps to NM_145034.4 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:179815517 G>A maps to NM_145034.4 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:130495566 G>A maps to NM_130459.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr9:130494960 A>G maps to NM_001085347.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr9:130494332 G>A maps to NM_001085347.1 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:130495839 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:179057213 C>T maps to NM_022371.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:59750720 G>A maps to NM_014729.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:59720726 T>C maps to NM_014729.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:59728013 C>T maps to NM_014729.2 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:42683123 C>T maps to ENST00000348077 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:42697356 T>G maps to ENST00000413823 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V6-01A-11D-A122-09 chr20:42679965 G>A maps to ENST00000348077 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:52473640 C>T maps to ENST00000407228 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:52479985 G>A maps to ENST00000407228 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr16:52484449 G>A maps to ENST00000407228 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:52473274 C>T maps to ENST00000407228 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:21956840 G>A maps to NM_014828.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:21961058 A>T maps to NM_014828.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr17:7579329 G>C maps to NM_001126112.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr17:7574033 C>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:7579882 G>A maps to NM_001126112.1 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:43784214 C>A maps to NM_001141980.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:43714111 G>A maps to NM_001141980.1 S1347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:43738608 C>A maps to NM_001141980.1 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:43748581 C>A maps to NM_001141980.1 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:43712599 G>A maps to NM_001141980.1 Y1528Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:43771616 C>A maps to NM_001141980.1 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:43699768 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:43748903 C>T maps to NM_001141980.1 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:43773164 C>A maps to NM_001141980.1 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:43749044 A>G maps to NM_001141980.1 N587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr15:43712844 G>A maps to NM_001141980.1 R1447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:223971969 C>T maps to NM_001031685.2 A1070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:223971815 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:224008969 C>A maps to NM_001031685.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:223991076 C>A maps to NM_001031685.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:44959841 C>T maps to NM_006034.3 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:27898637 C>A maps to NM_138349.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:24305998 A>G maps to NM_147184.1 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:24307142 C>T maps to NM_147184.1 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:44003797 G>A maps to NM_014477.2 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:44002555 G>T maps to NM_014477.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:44004137 G>A maps to NM_014477.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:189607201 C>G maps to NM_003722.4 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:189455531 C>T maps to NM_003722.4 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:189586458 G>A maps to NM_003722.4 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:189612027 C>T maps to NM_003722.4 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:189612027 C>T maps to NM_003722.4 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:189455531 C>T maps to NM_003722.4 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:189526188 G>A maps to NM_003722.4 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:189586503 C>T maps to NM_003722.4 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:189612035 G>A maps to NM_003722.4 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:3647611 C>T maps to NM_005427.2 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr1:3646581 G>A maps to NM_005427.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr6:83075635 C>A maps to NM_006670.4 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:113716008 C>T maps to NM_001143819.1 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:113664686 G>A maps to NM_001143819.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:113727974 C>T maps to NM_001143819.1 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:113730878 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr12:113724869 C>T maps to NM_001143819.1 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:113716017 C>T maps to NM_001143819.1 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:113726108 C>T maps to ENST00000428632 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:68822732 C>T maps to NM_139075.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:68831407 C>T maps to NM_139075.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:68846005 C>T maps to NM_139075.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:80950386 C>T maps to NM_001025252.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:80976723 C>A maps to NM_001025252.1 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:125541214 T>C did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr20:62505019 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:6328634 G>T maps to NM_033516.5 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:18047154 G>A maps to ENST00000341556 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:18042710 C>A maps to ENST00000341556 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:18042710 C>A maps to ENST00000341556 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:18050710 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:18054915 C>A maps to ENST00000341556 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:72338071 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:72338169 G>T maps to ENST00000389376 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr12:72388230 T>C maps to ENST00000389376 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:72372831 C>T maps to ENST00000389376 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:6978531 C>T maps to NM_001159287.1 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:144364829 G>A maps to ENST00000378099 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:144364916 C>T maps to ENST00000378099 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr15:63354418 G>A maps to ENST00000357980 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35682155 G>T maps to ENST00000329305 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:35684829 G>A maps to ENST00000378309 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:35685535 G>T maps to ENST00000329305 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:35685648 G>A maps to ENST00000329305 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:16212071 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr19:16178514 G>A maps to NM_001145160.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:16198908 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:18143900 C>A maps to NM_000367.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:1418269 T>G maps to NM_000547.5 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:1544422 C>T maps to NM_000547.5 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:1546233 G>A maps to NM_000547.5 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:1500506 G>T maps to NM_000547.5 G786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr2:1491693 C>T maps to NM_000547.5 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:1488573 C>T maps to NM_000547.5 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:1507738 C>T maps to NM_000547.5 D802D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:1499886 C>T maps to NM_000547.5 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6637731 G>T maps to ENST00000453338 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:6638352 T>C maps to ENST00000453338 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:6636545 C>T maps to ENST00000453338 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:6636678 T>G maps to ENST00000453338 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:6638261 A>G maps to ENST00000453338 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:6640115 A>G maps to ENST00000453338 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:103297308 C>T maps to ENST00000376052 Y781Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr13:103299695 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:103292683 C>T maps to ENST00000376052 R660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:103292683 C>T maps to ENST00000376052 R660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:103292683 C>T maps to ENST00000376052 R660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:103292683 C>T maps to ENST00000376052 R660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr13:103295701 A>G maps to ENST00000376052 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:103279485 A>G maps to ENST00000376052 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:103301292 C>T maps to ENST00000376052 R889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:103249411 G>A maps to ENST00000376052 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:103257237 T>C maps to ENST00000376052 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:103317179 G>A maps to ENST00000376052 A1092A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:103292683 C>T maps to ENST00000376052 R660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:103290641 G>A maps to ENST00000376052 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr5:666192 C>T maps to NM_007030.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:665246 G>T maps to NM_007030.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:67424181 G>A maps to NM_016140.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:67424229 C>T maps to NM_016140.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:186342563 C>T maps to NM_003292.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr1:186331434 C>T maps to NM_003292.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:186322944 G>A maps to NM_003292.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:186314783 T>C maps to NM_003292.2 V1047V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:186312592 T>C maps to NM_003292.2 R1205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:186329128 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:186313626 C>T maps to NM_003292.2 A1099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:186322944 G>A maps to NM_003292.2 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:186301392 G>T maps to NM_003292.2 V1846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:186304555 G>A maps to NM_003292.2 R1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:127294316 G>A maps to NM_001136053.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr3:127292498 T>C maps to NM_001136053.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:127295856 C>T maps to NM_001136053.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr3:188925280 G>A maps to NM_198485.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:3542046 C>T maps to NM_182752.3 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:3545082 C>T maps to NM_182752.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:3542421 G>T maps to NM_182752.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:3542421 G>T maps to NM_182752.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr1:3545118 C>T maps to NM_182752.3 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:3545046 G>A maps to NM_182752.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:73961662 C>A maps to ENST00000409716 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr9:140093603 G>T maps to NM_001128228.2 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:140093785 C>A maps to NM_001128228.2 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:48305550 G>A maps to NM_198479.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr19:48305637 T>C maps to NM_198479.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:48305781 C>A maps to NM_198479.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:65705855 G>A maps to NM_003596.3 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr22:26932448 G>T maps to NM_003595.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:26928690 T>C maps to NM_003595.3 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:10942759 T>C maps to NM_199261.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:10920142 C>A maps to NM_199261.2 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:10942767 C>A maps to NM_199261.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr21:10971323 C>T maps to NM_199261.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr21:10970031 G>A maps to NM_199261.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:20012252 G>A maps to NM_199254.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:20024237 C>T maps to NM_199254.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:19999157 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:20006718 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:19999127 T>G maps to NM_199254.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:20048215 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr13:20067595 C>T maps to NM_199254.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:30347858 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:30380609 C>T maps to ENST00000340513 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:30380609 C>T maps to ENST00000340513 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:30380609 C>T maps to ENST00000340513 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr20:30381809 G>T maps to ENST00000340513 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr20:30386282 G>A maps to ENST00000340513 Q723Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:23545860 G>A maps to NM_013293.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:23545854 G>A maps to NM_013293.3 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:50635731 G>A maps to NM_025204.2 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:123671570 C>T maps to NM_001190945.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:123675644 G>A maps to NM_001190945.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr9:139804379 C>T maps to ENST00000359662 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr9:139818322 C>T maps to ENST00000359662 Y438Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr14:103352602 C>T maps to NM_145725.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr14:103369605 C>T maps to NM_145725.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:239261824 G>T maps to NM_015650.3 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:239234448 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:239237889 G>A maps to NM_015650.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:111901545 C>T maps to ENST00000340026 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr6:111901455 G>A maps to ENST00000340026 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr6:111912626 C>A maps to ENST00000340026 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:209955412 C>T maps to NM_025228.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:209950782 C>T maps to NM_025228.2 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:209946342 C>T maps to NM_025228.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:27075638 C>T maps to NM_004295.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:211533364 C>T maps to ENST00000427925 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:211545546 C>T maps to ENST00000427925 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:211545546 C>T maps to ENST00000427925 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:36511924 G>A maps to NM_145803.1 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:36511924 G>A maps to NM_145803.1 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:36511953 G>A maps to NM_145803.1 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:2221577 G>A maps to NM_032271.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:2223260 G>A maps to NM_032271.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:112589776 G>A maps to NM_006700.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:49885611 T>A maps to NM_005879.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:49866926 G>A maps to NM_005879.2 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:49881329 G>A maps to NM_005879.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:42201897 C>T maps to ENST00000396175 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:42264715 G>A maps to NM_001042646.1 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:42132981 C>T maps to NM_001042646.1 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:42229628 C>A maps to NM_001042646.1 C191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:42264628 C>T maps to NM_001042646.1 Y754Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:42264715 G>A maps to NM_001042646.1 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:42132981 C>T maps to NM_001042646.1 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:202260101 G>A maps to NM_015049.2 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:202263031 G>A maps to NM_015049.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:71512311 C>T maps to NM_014294.5 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:118005616 T>C maps to NM_152402.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:52368063 G>A maps to NM_012288.3 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:36874839 C>T maps to NM_014831.2 E2034E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:36897167 C>A maps to NM_014831.2 E1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:36905971 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:36898113 G>A maps to NM_014831.2 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:36899433 C>T maps to NM_014831.2 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:36893314 C>T maps to NM_014831.2 E1550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:36897246 C>T maps to NM_014831.2 T1278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr3:36873543 G>C maps to NM_014831.2 Y2466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:36893782 C>A maps to NM_014831.2 E1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:3725387 C>T maps to NM_016292.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr16:3721733 G>A maps to NM_016292.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr21:45511917 G>A maps to NM_003274.4 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:45496478 G>A maps to NM_003274.4 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:45503038 C>T maps to NM_003274.4 N698N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:45507664 G>T maps to NM_003274.4 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr21:45502960 C>T maps to NM_003274.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr21:45499916 C>T maps to NM_003274.4 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr21:45522764 G>A maps to NM_003274.4 P1151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr21:45511917 G>A maps to NM_003274.4 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:45479369 C>A maps to ENST00000380221 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:13734158 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:13732583 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:88925064 C>T maps to NM_016209.3 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:36602862 C>A maps to NM_014408.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:36603480 C>A maps to NM_014408.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:36602872 G>A maps to NM_014408.3 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr11:118889982 C>T maps to NM_016146.4 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:7747471 C>T maps to NM_001042461.1 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr19:45667268 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:140743387 G>A maps to NM_031466.5 H1219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:141262945 C>T maps to NM_031466.5 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:108572510 C>T maps to NM_016388.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:17195498 C>T maps to ENST00000488990 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:123760142 C>A maps to NM_006073.2 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:123687295 C>T maps to NM_006073.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:123869680 G>T maps to NM_006073.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:123581762 C>A maps to NM_006073.2 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:123869740 C>T maps to NM_006073.2 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:123581762 C>A maps to NM_006073.2 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:123653060 C>T maps to NM_006073.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:123759261 C>A maps to NM_006073.2 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:123837339 C>A maps to NM_006073.2 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:123592328 C>A maps to NM_006073.2 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:118532112 G>A maps to ENST00000264029 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:118534069 G>A maps to ENST00000264029 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:118533510 G>A maps to ENST00000450700 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:118530560 C>T maps to ENST00000264029 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:118531434 C>T maps to ENST00000264029 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr11:118531286 G>A maps to ENST00000264029 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:41243961 C>T maps to NM_018643.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:41250489 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr6:41250406 C>T maps to NM_018643.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:41250160 G>A maps to NM_018643.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:41126471 C>A maps to ENST00000373122 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:41126764 G>T maps to NM_018965.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr6:41162431 G>T maps to ENST00000373108 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:42231303 C>T maps to NM_033502.2 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr6:42237130 G>A maps to NM_033502.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:42200617 G>A maps to NM_033502.2 R1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:42330683 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152713212 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:152710722 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:152710759 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:152710735 T>C did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:152710421 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr23:152710629 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:152710646 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:129695581 G>A maps to NM_007117.3 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:73046894 C>A maps to NM_013381.2 A936A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:73050755 G>T maps to NM_013381.2 E967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:73046868 C>T maps to NM_013381.2 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr12:72893297 C>T maps to NM_013381.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr12:72666728 C>T maps to NM_013381.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:72936114 A>C maps to NM_013381.2 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:110131530 C>T maps to NM_003301.4 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06B-01A-11W-A027-09 chr8:110100247 C>T maps to NM_003301.4 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:126445608 G>A maps to NM_025195.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:126448434 C>T maps to NM_025195.2 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:126445743 C>T maps to NM_025195.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:126445830 C>T maps to NM_025195.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:12863393 T>C maps to NM_021643.3 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:12880832 G>A maps to NM_021643.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:12858459 C>A maps to NM_021643.3 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:12863519 G>A maps to NM_021643.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:12880551 G>T maps to NM_021643.3 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:12880961 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:12863534 C>T maps to NM_021643.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:12880832 G>A maps to NM_021643.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:12880995 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:12880716 C>T maps to NM_021643.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr2:12880965 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:12880832 G>A maps to NM_021643.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:368788 C>A maps to ENST00000422053 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:372073 C>T maps to ENST00000422053 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:368759 C>T maps to ENST00000422053 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:368657 C>T maps to ENST00000422053 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr6:30128422 G>T maps to NM_006778.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:228584650 G>A maps to NM_145214.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:50586174 C>T maps to NM_001007278.1 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:50586282 G>A maps to NM_001007278.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:100849611 G>A maps to ENST00000311688 H236H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:30131748 C>T maps to NM_033229.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:18638424 C>T maps to NM_001037330.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr17:18638274 G>A maps to NM_001037330.1 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:228598868 C>T maps to NM_016102.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:228598739 G>A maps to NM_016102.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:154215567 G>A maps to NM_015271.3 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr4:154216613 C>T maps to NM_015271.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:4409564 G>A maps to NM_003141.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:4411570 G>A maps to NM_003141.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:4409564 G>A maps to NM_003141.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:5729463 C>T maps to NM_006074.4 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:5730766 C>T maps to NM_006074.4 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:5730490 C>T maps to NM_006074.4 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:5717531 G>T maps to NM_006074.4 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:5730451 G>A maps to NM_006074.4 W357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:5719603 C>A maps to NM_006074.4 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:5717809 C>A maps to NM_006074.4 C116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:5717566 C>T maps to NM_006074.4 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:64906801 C>T maps to NM_001656.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:64887675 G>A maps to NM_001656.3 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:64909947 C>A maps to NM_001656.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:138239476 A>G maps to NM_015905.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:138262237 C>T maps to NM_015905.2 R721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:54985912 C>T maps to NM_005082.4 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:54969126 C>T maps to NM_005082.4 E609E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:54991310 G>T maps to NM_005082.4 C13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr17:54969558 G>A maps to NM_005082.4 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15V-01A-11D-A122-09 chr17:54991091 G>A maps to NM_005082.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr6:30154270 G>A maps to NM_003449.3 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:30157215 G>A maps to NM_003449.3 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:28887992 C>T maps to NM_006510.4 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:59060513 A>G maps to NM_005762.2 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:59060960 G>A maps to NM_005762.2 Q642Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:59056843 G>A maps to NM_005762.2 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:59059680 G>A maps to NM_005762.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr19:59061210 C>A maps to NM_005762.2 S697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:119993731 C>T maps to NM_012101.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:120008340 C>T maps to NM_012101.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:119998142 C>A maps to NM_012101.3 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:120008667 G>T maps to NM_012101.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr11:119998184 C>T maps to NM_012101.3 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:6470404 G>A maps to NM_033278.2 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:6479074 C>T maps to NM_033278.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:6470615 G>A maps to NM_033278.2 Q668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:6470628 G>A maps to NM_033278.2 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:30080282 C>T maps to NM_007028.3 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:30078404 C>T maps to NM_007028.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:119460896 A>G maps to NM_012210.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:119460167 G>A maps to NM_012210.3 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:119460596 G>A maps to NM_012210.3 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:114976294 C>T maps to NM_015906.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:114970386 G>A maps to NM_015906.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:114945408 C>T maps to NM_015906.3 A955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:114964081 C>T maps to NM_015906.3 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:114945455 C>A maps to NM_015906.3 E940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:114948206 G>A maps to NM_015906.3 R865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:114973521 T>C maps to NM_015906.3 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:5662428 G>A maps to NM_130390.2 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:5662456 T>C maps to NM_130390.2 *271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr8:27145294 C>T maps to NM_171982.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr8:27145186 G>A maps to NM_171982.3 H454H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:114462355 T>G maps to NM_018700.3 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:114473236 G>T maps to NM_018700.3 S315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:114482893 C>A maps to NM_018700.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:114469586 C>A maps to NM_018700.3 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:114513446 C>A maps to NM_001017398.1 *62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:114469701 C>T maps to NM_018700.3 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:57094719 G>A maps to NM_015294.3 R775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:57119251 C>A maps to NM_015294.3 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:57105820 C>A maps to NM_015294.3 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:57079064 G>A maps to NM_015294.3 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:57134350 C>A maps to NM_015294.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:57094719 G>A maps to NM_015294.3 R775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:25966975 C>T maps to NM_006355.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr6:25967118 G>A maps to NM_006355.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:25967010 G>A maps to NM_006355.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:30308066 C>T maps to NM_021253.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:99501221 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:180662361 G>T maps to NM_201627.1 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:180661714 G>A maps to NM_033549.3 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:180659801 T>C maps to NM_033549.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr5:180651511 G>A maps to NM_033549.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:180651055 G>A maps to NM_033549.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr5:180660758 G>A maps to NM_033549.3 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:140397088 C>T maps to NM_152616.4 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:140401945 C>T maps to NM_152616.4 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:140397403 C>T maps to NM_152616.4 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:140401333 C>T maps to NM_152616.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:140406663 T>C maps to NM_152616.4 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:96265134 C>A maps to NM_138800.1 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:96260043 A>G maps to NM_138800.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:35684883 G>A maps to NM_017583.4 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:117661184 G>T maps to NM_025188.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:117659365 G>A maps to NM_025188.3 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr17:73871013 G>A maps to NM_033452.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:73872483 G>T maps to NM_033452.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:55038045 G>A maps to ENST00000357530 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr11:55038009 C>A maps to ENST00000357530 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr11:55036789 G>A maps to ENST00000357530 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr11:55032642 T>C maps to ENST00000357530 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:89531585 G>T maps to NM_020358.2 V357V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A056-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:5686428 G>A maps to NM_033034.2 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:5699532 C>T maps to NM_033034.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:5687249 G>A maps to NM_033034.2 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:5687301 G>A maps to NM_033034.2 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:72727000 C>T maps to NM_178125.2 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr7:72738452 G>A maps to NM_178125.2 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27522226 C>T maps to NM_032546.3 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:67064610 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:67064667 G>T maps to NM_184085.1 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:67066355 G>A maps to NM_184085.1 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:100732582 C>T maps to NM_030961.1 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:100732044 C>A maps to NM_030961.1 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100732536 C>T maps to NM_030961.1 F648F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248023986 C>T maps to NM_015431.3 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:248039311 C>T maps to NM_015431.3 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:248023954 G>T maps to NM_015431.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:160156466 C>A maps to ENST00000483754 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:160156382 C>A maps to ENST00000483754 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:160156627 A>C maps to ENST00000483754 L115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:5625798 C>T maps to NM_001003819.3 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:165962175 C>T maps to NM_152620.2 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:165961268 C>T maps to NM_152620.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:165962615 C>A maps to NM_152620.2 C464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:165961439 T>A maps to NM_152620.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:165962354 T>C maps to NM_152620.2 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:165961529 G>A maps to NM_152620.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr4:165891118 T>C maps to NM_001012414.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:165890659 T>C maps to NM_001012414.2 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr1:231349680 C>T maps to NM_001004342.3 D748D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:231344780 C>T maps to NM_001004342.3 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:231335910 C>T maps to NM_001004342.3 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr11:4621921 G>A maps to NM_018073.5 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:4621685 G>A maps to NM_018073.5 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr15:45047235 C>T maps to NM_182985.3 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr15:45051857 T>C maps to NM_182985.3 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:180630634 G>T maps to NM_203293.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:32933260 C>T maps to NM_001039111.1 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:32932741 C>T maps to NM_001039111.1 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr16:31235526 G>A maps to NM_001008274.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:75028411 C>T maps to ENST00000430211 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:75034120 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr7:72430722 C>T maps to ENST00000285805 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:72436493 G>A maps to ENST00000285805 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr14:51489582 G>A maps to ENST00000338969 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:51475870 C>T maps to ENST00000338969 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:51561051 C>T maps to ENST00000338969 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:51448588 G>A maps to ENST00000338969 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr14:51561075 G>A maps to ENST00000338969 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:51444041 G>A maps to NM_015163.5 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr14:51560934 G>A maps to ENST00000338969 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr14:51467493 G>A maps to ENST00000338969 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:51446185 G>A maps to ENST00000338969 N744N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr4:189063617 G>A maps to NM_178556.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:189068027 G>A maps to NM_178556.3 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:189067985 G>A maps to NM_178556.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:189065192 C>T maps to NM_178556.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr4:189060957 G>A maps to NM_178556.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:189061726 G>T maps to NM_178556.3 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:14366970 G>A maps to NM_007118.2 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:14389399 G>A maps to NM_007118.2 T1317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:14399068 C>T maps to NM_007118.2 R1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:14508110 C>T maps to NM_007118.2 F2958F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:14387900 C>T maps to NM_007118.2 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:14387900 C>T maps to NM_007118.2 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:14359640 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:14482806 C>T maps to NM_007118.2 I2194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr5:14504622 C>T maps to NM_007118.2 Q2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr5:14369541 C>T maps to NM_007118.2 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:14363896 C>T maps to NM_007118.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:14482806 C>T maps to NM_007118.2 I2194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:14290917 G>T maps to NM_007118.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:14389472 G>T maps to NM_007118.2 G1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr5:14462946 C>T maps to NM_007118.2 G1860G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:14291189 G>A maps to NM_007118.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr5:14498738 G>A maps to NM_007118.2 L2774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:38121175 C>T maps to NM_001039141.2 C871C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr22:38120882 C>T maps to NM_001039141.2 R774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:38119409 C>T maps to NM_001039141.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:38122300 G>A maps to NM_001039141.2 P1246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr22:38130947 T>A maps to NM_001039141.2 T1535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:6743799 C>T maps to ENST00000313244 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:6743230 G>A maps to ENST00000313244 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:6743843 C>T maps to ENST00000313244 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:6750326 C>T maps to ENST00000313244 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:92461858 G>A maps to NM_004239.3 S1631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:92470419 A>G maps to NM_004239.3 N1300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:92482108 G>A maps to NM_004239.3 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:92466408 G>T maps to NM_004239.3 S1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:92488058 T>G maps to NM_004239.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:92469839 G>A maps to NM_004239.3 R1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:92470806 G>A maps to NM_004239.3 I1171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:92454679 A>G maps to NM_004239.3 L1736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:230654349 G>A maps to ENST00000389044 R1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:230633359 C>T maps to ENST00000389044 V1966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:230673085 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:230675761 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:230678648 C>T maps to ENST00000389044 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:230668713 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:230656766 T>G maps to ENST00000389044 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:912005 C>T maps to NM_004237.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:901541 C>T maps to NM_004237.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr5:908177 C>T maps to NM_004237.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:916036 C>T maps to NM_004237.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:914626 A>G maps to NM_004237.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:64737305 C>A maps to NM_016213.4 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:100468035 G>A maps to NM_003302.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100468074 G>T maps to NM_003302.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:13218618 G>A maps to NM_001136035.2 N484N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:126317186 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:126359981 A>G maps to NM_001031712.2 *464W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:126332534 C>T maps to NM_001031712.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:126319385 G>A maps to NM_001031712.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:64084573 C>A maps to NM_016404.1 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:125464043 A>G maps to NM_017956.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:125463743 G>A maps to NM_017956.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:125463270 G>T maps to NM_017956.3 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:20101084 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr22:20100338 G>A maps to ENST00000404751 D549D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr22:20102108 G>A maps to ENST00000439169 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100297035 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:100274034 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:100278535 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:100276155 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100275577 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:100292925 G>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:100276154 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:100297104 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr14:61445997 A>G maps to NM_020810.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:61446305 C>A maps to NM_020810.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:61442712 C>T maps to NM_020810.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:61442840 G>A maps to NM_020810.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:5927166 G>A maps to NM_015939.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:5927139 G>A maps to NM_015939.3 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:103996557 G>A maps to ENST00000299201 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:103998943 C>T maps to ENST00000299201 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:103999150 C>A maps to ENST00000299201 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:29092450 G>A maps to NM_017910.3 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:29093119 A>T maps to NM_017910.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr2:29092939 T>C maps to NM_017910.3 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:46748196 G>T maps to NM_018006.4 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:28887749 G>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:3188245 T>C maps to NM_182916.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:3188257 A>C maps to NM_182916.2 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr23:54950036 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:54957200 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:54950962 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:54955293 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:54956513 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54955316 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54956157 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54956840 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr23:54949317 C>A did not map to a codon.
Sequencing variant TCGA-AP-A05P-01A-11W-A062-09 chr23:54950961 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:54955295 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:54955967 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:54957287 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:54950012 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:54949837 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54949729 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54951444 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:54949113 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:54950190 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:54957330 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:54949722 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:54957378 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:54950196 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:54954150 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:54955913 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:54952859 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:54956456 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:54957705 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54948707 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54951444 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54954150 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54956552 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54956894 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54957092 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:54956373 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr23:54956904 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:54955420 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:54955760 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:54957638 T>G did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:54950195 C>T did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:54955609 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:49724676 C>T maps to NM_005480.3 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:49723685 C>A maps to NM_005480.3 S404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:49723929 C>T maps to NM_005480.3 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:49722783 T>C maps to NM_005480.3 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:49724136 C>A maps to NM_005480.3 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr12:49717770 G>A maps to NM_005480.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:193051777 T>A maps to NM_004600.5 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:193045116 G>T maps to NM_004600.5 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:193051324 C>T maps to NM_004600.5 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:193038387 C>T maps to NM_004600.5 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr1:193051374 A>G maps to NM_004600.5 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:72967961 G>T maps to NM_007332.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:72970030 G>T maps to NM_007332.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:72946022 G>T maps to NM_007332.2 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:72959393 G>A maps to NM_007332.2 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr8:72959418 C>T maps to NM_007332.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:72948638 C>T maps to NM_007332.2 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:142503812 G>T maps to ENST00000476941 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:142511766 C>A maps to ENST00000476941 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:142522878 C>A maps to ENST00000476941 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:142499811 T>C maps to ENST00000476941 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:142521009 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:142499852 C>A maps to ENST00000476941 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:142522824 T>C maps to ENST00000476941 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr4:122833212 A>G maps to NM_001130698.1 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:122853626 C>T maps to NM_001130698.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:122833041 G>T maps to NM_001130698.1 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:122824086 G>A maps to NM_001130698.1 R795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:122854058 G>A maps to NM_001130698.1 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr4:122853512 G>A maps to NM_001130698.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr4:122824086 G>A maps to NM_001130698.1 R795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:122853674 G>A maps to NM_001130698.1 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr4:122824150 T>C maps to NM_001130698.1 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr4:122853689 C>T maps to NM_001130698.1 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:122825494 G>A maps to NM_001130698.1 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr4:122853581 C>T maps to NM_001130698.1 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:38211357 A>G maps to NM_003306.1 A877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:38213432 G>A maps to NM_003306.1 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:38248504 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:38266253 G>T maps to NM_003306.1 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:38320490 G>T maps to NM_003306.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:38357203 G>T maps to NM_003306.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:38211453 G>A maps to NM_003306.1 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:38211213 C>T maps to NM_003306.1 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:38211558 C>T maps to NM_003306.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr13:38211669 C>T maps to NM_003306.1 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:38266228 G>A maps to NM_003306.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr13:38266397 T>C maps to NM_003306.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr13:38320454 G>A maps to NM_003306.1 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:38229287 G>A maps to NM_003306.1 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:33591287 G>A maps to NM_015638.2 N727N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:33609000 G>A maps to NM_015638.2 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:33603861 T>C maps to NM_015638.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:33645344 C>T maps to NM_015638.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:111097275 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:111195412 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:111097010 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:111097015 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:111019652 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:111019933 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:111078340 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:111090421 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:111090572 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:111025181 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:111019923 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:111025181 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:111090572 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:111020010 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:111022276 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:111025348 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:111090400 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:111019999 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:111195384 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:111078261 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:111090542 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:111095541 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:111195592 G>A did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:111095666 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:111020171 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:111090572 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:111195455 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr11:101347128 C>T maps to NM_004621.5 W549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr11:101347071 C>T maps to NM_004621.5 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr5:135651464 G>A maps to NM_020389.2 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:135651308 G>A maps to NM_020389.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:135610522 G>A maps to NM_020389.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:135610522 G>A maps to NM_020389.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:135610444 G>A maps to NM_020389.2 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:135610369 C>T maps to NM_020389.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:135587487 G>A maps to NM_020389.2 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:135692648 C>A maps to NM_020389.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:135587469 G>A maps to NM_020389.2 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr5:135692559 C>T maps to NM_020389.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:135651365 A>G maps to NM_020389.2 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr15:31318415 C>T maps to NM_002420.4 V1163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr15:31329969 C>A maps to NM_002420.4 G817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:31355349 G>T maps to NM_002420.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:31327796 C>T maps to NM_002420.4 W862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:31294516 G>A maps to NM_002420.4 F1440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr15:31294506 G>T maps to NM_002420.4 R1444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:31325050 T>G maps to NM_002420.4 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:31358372 G>A maps to NM_002420.4 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:31329958 G>T maps to NM_002420.4 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:31294219 T>G maps to NM_002420.4 P1539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr15:31294425 G>A maps to NM_002420.4 Q1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr15:31339454 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:31294123 T>G maps to NM_002420.4 G1571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:31295038 G>A maps to NM_002420.4 S1266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:31352800 C>T maps to NM_002420.4 W381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:31294998 C>A maps to NM_002420.4 E1280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:31319217 C>T maps to NM_002420.4 P1110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:45810909 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:45817703 G>A maps to ENST00000397932 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:45820225 C>T maps to ENST00000397932 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:45825803 C>T maps to ENST00000397932 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:45810793 G>A maps to ENST00000397932 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:45845643 G>A maps to ENST00000397932 R1293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr21:45855082 G>A maps to ENST00000397932 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:45795894 A>C maps to ENST00000397932 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr21:45825041 C>T maps to ENST00000397932 D852D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:45833852 G>A maps to ENST00000397932 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:45837983 G>A maps to ENST00000397932 K1107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:45833849 G>A maps to ENST00000397932 A1013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:73151291 G>T maps to ENST00000419692 A1533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr9:73218281 G>A maps to ENST00000419692 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:73457903 G>T maps to ENST00000377097 C161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:73240118 G>A maps to ENST00000419692 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:73151012 G>A maps to ENST00000419692 L1626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:73399022 G>A maps to ENST00000419692 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:73151989 G>A maps to ENST00000419692 R1301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:73213424 G>A maps to ENST00000419692 C940C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:73151866 C>A maps to ENST00000419692 E1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:73213484 G>A maps to ENST00000419692 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr9:73426149 C>T maps to ENST00000419692 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:49705362 C>T maps to NM_017636.3 N1032N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:49671308 C>T maps to NM_017636.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49674875 C>T maps to NM_017636.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49705353 C>T maps to NM_017636.3 L1029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:49671814 G>A maps to NM_017636.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:49714015 G>A maps to NM_017636.3 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:49713495 C>T maps to NM_017636.3 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:49686387 C>T maps to NM_017636.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:2439408 G>C maps to ENST00000452833 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:2428999 G>A maps to ENST00000452833 I977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:2439525 G>A maps to ENST00000452833 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:2439058 G>A maps to ENST00000452833 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:2432666 G>A maps to ENST00000452833 D901D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:77376927 G>T maps to NM_017662.4 I1553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:77400933 G>A maps to NM_017662.4 F925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:77376984 C>T maps to NM_017662.4 R1534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:77457147 C>T maps to NM_017662.4 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr9:77353321 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:77377104 G>T maps to NM_017662.4 A1494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:77354916 C>A maps to NM_017662.4 E1737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr9:77386634 G>A maps to NM_017662.4 R1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr9:77411797 G>A maps to NM_017662.4 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:77353421 C>A maps to NM_017662.4 E1893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:77367278 C>A maps to NM_017662.4 E1638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:77457138 T>C maps to NM_017662.4 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:50929676 C>T maps to NM_017672.4 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:50862084 T>C maps to NM_017672.4 P1822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:50853902 G>T maps to NM_017672.4 S1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr15:50906373 G>T maps to NM_017672.4 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:50886631 C>A maps to NM_017672.4 G1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:234916723 C>T maps to NM_024080.4 R1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:234839347 A>G maps to NM_024080.4 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr2:234846017 C>T maps to NM_024080.4 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:234854618 C>T maps to NM_024080.4 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:234878943 C>A maps to NM_024080.4 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:234891821 C>T maps to NM_024080.4 Y905Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:234869643 G>A maps to NM_024080.4 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:234869434 G>T maps to NM_024080.4 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:234854660 G>A maps to NM_024080.4 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:234835298 C>T maps to NM_024080.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:234835299 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:234858645 G>A maps to NM_024080.4 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:116631463 G>A maps to NM_014112.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:116426928 A>G maps to NM_014112.2 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:116430563 A>G maps to NM_014112.2 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr8:116426721 C>T maps to NM_014112.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:116599719 T>C maps to NM_014112.2 T736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:116616217 C>A maps to NM_014112.2 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:116616230 C>T maps to NM_014112.2 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:116616418 C>A maps to NM_014112.2 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:116616593 C>T maps to NM_014112.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:116632179 C>A maps to NM_014112.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr8:116631583 G>A maps to NM_014112.2 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr8:116631583 G>A maps to NM_014112.2 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:63991769 G>T maps to NM_001160393.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr11:63993013 G>A maps to NM_001160393.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:3493235 C>T maps to ENST00000399756 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:3493235 C>T maps to ENST00000399756 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr17:3493226 C>T maps to ENST00000399756 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:16338242 G>A maps to NM_016113.4 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:16335352 G>A maps to NM_016113.4 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr17:16326861 C>T maps to NM_016113.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:16327044 G>A maps to NM_016113.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:16330085 G>A maps to NM_016113.4 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:16326201 C>T maps to NM_016113.4 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr17:3436190 G>A maps to ENST00000381913 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:3433497 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:3445839 C>A maps to ENST00000381913 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:3458051 C>T maps to ENST00000381913 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:3431411 C>T maps to ENST00000381913 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr12:110232160 G>A maps to NM_021625.4 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr12:110232235 C>T maps to NM_021625.4 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:110230201 G>A maps to NM_021625.4 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:142612681 G>A maps to NM_019841.4 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:142575032 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr7:98609013 G>A maps to ENST00000359863 A3717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:98608829 C>T maps to ENST00000359863 F3684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:98586432 C>T maps to ENST00000359863 H3149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:98609023 C>T maps to ENST00000359863 L3721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:98513383 C>T maps to ENST00000359863 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:98534827 C>T maps to ENST00000359863 I1387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:98560012 C>T maps to ENST00000359863 Y2257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:98609887 C>T maps to ENST00000359863 G3830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr7:98576478 C>T maps to ENST00000359863 C2855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:98507683 C>T maps to ENST00000359863 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:98579408 G>A maps to ENST00000359863 P2877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:98524885 C>T maps to ENST00000359863 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:98529152 C>T maps to ENST00000359863 H1239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:98581896 C>T maps to ENST00000359863 I3072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:98508890 T>G maps to ENST00000359863 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:98581837 C>T maps to ENST00000359863 L3053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:98581896 C>T maps to ENST00000359863 I3072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:98601885 C>A maps to ENST00000359863 I3447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:98527691 G>T maps to ENST00000359863 G1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr7:98562315 C>T maps to ENST00000359863 S2291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:98487989 C>T maps to ENST00000359863 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:98579408 G>A maps to ENST00000359863 P2877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:98601945 C>T maps to ENST00000359863 F3467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr7:98552893 C>G maps to ENST00000359863 V1961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr7:98609764 G>A maps to ENST00000359863 T3789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:98609881 C>T maps to ENST00000359863 F3828F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:98609050 C>T maps to ENST00000359863 R3730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZR-01A-21D-A10M-09 chr7:98574218 G>A maps to ENST00000359863 P2684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:98478802 G>A maps to ENST00000359863 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr7:98591317 C>T maps to ENST00000359863 I3321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:116734972 G>A maps to NM_139169.4 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:116734978 T>C maps to NM_139169.4 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:116731929 G>A maps to NM_139169.4 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:116731929 G>A maps to NM_139169.4 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:131073847 G>A maps to NM_015679.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr9:135780990 G>A maps to NM_000368.4 D658D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:135778015 G>A maps to NM_000368.4 F789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:135787795 G>T maps to NM_000368.4 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr9:135771936 G>A maps to NM_000368.4 S1060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:135777990 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:2129044 G>A maps to NM_000548.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:2134954 C>T maps to NM_000548.3 F1499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:2129134 G>A maps to NM_000548.3 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr16:2134620 G>A maps to NM_000548.3 S1466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:2138109 C>T maps to NM_000548.3 F1710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:2133795 G>A maps to NM_000548.3 R1328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:2106649 C>A maps to NM_000548.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:45148995 C>T maps to NM_183422.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:45147543 C>T maps to NM_183422.2 Q889Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr13:45009013 T>C maps to NM_183422.2 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W2-01A-11D-A117-09 chr3:150176209 A>G maps to NM_014779.2 E710E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A187-01A-11D-A12J-09 chr3:150127625 C>T maps to NM_014779.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:106957872 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:106957841 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:106959935 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:106957754 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:106959997 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:107018547 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:106957810 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:107018367 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:100071933 A>G maps to NM_030935.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:12560644 C>T maps to NM_025265.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:12545082 C>T maps to NM_025265.3 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:54695636 G>A maps to NM_001077446.2 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:73518242 C>T maps to NM_207346.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:58190113 G>A maps to NM_001172696.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:58190113 G>A maps to NM_001172696.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:58190078 C>T maps to NM_001172696.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:58189999 G>A maps to NM_001172696.1 W225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:18503299 G>A maps to NM_006292.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:18503233 G>T maps to NM_006292.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:18503317 G>A maps to NM_006292.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:18528465 G>T maps to NM_006292.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:18503370 C>A maps to NM_006292.2 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:18536386 A>G maps to NM_006292.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:99634675 G>A maps to NM_025244.2 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:99651697 C>A maps to NM_025244.2 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:99651703 C>A maps to NM_025244.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:99681553 G>A maps to NM_025244.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:99688281 G>A maps to NM_025244.2 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr2:99685395 A>G maps to NM_025244.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:99688246 G>A maps to NM_025244.2 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:65726762 G>T maps to NM_152762.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:115576027 T>C maps to NM_000549.3 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:115576075 C>T maps to NM_000549.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:81609295 C>A maps to NM_000369.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:81610123 C>T maps to NM_000369.2 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:81422083 C>T maps to NM_000369.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:81554298 G>T maps to NM_000369.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:81574910 C>A maps to NM_001142626.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr14:81609928 G>T maps to NM_000369.2 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:72998642 G>A maps to NM_005786.4 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:72998831 C>T maps to NM_005786.4 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:72998426 G>A maps to NM_005786.4 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:72999725 C>T maps to NM_005786.4 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:73000151 G>A maps to NM_005786.4 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr18:72998159 C>T maps to NM_005786.4 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr18:72999689 G>A maps to NM_005786.4 K731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:72999755 C>T maps to NM_005786.4 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr18:72998007 C>T maps to NM_005786.4 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:72999404 G>A maps to NM_005786.4 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:73000079 G>A maps to NM_005786.4 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr20:51872366 C>T maps to NM_173485.5 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:51872036 C>T maps to NM_173485.5 C680C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:51870392 C>T maps to NM_173485.5 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:51872330 G>A maps to NM_173485.5 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:51872192 G>A maps to NM_173485.5 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:51870398 G>A maps to NM_173485.5 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:51872342 T>G maps to NM_173485.5 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:51870086 G>A maps to NM_173485.5 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr20:51870059 G>A maps to NM_173485.5 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr20:51870938 G>A maps to NM_173485.5 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr20:51870695 C>T maps to NM_173485.5 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr19:31768040 C>T maps to NM_020856.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:31769198 G>T maps to NM_020856.2 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:31770553 C>A maps to NM_020856.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:31767943 C>A maps to NM_020856.2 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:31768154 G>A maps to NM_020856.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr19:31768349 G>A maps to NM_020856.2 H783H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:31767473 G>T maps to NM_020856.2 V1075V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr19:31769276 G>A maps to NM_020856.2 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr19:31768805 C>T maps to NM_020856.2 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:31768040 C>T maps to NM_020856.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:31767826 G>A maps to NM_020856.2 R958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr19:31770269 C>T maps to NM_020856.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:31767494 C>T maps to NM_020856.2 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:31769345 G>A maps to NM_020856.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:50245276 G>A maps to NM_021733.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr19:50248523 G>A maps to NM_021733.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:50247576 G>A maps to NM_021733.1 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr19:50250004 C>T maps to NM_021733.1 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:76507208 G>A maps to NM_015516.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr8:143395762 C>T maps to ENST00000445818 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:143381918 C>T maps to ENST00000445818 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:143412290 C>T maps to ENST00000445818 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:143381960 G>A maps to ENST00000445818 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:143413181 G>A maps to ENST00000445818 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:143425606 G>A maps to ENST00000445818 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:143425651 C>T maps to ENST00000445818 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:143395783 G>T maps to ENST00000445818 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr1:231696949 T>A maps to NM_005999.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr16:67859093 C>T maps to ENST00000339830 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:67855086 C>T maps to ENST00000339830 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:67855109 C>A maps to ENST00000339830 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:67854846 C>T maps to ENST00000339830 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:31106945 G>A maps to NM_001080509.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:31132559 C>A maps to NM_001080509.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:31106951 C>T maps to NM_001080509.2 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:120446661 C>A maps to NM_012338.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:82269208 C>T maps to NM_030927.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr10:82276000 C>T maps to NM_030927.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:71264231 C>T maps to NM_012339.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:11411947 C>T maps to NM_012466.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr5:176079856 C>T maps to NM_012171.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:176082005 C>T maps to NM_012171.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:44948229 T>C maps to ENST00000425677 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:44948289 C>T maps to ENST00000425677 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:44941474 A>G maps to ENST00000425677 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr11:44948253 C>T maps to ENST00000425677 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr12:85421801 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:85408289 C>T maps to NM_001100917.1 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:115595999 C>T maps to NM_005725.4 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:115604773 C>T maps to NM_005725.4 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:77339191 G>A maps to NM_005724.5 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:77345213 C>A maps to NM_005724.5 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr12:58139529 G>A maps to NM_005981.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr23:99889013 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:99887530 G>A did not map to a codon.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr23:99890694 G>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:99891679 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:99890194 C>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:99890721 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:99891635 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:38420870 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:38530644 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:38530696 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:38534998 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:38540517 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:38540528 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:3390925 G>A maps to ENST00000407263 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:3390437 C>T maps to ENST00000407263 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr22:43558924 C>T maps to NM_000714.4 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr23:53115134 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:53115178 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53112015 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53112403 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:53115126 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:53112307 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:53112182 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:53115362 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53114482 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:53115255 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:53114261 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:53115118 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:53112456 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53115070 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53115192 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:53115433 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:53115250 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:53114231 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:116573927 T>C maps to ENST00000368611 *465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:116575056 C>A maps to ENST00000368611 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:116574037 C>T maps to ENST00000368611 W428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:98289538 C>T maps to NM_033512.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:98289481 C>T maps to NM_033512.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:98289556 C>T maps to NM_033512.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr8:98288863 C>T maps to NM_033512.2 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:98289178 G>A maps to NM_033512.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr2:54482502 C>T maps to NM_001003937.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:2237911 G>A maps to NM_018128.4 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr17:2237911 G>A maps to NM_018128.4 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:54470890 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr23:54470968 C>T did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr23:54469840 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:2424339 C>T maps to NM_005706.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:2423907 C>T maps to NM_005706.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:2424405 C>T maps to NM_005706.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:112769885 G>A maps to NM_032028.3 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr5:112770527 G>A maps to NM_032028.3 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:112770238 C>A maps to NM_032028.3 E100*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-AX-A064-01A-11W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:19118944 T>C maps to NM_053006.4 G11G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A0JY-01A-11D-A10B-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D1-A103-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D1-A167-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:19625999 G>A maps to NM_032037.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:144696804 G>A maps to NM_003313.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:144698735 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:100387985 G>T maps to NM_139246.4 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:100367863 G>A maps to NM_139246.4 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:43230556 G>A maps to NM_032538.1 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:43220487 C>T maps to NM_032538.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr15:43109244 G>A maps to ENST00000263802 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:43093268 G>T maps to ENST00000263802 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr15:43093313 A>G maps to ENST00000263802 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:43067785 G>T maps to ENST00000263802 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr15:43038148 G>A maps to ENST00000263802 S1598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:43044592 C>A maps to ENST00000263802 E1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:43044671 T>C maps to ENST00000263802 E1329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:43075754 G>A maps to ENST00000263802 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr15:43069416 G>A maps to ENST00000263802 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:159492044 C>T maps to NM_003314.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:113234588 C>T maps to NM_017868.3 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:113209522 G>T maps to NM_017868.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:113211428 C>A maps to NM_017868.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:113235611 C>T maps to NM_017868.3 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:113235728 C>T maps to NM_017868.3 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr11:113196253 G>T maps to NM_017868.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:231093978 C>A maps to NM_024525.4 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:231060653 G>A maps to NM_024525.4 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:180321041 C>T maps to NM_133462.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:180322126 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr3:180320985 C>T maps to NM_133462.3 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:180325453 G>A maps to NM_133462.3 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:180327726 G>A maps to NM_133462.3 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:180321102 G>T maps to NM_133462.3 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr3:180322093 C>T maps to NM_133462.3 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:130482442 C>A maps to NM_144965.1 C171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:43419564 C>T maps to NM_018259.5 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:43413474 T>C maps to NM_018259.5 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr11:43419013 C>T maps to NM_018259.5 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr11:43419564 C>T maps to NM_018259.5 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:43513658 C>T maps to NM_018259.5 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr11:43469633 C>T maps to NM_018259.5 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:75034273 G>A maps to NM_145170.3 R988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:75082792 C>T maps to NM_145170.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:75056811 T>C maps to NM_145170.3 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:75082831 C>T maps to NM_145170.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:75038023 C>A maps to NM_145170.3 E841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:75095276 G>A maps to NM_145170.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:39170390 C>T maps to ENST00000301819 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:39178515 C>T maps to ENST00000301819 G1082G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:39167795 C>T maps to ENST00000301819 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:39150694 C>T maps to ENST00000301819 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:39170603 C>T maps to ENST00000301819 F654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:166747442 G>A maps to NM_024753.3 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:166797631 G>A maps to NM_024753.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr2:166747049 A>G maps to NM_024753.3 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr15:99740198 T>C maps to NM_022905.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr15:99679550 G>C maps to NM_022905.4 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:34896882 G>A maps to NM_144725.3 *362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:34850316 C>T maps to NM_144725.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:34896873 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:34850288 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:34864599 G>T maps to NM_144725.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156552137 A>G maps to NM_001105669.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:156551506 C>T maps to NM_001105669.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:156555562 G>A maps to NM_001105669.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:40117195 G>T maps to ENST00000377543 G572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:40117456 G>T maps to ENST00000377543 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr7:138864317 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:138863040 C>A maps to NM_024926.2 S384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:32903921 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:32865407 G>A maps to NM_017735.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:32897400 C>T maps to NM_017735.4 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:33036242 C>T maps to NM_017735.4 H717H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:33036269 G>A maps to NM_017735.4 K726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:33042569 A>G maps to NM_017735.4 V785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:33012049 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:147830229 T>C maps to ENST00000513335 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:147824740 C>A maps to ENST00000513335 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr21:38463678 T>C maps to NM_003316.3 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:38460137 G>A maps to NM_003316.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:38507759 C>T maps to NM_003316.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr21:38539916 C>T maps to NM_003316.3 R1488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr21:38525299 A>G maps to NM_003316.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:38461123 T>C maps to NM_003316.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr21:38537933 G>T maps to NM_003316.3 E1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr21:38529137 G>A maps to NM_003316.3 W974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:38538229 A>G maps to NM_003316.3 K1238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:38467694 G>T maps to NM_003316.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:38534365 G>T did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr21:38507789 C>T maps to NM_003316.3 N518N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:38519804 G>T maps to NM_003316.3 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr21:38538119 C>T maps to NM_003316.3 R1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:178483168 C>T maps to NM_152275.3 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:178482487 T>C maps to NM_152275.3 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:178482000 C>A maps to NM_152275.3 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:178482946 A>G maps to NM_152275.3 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:178417029 G>A maps to NM_152517.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:178415763 T>C maps to NM_152517.2 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:178415660 C>A maps to NM_152517.2 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:40728532 C>A maps to NM_012382.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:40746975 C>A maps to NM_012382.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:40716593 G>A maps to NM_012382.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:109482081 C>T maps to NM_014673.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:109488180 C>T maps to NM_014673.3 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:109482342 G>T maps to NM_014673.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:94876476 C>A maps to NM_014639.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:94818226 C>A maps to NM_014639.3 E1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:94800317 G>C maps to NM_014639.3 S1563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:94865913 C>T maps to NM_014639.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:94864789 A>G maps to NM_014639.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:94838672 C>T maps to NM_014639.3 E1084E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:46669894 G>A maps to NM_017931.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr22:46677539 C>T maps to NM_017931.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr22:46671211 C>T maps to NM_017931.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:46681151 C>T maps to NM_017931.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:51787797 A>C maps to ENST00000447632 P12P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AX-A0J0-01A-11D-A117-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr1:51787809 G>A maps to ENST00000447632 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:51755768 G>A maps to ENST00000447632 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:15188067 G>T maps to NM_152574.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:15307231 C>T maps to NM_152574.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:15186967 C>T maps to NM_152574.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr9:15192656 G>A maps to NM_152574.2 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:15186967 C>T maps to NM_152574.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y8-01A-11D-A159-09 chr9:15203832 G>C maps to NM_152574.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:21705425 G>A maps to NM_001135993.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:21644102 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:21698105 G>T maps to NM_001135993.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:21644102 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:21708874 T>C maps to NM_001135993.1 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:55182301 G>A maps to NM_004623.4 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr1:55183249 C>G maps to NM_004623.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:47249101 C>T maps to ENST00000394850 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:47256502 C>T maps to ENST00000394850 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:47184033 C>T maps to ENST00000394850 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11X-01A-11D-A10M-09 chr2:47177664 G>A maps to ENST00000394850 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr2:47233182 C>T maps to ENST00000394850 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr14:91110423 G>A maps to NM_001010854.1 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr14:91113309 A>G maps to NM_001010854.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr14:91142992 G>A maps to NM_001010854.1 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:91077133 G>A maps to NM_001010854.1 R640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr14:91059965 G>T maps to NM_001010854.1 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:91121427 T>C maps to NM_001010854.1 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:89307530 G>A maps to NM_144596.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:89307767 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:89310166 C>A maps to NM_144596.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:89336428 A>C maps to NM_144596.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:62502897 G>T maps to NM_173810.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:135251376 G>A maps to NM_007344.2 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr9:135277917 G>A maps to NM_007344.2 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:135275575 T>G maps to NM_007344.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:135251432 G>A maps to NM_007344.2 R863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:135276896 G>A maps to NM_007344.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:135271859 G>A maps to NM_007344.2 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:135277802 A>G maps to NM_007344.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:117631595 G>A maps to NM_003594.3 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:117617782 G>T maps to NM_003594.3 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:117618327 G>A maps to NM_003594.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:117626649 C>T maps to NM_003594.3 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:80715831 A>G maps to ENST00000509313 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:80718109 G>T maps to NM_003318.4 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:80715658 T>C maps to NM_003318.4 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:80717676 G>A maps to NM_003318.4 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:80717676 G>A maps to NM_003318.4 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:113251760 G>A maps to NM_153712.4 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:113251908 A>G maps to NM_153712.4 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:113240001 G>A maps to NM_153712.4 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr2:113240043 G>A maps to NM_153712.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:1116114 G>A maps to NM_001130045.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:124752049 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:124736404 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:124751689 G>A maps to NM_001139442.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:43575961 G>A maps to NM_015140.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:43575961 G>A maps to NM_015140.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:43568479 G>A maps to NM_015140.3 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:90801324 C>T maps to ENST00000438251 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr15:90800386 C>T maps to ENST00000438251 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:167754698 C>T maps to NM_031949.4 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:167754338 T>C maps to NM_031949.4 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:9859435 C>A maps to NM_001025930.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:9874861 G>A maps to NM_001025930.3 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:9857780 C>A maps to ENST00000443148 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:219609834 C>T maps to NM_014640.4 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:219614017 A>G maps to NM_014640.4 R881R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:219604832 G>T maps to NM_014640.4 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:219604832 G>T maps to NM_014640.4 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:219610492 C>T maps to NM_014640.4 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:219616454 C>T maps to NM_014640.4 R968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:219618317 G>A maps to NM_014640.4 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:76165558 G>A maps to NM_015072.4 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:76286441 G>A maps to NM_015072.4 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:76184215 G>A maps to NM_015072.4 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:76243106 T>C maps to NM_015072.4 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr14:76211871 C>T maps to NM_015072.4 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:46847315 C>T maps to NM_001130918.1 K728K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:46846440 G>A maps to NM_001130918.1 H862H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr17:46865186 C>T maps to NM_001130918.1 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:46874455 C>T maps to NM_001130918.1 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:84372115 C>A maps to NM_024686.4 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:84394906 G>T maps to NM_024686.4 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50469134 C>A maps to NM_001080447.1 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:30530751 C>T maps to NM_001008409.2 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr20:30530757 C>T maps to NM_001008409.2 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:30458943 G>A maps to NM_001008409.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:30475040 C>T maps to NM_001008409.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:179410817 G>T maps to NM_133378.4 L29147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:179553407 G>A maps to NM_133378.4 H9487H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:179399239 G>A maps to NM_133378.4 F31466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:179403859 G>A maps to NM_133378.4 I30366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:179417256 C>A maps to NM_133378.4 E27556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:179421848 G>T maps to NM_133378.4 I26776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:179553440 G>A maps to NM_133378.4 F9476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:179580421 G>A maps to NM_133378.4 I7329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr2:179393346 G>A maps to NM_133378.4 Q33143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr2:179478884 G>T maps to NM_133378.4 T13845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GU-01A-11W-A062-09 chr2:179464473 C>T maps to NM_133378.4 W16150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr2:179664275 C>T maps to NM_133378.4 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:179453922 T>C maps to NM_133378.4 V18275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179396826 G>A maps to NM_133378.4 R32271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179402567 G>A maps to NM_133378.4 C30554C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179426831 G>A maps to NM_133378.4 V25441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179455158 G>T maps to NM_133378.4 A17863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179457610 G>T maps to NM_133378.4 T17177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179481259 C>T maps to NM_133378.4 P13518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179534098 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179588300 C>A maps to NM_133378.4 E5932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179643788 G>A maps to NM_133378.4 D1340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:179647024 G>A maps to NM_133378.4 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:179437784 A>G maps to NM_133378.4 Y21790Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:179612282 C>T maps to ENST00000375038 V4950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:179640623 T>C maps to NM_133378.4 K1989K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179412800 G>A maps to NM_133378.4 F28616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179423350 T>C maps to NM_133378.4 P26377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179441977 C>T maps to NM_133378.4 T20460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179447703 A>G maps to NM_133378.4 S19374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179467273 C>T maps to NM_133378.4 T15717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179476303 G>T maps to NM_133378.4 I14316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179481732 T>G maps to NM_133378.4 P13393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179485206 G>A maps to NM_133378.4 V12779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179523193 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179527746 C>A maps to NM_133378.4 E10507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179552940 C>T maps to NM_133378.4 E9492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179569634 G>T maps to NM_133378.4 S8644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179585823 G>T maps to NM_133378.4 S6397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179587599 T>C maps to NM_133378.4 L6098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179594438 G>A maps to NM_133378.4 R4937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179594649 C>T maps to NM_133378.4 K4866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179595481 C>T maps to NM_133378.4 K4682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179613328 C>A maps to ENST00000375038 E4602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:179623846 G>A maps to NM_133378.4 F3389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179395518 C>A maps to NM_133378.4 E32707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179396724 C>A maps to NM_133378.4 E32305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179398594 G>A maps to NM_133378.4 D31681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179432594 G>T maps to NM_133378.4 P23520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179477785 G>T maps to NM_133378.4 P13986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179482119 G>A maps to NM_133378.4 R13330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179501149 G>T maps to NM_133378.4 T11200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179629356 C>T maps to NM_133378.4 T3295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179640596 G>A maps to NM_133378.4 R1998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:179643818 G>A maps to NM_133378.4 R1330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr2:179413967 G>T maps to NM_133378.4 V28227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179395861 C>T maps to NM_133378.4 V32592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179396059 G>T maps to NM_133378.4 S32526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179405007 C>A maps to NM_133378.4 G30061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179408015 G>A maps to NM_133378.4 Y29660Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179425601 G>A maps to NM_133378.4 D25851D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179440280 G>A maps to NM_133378.4 P20958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179442355 C>A maps to NM_133378.4 E20365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179470278 G>A maps to NM_133378.4 R15347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179480172 G>A maps to NM_133378.4 R13599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179504784 C>T maps to NM_133378.4 K11024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179528070 C>A maps to ENST00000392423 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179559598 C>T maps to NM_133378.4 K9191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179581891 G>A maps to NM_133378.4 A7279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179582781 G>A maps to NM_133378.4 N7073N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:179593049 C>A maps to NM_133378.4 E5257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr2:179408964 G>A maps to NM_133378.4 S29429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr2:179469885 T>C maps to NM_133378.4 V15438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179399935 G>T maps to NM_133378.4 V31234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179410324 C>A maps to NM_133378.4 E29270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179417100 C>A maps to NM_133378.4 E27608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179428333 G>A maps to NM_133378.4 R24941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179459337 C>A maps to NM_133378.4 E16727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179463538 G>T maps to NM_133378.4 I16398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179526522 C>T maps to ENST00000392423 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179569675 C>T maps to NM_133378.4 E8630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179575834 T>C maps to NM_133378.4 T8132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179575972 G>T maps to NM_133378.4 I8086I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179577955 C>A maps to NM_133378.4 G7725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179604978 G>T maps to NM_133437.3 S4156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179612893 C>A maps to ENST00000375038 E4747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179614363 C>A maps to ENST00000375038 E4257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179623810 C>A maps to NM_133378.4 L3401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:179641739 G>A maps to NM_133378.4 I1617I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179422467 C>A maps to NM_133378.4 G26637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179425591 G>A maps to NM_133378.4 R25855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179443653 G>T maps to NM_133378.4 T20133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179444447 A>G maps to NM_133378.4 T19924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179472161 A>G maps to NM_133378.4 G15183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179486672 C>T maps to NM_133378.4 K12424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179534400 T>C maps to ENST00000392423 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179553410 C>T maps to NM_133378.4 R9486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179612201 A>G maps to ENST00000375038 S4977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:179640245 A>G maps to NM_133378.4 G2115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr2:179632508 G>A maps to NM_133378.4 R3150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr2:179466475 C>T maps to NM_133378.4 P15879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179391749 G>A maps to NM_133378.4 R33421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179426305 G>A maps to NM_133378.4 R25617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179454956 G>A maps to NM_133378.4 R17931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179458403 A>C maps to NM_133378.4 V16973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179470312 A>G maps to NM_133378.4 R15335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179477259 T>G maps to NM_133378.4 T14096T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179480412 C>A maps to NM_133378.4 E13571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179494170 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179548795 C>T maps to NM_133378.4 P9668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179579172 G>A maps to NM_133378.4 I7532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179586801 C>A maps to NM_133378.4 E6286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179589095 G>T maps to NM_133378.4 I5758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179611024 C>A maps to ENST00000375038 E5370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179612776 C>A maps to ENST00000375038 E4786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179612903 T>C maps to ENST00000375038 A4743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179614135 C>A maps to ENST00000375038 E4333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:179647146 C>A maps to NM_133378.4 E1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:179430272 G>A maps to NM_133378.4 S24294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:179431169 G>A maps to NM_133378.4 V23995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:179444945 C>T maps to NM_133378.4 G19788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:179473627 C>T maps to NM_133378.4 P14802P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:179550286 G>A maps to NM_133378.4 L9540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr2:179501284 A>G maps to NM_133378.4 G11155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:179495572 G>A maps to NM_133378.4 H12136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179428757 A>G maps to NM_133378.4 L24799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179428916 T>C maps to NM_133378.4 K24746K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179434700 T>C maps to NM_133378.4 G22818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179442497 C>T maps to NM_133378.4 S20317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179459169 C>A maps to NM_133378.4 E16783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179485032 G>A maps to NM_133378.4 F12837F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179489371 C>A maps to NM_133378.4 E12311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179500777 G>A maps to NM_133378.4 N11272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179516906 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179571203 G>A maps to NM_133378.4 G8555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179587192 G>A maps to NM_133378.4 R6197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179596657 G>T maps to NM_133378.4 V4404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179613013 G>T maps to ENST00000375038 R4707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179614946 T>C maps to ENST00000375038 A4062A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179641892 A>G maps to NM_133378.4 H1599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:179655481 C>A maps to NM_133378.4 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr2:179594418 C>T maps to NM_133378.4 A4943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr2:179639057 T>C maps to NM_133378.4 K2311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:179438797 T>G maps to NM_133378.4 R21453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr2:179634514 C>T maps to NM_133378.4 V2931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179434058 G>A maps to NM_133378.4 D23032D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179451258 C>A maps to NM_133378.4 G18889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179458351 G>A maps to NM_133378.4 L16991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179472398 C>A maps to NM_133378.4 V15104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179481259 C>T maps to NM_133378.4 P13518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179560664 G>A maps to NM_133378.4 D9134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179567298 A>G maps to NM_133378.4 D8861D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179610830 C>T maps to ENST00000375038 E5434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179629331 C>A maps to NM_133378.4 E3304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:179640647 C>T maps to NM_133378.4 R1981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:179413565 T>C maps to NM_133378.4 A28361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:179427976 C>A maps to NM_133378.4 G25060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:179598098 G>A maps to NM_133378.4 Y4063Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:179659828 A>G maps to NM_133378.4 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:179426049 G>T maps to NM_133378.4 S25702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:179430976 G>A maps to NM_133378.4 R24060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:179436929 A>G maps to NM_133378.4 D22075D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:179458784 C>T maps to NM_133378.4 E16877E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:179506964 G>A maps to NM_133378.4 S10951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:179516391 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:179588751 A>G maps to NM_133378.4 F5834F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:179644116 C>A maps to NM_133378.4 E1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr2:179535832 T>C maps to NM_133378.4 K10463K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:179395331 G>C maps to NM_133378.4 S32769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr2:179596507 C>T maps to NM_133378.4 K4454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr2:179595379 T>C maps to NM_133378.4 S4716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr2:179485146 A>G maps to NM_133378.4 D12799D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr2:179599283 T>C maps to NM_133378.4 G3845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr2:179594421 C>T maps to NM_133378.4 T4942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr2:179584020 C>T maps to NM_133378.4 Q6788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:179418273 C>A maps to NM_133378.4 E27252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:179434108 C>A maps to NM_133378.4 E23016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:179602934 G>A maps to NM_133378.4 R3505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:179613946 C>A maps to ENST00000375038 E4396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:179631336 G>T maps to NM_133378.4 V3158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:179632554 G>A maps to NM_133378.4 N3134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:179633571 G>T maps to NM_133378.4 I2997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr2:179410568 T>C maps to NM_133378.4 P29230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr2:179460303 C>T maps to NM_133378.4 A16691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr2:179643730 C>A maps to NM_133378.4 G1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179412571 G>A maps to NM_133378.4 R28693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179438144 C>T maps to NM_133378.4 S21670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179439333 G>T maps to NM_133378.4 S21274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179465830 C>T maps to NM_133378.4 W16032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179501356 G>A maps to NM_133378.4 F11131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179504515 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179536868 C>A maps to NM_133378.4 E10385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179584793 C>A maps to NM_133378.4 E6615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179588271 G>T maps to NM_133378.4 I5941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179610758 C>A maps to ENST00000375038 V5458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179615407 C>A maps to ENST00000375038 E3909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179615605 C>A maps to ENST00000375038 E3843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:179641985 C>T maps to NM_133378.4 K1568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:179414324 A>C maps to NM_133378.4 S28140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:179437214 A>G maps to NM_133378.4 G21980G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:179446418 G>T maps to NM_133378.4 L19624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:179604345 A>G maps to NM_133437.3 F4367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:179435389 G>A maps to NM_133378.4 R22589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:179481952 T>C maps to NM_133378.4 G13355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:179499951 G>A maps to NM_133378.4 I11420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:179590253 C>A maps to NM_133378.4 E5649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:179605674 C>T maps to NM_133437.3 E3924E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr2:179647563 G>C maps to NM_133378.4 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr2:179489417 C>T maps to NM_133378.4 T12295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:179401680 G>T maps to NM_133378.4 I30817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:179451433 G>A maps to NM_133378.4 I18830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:179456347 C>T maps to NM_133378.4 P17498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:179528225 C>A maps to ENST00000392423 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:179579177 C>A maps to NM_133378.4 E7531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:179593296 G>A maps to NM_133378.4 S5208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:179410963 G>A maps to NM_133378.4 A29130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:179435162 A>G maps to NM_133378.4 D22664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:179647598 G>A maps to NM_133378.4 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:179650670 G>A maps to NM_133378.4 H758H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr2:179466063 G>A maps to NM_133378.4 R15986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr2:179499272 G>A maps to NM_133378.4 R11511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr2:179571347 G>A maps to NM_133378.4 G8507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:179640428 G>A maps to NM_133378.4 A2054A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:179547472 G>A maps to NM_133378.4 Y9771Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:179645962 G>A maps to NM_133378.4 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:179410151 G>A maps to NM_133378.4 S29327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:179393278 G>A maps to NM_133378.4 I33165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:179426603 G>A maps to NM_133378.4 C25517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:179431564 G>A maps to NM_133378.4 R23864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:179438297 G>T maps to NM_133378.4 L21619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:179592992 C>A maps to NM_133378.4 E5276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:179599204 G>A maps to NM_133378.4 R3872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:179485077 C>T maps to NM_133378.4 P12822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr2:179610791 A>C maps to ENST00000375038 L5447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr2:179587192 G>A maps to NM_133378.4 R6197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr2:179422831 G>A maps to NM_133378.4 V26515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179391828 C>T maps to NM_133378.4 Q33394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179397259 T>C maps to NM_133378.4 S32126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179431219 G>A maps to NM_133378.4 R23979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179435048 A>G maps to NM_133378.4 L22702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179451433 G>A maps to NM_133378.4 I18830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179455520 G>A maps to NM_133378.4 R17743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179472161 A>G maps to NM_133378.4 G15183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179577514 G>A maps to NM_133378.4 F7835F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179584977 G>A maps to NM_133378.4 F6553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179592509 C>A maps to NM_133378.4 G5355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:179593263 G>A maps to NM_133378.4 F5219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:179523750 C>T maps to NM_133378.4 P10574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr2:179633487 C>A maps to NM_133378.4 L3025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:63976797 G>A maps to NM_000370.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:63985566 G>A maps to NM_000370.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr20:43108644 C>T maps to NM_024331.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:43118136 C>T maps to NM_024331.3 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:43108804 C>T maps to NM_024331.3 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:43109010 C>T maps to NM_024331.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:43108747 G>T maps to NM_024331.3 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:29178616 C>T maps to ENST00000432547 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:54930462 C>T maps to ENST00000391739 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:54933405 G>T maps to ENST00000391739 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:54947306 T>G maps to ENST00000391739 *452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:54942318 G>T maps to ENST00000391739 G359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:54942080 C>T maps to ENST00000391739 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:54930462 C>T maps to ENST00000391739 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:72233434 T>A maps to NM_032646.5 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:72249358 C>T maps to NM_032646.5 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:72249396 C>T maps to NM_032646.5 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:2696036 C>T maps to NM_025250.2 Y373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:8118304 A>G maps to NM_003320.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr11:8119341 C>T maps to NM_003320.4 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:8123159 C>T maps to NM_003320.4 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:49580442 G>A maps to NM_006009.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:19751170 A>G maps to NM_006001.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:19748010 C>A maps to NM_006001.1 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:19751423 C>T maps to NM_006001.1 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr13:19753562 G>T maps to NM_006001.1 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:132238048 G>A maps to NM_080386.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:132237697 C>T maps to NM_080386.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:130952039 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:130953815 G>A maps to NM_207312.2 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:130951756 C>A maps to NM_207312.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:130949507 C>A maps to NM_207312.2 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr2:130951558 G>A maps to NM_207312.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr2:130949415 G>A maps to NM_207312.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr2:130953800 G>A maps to NM_207312.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:130951946 C>T maps to NM_207312.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:220116736 C>T maps to NM_006000.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:220115763 G>A maps to NM_006000.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:220116328 G>A maps to NM_006000.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:220116817 G>A maps to NM_006000.1 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr2:220115496 C>T maps to NM_006000.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr22:18604310 C>T maps to NM_018943.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:18604248 G>T maps to NM_018943.2 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr22:18613801 G>T maps to NM_018943.2 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:5435830 C>T maps to NM_024803.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:5435794 C>T maps to NM_024803.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:5435509 C>T maps to NM_024803.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Z-01A-11D-A10M-09 chr10:5436058 G>A maps to NM_024803.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:30691402 C>T maps to NM_178014.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr6:30691165 C>T maps to NM_178014.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:57598886 C>T maps to NM_030773.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:3156299 G>A maps to NM_001069.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr6:3154174 G>T maps to NM_001069.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:3154822 G>A maps to NM_001069.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr6:3156347 G>A maps to NM_001069.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:3225095 G>A maps to NM_178012.4 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:3225014 G>A maps to NM_178012.4 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:3225014 G>A maps to NM_178012.4 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:3226474 G>A maps to NM_178012.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:90001641 G>A maps to ENST00000304984 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr16:90001902 C>T maps to ENST00000304984 N695N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:90001590 C>T maps to ENST00000304984 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:93845 C>T maps to NM_177987.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:57944105 A>G maps to NM_016261.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:112400935 G>A maps to NM_016262.4 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:112400953 G>A maps to NM_016262.4 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:40766525 T>C maps to NM_001070.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:40765675 C>T maps to NM_001070.4 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A186-01A-11D-A12J-09 chr17:40766430 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:40811921 C>T maps to NM_016437.2 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:135094913 C>T maps to NM_006659.2 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:135116411 C>A maps to NM_006659.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:113174283 T>G maps to NM_006322.4 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr13:113200144 G>A maps to NM_006322.4 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:113143947 C>A maps to NM_006322.4 E838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr13:113208489 G>A maps to NM_006322.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr13:113176743 C>T maps to NM_006322.4 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:113143993 C>T maps to NM_006322.4 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:43669265 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:43668300 G>A maps to ENST00000399460 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:43687328 G>T maps to ENST00000399460 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:22866909 G>A maps to NM_052903.4 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:22848883 C>T maps to NM_052903.4 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:22836065 T>C maps to NM_052903.4 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:22835914 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:22836061 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:22851109 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr22:50664610 C>T maps to NM_020461.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:50657049 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50657308 C>T maps to NM_020461.3 T1548T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr22:50664797 G>A maps to NM_020461.3 H537H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr22:50662686 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr22:50662993 C>A maps to NM_020461.3 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:50656649 C>T maps to NM_020461.3 A1712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:50660063 C>T maps to NM_020461.3 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:50662993 C>A maps to NM_020461.3 E671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr22:50662576 T>A maps to NM_020461.3 K755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50656428 C>T maps to NM_020461.3 P1762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:151552189 C>T maps to NM_020127.2 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:35480610 G>A maps to NM_003322.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:35478731 C>T maps to NM_003322.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:35477676 C>T maps to NM_003322.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:49391445 C>A maps to NM_003323.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:49385367 G>A maps to NM_003323.2 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:49388730 G>A maps to NM_003323.2 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:158873286 C>T maps to NM_020245.3 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:158923868 C>T maps to NM_020245.3 S1058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:158870179 G>A maps to NM_020245.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A169-01A-11D-A12J-09 chr6:158923538 C>T maps to NM_020245.3 V948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:62343615 G>A maps to NM_022830.2 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:62346502 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62327832 G>A maps to ENST00000378019 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:62348951 C>T maps to NM_022830.2 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:62358995 G>A maps to NM_022830.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:62343183 G>A maps to NM_022830.2 C707C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:44196086 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:52265980 G>T maps to NM_007284.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52263753 G>A maps to ENST00000494383 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:52269096 A>G maps to NM_007284.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:19748422 C>A maps to NM_001002926.1 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:19738334 G>T maps to NM_001002926.1 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:19738154 C>T maps to NM_001002926.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:19738109 T>C maps to NM_001002926.1 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:9396407 C>T maps to NM_020648.5 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:9396291 C>T maps to NM_020648.5 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:48088526 G>T maps to NM_003328.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:32647119 C>T maps to NM_175852.3 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:139609997 T>C maps to ENST00000358430 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:139581477 G>A maps to ENST00000358430 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:139564406 G>A maps to ENST00000358430 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:139564432 C>A maps to ENST00000358430 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:16852419 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:16855742 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:16836763 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:16836783 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:16836903 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:16859598 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:16836937 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:16836795 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:16850790 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:16859705 G>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:16859705 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:16836783 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:16847869 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:113013685 G>A maps to NM_003329.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:36863922 G>A maps to NM_012473.3 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:36863943 C>T maps to NM_012473.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr16:11785668 G>A maps to ENST00000356957 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:11781720 A>T maps to ENST00000356957 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:11824587 G>T maps to ENST00000356957 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr5:134223685 C>T maps to NM_024715.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr14:52899167 T>A maps to NM_020784.2 K778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:52899099 C>T maps to NM_020784.2 W800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:53010215 A>G maps to NM_020784.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:9887208 G>T maps to NM_001098529.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:9887208 G>T maps to NM_001098529.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:9886800 G>T maps to NM_001098529.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:9887678 G>A maps to NM_001098529.1 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr18:9887028 G>T maps to NM_001098529.1 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:9887129 G>A maps to NM_001098529.1 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:37901670 G>A maps to NM_016616.4 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:37905182 A>G maps to NM_016616.4 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:37927896 G>A maps to NM_016616.4 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:37903063 C>T maps to NM_016616.4 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:37907311 C>T maps to NM_016616.4 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:37901700 C>T maps to NM_016616.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:37890037 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:37923978 G>T maps to NM_016616.4 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:37907311 C>T maps to NM_016616.4 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:7883468 G>A maps to NM_030810.3 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr6:7883468 G>T maps to NM_030810.3 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:7886243 G>A maps to NM_030810.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr6:7899811 T>C maps to NM_030810.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:113096600 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:99938614 T>C maps to NM_005783.3 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:54270180 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:54278313 C>T maps to NM_004786.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:72120628 G>T maps to NM_001142318.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:104645330 T>C maps to NM_001093771.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr12:104742190 T>C maps to NM_001093771.1 *648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:104713268 G>T maps to NM_001093771.1 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:104725407 G>T maps to NM_001093771.1 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:19898967 G>A maps to NM_006440.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:10464730 G>A maps to NM_003331.4 C965C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:10476447 C>T maps to NM_003331.4 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:10475408 G>A maps to NM_003331.4 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:10472849 G>T maps to NM_003331.4 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:10476375 G>A maps to NM_003331.4 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:10476339 C>T maps to NM_003331.4 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr19:10464802 G>C maps to NM_003331.4 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr19:10475378 C>A maps to NM_003331.4 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:50966942 G>A maps to ENST00000395681 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:50967758 G>A maps to ENST00000395681 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr18:670815 C>T maps to NM_001071.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:89018027 C>A maps to NM_000372.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:88911246 C>T maps to NM_000372.4 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:88924504 G>T maps to NM_000372.4 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr15:41864677 C>A maps to NM_006293.3 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr15:41870440 G>A maps to NM_006293.3 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:41859735 G>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr15:41863263 G>A maps to NM_006293.3 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr15:41870245 G>A maps to NM_006293.3 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:41854875 C>T maps to NM_006293.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr15:41861186 C>T maps to NM_006293.3 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:36398351 C>T maps to NM_003332.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:12698512 C>A maps to NM_000550.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:12698560 T>C maps to NM_000550.2 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:12709022 C>T maps to NM_000550.2 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr9:12695617 C>T maps to NM_000550.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr10:71903690 G>A maps to NM_173555.2 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:66703326 C>T maps to NM_018264.2 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:66463178 G>A maps to NM_018264.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr7:66703425 G>A maps to NM_018264.2 W703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr7:66660158 C>T maps to NM_018264.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:75204396 T>C maps to NM_138467.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr1:75229757 T>C maps to NM_138467.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:75202287 T>C maps to NM_138467.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr21:44513331 C>T maps to NM_001025203.1 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:56175096 C>T maps to NM_007279.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:56173962 C>T maps to NM_007279.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:56181009 C>T maps to NM_007279.2 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:70960610 T>C maps to NM_018003.2 V804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:70961254 G>A maps to NM_018003.2 R590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:70959097 C>A maps to NM_018003.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:70961252 T>A maps to NM_018003.2 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr15:70960979 G>A maps to NM_018003.2 H681H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr15:70961644 G>T maps to NM_018003.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:70959097 C>A maps to NM_018003.2 E1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:70960378 C>A maps to NM_018003.2 E882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:70959637 C>A maps to NM_018003.2 E1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:162569087 G>T maps to ENST00000367925 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:162546565 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47060742 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:47060331 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:47074322 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:47062183 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47060759 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47060912 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47069479 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:47061877 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:47074235 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47068948 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:47062425 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47060331 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:47060383 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:47069478 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47062946 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47062996 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47072253 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47074219 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:47058448 A>G did not map to a codon.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr23:47062082 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:34935950 T>C maps to NM_005499.2 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:34945253 C>A maps to NM_005499.2 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:34929584 G>A maps to NM_005499.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:34942895 G>A maps to NM_005499.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr19:34919390 C>T maps to NM_005499.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:34929584 G>A maps to NM_005499.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:132390940 G>T maps to NM_024818.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:132394463 C>T maps to NM_024818.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:132394463 C>T maps to NM_024818.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:68543397 G>A maps to NM_018227.5 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:68536259 G>A maps to NM_018227.5 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:68530939 A>G maps to NM_018227.5 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:68534316 C>A maps to NM_018227.5 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr4:68527864 T>C maps to ENST00000420827 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:49846846 C>T maps to NM_003335.2 Q713Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:49848720 G>T maps to NM_003335.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:49851199 C>T maps to NM_003335.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:49851199 C>T maps to NM_003335.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:138847228 A>G maps to NM_016172.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:100037561 C>T maps to NM_001144072.1 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:33989067 T>C maps to NM_018449.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:33927930 C>T maps to NM_018449.2 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:33922843 C>T maps to NM_018449.2 T1035T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:33922582 C>T maps to NM_018449.2 Q1093Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:33943428 C>T maps to NM_018449.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr9:33922846 C>T maps to NM_018449.2 G1034G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:33944511 G>A maps to NM_018449.2 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:33989033 C>A maps to NM_018449.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr9:33923437 G>C maps to NM_018449.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr1:154228161 G>A maps to NM_014847.3 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:154233485 C>T maps to NM_014847.3 N899N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:154241363 C>T maps to NM_014847.3 H1034H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:154229705 G>A maps to NM_014847.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:154235615 G>A maps to NM_001127320.1 T980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:154228170 G>A maps to NM_014847.3 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:43838559 G>A maps to NM_018961.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:43836554 C>T maps to NM_018961.2 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:43857601 C>T maps to NM_018961.2 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:43867196 G>T maps to NM_018961.2 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:122650320 C>T maps to NM_032873.4 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:122678799 C>T maps to NM_032873.4 H576H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:122680508 G>A maps to NM_032873.4 W622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:122647893 C>T maps to NM_032873.4 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:16285548 G>T maps to NM_018955.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:125398193 T>G maps to NM_021009.5 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:118716598 G>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:118715532 T>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:118717175 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:118717207 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:133724056 C>T maps to NM_003337.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:133716429 G>T maps to NM_003337.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:44444139 C>T maps to NM_181799.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:44444208 G>A maps to NM_007019.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:44444361 C>A maps to NM_007019.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:139006339 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:43990204 G>A maps to NM_015983.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr3:23929189 G>A maps to NM_003341.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:23258751 G>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:181925491 C>A maps to NM_182678.1 S160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr2:181927518 G>A maps to NM_182678.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:238934008 G>A maps to NM_080678.1 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:238925173 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:1370181 C>T maps to NM_194259.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:1370572 C>T maps to ENST00000402301 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr16:1370635 C>A maps to ENST00000402301 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:90053413 C>T maps to NM_016021.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:90039499 A>G maps to NM_016021.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:90052042 C>T maps to NM_016021.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:1190693 G>A maps to NM_194315.1 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr22:21975916 G>T maps to ENST00000458578 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:57319962 C>A maps to NM_004223.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr12:93835633 G>A maps to NM_003348.3 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:142967262 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:142967508 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:142967582 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr23:142967524 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:142967647 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Q-01A-12D-A12J-09 chr23:142967346 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:74387293 G>A maps to NM_022066.3 G1203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:74396257 G>A maps to NM_022066.3 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:74395861 A>G maps to NM_022066.3 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:74392497 C>T maps to NM_022066.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:74388044 G>A maps to NM_022066.3 N1032N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:74387398 C>T maps to NM_022066.3 S1168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:74395594 C>T maps to NM_022066.3 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:74396365 G>A maps to NM_022066.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:74398171 G>A maps to NM_022066.3 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr15:76171447 T>C maps to NM_173469.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:76183283 G>T maps to NM_173469.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:76175736 C>T maps to NM_173469.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr15:76183288 G>A maps to NM_173469.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:33912024 C>T maps to NM_017811.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:64671403 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:64709811 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr20:48700775 G>A maps to NM_199203.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:48955713 G>A maps to NM_003350.2 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:48973337 G>T maps to NM_003350.2 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:48962498 A>G maps to NM_003350.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:74742624 G>T maps to NM_001001481.1 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:74722768 C>T maps to NM_001001481.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr17:47000241 C>T maps to NM_023079.4 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:47000241 C>T maps to NM_023079.4 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:25616711 G>A maps to NM_000462.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:25620852 G>T maps to NM_000462.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:25615954 C>A maps to NM_000462.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr15:25620630 G>A maps to NM_000462.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:25616213 C>T maps to NM_000462.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:109921750 C>T maps to NM_183415.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:109928914 T>G maps to NM_183415.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:109945513 C>T maps to NM_183415.1 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:109961889 C>T maps to NM_183415.1 S824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:109958987 C>T maps to NM_183415.1 H704H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:109971272 C>T maps to NM_183415.1 F975F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:109921497 C>T maps to NM_183415.1 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:109939238 C>T maps to NM_183415.1 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:157016036 C>T maps to NM_014671.2 R698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:157000199 T>C maps to NM_014671.2 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:156975018 T>C maps to NM_014671.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr7:156975018 T>C maps to NM_014671.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr7:157049656 G>T maps to NM_014671.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:157000205 A>C maps to NM_014671.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:156963053 C>T maps to NM_014671.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:118267106 C>A maps to NM_004788.2 I1058I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:118239406 C>T maps to NM_004788.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:118243913 C>T maps to NM_004788.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:118239406 C>T maps to NM_004788.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:118235809 G>A maps to NM_004788.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:118255635 C>A maps to NM_004788.2 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:118250337 C>T maps to NM_004788.2 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:10240004 C>T maps to NM_001105562.2 S1300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:10166440 C>T maps to NM_001105562.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:10163146 G>T maps to NM_001105562.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:10155591 G>A maps to NM_001105562.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:10195146 G>A maps to NM_001105562.2 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:10218426 C>T maps to NM_001105562.2 T980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:10190864 C>T maps to NM_001105562.2 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:10190801 G>A maps to NM_001105562.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:10209261 C>A maps to NM_001105562.2 S871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:23569565 C>A maps to ENST00000219638 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr1:11333812 C>T maps to NM_013319.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:30341436 C>T maps to NM_007106.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:153714217 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:153714141 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:153714302 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr23:153714207 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:153713946 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:153714110 C>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:153714190 C>A did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:110655662 G>A maps to NM_203412.1 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:158705274 G>A maps to NM_145049.3 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:158710264 G>T maps to NM_145049.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr16:4903004 T>C maps to NM_016936.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:4911054 C>T maps to NM_016936.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:4926966 G>A maps to NM_016936.3 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:4920911 G>T maps to NM_016936.3 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:138968317 T>C maps to NM_173569.3 T889T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:138946315 C>T maps to NM_173569.3 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:3102383 G>A maps to NM_014948.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr20:3102486 G>T maps to NM_014948.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:33434836 A>G maps to NM_001128161.1 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:33467130 C>T maps to NM_001128161.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr3:33434922 C>A maps to NM_001128161.1 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:86294874 G>A maps to NM_013438.4 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:86322432 C>T maps to NM_013438.4 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:56591126 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:56590893 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:56591328 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:56590845 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:56590435 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:56590892 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MU-01A-11D-A10B-09 chr23:56591468 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr23:56590463 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:56590955 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:56592176 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:56591401 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:56590892 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:56590443 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:56591085 C>T did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:5530047 A>G maps to NM_017481.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:5529852 G>A maps to NM_017481.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:5529393 C>T maps to NM_017481.2 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:5529348 C>T maps to NM_017481.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:5528820 C>A maps to NM_017481.2 *656Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:5529303 T>C maps to NM_017481.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:5529179 C>A maps to NM_017481.2 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:156018387 G>T maps to NM_020131.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:156011742 A>G maps to NM_020131.3 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:156012660 G>T maps to NM_020131.3 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr15:43352005 G>A maps to NM_174916.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:43250251 A>G maps to NM_174916.2 P1598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:43307910 C>A maps to NM_174916.2 E1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:43308051 C>A maps to NM_174916.2 E1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:43339389 A>C maps to NM_174916.2 L546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:43347064 G>T maps to NM_174916.2 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:43324802 T>C maps to NM_174916.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:42658784 A>G maps to NM_015255.2 L1714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:42573591 C>T maps to NM_015255.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr6:42646396 C>T maps to NM_015255.2 P1533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:42541551 T>C maps to NM_015255.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:42652554 T>G maps to NM_015255.2 L1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr6:42584988 G>A maps to NM_015255.2 Q398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:42643897 C>T maps to NM_015255.2 H1452H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:42600363 A>G maps to NM_015255.2 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:42656091 C>T maps to NM_015255.2 Y1664Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:42600361 C>T maps to NM_015255.2 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:170843264 C>T maps to ENST00000442603 R1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:170762557 C>T maps to ENST00000442603 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:170912048 C>T maps to ENST00000442603 S1609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:170751734 G>T maps to ENST00000442603 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:170917696 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LQ-01A-12D-A10B-09 chr1:19482147 A>G maps to ENST00000375267 C2029C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:19404481 G>A maps to ENST00000375267 Y5104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:19444358 G>A maps to ENST00000375267 S3529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:19415317 G>T maps to ENST00000375267 R4789R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:19440524 G>A maps to ENST00000375267 R3748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:19482762 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:19408036 G>A maps to ENST00000375267 N5013N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:19442121 G>T maps to ENST00000375267 R3611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:19470545 G>A maps to ENST00000375267 R2703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:19452987 G>T maps to ENST00000375267 T3130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:19455504 G>A maps to ENST00000375267 N2990N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:19487587 C>T maps to ENST00000375267 S1743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr1:19415444 C>T maps to ENST00000375267 P4746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:19439187 C>T maps to ENST00000375267 S3877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:103283450 G>A maps to NM_015902.4 N2332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:103284936 G>A maps to NM_015902.4 R2265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:103298659 G>A maps to NM_015902.4 Q1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:103311161 A>G maps to NM_015902.4 D1080D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:103354778 C>T maps to NM_015902.4 E340E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:103324016 G>A maps to NM_015902.4 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:103326030 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:103323705 G>A maps to NM_015902.4 R813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:93686657 G>T maps to NM_175748.3 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:93684945 A>G maps to NM_175748.3 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:93676167 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr10:99327803 G>A maps to NM_024954.3 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr10:99329913 C>T maps to NM_024954.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:171639136 G>A maps to NM_152277.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:171639219 C>A maps to NM_152277.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:171638917 G>A maps to NM_152277.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:42285113 G>T maps to NM_014233.2 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:42293321 G>A maps to NM_014233.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:42286767 G>A maps to NM_014233.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:42290608 G>A maps to NM_014233.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:42293102 C>T maps to NM_014233.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:89819593 A>G maps to NM_001143975.1 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:62445740 C>T maps to ENST00000436354 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr11:62445881 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr11:62445052 A>C maps to NM_015853.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:20517119 T>C maps to NM_152376.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:20517176 C>T maps to NM_152376.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:26612418 G>A maps to NM_183008.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:26629320 C>T maps to NM_183008.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr8:59359974 A>G maps to NM_001077619.1 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:59347022 G>T maps to NM_001077619.1 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:136511772 G>T maps to NM_014607.3 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:136519481 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:196083702 G>A maps to NM_015562.1 H441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr3:196096310 G>A maps to NM_015562.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:30614365 G>T maps to ENST00000265616 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:30608997 G>A maps to ENST00000265616 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05J-01A-11W-A027-09 chr4:41270033 G>T maps to NM_004181.4 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:41270024 G>T maps to NM_004181.4 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:192992121 A>G maps to ENST00000367450 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:192993051 A>G maps to ENST00000367450 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:193018893 C>T maps to ENST00000367450 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:192998687 C>A maps to ENST00000367450 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:134404647 C>T maps to NM_031432.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:134404900 C>T maps to NM_031432.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr9:134400585 C>T maps to NM_031432.2 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:165860500 G>T maps to NM_012474.4 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:165860500 G>T maps to NM_012474.4 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:62571334 C>T maps to NM_017859.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:62577277 G>A maps to NM_017859.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:62577253 G>A maps to NM_017859.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr20:62572182 C>T maps to NM_017859.3 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:13271632 G>A maps to NM_145314.1 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:13275753 C>T maps to NM_145314.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:13271667 C>A maps to NM_145314.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr10:5415796 C>T maps to NM_053049.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:141483480 G>A maps to NM_021833.4 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:73686068 G>A maps to NM_003355.2 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:73717277 G>A maps to NM_003356.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr11:73717301 G>A maps to NM_003356.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:18553959 A>G maps to NM_001040697.1 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:18568442 G>A maps to NM_001040697.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:161123796 G>T maps to NM_016406.3 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:19445662 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:19455393 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:19443291 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:38924256 C>T maps to ENST00000379641 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:186337021 C>T did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr4:186336329 G>A maps to NM_018359.3 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:186336326 C>T maps to NM_018359.3 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:186329435 C>A maps to NM_018359.3 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:186329435 C>A maps to NM_018359.3 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:39523093 G>A maps to NM_003359.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:39523017 C>A maps to NM_003359.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:39506054 A>C maps to NM_003359.3 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr2:128918110 C>T maps to NM_020120.3 C880C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:128880798 C>T maps to NM_020120.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:128918752 C>T maps to NM_020120.3 D912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:128913099 C>A maps to NM_020120.3 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr2:128877941 C>T maps to NM_020120.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr13:96599290 G>A maps to NM_020121.3 H559H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:96506701 G>A maps to NM_020121.3 R1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:96589188 C>A maps to NM_020121.3 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:96622495 A>C maps to NM_020121.3 L402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:96622455 G>T maps to NM_020121.3 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:96506701 G>A maps to NM_020121.3 R1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:96489363 T>C maps to NM_020121.3 K1459K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:234669400 C>T maps to NM_000463.2 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:234545485 T>C maps to NM_019075.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr2:234545245 G>A maps to NM_019075.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:234637888 C>T maps to NM_019093.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:234638458 T>C maps to NM_019093.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr2:234676535 G>A maps to ENST00000373460 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:234602186 G>A maps to NM_001072.3 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:234602381 C>A maps to NM_001072.3 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:234590990 C>A maps to ENST00000373460 Y137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:234580708 G>A maps to ENST00000373460 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:70513121 C>A maps to ENST00000514019 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:70513121 C>A maps to ENST00000514019 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:70513299 C>A maps to ENST00000514019 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:70504704 C>T maps to ENST00000514019 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:70504706 T>G maps to ENST00000514019 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:70505285 C>A maps to NM_001105677.1 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:69795755 C>T maps to NM_024743.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr4:69682455 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:69681866 G>T maps to NM_001075.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:69682378 C>A maps to NM_001075.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:69681827 G>T maps to NM_001075.4 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:70080139 G>A maps to NM_001073.1 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:70070317 G>T maps to NM_001073.1 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:70078385 G>A maps to NM_001073.1 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr4:69879872 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:69519924 G>A maps to NM_001076.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:69535816 G>A maps to NM_001076.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr4:69512911 G>A maps to NM_001076.2 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr4:69536170 A>G maps to NM_001076.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:69536054 G>A maps to NM_001076.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:69403405 T>C maps to NM_001076.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:69433500 G>A maps to NM_001076.2 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:69403614 C>A maps to NM_001076.2 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:70146641 G>T maps to NM_053039.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:70284670 A>G maps to ENST00000381079 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:70352374 C>A maps to NM_021139.2 G348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr4:70361302 G>A maps to NM_021139.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:69978238 C>T maps to NM_001074.2 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:69962909 C>T maps to NM_001074.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr4:69962465 T>C maps to NM_001074.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:69962816 C>T maps to NM_001074.2 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr4:69962537 T>C maps to NM_001074.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:35966014 C>A maps to NM_152404.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:35991230 C>A maps to ENST00000515801 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:35965778 A>G maps to NM_152404.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:36052020 C>A maps to NM_174914.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:36051987 C>A maps to NM_174914.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:115589340 A>G maps to NM_003360.3 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:115544570 G>T maps to NM_003360.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:115544423 G>T maps to NM_003360.3 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:115544116 G>A maps to NM_003360.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:115597144 C>T maps to NM_003360.3 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:162470776 C>T maps to NM_175866.4 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:162470890 G>A maps to NM_175866.4 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:162487911 G>T maps to NM_175866.4 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:162492195 C>A maps to NM_175866.4 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:162467921 C>T maps to NM_175866.4 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:4941563 G>T maps to ENST00000398240 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr19:4950881 C>T maps to ENST00000398240 Y577Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:34840164 G>T maps to NM_017754.3 E1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:34840116 G>T maps to NM_017754.3 E1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr6:34825152 C>A maps to NM_017754.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:34826257 G>T maps to NM_017754.3 E709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr6:34835098 G>A maps to NM_017754.3 G1170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:100478259 G>A maps to NM_015054.1 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:100452993 A>C maps to NM_015054.1 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:100466588 G>T maps to NM_015054.1 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:100492309 G>A maps to NM_015054.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr12:100451402 C>A maps to NM_015054.1 E1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr12:100431415 A>T maps to NM_015054.1 *1465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr12:100491267 C>A maps to NM_015054.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr12:100480136 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:6482095 T>C maps to NM_152896.1 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:6434146 C>T maps to NM_152896.1 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr9:6481663 T>C maps to NM_152896.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:6506172 A>G maps to NM_152896.1 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:6420973 A>T maps to NM_152896.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:176370377 G>A maps to ENST00000377219 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr5:176396233 G>A maps to ENST00000377219 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:150289944 C>T maps to NM_025218.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:150290007 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:150266443 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:150386729 G>A maps to NM_024518.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:132393455 C>T maps to NM_003565.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:132395278 G>A maps to NM_003565.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:132380232 C>T maps to NM_003565.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr12:132392047 C>T maps to NM_003565.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:132393772 G>A maps to NM_003565.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:19683921 G>A maps to NM_014683.3 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:19689301 A>G maps to NM_014683.3 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:19700870 G>A maps to NM_014683.3 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:19769129 C>T maps to NM_014683.3 W34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:19769054 G>T maps to NM_014683.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:19700870 G>A maps to NM_014683.3 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:75134533 C>T maps to NM_001099436.1 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr15:75131903 G>A maps to NM_001099436.1 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:75133824 T>C maps to NM_001099436.1 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:41841694 C>A maps to NM_017886.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:41977372 C>A maps to NM_017886.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:41957544 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:41977372 C>A maps to NM_017886.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:41961286 C>A maps to NM_017886.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:20352410 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:20355443 C>T maps to ENST00000424589 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr16:20352633 C>T maps to ENST00000424589 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr16:20344656 G>T maps to ENST00000424589 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:43496219 C>T maps to NM_173568.3 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:43531689 G>A maps to NM_173568.3 W786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:43546483 G>A maps to NM_173568.3 T1187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:43547181 C>T maps to NM_173568.3 I1248I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:43539357 G>A maps to NM_173568.3 E999E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr21:43543235 C>T maps to NM_173568.3 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:124456472 A>G maps to NM_000373.3 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:124456508 T>G maps to NM_000373.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:124456784 C>T maps to NM_000373.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:124458953 G>T maps to NM_000373.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr3:124453941 T>C maps to NM_000373.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:121157828 C>A maps to NM_001080533.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:121154542 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:17751382 G>A maps to ENST00000428389 Y996Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:17785551 C>T maps to ENST00000428389 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:17735751 G>T maps to ENST00000428389 L1449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:17741004 G>A maps to ENST00000428389 L1294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:17756633 G>A maps to ENST00000428389 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:17746840 G>A maps to ENST00000428389 C1157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr19:17738352 G>A maps to ENST00000428389 N1383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:17756816 A>C maps to ENST00000428389 Y804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:17738358 G>T maps to ENST00000428389 L1381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:17728528 G>A maps to ENST00000428389 Q1602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:35399223 C>T maps to ENST00000396787 R1310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:35376077 C>T maps to ENST00000396787 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:35381181 A>G maps to ENST00000396787 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:35403480 C>A maps to ENST00000396787 R1490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:35377570 C>A maps to ENST00000396787 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:54307577 C>A maps to ENST00000260323 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr15:54306539 C>G maps to ENST00000260323 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:54305829 G>T maps to ENST00000260323 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:54860137 C>A maps to ENST00000260323 T2033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:54307944 G>T maps to ENST00000260323 E949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:54307905 G>T maps to ENST00000260323 E936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:54308019 G>T maps to ENST00000260323 E974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:54592512 G>T maps to ENST00000260323 E1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:54305624 C>A maps to ENST00000260323 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:54919044 C>T maps to ENST00000260323 R2127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:54306860 G>A maps to ENST00000260323 W587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:54435231 G>T maps to ENST00000260323 E1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:54825156 C>T maps to ENST00000260323 F1863F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr15:54817776 G>T maps to ENST00000260323 E1830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:54305141 T>C maps to ENST00000260323 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:54792275 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:73836862 C>T maps to ENST00000412096 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:73827220 G>A maps to ENST00000412096 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:73839253 G>A maps to ENST00000412096 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:73836362 A>G maps to ENST00000412096 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:73832756 T>G maps to ENST00000412096 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:91483616 C>T maps to NM_018671.3 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr17:33504091 C>T maps to NM_173167.2 H696H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:33481675 G>A maps to NM_173167.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:99227272 G>T maps to ENST00000409347 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:99226440 G>A maps to ENST00000409347 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr2:99227328 C>T maps to ENST00000409347 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:176306787 G>A maps to NM_133369.2 R810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:176305321 C>A maps to NM_133369.2 Y649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:176295176 C>T maps to NM_133369.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr5:176305243 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr5:176305473 A>G did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr5:176295129 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:73044510 G>A maps to NM_170744.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:73047499 C>T maps to NM_170744.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:73045098 C>T maps to NM_170744.3 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr4:96140216 G>A maps to NM_003728.3 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:96140195 T>C maps to NM_003728.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:96140240 C>T maps to NM_003728.3 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:96163727 C>T maps to NM_003728.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:96124040 G>T maps to NM_003728.3 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr4:96090516 T>C maps to NM_003728.3 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:41002497 G>A maps to NM_173561.2 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:41002632 C>A maps to NM_173561.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr8:35402006 T>C maps to ENST00000453357 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:35406936 G>A maps to ENST00000416672 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:35425653 C>T maps to ENST00000416672 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:35608254 C>A maps to ENST00000416672 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:35579743 C>T maps to ENST00000416672 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:35583874 C>T maps to ENST00000416672 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:35631833 C>A maps to ENST00000416672 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:35647891 C>T maps to ENST00000416672 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:35425742 C>A maps to ENST00000416672 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:35544222 C>A maps to ENST00000416672 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:35583820 C>T maps to ENST00000416672 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr8:35608224 C>T maps to ENST00000416672 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:35606044 C>T maps to ENST00000416672 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr8:35579761 G>A maps to ENST00000416672 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:35631842 C>T maps to ENST00000416672 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:167719500 C>A maps to NM_018974.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:167717572 G>A maps to NM_018974.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:67764105 G>A maps to NM_030930.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr11:67765850 C>T maps to NM_030930.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:73808285 G>A maps to NM_001080419.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr17:73814742 C>T maps to NM_001080419.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:73805898 C>T maps to NM_001080419.1 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:1463995 C>T maps to ENST00000508903 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:24909329 C>A maps to NM_016327.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:18966853 G>T maps to ENST00000418384 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:18968260 C>T maps to ENST00000418384 Q712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:18963848 C>T maps to ENST00000418384 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr19:18967729 G>A maps to ENST00000418384 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:18964070 C>T maps to ENST00000418384 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr19:18965997 G>A maps to ENST00000418384 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:18965729 G>A maps to ENST00000418384 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:12070816 C>A maps to NM_015542.2 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:12043815 C>A maps to NM_015542.2 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:11997262 G>A maps to NM_015542.2 R940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:12001307 G>A maps to NM_015542.2 Y744Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:11994104 C>T maps to NM_015542.2 R998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:12077194 G>A maps to NM_015542.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr13:115067485 C>T maps to NM_023011.2 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr13:115064475 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:118971926 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:118972369 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:118975044 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:118974639 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:118977173 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr23:118977239 T>A did not map to a codon.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr23:118977240 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:118977167 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:118968979 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118971829 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:118985490 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:118985768 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:118972447 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:118986858 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:118986751 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:118968881 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:118975092 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:118975121 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:118977249 T>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:118979166 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr23:118971919 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:36166744 G>T maps to NM_007000.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:118917920 C>T maps to NM_006952.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17L-01A-11D-A12J-09 chr3:118913097 C>T maps to NM_006952.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:118828378 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:45691467 G>A maps to NM_006953.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:76140313 C>T maps to NM_030570.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:48141470 C>T maps to NM_003364.2 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:158978092 C>A maps to NM_001135098.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:74494096 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:74494342 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:74519605 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr23:74494253 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr23:74516199 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:74519614 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:74494388 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:74494212 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr23:74523320 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:74494185 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:74520816 G>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:74519568 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:33894506 G>A maps to NM_018244.4 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:97244123 C>A maps to NM_006294.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:97245420 T>C maps to NM_006294.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:48638129 G>A maps to NM_003365.2 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:48641051 G>A maps to NM_003365.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:21983355 C>T maps to NM_003366.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:29698966 C>A maps to NM_006003.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr19:29698565 G>A maps to NM_006003.2 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:132203178 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:229783375 C>T maps to NM_014777.2 H1342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:229783375 C>T maps to NM_014777.2 H1342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:229772192 C>A maps to NM_014777.2 Y611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:229773773 C>T maps to NM_014777.2 D1138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:229795001 C>A maps to NM_014777.2 Y1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:229773749 G>A maps to NM_014777.2 Q1130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:229772855 T>C maps to NM_014777.2 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:229773725 G>A maps to NM_014777.2 T1122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:229773869 A>G maps to NM_014777.2 G1170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:229794923 C>T maps to NM_014777.2 D1485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:43917455 G>A maps to NM_001077663.1 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr7:43918299 G>A maps to NM_001077663.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:43918073 C>A maps to NM_001077663.1 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:43927410 C>A maps to NM_001077663.1 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:43916865 G>T maps to NM_001077663.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:131140354 C>T maps to NM_001135947.1 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:131151566 C>T maps to NM_001135947.1 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:126208140 G>A maps to NM_001165974.1 Y622Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:126218196 A>G maps to NM_001165974.1 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:126219596 C>T maps to NM_001165974.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:126229550 G>A maps to NM_001165974.1 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:126220074 G>A maps to NM_001165974.1 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:126224817 G>A maps to NM_001165974.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr3:126216966 C>T maps to NM_001165974.1 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:45479412 C>T maps to NM_000374.4 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0YU-01A-21D-A10M-09 chr1:45479418 C>T maps to NM_000374.4 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:127486631 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:17330165 C>T maps to NM_018467.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161010027 G>A maps to NM_007122.3 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:161009799 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:161012650 C>T maps to NM_007122.3 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:35761708 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:17547985 G>A maps to NM_153676.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:17544790 G>A maps to NM_153676.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:17548863 G>A maps to NM_153676.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:17527468 G>A maps to NM_153676.3 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:17552745 G>T maps to NM_153676.3 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:17547985 G>A maps to NM_153676.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr11:17517180 G>A maps to NM_153676.3 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:72915757 C>T maps to NM_173477.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr17:72916297 C>T maps to NM_173477.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:215822096 G>A maps to ENST00000366943 G4785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:216390783 A>C maps to ENST00000366943 A1034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:216246481 T>C maps to ENST00000366943 G1911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:215807887 C>T maps to ENST00000366943 E5070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:216019295 G>T maps to ENST00000366943 I2975I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr1:215847526 C>A maps to ENST00000366943 E4576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:215813956 G>A maps to ENST00000366943 R4971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:215844436 G>A maps to ENST00000366943 Y4670Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:215853658 A>G maps to ENST00000366943 G4042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:216017731 A>C maps to ENST00000366943 S3054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:215844358 A>G maps to ENST00000366943 S4696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:216380714 G>T maps to ENST00000366943 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:216424431 T>C maps to ENST00000366943 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:215824056 G>A maps to ENST00000366943 A4740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:215956214 G>A maps to ENST00000366943 R3484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:216011418 G>A maps to ENST00000366943 C3095C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:216019217 A>G maps to ENST00000366943 N3001N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:216074236 G>A maps to ENST00000366943 G2437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:216138760 G>A maps to ENST00000366943 Q2340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:216246285 C>T maps to ENST00000366943 S1934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:215953199 G>A maps to ENST00000366943 Q3642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:216258045 C>A maps to ENST00000366943 G1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:215847676 G>A maps to ENST00000366943 R4526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:215853544 G>A maps to ENST00000366943 G4080G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr1:215953191 C>T maps to ENST00000366943 T3644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:215940125 G>A maps to ENST00000366943 L3648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:216073528 G>A maps to ENST00000366943 S2494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:216498706 G>A maps to ENST00000366943 N361N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr1:216369978 A>G maps to ENST00000366943 V1389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr1:216019172 G>A maps to ENST00000366943 C3016C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18C-01A-11D-A12J-09 chr1:216019376 T>C did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:215821979 G>T maps to ENST00000366943 T4824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:215847676 G>A maps to ENST00000366943 R4526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:216221912 C>T maps to ENST00000366943 E2042E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:216371854 G>A maps to ENST00000366943 R1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:216595195 T>C maps to ENST00000366943 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:215848349 T>C maps to ENST00000366943 Q4301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:215932005 C>A maps to ENST00000366943 E3774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:215848262 G>A maps to ENST00000366943 S4330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:215953251 C>T maps to ENST00000366943 Q3624Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:215963419 G>T maps to ENST00000366943 S3388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr1:215807815 C>T maps to ENST00000366943 P5094P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:215972456 G>T maps to ENST00000366943 C3250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:215848631 G>A maps to ENST00000366943 A4207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:215916639 G>T maps to ENST00000366943 V3809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:216040512 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:17369127 G>A maps to NM_031941.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:17375053 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:105152016 G>A maps to NM_032747.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:76695902 C>T maps to NM_003715.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:76695830 C>T maps to NM_003715.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:62910553 G>T maps to NM_003368.4 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:84793793 C>T maps to NM_005153.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:84778962 C>A maps to NM_005153.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:84801925 G>T maps to NM_005153.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr16:84806214 C>T maps to NM_005153.2 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:84778269 C>T maps to NM_005153.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:84806232 T>G maps to NM_005153.2 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:84793793 C>T maps to NM_005153.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:47100806 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47098789 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47098845 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47101615 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47098852 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:47098765 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:47099746 C>T did not map to a codon.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr23:47099825 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47092433 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47100186 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47100773 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:47107323 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47100701 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47107094 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47092371 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47098871 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47101533 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47102116 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47104842 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47104770 C>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:47092477 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:47107094 C>T did not map to a codon.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr23:47101046 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:27645219 G>A maps to NM_182488.3 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:179462840 C>T maps to NM_003940.2 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:179426674 G>A maps to NM_003940.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:179437788 G>A maps to NM_003940.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr3:179418823 C>T maps to NM_003940.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:179418823 C>T maps to NM_003940.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:179426713 G>T maps to NM_003940.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:179472563 C>T maps to NM_003940.2 R615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr12:62777894 C>T maps to ENST00000280377 R429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:30426134 G>T maps to NM_006447.2 E736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr21:30403006 T>C maps to NM_006447.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:30411451 G>T maps to NM_006447.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:30419196 C>T maps to NM_006447.2 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr21:30403057 G>A maps to NM_006447.2 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:11995978 G>T maps to NM_201402.2 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:11995198 A>G maps to NM_201402.2 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:18644562 G>A maps to NM_017414.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr22:18644665 G>T maps to NM_017414.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr22:18652699 G>A maps to NM_017414.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr3:49154343 C>A maps to ENST00000434032 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:49152922 G>A maps to ENST00000434032 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:49153594 C>T maps to ENST00000434032 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr3:49152249 C>A maps to ENST00000434032 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:119228770 G>A maps to NM_004205.4 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:119243602 G>A maps to NM_004205.4 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:119229486 G>A maps to NM_004205.4 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:119243602 G>A maps to NM_004205.4 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:132641900 C>T maps to NM_001008563.3 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:132635785 G>A maps to NM_001008563.3 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:132632093 G>A maps to NM_001008563.3 W512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:132641861 G>A maps to NM_001008563.3 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr9:132636940 G>A maps to NM_001008563.3 G609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr9:132625467 G>A maps to NM_001008563.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:161132832 G>T maps to NM_012475.4 G340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:161130577 C>T maps to NM_012475.4 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:20914477 C>T maps to ENST00000455117 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:20931876 C>T maps to ENST00000455117 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:20931876 C>T maps to ENST00000455117 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:20919074 T>C maps to ENST00000455117 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:20921416 A>G maps to ENST00000455117 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr17:20919196 G>T maps to ENST00000455117 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:55627937 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:55638129 A>G maps to NM_015306.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:55560967 G>A maps to NM_015306.2 R2055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:55562743 G>A maps to NM_015306.2 G1939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:55637240 C>T maps to NM_015306.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:55560962 G>A maps to NM_015306.2 V2056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:55545261 C>T maps to NM_015306.2 E2383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:55591132 G>A maps to NM_015306.2 R1274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:55590187 A>G maps to NM_015306.2 S1358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:55557778 A>C maps to NM_015306.2 Y2157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:55590162 G>A maps to NM_015306.2 R1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr1:55563318 C>T maps to NM_015306.2 G1889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:55589212 G>A maps to NM_015306.2 R1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr21:17203949 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr21:17202856 G>A maps to ENST00000285681 Q567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr21:17250737 G>T maps to ENST00000285681 E1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:17163914 A>C maps to ENST00000285681 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr21:17250135 G>T maps to ENST00000285681 E973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr21:17250740 C>T maps to ENST00000285681 R1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr21:17202851 T>C maps to ENST00000285681 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:17135239 G>T maps to ENST00000285681 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:17199506 G>T maps to ENST00000285681 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr21:17250144 G>T maps to ENST00000285681 E976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr21:17203947 G>T maps to ENST00000285681 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:17191117 G>T maps to ENST00000285681 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr21:17214747 G>A maps to ENST00000285681 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:132160081 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr23:132160572 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:132160506 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:132159804 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:132160873 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:132162146 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:132160873 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:132161430 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:132161833 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:132161659 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:132161330 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:132161980 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:132159804 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:132160041 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:132161572 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:132161703 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:132159905 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:132161035 A>G did not map to a codon.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr23:132162228 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:132160339 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:132159589 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:132162115 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:113675638 G>A maps to NM_020886.2 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:113672229 G>T maps to NM_020886.2 C1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:113675638 G>A maps to NM_020886.2 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:113673912 G>A maps to NM_020886.2 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:113704981 G>A maps to NM_020886.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr11:113705057 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:57640546 G>A maps to NM_020903.2 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:57640711 A>G maps to NM_020903.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr19:57642511 C>T maps to NM_020903.2 Y823Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:57641240 G>T maps to NM_020903.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:57641962 C>T maps to NM_020903.2 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:63883012 G>A maps to NM_006537.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:63852160 T>C maps to NM_006537.2 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:109522830 G>A maps to NM_032663.3 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:109522839 G>A maps to NM_032663.3 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:109523640 C>T maps to NM_032663.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:109523470 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:23080566 C>T maps to NM_020718.3 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:23080764 C>T maps to NM_020718.3 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:58284444 A>G maps to NM_032582.3 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:58313498 G>A maps to NM_032582.3 Y413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:58282843 G>T maps to NM_032582.3 P1071P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:78205035 C>A maps to NM_015017.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:78163049 A>G maps to NM_015017.3 D927D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:78180398 G>A maps to NM_015017.3 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:61492624 G>A maps to NM_014709.3 G1895G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:61607464 G>A maps to NM_014709.3 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:61484359 G>A maps to NM_014709.3 I1990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:61455833 C>T maps to NM_014709.3 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:61512019 G>A maps to NM_014709.3 L1608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr2:61447507 G>A maps to NM_014709.3 Q2662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:61441704 T>C maps to NM_014709.3 L2724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:61546450 C>A maps to NM_014709.3 E1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:61433185 G>A maps to NM_014709.3 S3040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:61538989 A>G maps to NM_014709.3 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:61415278 G>T maps to NM_014709.3 V3533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:61541829 C>T maps to NM_014709.3 E1144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:61575498 G>A maps to NM_014709.3 H597H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:61431441 C>T maps to NM_014709.3 P3111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:61597700 C>A maps to NM_014709.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr11:77919934 C>T maps to NM_020798.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:76803223 C>T maps to NM_025090.3 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:76794558 C>A maps to NM_025090.3 R1105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:76802269 G>A maps to NM_025090.3 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr17:76802344 G>A maps to NM_025090.3 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:76809058 G>A maps to NM_025090.3 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr17:76798403 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:76798595 A>G maps to NM_025090.3 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:76809945 C>A maps to NM_025090.3 G392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr17:76832319 G>A maps to NM_025090.3 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:76794531 T>C maps to NM_025090.3 A1114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:76825009 G>T maps to NM_025090.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr17:76823322 G>A maps to ENST00000432878 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:219339437 G>A maps to NM_020935.2 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:219350459 C>A maps to NM_020935.2 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M6-01A-31D-A10B-09 chr2:219399410 T>G maps to NM_020935.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr2:219344431 T>C maps to NM_020935.2 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:144135072 C>A maps to NM_032557.5 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:144106795 C>T maps to NM_032557.5 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:144118977 T>A maps to NM_032557.5 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:144130760 C>A maps to NM_032557.5 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr2:85848613 G>A maps to NM_006590.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:49337970 G>A maps to NM_003363.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:49354741 C>A maps to ENST00000415188 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:49321511 G>A maps to NM_003363.3 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr3:49348984 A>G maps to NM_003363.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr2:234394541 G>A maps to NM_018218.2 N1104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:234421266 A>G maps to NM_018218.2 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:234457782 A>G maps to NM_018218.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:234436070 G>T maps to NM_018218.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:234394436 G>A maps to NM_018218.2 F1139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:234394436 G>A maps to NM_018218.2 F1139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:234399884 C>T maps to NM_018218.2 A991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:234428236 G>A maps to ENST00000452724 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:6189539 G>A maps to ENST00000404835 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:6187480 G>A maps to ENST00000404835 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr7:6187411 C>A maps to ENST00000404835 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:9580182 C>T maps to NM_153210.3 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:9590171 G>A maps to NM_153210.3 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:95927366 C>T maps to NM_032147.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:95922630 C>A maps to NM_032147.2 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:95927918 A>G maps to NM_032147.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:95922738 C>A maps to NM_032147.2 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr12:95927035 G>A maps to NM_032147.2 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr12:95927651 A>G maps to NM_032147.2 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr12:95927845 C>A maps to NM_032147.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:99936645 C>A maps to NM_001080481.1 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:99893832 C>T maps to NM_001080481.1 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:99912963 C>A maps to NM_001080481.1 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:99936645 C>A maps to NM_001080481.1 E177*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BS-A0UL-01A-11D-A10G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:99914627 C>A maps to NM_001080481.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:53463853 T>C maps to NM_022832.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:53463865 C>T maps to NM_022832.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:53463882 C>A maps to NM_022832.3 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:11964231 C>T maps to ENST00000399455 I895I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:11951045 T>G maps to ENST00000399455 Y491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr11:11974390 C>T maps to ENST00000399455 S1236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:11955419 G>T maps to ENST00000399455 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr11:11906128 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr11:11964495 G>T maps to ENST00000399455 T983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:22041926 C>A maps to NM_032236.5 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:22078088 C>A maps to NM_032236.5 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr1:22078003 A>T maps to NM_032236.5 L257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:41773722 G>A maps to ENST00000373009 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:6965951 C>T maps to NM_001098536.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:6971693 C>T maps to NM_001098536.1 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr12:6972494 C>T maps to NM_001098536.1 N636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:6972348 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:50830994 A>G maps to ENST00000456636 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:50833338 G>T maps to ENST00000456636 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr15:50835872 T>G maps to ENST00000456636 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:50833254 G>A maps to ENST00000456636 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:55514687 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:55514202 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:55513272 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:55514859 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:55513613 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:55514104 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:55514785 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LN-01A-11W-A062-09 chr23:55515339 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:55513395 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:55513393 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:55513477 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:55514675 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:55513611 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:55514188 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:120193172 G>T maps to NM_019050.2 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:120193172 G>T maps to NM_019050.2 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:120213568 G>T maps to NM_019050.2 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:120192461 G>T maps to NM_019050.2 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:75276511 C>T maps to NM_152586.3 Q1224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:75276310 A>G maps to NM_152586.3 H1291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:75302840 C>A maps to NM_152586.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:75335365 C>A maps to NM_152586.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:75289571 C>T maps to NM_152586.3 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr10:75276157 G>A maps to NM_152586.3 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr10:75335311 A>G maps to NM_152586.3 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:5072304 A>T maps to NM_004505.2 K1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:5073924 G>A maps to NM_004505.2 K1223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr17:5072276 G>A maps to NM_004505.2 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:5042664 G>A maps to NM_004505.2 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:5071322 G>T maps to NM_004505.2 E1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr17:5074101 C>T maps to NM_004505.2 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:5048041 G>T maps to NM_004505.2 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:5058808 G>T maps to NM_004505.2 R912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:5073772 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr17:5049439 C>T maps to NM_004505.2 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:5041491 C>T maps to NM_004505.2 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr17:5038538 C>T maps to NM_004505.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:11560538 C>A maps to NM_001080491.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:8995050 C>T maps to NM_003470.2 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:8996252 G>A maps to NM_003470.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:8994475 C>T maps to NM_003470.2 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:8988926 G>A maps to NM_003470.2 F1000F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0IS-01A-12D-A10M-09 chr16:9017169 C>T maps to NM_003470.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:8989513 C>T maps to NM_003470.2 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:8994475 C>T maps to NM_003470.2 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:8996317 G>T maps to NM_003470.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:8993561 G>A maps to NM_003470.2 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:50769530 G>A maps to NM_005154.3 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:50731297 G>T maps to NM_005154.3 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:50751274 G>A maps to NM_005154.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr15:50769542 T>C maps to NM_005154.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr15:50788199 A>G maps to NM_005154.3 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:50788071 G>T maps to NM_005154.3 E896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:41043674 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:41031195 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:41060456 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:41073933 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:41077683 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:41002674 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:41055876 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:41075688 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:40996171 T>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:40999933 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:41002633 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:41012232 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:41012293 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:41077838 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:41084092 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41029486 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41057990 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41076539 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41077650 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41084139 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:41089022 T>C did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:40996187 T>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:41055530 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:41075903 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:41010203 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:41031206 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:41055876 C>T did not map to a codon.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr23:41073893 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:41025142 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:41043260 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:40994074 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:40988332 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:40996172 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41003880 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41073962 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:41078376 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:40990751 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:41029254 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:41075315 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr23:40996248 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:41089042 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:41000332 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:41002633 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:41075374 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:41047317 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:41060376 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:41027379 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:41029421 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:41057932 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:41007708 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr23:41026799 G>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:41029341 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:31232784 C>A maps to NM_005800.4 T857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:31233425 T>G maps to NM_005800.4 L1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:31232959 C>T maps to NM_005800.4 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr13:31195354 C>T maps to NM_005800.4 H26H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:149342550 C>T maps to NM_005715.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:129045083 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129053154 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129063351 T>C did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:129055244 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:129055509 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:129058979 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:129055268 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:129055509 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:129040193 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:129054480 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:129055252 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:129041356 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:129054654 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:129055451 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:129060300 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:129059968 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:129060040 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:129059937 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:129063377 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:52604491 G>T maps to NM_021645.5 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:72864259 C>A maps to NM_032175.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:72875810 C>T maps to NM_032175.2 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:49357441 A>G maps to NM_016001.2 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:49357755 G>T maps to NM_016001.2 E374*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D1-A174-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:101766693 G>A maps to NM_014503.2 L2277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:101706033 G>A maps to NM_014503.2 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:101680224 G>A maps to NM_014503.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:101777000 C>T maps to NM_014503.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:101739447 C>T maps to NM_014503.2 F1574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:101767490 C>T maps to NM_014503.2 L2359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:101777015 G>A maps to NM_014503.2 T2618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:101750827 G>T maps to NM_014503.2 E1887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:101757431 C>T maps to NM_014503.2 R1957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr12:101685756 C>T maps to NM_014503.2 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:101727146 C>A maps to NM_014503.2 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:101750394 C>T maps to NM_014503.2 R1820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:101761708 T>A maps to NM_014503.2 P2113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:101774983 G>T maps to NM_014503.2 E2551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:101705568 G>A maps to NM_014503.2 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr12:101777343 C>T maps to NM_014503.2 L2651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:71554546 T>C maps to NM_020368.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:71554871 G>T maps to NM_020368.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:71555123 C>T maps to NM_020368.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:30226733 C>T maps to NM_018428.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:30200436 G>A maps to NM_018428.2 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:30207637 C>T maps to NM_018428.2 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr17:30207652 G>A maps to NM_018428.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr6:145069598 C>T maps to NM_007124.2 P2719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:144814580 C>T maps to NM_007124.2 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:144745219 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:144780419 C>T maps to NM_007124.2 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:145157442 A>G maps to NM_007124.2 L3277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr6:144837408 T>C maps to NM_007124.2 T1763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:144747466 G>A maps to NM_007124.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:144759925 G>A maps to NM_007124.2 Q429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:144779922 G>T maps to NM_007124.2 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:144779922 G>T maps to NM_007124.2 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:144869957 G>T maps to NM_007124.2 E2260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:145160323 C>T maps to NM_007124.2 R3361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:144795846 G>A maps to NM_007124.2 Q1096Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:144838030 G>T maps to NM_007124.2 E1830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:144724320 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:144794935 C>T maps to NM_007124.2 D1049D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:144843240 G>A maps to NM_007124.2 S1889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr6:144858753 G>A maps to NM_007124.2 R2090R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr6:145093072 T>C maps to NM_007124.2 H2842H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:144783843 G>T maps to NM_007124.2 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:145110328 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr17:80332319 C>A maps to NM_018949.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:75590930 G>A maps to NM_003369.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr11:75562960 C>A maps to NM_003369.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr2:106729122 C>T maps to ENST00000283148 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:47517099 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:70834739 G>A maps to NM_018052.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:70778446 G>A maps to NM_018052.3 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:70721925 G>A maps to NM_018052.3 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr16:70765438 G>A maps to NM_018052.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:7837335 C>T maps to NM_004781.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:7837287 C>T maps to NM_004781.3 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:171688329 T>G maps to NM_003762.4 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:155119253 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:155119216 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:155149504 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:155171617 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:155119225 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:85808721 G>A maps to NM_003761.4 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:116226667 T>C maps to NM_001172412.1 H350H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MC-01A-21W-A062-09 chr1:160394930 G>A maps to NM_020335.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:9950414 T>C maps to NM_003574.5 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:9936134 G>A maps to NM_003574.5 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:9931855 G>A maps to NM_003574.5 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:31748673 G>A maps to NM_006295.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LO-01A-11W-A062-09 chr6:31750213 C>T maps to NM_006295.2 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:30883635 C>T maps to NM_001167734.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:77229328 C>T maps to NM_014909.4 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:213147325 G>A maps to NM_001136474.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr1:213145936 G>A maps to NM_001136474.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:213146176 C>T maps to NM_001136474.1 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:4432887 G>A maps to NM_138440.2 K670K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:41170654 G>A maps to NM_006373.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr17:41170143 C>T maps to NM_006373.3 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:77859198 C>T maps to NM_020927.1 C140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:77859145 G>T maps to NM_020927.1 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:77910269 C>A maps to NM_020927.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:77910269 C>A maps to NM_020927.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:78005745 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:6825375 C>T maps to NM_005428.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:6833917 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:6828715 C>T maps to NM_005428.2 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:6829811 C>T maps to NM_005428.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:6821685 G>A maps to NM_005428.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:6825390 C>T maps to NM_005428.2 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr19:6828646 C>T maps to NM_005428.2 C369C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr19:6772958 T>C maps to NM_005428.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:6772992 G>T maps to NM_005428.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:6822479 G>A maps to NM_005428.2 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr9:136637092 G>A maps to NM_001134398.1 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:136671261 G>A maps to NM_001134398.1 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:136662834 G>A maps to NM_001134398.1 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:136643934 C>T maps to NM_001134398.1 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:136637092 G>A maps to NM_001134398.1 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:108247211 A>G maps to NM_006113.4 C555C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:108292212 A>G maps to NM_006113.4 H421H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:108307784 G>A maps to NM_006113.4 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:108152584 C>T maps to NM_006113.4 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:108247216 C>A maps to NM_006113.4 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:118891803 T>C maps to NM_199131.2 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr10:118891746 G>A maps to NM_199131.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:118896102 C>T maps to NM_001112704.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:118893610 C>A maps to NM_001112704.1 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:154448529 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:154464562 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:154448562 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:154448518 G>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:154444816 C>T did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:154444802 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:154444766 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:101198073 G>A maps to NM_001078.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:101190237 C>T maps to NM_001078.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:101200263 G>T maps to NM_001078.3 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:101188880 G>T maps to NM_001078.3 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:101194834 G>A maps to NM_001078.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:82836873 C>T maps to NM_004385.4 D2684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:82786178 C>T maps to NM_004385.4 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:82789718 C>T maps to NM_004385.4 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:82808066 G>A maps to NM_004385.4 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:82789694 A>G maps to NM_004385.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:82816177 G>T maps to NM_004385.4 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr5:82815531 T>A maps to NM_004385.4 Y469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:82837314 C>A maps to NM_004385.4 I2831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:82841380 G>A maps to NM_004385.4 P3097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:82816084 G>T maps to NM_004385.4 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:82834561 G>T maps to NM_004385.4 E1914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:82836058 G>T maps to NM_004385.4 E2413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:82786220 G>A maps to NM_004385.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr5:82816084 G>T maps to NM_004385.4 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:82835821 G>T maps to NM_004385.4 E2334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:82835130 C>A maps to NM_004385.4 V2103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:82835989 G>T maps to NM_004385.4 E2390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:82815465 T>C maps to NM_004385.4 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr5:82834419 A>G maps to NM_004385.4 V1866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:82815577 G>T maps to NM_004385.4 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:82837830 G>T maps to NM_004385.4 T3003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:82837830 G>A maps to NM_004385.4 T3003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr5:82837065 G>A maps to NM_004385.4 Q2748Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:75868838 C>T maps to NM_014000.2 A890A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr10:75867084 G>A maps to NM_014000.2 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:75864807 G>T did not map to a codon.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr10:75874036 C>T maps to NM_014000.2 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr10:75843244 T>C maps to NM_014000.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:35067982 G>A maps to NM_007126.3 C69C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:35059201 C>T maps to NM_007126.3 E673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:35057146 G>A maps to NM_007126.3 Y796Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:35060842 G>A maps to NM_007126.3 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:67576598 T>C maps to NM_025054.4 S865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:67577933 G>T maps to NM_025054.4 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:67547427 T>G maps to NM_025054.4 R993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:67577000 T>C maps to NM_025054.4 K731K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr8:67576550 T>C maps to NM_025054.4 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:67576775 T>C maps to NM_025054.4 R806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:67577213 G>A maps to NM_025054.4 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:67577570 G>A maps to NM_025054.4 C541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:7811768 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:7811571 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr23:7811708 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:8138092 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:8138356 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr23:6451928 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:6452043 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:8434007 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:8433970 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:8434462 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:133311612 C>T maps to NM_003374.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:76982022 G>T maps to NM_001184783.1 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:42257212 G>A maps to ENST00000417062 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:42259477 C>T maps to ENST00000417062 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EO-A1Y5-01A-11D-A159-09 chr8:42256285 A>G maps to ENST00000417062 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr6:43748591 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:43745251 C>T maps to NM_001025366.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:64003396 C>T maps to NM_003377.3 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr11:64003312 C>T maps to NM_003377.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:64003776 G>T maps to NM_003377.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr11:64003285 G>A maps to NM_003377.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:177609029 G>A maps to NM_005429.2 H252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:177632698 G>A maps to NM_005429.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:157131701 T>G maps to NM_001167912.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:56058076 G>T maps to NM_007146.2 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:95693941 C>T maps to NM_017599.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr12:95694437 G>T maps to NM_017599.3 E777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:95656698 C>T maps to NM_017599.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:95688087 A>T maps to NM_017599.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:95681475 T>G maps to NM_017599.3 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:95660315 T>C maps to NM_017599.3 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:95676357 A>G maps to NM_017599.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:95681598 C>T maps to NM_017599.3 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:100808073 G>T maps to NM_003378.3 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:135630909 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:135631043 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:135631083 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:135630962 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:135632930 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:117586967 G>A maps to NM_182645.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr3:87018142 G>C maps to NM_016206.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr3:87027907 G>T maps to NM_016206.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:11600158 C>T maps to NM_014667.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr2:219295614 G>A maps to ENST00000441734 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr2:219294066 C>T maps to NM_007127.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:219294099 G>A maps to NM_007127.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:38048169 C>T maps to NM_015873.3 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:38044777 C>T maps to NM_015873.3 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:17271739 C>T maps to NM_003380.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr10:17278331 C>G maps to NM_003380.3 S438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:153075301 T>C maps to NM_003381.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:153077319 C>A maps to NM_003381.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:42569605 C>T maps to NM_004624.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:42569500 G>A maps to NM_004624.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:42568934 C>T maps to NM_004624.3 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:42576568 C>A maps to NM_004624.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:158824715 G>A maps to ENST00000402066 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:158826926 G>A maps to ENST00000402066 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:158896489 G>A maps to ENST00000402066 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:158824676 G>T maps to ENST00000402066 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:37032794 C>T maps to NM_053276.3 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:37032683 G>A maps to NM_053276.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:37032713 G>A maps to NM_053276.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:37035706 C>T maps to NM_053276.3 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:37035853 C>T maps to NM_053276.3 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:37014327 C>T maps to NM_053276.3 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:36986229 C>A maps to NM_001177972.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:65419230 C>T maps to NM_173517.3 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:2648667 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:2639886 C>T maps to NM_003383.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:2651925 T>G maps to NM_003383.3 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:2639886 C>T maps to NM_003383.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr9:2643727 C>T maps to NM_003383.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:150573425 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:150572169 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:150572135 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:5908921 C>A maps to NM_001017921.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:4688749 G>A maps to NM_182566.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:53761996 C>T maps to NM_173856.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:53762650 C>T maps to NM_173856.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:53770561 A>C maps to NM_173857.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr6:133013631 G>T maps to NM_004666.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr6:133013433 G>A maps to NM_004666.2 N372N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr6:133005623 A>G maps to NM_004666.2 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16S-01A-11D-A12J-09 chr6:133013589 G>A maps to NM_004666.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr6:133065597 A>G maps to NM_004665.2 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:133078956 A>G maps to NM_004665.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr6:133072349 C>T maps to NM_004665.2 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:51464926 C>T maps to ENST00000273612 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:51517748 T>C maps to ENST00000273612 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:51454239 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:51456330 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:51449892 G>A maps to ENST00000273612 C1384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:51440667 A>G maps to ENST00000273612 D1458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr3:51457722 G>T maps to ENST00000273612 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:51464926 C>T maps to ENST00000273612 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:51458365 G>T maps to ENST00000273612 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:51456221 C>T maps to ENST00000273612 G1115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr3:51456129 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:118951994 C>T maps to NM_021729.4 R877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:118949412 C>T maps to NM_021729.4 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:118951994 C>T maps to NM_021729.4 R877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:118949008 C>T maps to NM_021729.4 R629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:118949541 C>T maps to NM_021729.4 Q700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:118948605 C>T maps to NM_021729.4 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:79933485 G>A maps to ENST00000376646 L1764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:79952301 C>A maps to ENST00000376646 S2076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:79984283 G>T maps to ENST00000376646 E2876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:79934541 G>T maps to ENST00000376646 E1790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:79938055 C>T maps to ENST00000376646 H1968H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:79891127 G>T maps to ENST00000376646 E939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:79955363 T>C maps to ENST00000376646 I2308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:79836244 A>G maps to ENST00000376646 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:79980411 G>T maps to ENST00000376646 E2751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:79910751 C>T maps to ENST00000376646 R1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:79922875 G>T maps to ENST00000376646 E1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:79959118 C>T maps to ENST00000376646 V2359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr9:79968531 G>T maps to ENST00000376646 E2543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:79820293 G>T maps to ENST00000376646 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr9:79835224 T>C maps to ENST00000376646 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:79891016 G>T maps to ENST00000376646 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:79853067 T>C maps to ENST00000376646 C582C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:79829246 C>T maps to ENST00000376646 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:79972722 C>A maps to ENST00000376646 S2642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr8:100829916 C>T maps to NM_017890.3 Y2774Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:100866242 G>A maps to NM_017890.3 V3567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:100654662 C>T maps to NM_017890.3 R1974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:100147910 G>T maps to NM_017890.3 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:100654040 C>A maps to NM_017890.3 I1766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:100147277 G>A maps to NM_017890.3 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:100523718 G>T maps to NM_017890.3 E1563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr8:100403933 T>C did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:100123422 T>C maps to NM_017890.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:100147931 G>T maps to NM_017890.3 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:100847454 C>T maps to NM_017890.3 L3240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:100871589 C>T maps to NM_017890.3 I3667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:100155259 G>A maps to NM_017890.3 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:100866137 C>T maps to NM_017890.3 Y3532Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr8:100128026 G>T maps to NM_017890.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr8:100587946 C>T maps to NM_017890.3 R1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:100182284 G>T maps to NM_017890.3 G743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:100883723 C>T maps to NM_017890.3 D3873D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:100883846 C>T maps to NM_017890.3 I3914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:100533143 G>T maps to NM_017890.3 E1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:100589744 G>T maps to NM_017890.3 E1727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:100654223 A>G maps to NM_017890.3 S1827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:100871601 C>T maps to NM_017890.3 V3671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:100147861 G>A maps to NM_017890.3 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr8:100287477 T>C maps to NM_017890.3 N940N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr8:100874127 C>T maps to NM_017890.3 G3748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:100443864 G>A maps to NM_017890.3 W1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr8:100148969 T>C maps to NM_017890.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:62147104 G>A maps to NM_020821.2 R3709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:62238059 C>A maps to NM_020821.2 E1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:62276201 C>T maps to NM_020821.2 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:62302668 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:62147104 G>A maps to NM_020821.2 R3709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:62221802 T>G maps to NM_020821.2 A2061A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:62325666 C>A maps to NM_020821.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr15:62305294 G>A maps to NM_020821.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:62221753 C>A maps to NM_020821.2 E2078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:62217668 C>A maps to NM_020821.2 E2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:62270907 G>T maps to NM_020821.2 S736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:62219412 C>T maps to NM_020821.2 S2131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:62242597 C>A maps to NM_020821.2 E1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:62274681 C>A maps to NM_020821.2 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:62233999 A>G maps to NM_020821.2 D1805D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:62256040 C>T maps to NM_020821.2 K1108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:62226458 C>A maps to NM_020821.2 E1943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:62221753 C>A maps to NM_020821.2 E2078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:12336825 C>T maps to NM_015378.2 R1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:12408929 C>G maps to NM_015378.2 G3040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:12317132 G>A maps to NM_015378.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:12342964 C>A maps to NM_015378.2 T1602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:12371618 C>T maps to NM_015378.2 N2253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:12378383 C>T maps to NM_015378.2 V2468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:12402964 C>A maps to NM_015378.2 L2914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:12321132 G>A maps to NM_015378.2 Q447Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:12567074 G>A maps to NM_015378.2 V4321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr1:12422795 C>T maps to NM_015378.2 R3388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr1:12336998 G>A maps to NM_015378.2 T1118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:12415987 G>T maps to NM_015378.2 E3238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:12439595 G>A maps to NM_015378.2 T3712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:2845102 C>T maps to NM_022575.2 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:2843493 C>T maps to NM_022575.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:2844901 C>T maps to NM_022575.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr20:2846886 T>C maps to NM_022575.2 H767H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:2842489 C>T maps to NM_022575.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:2842290 C>T maps to NM_022575.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:2847075 C>T maps to NM_022575.2 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:41195413 A>T maps to NM_020857.2 K933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:41191585 C>T maps to NM_020857.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr15:41192977 C>T maps to NM_020857.2 N654N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:41192065 C>T maps to NM_020857.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:41191501 C>T maps to NM_020857.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:40926685 C>T maps to NM_032353.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:40925774 G>A maps to NM_032353.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:70892676 T>C maps to NM_004896.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:70892785 G>T maps to NM_004896.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr10:70930974 C>T maps to NM_004896.3 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:110930880 G>A maps to NM_057180.1 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:122745891 G>A maps to NM_022916.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr12:122735535 G>A maps to NM_022916.4 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:122716927 G>A maps to NM_022916.4 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr12:122726974 C>T maps to NM_022916.4 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:122723215 A>C maps to NM_022916.4 L407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:122724463 G>A maps to NM_022916.4 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:91549654 C>A maps to NM_018668.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr15:91543023 C>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr15:91543803 G>A maps to NM_018668.3 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:91553037 G>T maps to NM_018668.3 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:46695764 T>A maps to NM_018206.4 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:46711252 C>A maps to NM_018206.4 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:46712982 G>A maps to NM_018206.4 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:53000135 G>A maps to NM_016075.2 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr13:52990008 C>A maps to NM_016075.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr15:42470676 C>T maps to ENST00000348544 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:38937710 C>A maps to NM_014396.3 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr7:38813751 T>C maps to NM_014396.3 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:38796566 C>T maps to NM_014396.3 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:150054801 G>A maps to NM_007259.3 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:150049848 C>T maps to NM_007259.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:150044262 C>T maps to NM_007259.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr1:150064114 C>T maps to NM_007259.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:150082736 G>A maps to NM_007259.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:61067283 G>A maps to NM_004869.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:33234969 G>A maps to NM_022553.4 Q374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:33232200 G>A maps to NM_022553.4 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:33235078 C>T maps to NM_022553.4 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:33235039 G>A maps to NM_022553.4 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr6:33235093 G>A maps to NM_022553.4 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:489532 G>A maps to NM_001128159.2 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:440281 G>A maps to NM_001128159.2 C667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr17:602617 A>C maps to NM_001128159.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:559186 C>A maps to NM_001128159.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:565054 C>T maps to NM_001128159.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:64141313 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:64140408 T>C maps to NM_016516.2 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:64120623 G>T maps to NM_016516.2 A958A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:151149452 G>A maps to ENST00000354473 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:151156813 C>A maps to ENST00000354473 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr1:151149368 C>T maps to ENST00000354473 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:184584686 T>A maps to ENST00000437079 C473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Q-01A-11D-A122-09 chr3:184588533 C>T maps to ENST00000437079 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr14:97321622 C>T maps to NM_003384.2 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:97326982 G>T maps to NM_003384.2 G327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:97342378 G>T maps to NM_003384.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:58373542 C>A maps to NM_001130480.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:58373533 C>T maps to NM_001130480.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:50482458 C>T maps to NM_016440.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:50498068 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:50496209 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:107319370 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:107301302 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:107319386 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:107320555 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:107310300 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:107320329 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:107320310 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:107301374 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:107301383 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:118533533 G>T maps to NM_019086.5 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:118520205 G>A maps to NM_019086.5 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:118517220 G>A maps to NM_019086.5 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:124618540 G>A maps to NM_014312.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:65252404 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:65253669 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:65253369 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:65252503 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:65244970 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:159824794 C>T maps to NM_001013661.1 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:54610434 C>A maps to ENST00000404951 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:74706380 C>A maps to NM_182894.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr14:74727393 C>T maps to NM_182894.2 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:114428032 C>T maps to NM_145206.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:114575072 C>T maps to NM_145206.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr14:68126446 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:116046110 C>T maps to NM_198496.1 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:22144300 G>A maps to NM_173615.3 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:22149728 G>T maps to NM_173615.3 G730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:22108240 G>T maps to NM_173615.3 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:22111742 G>A maps to NM_173615.3 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:22134428 G>A maps to NM_173615.3 W460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:22142927 C>A maps to NM_173615.3 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:22149749 G>T maps to NM_173615.3 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:98797509 G>A maps to NM_144992.4 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:98828446 G>T maps to NM_144992.4 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:98928524 C>T maps to ENST00000451075 I1255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr2:98866864 C>T maps to NM_144992.4 R920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:98907170 G>T maps to ENST00000422503 *1081Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:98907107 C>T maps to ENST00000422503 F1060F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:98709731 C>T maps to NM_144992.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:98928360 A>T maps to NM_144992.4 R1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:98866890 C>A maps to NM_144992.4 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:98887175 G>T maps to NM_144992.4 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:98732124 G>A maps to NM_144992.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:123988963 C>T maps to NM_014622.4 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:123993766 C>T maps to NM_014622.4 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:124013233 C>T maps to NM_014622.4 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:124007321 C>A maps to NM_014622.4 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:123988494 C>T maps to NM_014622.4 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:123994388 C>T maps to NM_014622.4 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:49951735 C>T maps to NM_198570.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:215279087 C>T maps to NM_001080500.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:61053873 G>A maps to NM_152718.2 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:61026467 C>T maps to NM_152718.2 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr11:61026326 C>T maps to NM_152718.2 T896T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:61045928 G>A maps to NM_152718.2 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:6128761 C>T maps to NM_000552.3 R1274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:6161869 C>A maps to NM_000552.3 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:6120885 C>T maps to NM_000552.3 K1913K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:6125703 C>A maps to NM_000552.3 R1763R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:6128242 C>T maps to NM_000552.3 E1447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:6103288 C>A maps to NM_000552.3 E2113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:6145581 C>A maps to NM_000552.3 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:6103644 T>C maps to NM_000552.3 Q2064Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr12:6125769 A>G maps to NM_000552.3 I1741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:28903594 C>T maps to NM_016628.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:28903533 G>A maps to NM_016628.3 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:28884782 G>A maps to NM_016628.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:88227230 A>G maps to ENST00000342368 Y810Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr10:88260201 G>A maps to ENST00000342368 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:88260093 C>T maps to ENST00000342368 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:88206016 C>A maps to ENST00000342368 E1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:88260012 C>T maps to ENST00000342368 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:88277846 C>A maps to ENST00000342368 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:88260093 C>T maps to ENST00000342368 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:100809662 G>T maps to NM_173701.1 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr1:119588246 G>A maps to NM_015836.3 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48544140 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48549529 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:48542780 A>C did not map to a codon.
Sequencing variant TCGA-AX-A1CP-01A-11D-A135-09 chr23:48542705 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr23:48542342 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr23:48545264 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:48544513 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:48546787 T>C did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:48542774 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr23:48543954 A>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:48545284 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:110421753 C>A maps to NM_003931.2 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:110429777 G>A maps to NM_003931.2 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:110426646 C>A maps to NM_003931.2 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:110434531 C>A maps to NM_003931.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:27742592 G>A maps to NM_006990.2 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:27742484 C>T maps to NM_006990.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:27739148 C>T maps to NM_006990.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:123335900 A>G maps to NM_003941.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr7:123329183 A>T maps to NM_003941.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:74687759 G>A maps to ENST00000393972 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:14952593 T>C maps to NM_016312.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:14952637 G>A maps to NM_016312.2 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:14946665 T>C maps to NM_016312.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:14947915 G>T maps to NM_016312.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:14954302 A>C maps to NM_016312.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:14947558 G>A maps to NM_016312.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:73843003 G>A maps to NM_012478.3 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:42418277 C>A maps to NM_152613.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:42422926 C>T maps to NM_152613.2 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:41642767 G>T maps to NM_007187.3 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:102612898 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:102612897 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:74480411 G>A maps to NM_030798.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:74486520 C>T maps to NM_030798.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:70853358 C>A maps to NM_022479.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:71036363 G>T maps to NM_022479.1 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:71130526 C>A maps to NM_022479.1 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr7:70885902 G>A maps to NM_022479.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr7:71130574 G>A maps to NM_022479.1 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:73107983 G>A maps to ENST00000423497 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:73106927 C>T maps to ENST00000423497 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:73279465 C>T maps to NM_182504.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:224770670 G>A maps to NM_020830.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr2:224760303 G>C maps to NM_020830.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:224758955 C>A maps to NM_020830.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:224746656 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:224763759 G>A maps to NM_020830.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:224765928 G>A maps to NM_020830.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr13:52332384 C>T maps to NM_052950.3 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr13:52325481 G>A maps to NM_052950.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr13:52332384 C>T maps to NM_052950.3 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:52332408 G>T maps to NM_052950.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr13:52332384 C>T maps to NM_052950.3 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:85645692 G>A maps to NM_014991.4 R2443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:85731101 C>T maps to NM_014991.4 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:85654714 G>A maps to NM_014991.4 I2347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr4:85699712 A>G maps to NM_014991.4 H1487H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:85657352 A>G maps to NM_014991.4 S2295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr4:85594130 G>A maps to NM_014991.4 Q3491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:85715750 G>A maps to NM_014991.4 Y1136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:85605185 G>A maps to NM_014991.4 S3212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:85699689 G>T maps to NM_014991.4 S1495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:85600237 G>A maps to NM_014991.4 G3327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:85664915 C>A maps to NM_014991.4 E2004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:85694033 C>T maps to NM_014991.4 E1601E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr4:85600321 G>A maps to NM_014991.4 D3299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:85623568 C>A maps to NM_014991.4 E2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:55422348 C>A maps to NM_007086.3 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:55423801 C>A maps to NM_007086.3 E956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:55467295 C>T maps to NM_007086.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:10090251 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:10089429 G>A maps to NM_017491.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:10084713 C>T maps to NM_017491.3 S376S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A051-01A-21W-A027-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:122633378 C>T maps to NM_018117.11 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:122640386 C>T maps to NM_018117.11 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:122622322 T>G maps to NM_018117.11 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:122649474 T>G maps to NM_018117.11 L766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:122619654 C>T maps to NM_018117.11 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:203748384 C>T maps to NM_018256.3 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48457145 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:48458045 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48457831 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:48458063 C>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:48458736 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:48458813 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:48458723 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:48463353 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:48458717 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:9490151 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:9545079 G>T maps to NM_145054.4 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:9490145 C>T maps to NM_145054.4 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:9515757 T>A maps to NM_145054.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr17:9511491 C>T maps to NM_145054.4 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:9545079 G>T maps to NM_145054.4 E539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:177083277 C>T maps to NM_170710.4 R959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:177041042 C>A maps to NM_170710.4 C135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:177069290 C>T maps to NM_170710.4 R592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:177093533 A>G maps to NM_170710.4 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:177095771 C>T maps to NM_170710.4 R1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:177072988 C>A maps to NM_170710.4 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr4:177069469 C>T maps to NM_170710.4 H651H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:990979 C>T maps to NM_024100.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr4:39187360 C>T maps to NM_025132.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:39196162 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:39245930 C>T maps to NM_025132.3 R829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:39219610 C>T maps to NM_025132.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:39276563 C>T maps to NM_025132.3 I1234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:39230161 C>T maps to NM_025132.3 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:39267744 C>T maps to NM_025132.3 N1082N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:39278744 C>A maps to NM_025132.3 I1274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr4:39254825 C>T maps to NM_025132.3 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:39255648 T>C maps to NM_025132.3 I1000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:736078 C>T maps to ENST00000248142 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:737358 C>T maps to ENST00000248142 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:736815 C>T maps to ENST00000248142 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:735511 C>T maps to ENST00000248142 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:100995448 C>T maps to NM_001161476.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr14:100992271 C>T maps to NM_001161476.1 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:224606035 C>A maps to NM_025160.6 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:224588660 G>A maps to NM_025160.6 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JT-01A-21D-A122-09 chr1:224581650 T>A maps to NM_025160.6 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr6:170038632 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:118477157 A>C maps to NM_006784.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:118492749 A>G maps to NM_006784.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:118502045 G>A maps to NM_006784.2 E936E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:118477190 C>T maps to NM_006784.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:118492692 G>A maps to NM_006784.2 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr1:118482098 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:118495574 G>T maps to NM_006784.2 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:116091183 C>A maps to NM_001012361.2 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:116083830 C>A maps to NM_001012361.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:128522457 C>T maps to NM_018383.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:128467396 G>A maps to NM_018383.4 G1114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:128477377 G>A maps to NM_018383.4 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:128479415 A>C maps to NM_018383.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:128482483 A>G maps to NM_018383.4 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:128477180 C>T maps to NM_018383.4 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:128481932 G>C maps to NM_018383.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:128522060 C>A maps to NM_001006622.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr2:128477458 G>A maps to NM_018383.4 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:20133188 T>G maps to NM_001006657.1 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:20153637 C>A maps to NM_001006657.1 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr5:110461364 C>T maps to NM_139281.2 R860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:110456793 T>C maps to NM_139281.2 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:110440992 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:110446631 C>A maps to NM_139281.2 I585I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:110439579 A>G maps to NM_139281.2 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr5:110438069 G>A maps to NM_139281.2 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr5:110428091 A>T maps to NM_139281.2 K36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:110443023 C>A maps to NM_139281.2 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:1123909 G>T maps to ENST00000416775 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:1123903 G>T maps to ENST00000416775 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr10:1123943 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:127619015 C>T maps to NM_001045476.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:76785397 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr5:76729019 C>T maps to NM_018268.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr2:29152461 T>A maps to NM_015131.1 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:29137005 G>A maps to NM_015131.1 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:29169591 G>T maps to NM_015131.1 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:29169591 G>T maps to NM_015131.1 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:117566792 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:117577541 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:117526797 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:117528089 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:117526731 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:117575509 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:117576288 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:117577649 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:117566842 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:117540960 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:117480470 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117526697 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117526872 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:117532379 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:117521350 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:117577605 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:117577649 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:117529211 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117527194 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117566842 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117576531 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117582887 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:117528036 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:117543589 G>T did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:117540869 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:117582933 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:48934319 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:48933228 C>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:48932478 C>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:48932826 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr23:48932902 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:48934313 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:48934102 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:48933021 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:48932467 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:48933245 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:48932827 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:80574406 G>A maps to NM_019613.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:33247082 C>A maps to NM_005452.5 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:33248523 G>A maps to NM_005452.5 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:33254639 C>T maps to NM_005452.5 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:33256733 T>C maps to NM_005452.5 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:109566103 C>A maps to NM_001142550.1 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:39104555 C>T maps to NM_020839.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:39129638 C>T maps to NM_020839.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr3:39127063 G>A maps to NM_020839.2 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:137019586 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:137020840 G>A maps to NM_052821.3 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr9:137021644 A>G maps to NM_052821.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:113127957 G>A maps to NM_001164496.1 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:113092364 G>A maps to NM_001164496.1 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:113092330 G>A maps to NM_001164496.1 Q791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:113027011 G>A maps to NM_001164496.1 C1540C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:113082107 C>A maps to NM_001164496.1 E940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:113063554 G>A maps to NM_001164496.1 R1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:113010505 C>T maps to NM_001164496.1 S1821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:113115522 G>A maps to NM_001164496.1 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:113082107 C>A maps to NM_001164496.1 E940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:74650492 C>T maps to NM_032118.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:74652204 T>G maps to NM_032118.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:74650047 C>T maps to NM_032118.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:140048484 C>T maps to NM_017706.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:74908202 G>A maps to NM_030581.3 H943H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:74943480 C>T maps to NM_030581.3 A520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:74937955 C>T maps to NM_030581.3 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:74949883 C>A maps to NM_030581.3 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:74950049 G>A maps to NM_030581.3 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:122134000 A>G maps to NM_019069.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:49052140 G>A maps to NM_018031.3 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:49049980 G>A maps to NM_018031.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:49052591 C>T maps to NM_018031.3 T1109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:49050797 C>T maps to NM_018031.3 R641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:158695261 G>T maps to NM_018051.4 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:158698776 G>A maps to NM_018051.4 K485K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr7:158718992 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:78580722 G>A maps to NM_025234.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:78578399 G>A maps to NM_025234.1 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr15:78578444 G>A maps to NM_025234.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36593924 C>T maps to NM_001083961.1 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:36582181 C>T maps to NM_001083961.1 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr19:36592160 G>A maps to NM_001083961.1 Q971Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:36558827 G>A maps to NM_001083961.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:36590401 G>A maps to NM_001083961.1 K874K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:85548072 G>T maps to NM_145172.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:85550264 G>T maps to NM_145172.3 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:85564245 G>T maps to NM_145172.3 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:85547007 T>C maps to NM_145172.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:85570250 C>T maps to NM_145172.3 C508C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:85592390 C>A maps to NM_145172.3 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:241850885 C>T maps to NM_144625.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:241912990 C>A maps to NM_144625.4 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:241951277 G>T maps to NM_144625.4 E935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:241951196 C>T maps to NM_144625.4 R908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:241875151 C>A maps to NM_144625.4 Y331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr1:241946668 C>T maps to NM_144625.4 I887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:43675430 G>A maps to NM_001195831.1 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:43649452 C>A maps to NM_001195831.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:43672497 C>T maps to NM_001195831.1 C550C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:43638489 C>A maps to NM_001195831.1 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:43638510 C>A maps to NM_001195831.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:43665146 C>T maps to NM_001195831.1 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:43647256 G>A maps to NM_001195831.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:43647493 C>T maps to NM_001195831.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr12:122389384 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr12:122405988 C>T maps to NM_144668.4 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:122359259 G>T maps to NM_144668.4 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:124140709 C>T maps to NM_145647.3 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:124132354 C>T maps to NM_145647.3 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:124089349 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr8:124140594 G>A maps to NM_145647.3 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:124109566 T>C maps to NM_145647.3 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:228754596 G>T maps to NM_178821.1 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:228754596 G>T maps to NM_178821.1 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:228754646 C>T maps to NM_178821.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr2:228767818 C>A maps to NM_178821.1 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:54606618 C>T maps to NM_015285.2 I1353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:54423917 G>A maps to NM_015285.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:54361894 G>T maps to NM_015285.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:54547320 C>T maps to NM_015285.2 R1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:54547322 A>G maps to NM_015285.2 R1151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr18:54448876 C>T maps to NM_015285.2 H1060H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:54398697 C>A maps to NM_015285.2 S620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:54363621 G>T maps to NM_015285.2 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:54424065 G>T maps to NM_015285.2 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:54424197 G>T maps to NM_015285.2 E792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:54694425 C>T maps to NM_015285.2 R1487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr18:54339865 C>T maps to NM_015285.2 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:37392139 G>T maps to NM_018034.2 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:54008801 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:53992016 C>T maps to NM_182758.2 W565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:54003597 A>G maps to NM_182758.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:53994474 C>T maps to NM_182758.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:54005024 G>A maps to NM_182758.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JN-01A-11D-A10B-09 chr15:53992109 G>T maps to NM_182758.2 C534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:53901775 G>T maps to NM_182758.2 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:53994474 C>T maps to NM_182758.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:54005073 G>T maps to NM_182758.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:54005063 C>A maps to NM_182758.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:190331171 T>C maps to NM_032168.1 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:190327258 C>T maps to NM_032168.1 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr2:190334121 A>G maps to NM_032168.1 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr2:190339477 T>C maps to NM_032168.1 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:44134636 G>T maps to NM_024908.3 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:44149149 A>C maps to NM_024908.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:111985954 G>T maps to NM_024102.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:67306303 C>A maps to NM_024763.4 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:67356899 C>A maps to NM_024763.4 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:67313331 C>A maps to NM_024763.4 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:67356906 T>G maps to NM_024763.4 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr1:67340570 G>A maps to NM_024763.4 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:1630733 G>A maps to NM_001163809.1 Q827Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:1631033 C>T maps to NM_001163809.1 F927F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:1628984 C>T maps to NM_001163809.1 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr17:1630973 G>A maps to NM_001163809.1 Q907Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:52294457 G>A maps to NM_025222.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:52301020 G>T maps to NM_025222.3 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:12781089 C>T maps to NM_032332.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:12781593 C>T maps to NM_032332.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:12780837 C>T maps to NM_032332.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:140450083 C>T maps to NM_138778.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:140459601 G>A maps to NM_138778.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:151079029 G>A maps to ENST00000426624 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:33639781 C>T maps to NM_173479.3 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:33647372 C>T maps to NM_173479.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:33655168 A>T maps to NM_173479.3 K383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UT-01A-11D-A10B-09 chr14:64066161 C>A maps to NM_080666.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:708903 C>T maps to NM_145294.4 I968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:706823 C>T maps to NM_145294.4 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:703744 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:701234 G>A maps to NM_145294.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:711940 G>A maps to NM_145294.4 S1305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:701966 G>T maps to NM_145294.4 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr16:703522 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:134878102 C>T maps to NM_014149.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:134878066 G>A maps to NM_014149.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr7:134889079 C>T maps to NM_014149.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:134878135 C>T maps to NM_014149.3 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:68358370 C>T maps to NM_138458.2 *358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:68361859 G>A maps to NM_138458.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:90276354 C>A maps to NM_020212.1 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:90245148 C>T maps to NM_020212.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr15:90255327 C>T maps to NM_020212.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr15:90272310 C>T maps to NM_020212.1 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:160139541 G>A maps to NM_001128212.1 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:160112754 C>A maps to NM_001128212.1 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:160136296 G>A maps to NM_001128212.1 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:27620554 C>T maps to ENST00000319394 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr1:27631606 C>T maps to ENST00000319394 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:27631506 C>T maps to ENST00000319394 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:27631647 C>T maps to ENST00000319394 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:27624476 C>T maps to ENST00000319394 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:27623545 G>A maps to ENST00000319394 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:27618813 C>T maps to ENST00000319394 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:124442245 G>A maps to NM_018024.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:141430117 T>C maps to NM_001105558.1 *568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:141418916 G>T maps to NM_001105558.1 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:141418948 C>T maps to NM_001105558.1 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:44313594 G>T maps to NM_172131.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:44417597 A>G maps to NM_080614.1 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:43739417 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:44207873 G>A maps to NM_130896.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:44236748 C>A maps to NM_147198.2 *90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:681396 C>A maps to NM_053284.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:48917662 C>T maps to NM_175575.5 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr4:6302772 C>T maps to NM_006005.3 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:6303099 C>A maps to NM_006005.3 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:6304158 C>T maps to NM_006005.3 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:6304041 C>T maps to NM_006005.3 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:6303234 C>A maps to NM_006005.3 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr4:6302496 C>T maps to NM_006005.3 N325N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr15:83485472 T>G maps to NM_001080435.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:83495206 G>T maps to NM_001080435.1 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr15:83499454 G>A maps to NM_001080435.1 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11W-01A-12D-A122-09 chr15:83485535 C>T maps to NM_001080435.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr15:83499655 G>A maps to NM_001080435.1 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:1957480 C>T maps to NM_133335.3 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:1962829 C>T maps to NM_133335.3 H1108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:1957835 G>A maps to NM_133335.3 A934A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:1978323 C>T maps to NM_133335.3 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr4:1955183 C>T maps to NM_133335.3 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:1957435 C>A maps to NM_133335.3 C845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:1957782 G>T maps to NM_133335.3 E917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr8:38205428 C>T maps to NM_023034.1 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:38162249 A>T maps to NM_023034.1 C822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:38196053 T>C maps to NM_023034.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr8:38187282 C>T maps to NM_023034.1 Q398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:38133957 G>A maps to NM_023034.1 R1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:38146957 C>A maps to NM_023034.1 E1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:1985407 G>A maps to NM_005663.3 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:65445209 G>A maps to NM_007191.4 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr2:175436683 G>A maps to NM_003387.4 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:175446053 A>G maps to NM_003387.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:175437118 C>T maps to NM_003387.4 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:175436887 G>A maps to NM_003387.4 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr2:175436545 G>A maps to NM_003387.4 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:29915469 C>T maps to NM_001080529.1 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:29927726 G>A maps to NM_001080529.1 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:29928928 C>T maps to NM_001080529.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:29927789 G>A maps to NM_001080529.1 Q402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:66446991 G>A maps to NM_017983.5 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:66432540 A>C maps to NM_017983.5 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:66417925 C>T maps to NM_017983.5 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:66423282 C>T maps to NM_017983.5 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:66449098 G>A maps to NM_017983.5 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:5256784 C>T maps to NM_015610.3 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:5270544 C>T maps to NM_015610.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:5256815 T>C maps to NM_015610.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:134233034 C>T maps to NM_003882.2 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:134232914 C>T maps to NM_003882.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:134233037 C>T maps to NM_003882.2 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:134239739 A>G maps to NM_003882.2 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr8:134239937 A>G maps to NM_003882.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:134232839 C>T maps to NM_003882.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:134225252 C>T maps to NM_003882.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr8:134239874 T>C maps to NM_003882.2 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:43353475 C>T maps to NM_003881.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:112382253 G>T maps to NM_198239.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:112382253 G>T maps to NM_198239.1 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:15538195 C>T maps to ENST00000389282 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:15547878 G>A maps to ENST00000389282 F778F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr19:15537871 C>T maps to ENST00000389282 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:15538303 G>A maps to ENST00000389282 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:15559016 G>A maps to ENST00000389282 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05W-01A-21W-A027-09 chr1:68619221 G>A maps to NM_024911.6 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:68659872 C>A maps to NM_024911.6 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:68592012 G>A maps to NM_024911.6 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:68697916 G>A maps to NM_024911.6 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:68564356 C>T maps to NM_001002292.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr1:68610260 G>A maps to NM_024911.6 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:992689 G>T maps to NM_001184985.1 E1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr12:988776 A>G maps to NM_018979.3 E804E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:994529 A>G maps to NM_001184985.1 E1780E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:995024 G>A maps to NM_001184985.1 E1945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr12:1017741 C>T maps to NM_001184985.1 T2571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:1009726 G>A maps to NM_001184985.1 Q2438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:970505 T>C maps to NM_001184985.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:1005253 C>T maps to NM_001184985.1 D2127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr12:922854 T>C maps to NM_001184985.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:1005565 G>A maps to NM_001184985.1 K2231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:863406 G>T maps to NM_001184985.1 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:1005484 A>T maps to NM_001184985.1 G2204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:968539 G>A maps to NM_001184985.1 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:999659 A>G maps to NM_001184985.1 G2090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr12:1005415 G>A maps to NM_001184985.1 V2181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:922920 A>T maps to NM_001184985.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr12:992631 A>G maps to NM_001184985.1 K1447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:96051364 G>A maps to ENST00000297954 P1480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr9:96026308 G>A maps to ENST00000297954 T1230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr9:95992057 C>T maps to ENST00000297954 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr9:96009907 G>A maps to ENST00000297954 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:54224922 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:54324762 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54263452 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54337566 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:54359625 C>A did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:54264788 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:54337623 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54259320 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:54328243 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:54265350 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54228502 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54277992 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54328243 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54334476 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54337639 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54359799 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:54359972 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54264821 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54278071 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54321004 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54335575 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54335690 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:54337626 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:54278088 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:54228450 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:54263820 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:54277992 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:54265456 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:54275488 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:54275841 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:54360049 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:54259387 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:54224971 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:54228502 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:54335669 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:54360022 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:54319610 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:54337650 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:54359936 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:54263372 T>C did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr23:54282286 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17K-01A-11D-A12J-09 chr23:54319595 G>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:54319364 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr17:40936017 G>A maps to NM_032387.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:40934882 G>A maps to NM_032387.4 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr17:40936446 G>A maps to NM_032387.4 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:40933060 T>C maps to NM_032387.4 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr17:40936140 G>A maps to NM_032387.4 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:219754710 C>T maps to NM_025216.2 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:49361734 C>T maps to NM_003394.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:49364106 C>A maps to NM_003394.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr11:75898114 G>A maps to NM_004626.2 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:120979053 T>C maps to NM_057168.1 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:120969662 C>T maps to NM_057168.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr7:120969731 C>T maps to NM_057168.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:116937747 G>A maps to NM_003391.2 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:116963071 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:113057666 T>C maps to NM_024494.2 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr1:113059840 C>T maps to NM_024494.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:113057517 C>T maps to NM_024494.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:113052048 C>T maps to NM_024494.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:113057625 C>A maps to NM_024494.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:44846033 G>A maps to NM_030753.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:44846063 G>A maps to NM_030753.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:44846111 G>A maps to NM_030753.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:44845832 G>A maps to NM_030753.3 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:44846129 G>A maps to NM_030753.3 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:44846063 G>A maps to NM_030753.3 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:228210490 C>T maps to ENST00000366753 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:228246751 G>A maps to ENST00000366753 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:228210589 C>T maps to ENST00000366753 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr1:228210496 C>T maps to ENST00000366753 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MG-01A-21D-A10B-09 chr1:22456214 G>A maps to NM_030761.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:55504143 G>A maps to NM_003392.3 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:55504093 C>T maps to ENST00000442038 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr12:1755105 C>T maps to NM_032642.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:219736438 C>T maps to NM_006522.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr2:219736480 G>A maps to NM_006522.3 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:13860851 C>T maps to NM_004625.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C8-01A-11D-A135-09 chr3:13916618 G>T maps to NM_004625.3 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:13916570 G>A maps to NM_004625.3 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:228111879 G>A maps to NM_003395.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:228112048 G>A maps to NM_003395.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:7605345 T>C maps to ENST00000451908 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr17:7606421 G>A maps to NM_018081.2 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:7592916 C>T maps to NM_018081.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr17:7592199 C>T maps to NM_018081.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7592394 C>T maps to NM_018081.2 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr21:40763743 C>T maps to NM_004627.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:30945420 G>T maps to NM_000553.4 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:30938551 G>T maps to NM_000553.4 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:30933693 G>T maps to NM_000553.4 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AJ-A23M-01A-11D-A159-09 chr17:25639259 T>C maps to NM_015626.8 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:25639341 C>T maps to NM_015626.8 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:118476092 C>T maps to ENST00000441406 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr17:6023809 C>T maps to NM_015253.1 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr17:6023653 C>T maps to NM_015253.1 Y467Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr17:6023671 G>A maps to NM_015253.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr17:6023635 G>A maps to NM_015253.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr17:6023779 C>T maps to NM_015253.1 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:108634199 C>A maps to ENST00000261400 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:108603924 C>T maps to ENST00000261400 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:108620876 C>T maps to ENST00000261400 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:108634208 C>T maps to ENST00000261400 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:108641999 C>T maps to ENST00000261400 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr12:108634208 C>T maps to ENST00000261400 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:32421517 C>T maps to NM_024426.4 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr6:160164748 G>A maps to NM_004906.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr5:167851014 C>T maps to NM_001161661.1 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:167855747 C>T maps to NM_001161661.1 D652D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:167798536 C>A maps to NM_001161661.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr5:167858265 C>T maps to NM_001161661.1 R699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:167882369 G>T maps to NM_001161661.1 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:167881048 G>T maps to NM_001161661.1 E868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr5:167812372 G>A maps to NM_001161661.1 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr5:167858265 C>T maps to NM_001161661.1 R699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr5:167850638 C>A maps to NM_001161661.1 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:184201997 G>T maps to ENST00000448232 E878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:184182395 G>A maps to ENST00000448232 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:184204002 G>T maps to ENST00000448232 E967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:184186897 C>T maps to ENST00000448232 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:10096178 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:10106871 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:10096043 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:10102498 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:10085310 C>T did not map to a codon.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr23:10062227 A>G did not map to a codon.
Sequencing variant TCGA-AX-A0IW-01A-11W-A062-09 chr23:10035294 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:10047818 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:10085339 A>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:10093119 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:10058844 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:10104688 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:10085338 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:10109532 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:10035454 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:10035515 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr23:10085462 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr23:10096134 G>T did not map to a codon.
Sequencing variant TCGA-BK-A13C-01A-11D-A122-09 chr23:10093128 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:10102570 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr23:10085321 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:10096129 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:10085534 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:10090723 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:10085308 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:10062200 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:79245599 C>A maps to NM_016373.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:78312519 G>A maps to NM_130791.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr16:78458937 C>A maps to NM_016373.1 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr16:78420791 C>T maps to NM_016373.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:87410584 G>T maps to NM_007013.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:87473499 C>T maps to NM_007013.3 F849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:87473461 G>T maps to NM_007013.3 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr8:87460685 G>A maps to NM_007013.3 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:69963381 C>T maps to NM_007014.3 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:69965464 C>T maps to NM_007014.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:149260150 G>A maps to NM_001168278.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:149238744 G>T maps to NM_001168278.1 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:149260150 G>A maps to NM_001168278.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:7684869 G>A maps to NM_020196.2 D786D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:7687716 G>A maps to NM_020196.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:7691051 G>A maps to NM_020196.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:6674257 T>C maps to NM_017523.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:52895552 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:52842216 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:52842261 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr22:29191689 A>C maps to ENST00000403532 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:29193193 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:168550442 G>A maps to NM_002995.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:168511244 G>T maps to NM_003175.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:31587056 G>A maps to NM_000379.3 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:31624194 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:31569661 C>T maps to NM_000379.3 K1108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:31571205 G>A maps to NM_000379.3 Y1025Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:31590878 G>A maps to NM_000379.3 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:31620556 G>A maps to NM_000379.3 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr2:31609393 G>A maps to NM_000379.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:31590878 G>T maps to NM_000379.3 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:2688601 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:2712608 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:2726249 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:2712614 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:2700105 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:2726244 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:2726230 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:123019575 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:123034363 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:123019668 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:123019537 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr23:123020209 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123019597 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123020214 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:123040881 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:123019820 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123020015 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123034374 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:123034441 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:123025125 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:39229228 G>A maps to NM_194293.2 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:39229949 G>A maps to NM_194293.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr3:39228931 G>A maps to NM_194293.2 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:39229970 G>T maps to NM_194293.2 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:39229322 G>A maps to NM_194293.2 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr3:39230012 G>A maps to NM_194293.2 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr3:39228611 C>T maps to NM_194293.2 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:39226115 A>G maps to NM_194293.2 T1607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:168106317 G>T maps to NM_152381.5 E2806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:168102482 G>A maps to NM_152381.5 W1527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:167760390 C>T maps to NM_152381.5 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:168106475 C>T maps to NM_152381.5 I2858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LH-01A-11W-A062-09 chr2:168100145 G>A maps to NM_152381.5 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:168097236 C>T maps to NM_152381.5 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:168100490 A>G maps to NM_152381.5 Q863Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:167760390 C>T maps to NM_152381.5 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:168100134 A>C maps to NM_152381.5 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:168102642 C>T maps to NM_152381.5 R1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:168102905 T>C maps to NM_152381.5 S1668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr2:168107009 C>A maps to NM_152381.5 S3036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:168099824 G>A maps to NM_152381.5 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:168104751 G>T maps to NM_152381.5 E2284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:168107318 C>T maps to NM_152381.5 N3139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:168106475 C>T maps to NM_152381.5 I2858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CB-01A-32D-A10B-09 chr2:168105920 C>T maps to NM_152381.5 C2673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:168099252 G>T maps to NM_152381.5 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:168101525 C>A maps to NM_152381.5 S1208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:167992564 C>A maps to NM_152381.5 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:168100754 C>A maps to NM_152381.5 I951I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:168102395 T>G maps to NM_152381.5 T1498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr2:168099407 T>C maps to NM_152381.5 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr2:168104756 T>C maps to NM_152381.5 S2285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:37545299 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:37553542 T>G did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:37553587 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:37587469 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:37553758 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:37587548 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr23:37587533 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:37545375 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:37587521 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:37587684 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:17265005 C>A maps to NM_175878.3 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:17280678 C>A maps to NM_175878.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:56435861 C>T maps to NM_052898.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:56270265 C>T maps to NM_052898.1 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:56436548 C>A maps to NM_052898.1 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:56436606 G>T maps to NM_052898.1 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:56436131 C>T maps to NM_052898.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:56436606 G>T maps to NM_052898.1 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:6669627 G>A maps to NM_207411.4 P384P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:6669419 C>A maps to NM_207411.4 E454*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B5-A11E-01A-11D-A10M-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr8:6679393 G>A maps to NM_207411.4 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr8:6669182 C>A maps to NM_207411.4 G533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:10755857 G>A maps to NM_173683.3 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:10755610 G>A maps to NM_173683.3 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:10756281 G>T maps to NM_173683.3 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:10756220 G>A maps to NM_173683.3 F389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:10755782 C>A maps to NM_173683.3 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:10755464 G>T maps to NM_173683.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr8:10756040 G>T maps to NM_173683.3 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:10756022 G>T maps to NM_173683.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr20:30556400 C>A maps to NM_001011718.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0V8-01A-11D-A122-09 chr20:30584761 G>A maps to NM_001011718.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:71593383 A>C maps to NM_001011720.1 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:71646034 G>A maps to NM_001011720.1 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:71593551 G>T maps to NM_001011720.1 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100170054 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:100183303 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100169635 T>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100183118 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:100183196 A>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:100183166 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:100169569 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:100177995 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:100183176 G>T did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:100182966 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:100437715 A>C did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:100451873 C>A maps to NM_000380.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:14193882 C>T maps to NM_004628.4 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:14209785 C>T maps to NM_004628.4 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:111643888 C>A maps to NM_020383.3 G256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr10:111651531 G>T maps to NM_020383.3 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:128902373 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:128889281 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:128896668 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:128880222 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:128896670 A>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:128902331 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:128884475 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:128884524 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr23:128876139 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:128879180 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:128895222 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr23:128888463 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:128886209 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:128886248 C>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:128886195 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:128894499 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:41320406 C>T maps to NM_022098.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:41282486 C>T maps to NM_022098.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:41322426 C>T maps to NM_022098.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:41322438 A>G maps to NM_022098.2 *508W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr22:41278090 C>T maps to NM_022098.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr22:41322324 T>C maps to NM_022098.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr2:61760990 A>C maps to NM_003400.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:61713061 T>C maps to NM_003400.3 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr2:61717815 A>C maps to NM_003400.3 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr2:61726915 C>T maps to NM_003400.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:21374455 C>T maps to NM_022459.4 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:21374437 G>A maps to NM_022459.4 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr13:21370323 C>T maps to NM_022459.4 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:21370949 C>A maps to NM_022459.4 E857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:21383303 G>A maps to NM_022459.4 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr13:21383303 G>A maps to NM_022459.4 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr13:21361120 A>G maps to NM_022459.4 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:21383303 G>A maps to NM_022459.4 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:43491715 C>A maps to NM_020750.2 E1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:43496592 G>A maps to NM_020750.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:43528732 A>C maps to NM_020750.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:43501718 C>A maps to NM_020750.2 E790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:43519109 G>A maps to NM_020750.2 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr16:28188615 G>T maps to NM_015171.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:28115977 C>T maps to NM_015171.2 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr16:28167675 G>A maps to NM_015171.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr16:28117747 A>G maps to NM_015171.2 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:21849469 C>T maps to ENST00000434536 N720N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:21856722 C>T maps to ENST00000434536 F859F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:21861512 C>T maps to ENST00000434536 R1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:21832233 C>T maps to ENST00000434536 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:21856272 C>T maps to ENST00000434536 R794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr8:21856656 G>A maps to ENST00000434536 K837K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:21832254 C>A maps to ENST00000434536 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr8:21843130 A>G maps to ENST00000434536 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr12:64827363 C>T maps to NM_007235.3 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:64810486 T>C maps to NM_007235.3 H51H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr12:64808769 G>T did not map to a codon.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:180832952 C>T maps to NM_004736.3 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:180794045 G>A maps to NM_004736.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:180794299 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44056176 C>T maps to NM_006297.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:44056352 G>A maps to NM_006297.2 R300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:152346092 G>A maps to NM_005431.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:104165907 G>T maps to NM_005432.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr14:104165286 G>A maps to NM_005432.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr5:82400875 A>G maps to NM_022406.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:82499527 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:82406985 T>C maps to NM_022406.2 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:82649019 C>T maps to NM_022406.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:217055058 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr22:42059624 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr22:42046866 C>T maps to NM_001469.3 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:58350526 G>T maps to NM_033276.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:58347430 G>T maps to NM_033276.2 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr3:142151539 G>A maps to NM_019001.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:142137371 C>T maps to NM_019001.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:142142426 G>A maps to NM_019001.3 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:142145633 C>A maps to NM_019001.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:142142426 G>A maps to NM_019001.3 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr3:142116260 G>T maps to NM_019001.3 S750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:21312263 G>A maps to NM_012255.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:21312418 T>C maps to NM_012255.3 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:21314628 T>C maps to NM_012255.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:21312979 G>T maps to NM_012255.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:21311339 G>A maps to NM_012255.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:21312957 G>A maps to NM_012255.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:21314237 G>A maps to NM_012255.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:21367508 C>T maps to NM_012255.3 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:21312957 G>A maps to NM_012255.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:21336796 C>T maps to NM_012255.3 Y700Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr20:21324735 G>A maps to NM_012255.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr20:21327148 C>T maps to NM_012255.3 Y542Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:21312957 G>A maps to NM_012255.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:21329004 G>A maps to NM_012255.3 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr20:21306922 G>T maps to NM_012255.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr11:74563070 G>A maps to NM_182969.1 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:74562191 G>A maps to NM_182969.1 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:74562191 G>A maps to NM_182969.1 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:74562191 G>A maps to NM_182969.1 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:74632335 A>G maps to NM_182969.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:38437042 G>T maps to NM_005108.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:38454497 G>A maps to NM_005108.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:38415956 G>A maps to NM_005108.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:38438621 T>C maps to NM_005108.3 C470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:17353331 C>T maps to NM_022166.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:17202581 C>T maps to NM_022166.3 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:17353133 G>A maps to NM_022166.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:17228421 G>A maps to NM_022166.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:17292169 G>A maps to NM_022166.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:17252766 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr16:17232373 C>T maps to NM_022166.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M8-01A-12D-A10B-09 chr16:17202803 G>A maps to NM_022166.3 N876N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr16:17353037 C>T maps to NM_022166.3 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:48434474 C>T maps to NM_022167.2 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11I-01A-11D-A10M-09 chr17:48433312 G>A maps to NM_022167.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:48434011 C>T maps to NM_022167.2 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:33251992 G>A maps to NM_003680.3 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:33276553 C>T maps to NM_003680.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:33245792 G>A maps to NM_003680.3 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:33252603 C>A maps to NM_003680.3 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr12:32903672 T>C maps to NM_001040436.1 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:43162437 A>G maps to NM_004559.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:7193323 G>A maps to NM_015982.3 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:7193312 C>T maps to NM_015982.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:183521962 C>T maps to NM_018023.4 I1257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:183508631 G>A maps to NM_018023.4 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:183521092 C>T maps to NM_018023.4 G1184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:183515762 G>A maps to NM_018023.4 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr3:183490340 C>T maps to NM_018023.4 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr3:183508703 C>T maps to NM_018023.4 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:183504073 C>T maps to NM_018023.4 N966N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:69764572 G>T maps to NM_006530.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:739755 C>T maps to NM_005433.3 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:745804 C>A maps to NM_005433.3 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:66055716 G>A maps to ENST00000376904 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr11:66052850 C>T maps to ENST00000431556 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:54332034 C>T maps to NM_018982.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:11034824 G>A maps to NM_024029.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:11036371 C>T maps to NM_024029.3 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:32515563 C>A maps to NM_032312.3 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:32523377 G>T maps to NM_032312.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:143545122 A>G maps to NM_030799.7 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr5:143543733 C>A maps to NM_030799.7 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:67731770 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:67738634 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:67731785 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:67733196 A>C did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:67731807 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr23:67718948 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:67731807 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:67738634 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:67741325 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:67731802 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:67741236 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:67733243 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr4:44624496 C>T maps to NM_182592.2 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44250648 C>T maps to NM_006555.3 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:44250648 C>T maps to NM_006555.3 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr14:75266119 C>T maps to NM_019589.2 R1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:75265441 C>T maps to NM_019589.2 R1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:75283968 G>T maps to NM_019589.2 E1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr14:75283970 A>G maps to NM_019589.2 E1979E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr14:75245170 C>T maps to NM_019589.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr14:75245268 A>G maps to NM_019589.2 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr14:75248809 G>A maps to NM_019589.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr14:75278373 T>A maps to NM_019589.2 G1760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:75230707 C>T maps to NM_019589.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr14:75265953 A>G maps to NM_019589.2 E1318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr14:75302092 C>T maps to NM_019589.2 L2140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:27406636 C>A maps to NM_139312.1 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:27425210 G>A maps to NM_139312.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:27409411 G>A maps to NM_139312.1 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:27434387 G>T maps to NM_139312.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:27425210 G>A maps to NM_139312.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:27409411 G>A maps to NM_139312.1 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:207222526 T>C maps to NM_018566.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:207222904 G>A maps to NM_018566.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr16:30106211 G>A maps to NM_031477.4 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr1:38270002 G>A maps to NM_024640.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:135739043 T>C maps to NM_025052.3 K1089K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:135739082 G>T maps to NM_025052.3 Y1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:135745100 G>T maps to NM_025052.3 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:135744242 T>C maps to NM_025052.3 K733K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:135749142 C>T maps to NM_025052.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:135757537 C>A maps to NM_025052.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr2:135743404 C>A maps to NM_025052.3 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:135743578 C>A maps to NM_025052.3 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:135744686 C>T maps to NM_025052.3 W585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:135745214 C>T maps to NM_025052.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:135763095 G>A maps to NM_025052.3 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:135738809 C>T maps to NM_025052.3 T1167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:69202852 C>A maps to NM_001031732.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr4:69202889 T>C maps to NM_001031732.2 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:69202889 T>C maps to NM_001031732.2 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:69203378 C>A maps to NM_001031732.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr4:69184260 T>C maps to NM_001031732.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:112862428 G>T maps to NM_022828.3 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:112874796 G>T maps to NM_022828.3 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr5:112876807 C>T maps to NM_022828.3 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:112874844 G>T maps to NM_022828.3 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:112851059 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:112889716 G>T maps to NM_022828.3 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:112927876 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:112889296 A>G maps to NM_022828.3 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:112896881 G>A maps to NM_022828.3 Q774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr5:112888985 C>T maps to NM_022828.3 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:112862455 G>T maps to NM_022828.3 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:61834118 C>T maps to NM_017798.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:61834907 C>T maps to NM_017798.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:61834979 A>C maps to NM_017798.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr20:61833722 G>T maps to NM_017798.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:43533618 G>A maps to NM_139323.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:43530281 T>C maps to NM_139323.2 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:1248738 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:1303471 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:1265278 G>A maps to NM_006761.4 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr17:1303459 G>A did not map to a codon.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr17:1257521 G>C maps to NM_006761.4 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr2:9770349 G>A maps to NM_006826.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:21875042 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:21874823 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:21875613 G>A did not map to a codon.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr23:21875590 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:21874824 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:21874874 C>T did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:21874610 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:21875230 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr23:21875369 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:74078610 C>T maps to NM_180990.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr17:74076479 C>G maps to NM_180990.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr18:72914044 G>A maps to NM_175907.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr18:72913820 G>A maps to NM_175907.4 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:72913781 G>A maps to NM_175907.4 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:174086218 C>T maps to NM_133646.2 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:174130853 C>T maps to NM_016653.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:174104148 T>G maps to NM_016653.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:174131366 C>T maps to NM_016653.2 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:174096921 T>G maps to NM_016653.2 Y345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:174081896 C>T maps to NM_016653.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:100349947 C>T maps to ENST00000349350 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:100371046 C>A maps to ENST00000349350 I1855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:100350625 G>A maps to ENST00000349350 T966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:100336165 G>A maps to ENST00000349350 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:100377077 C>A maps to ENST00000349350 V2109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:100386926 G>A maps to ENST00000349350 P2438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr7:100344203 G>A maps to ENST00000349350 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:100373122 G>A maps to ENST00000349350 R1984R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:100364269 C>A maps to ENST00000349350 I1531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr7:100352873 C>T maps to ENST00000349350 Y1050Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100382412 G>T maps to ENST00000349350 E2264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:100385678 G>T maps to ENST00000349350 G2383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:100348353 C>T maps to ENST00000349350 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:100349891 G>T maps to ENST00000349350 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:100358099 G>A maps to ENST00000349350 T1261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:100365542 G>A maps to ENST00000349350 T1650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr7:100334136 C>T maps to ENST00000349350 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:100352897 G>A maps to ENST00000349350 S1058S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:100369587 G>A maps to ENST00000349350 A1790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:100346070 T>C maps to ENST00000349350 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:100348428 G>A maps to ENST00000349350 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:100350521 G>T maps to ENST00000349350 E932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:98351823 C>T maps to NM_001079.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:98354218 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:98354296 C>T maps to NM_001079.3 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:98354266 C>T maps to NM_001079.3 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:98355880 C>T maps to NM_001079.3 R594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:167000226 C>A maps to ENST00000307529 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:167023501 C>A maps to ENST00000307529 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr3:167083709 T>C maps to ENST00000307529 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:167000226 C>A maps to ENST00000307529 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr3:167023445 A>G maps to ENST00000307529 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:2408657 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:2408501 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr23:2407559 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:2408411 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:2407461 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:2408330 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:2408422 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:2407050 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:2406843 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr23:2407646 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:2406914 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:2408666 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:2408223 G>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:2407159 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:2407350 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:2408666 C>T did not map to a codon.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr23:2408380 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:2408725 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr22:50277354 C>T maps to NM_014838.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:50278323 C>T maps to NM_014838.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr22:50277471 C>T maps to NM_014838.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:50280051 C>T maps to NM_014838.2 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:50280474 G>A maps to NM_014838.2 S1055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:50277354 C>T maps to NM_014838.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:50278881 G>A maps to NM_014838.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50278338 C>T maps to NM_014838.2 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:50280105 C>T maps to NM_014838.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr22:50277522 G>A maps to NM_014838.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:56188258 G>A maps to NM_030776.2 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:56195324 G>A maps to NM_030776.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr20:56188297 C>T maps to NM_030776.2 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr20:56190116 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:64989824 C>T maps to NM_001123329.1 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr14:64988837 G>T maps to NM_001123329.1 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:64989824 C>T maps to NM_001123329.1 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:64990033 A>G maps to NM_001123329.1 K604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:81399980 C>A maps to NM_001105539.1 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:81411757 C>A maps to NM_001105539.1 Y334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:101373566 G>A maps to NM_014415.3 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:101370426 G>T maps to NM_014415.3 V915V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:101390112 G>A maps to NM_014415.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:101390046 A>G maps to NM_014415.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:31867945 G>A maps to NM_181842.2 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:31868050 G>A maps to NM_181842.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr6:31868977 C>A maps to NM_181842.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:113935068 G>A maps to NM_001018011.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06L-01A-11D-A122-09 chr11:114118016 C>T maps to NM_001018011.1 Y574Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:113934435 C>A maps to NM_001018011.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:114118079 G>A maps to NM_001018011.1 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr11:114113009 C>T maps to NM_001018011.1 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:114121045 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr11:113934831 C>T maps to NM_001018011.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:113934590 C>A maps to NM_001018011.1 S190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:114121231 C>T maps to NM_001018011.1 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr11:114057689 T>C maps to NM_001018011.1 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZU-01A-11D-A10M-09 chr11:114121228 G>A maps to NM_001018011.1 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr1:16269681 G>A maps to ENST00000375733 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr1:16270713 C>T maps to ENST00000448462 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr1:16270875 G>A maps to ENST00000375733 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:114070276 G>A maps to NM_001164342.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:114069853 C>T maps to NM_001164342.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:114070336 G>A maps to NM_001164342.1 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr3:114069376 G>A maps to NM_001164342.1 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr3:114070441 G>A maps to NM_001164342.1 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr6:33283316 C>T maps to NM_001145338.1 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr6:33283316 C>T maps to NM_001145338.1 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:109787239 G>A maps to NM_014797.2 H636H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:109803013 G>A maps to NM_014797.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:109787506 C>T maps to NM_014797.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:109802475 G>A maps to NM_014797.2 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr14:64954441 C>T maps to NM_006977.2 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:125681426 G>A maps to NM_020924.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:125681979 G>T maps to NM_020924.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:125681211 G>T maps to NM_020924.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr9:125681487 A>C maps to NM_020924.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr11:62521012 G>A maps to NM_024784.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:62520614 A>C maps to NM_024784.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:119387828 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:119388329 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:119389156 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:119387311 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:119388838 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0L9-01A-11W-A062-09 chr23:119388180 C>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:119387497 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:119388441 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:119388970 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:119387282 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:119387604 T>A did not map to a codon.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr23:119388101 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:119387925 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:119388878 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:119389183 G>T did not map to a codon.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr23:119388864 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:119387719 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:119388191 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:119389072 C>T did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:119388272 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:119388858 T>C did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:119387391 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr9:129642385 C>T maps to ENST00000319119 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr9:129642241 G>A maps to ENST00000319119 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:129642106 C>T maps to ENST00000319119 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr9:129642961 T>C maps to ENST00000319119 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:173855042 T>C maps to NM_001122770.1 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr3:141161980 G>T maps to NM_001080412.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr3:141161550 C>T maps to NM_001080412.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:141162655 C>T maps to NM_001080412.2 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:141163680 C>T maps to NM_001080412.2 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:141161944 G>T maps to NM_001080412.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:141164427 C>T maps to NM_001080412.2 F1066F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr3:141163623 T>C maps to NM_001080412.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:57397159 C>T maps to NM_014830.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr12:57398044 C>T maps to NM_014830.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:57397485 C>A maps to NM_014830.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:57397593 G>A maps to NM_014830.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr12:57397201 C>T maps to NM_014830.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M9-01A-21W-A10C-09 chr17:7366742 G>A maps to NM_020899.3 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:7366932 C>T maps to NM_020899.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr1:22848119 G>A maps to NM_014870.3 E1060E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05N-01A-11W-A027-09 chr1:22850798 G>A maps to NM_014870.3 K1129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:22839447 C>T maps to NM_014870.3 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:22832621 G>A maps to NM_014870.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:22816926 G>A maps to NM_014870.3 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr1:22816704 C>T maps to NM_014870.3 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:22817917 G>T maps to NM_014870.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr1:22838598 C>A maps to NM_014870.3 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:22838266 G>T maps to NM_014870.3 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:197147551 C>T maps to NM_194314.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:197168756 C>A maps to NM_194314.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:197128827 C>T maps to NM_194314.2 T797T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:197141301 G>A maps to NM_194314.2 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:197169030 T>C maps to NM_194314.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:129595862 G>T maps to NM_014007.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:130131747 A>T maps to ENST00000397753 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GE-01A-11W-A062-09 chr20:62421795 C>T maps to NM_025224.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:62421317 G>A maps to NM_025224.2 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:62421747 G>A maps to NM_025224.2 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:62421759 G>A maps to NM_025224.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:42704540 C>T maps to NM_145166.3 C553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr3:42700437 C>T maps to NM_145166.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:42699891 C>T maps to NM_145166.3 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:42700000 C>T maps to NM_145166.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:6641116 G>T maps to NM_005341.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:4322890 C>T maps to NM_145291.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:37441318 C>T maps to NM_014872.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:125673603 C>A maps to NM_006626.4 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr9:125673590 G>T maps to NM_006626.4 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:4048100 G>A maps to NM_015898.2 C468C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:4054696 G>A maps to NM_015898.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:154987480 C>T maps to ENST00000417934 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:154987591 C>T maps to ENST00000417934 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:154987339 C>T maps to ENST00000417934 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr1:154987430 C>T maps to ENST00000417934 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:154988065 C>T maps to ENST00000417934 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:154988026 G>A maps to ENST00000417934 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:154988263 C>T maps to ENST00000417934 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:154988279 C>T maps to ENST00000417934 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:45556116 C>T maps to NM_001039360.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:45556221 G>T maps to NM_001039360.2 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr18:45567178 G>A maps to NM_001039360.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:45566719 C>T maps to NM_001039360.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:45566719 C>A maps to NM_001039360.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:45566719 C>T maps to NM_001039360.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:45567082 G>A maps to NM_001039360.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr18:45567237 G>A maps to NM_001039360.2 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:33058633 C>A maps to NM_001040441.1 V34V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:33060818 C>T maps to NM_001040441.1 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:33099711 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:33423746 C>T maps to NM_152735.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:33423746 C>T maps to NM_152735.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr12:56515042 C>T maps to NM_032786.1 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr12:56514987 C>T maps to NM_032786.1 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:56514921 C>A maps to NM_032786.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:203819658 C>T maps to NM_014827.4 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:203798951 C>T maps to NM_014827.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:203798690 C>T maps to NM_014827.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr1:203816651 T>C maps to NM_014827.4 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:37941297 C>T maps to NM_025079.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:37947262 C>T maps to NM_025079.2 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:37945971 C>A maps to NM_025079.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:37948350 C>A maps to NM_025079.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:64717098 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:64719764 T>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:64722359 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:64722505 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:64719831 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:64722147 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:64722233 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:64722313 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:64722692 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:64718906 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:64708942 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:64722448 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:64709261 T>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:64708824 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:64717032 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:64718963 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:64709024 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:64719015 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:64719855 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:64722747 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:64722183 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0M7-01A-11W-A062-09 chr23:64717129 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:64719097 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:64719816 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:64722071 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:64717087 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:64722043 C>T did not map to a codon.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr23:64708987 G>C did not map to a codon.
Sequencing variant TCGA-FI-A2EX-01A-11D-A17D-09 chr23:64718967 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr11:110036164 C>T maps to NM_033390.1 D785D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:110035729 C>T maps to NM_033390.1 Y640Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr11:110023766 T>C maps to NM_033390.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:110007470 G>A maps to NM_033390.1 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr6:149795379 C>T maps to NM_207360.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr6:149777857 G>A maps to NM_207360.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:149773788 C>T maps to NM_207360.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:149795673 C>T maps to NM_207360.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:46554133 G>A maps to ENST00000242848 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:46543969 C>T maps to ENST00000242848 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:46616330 G>A maps to ENST00000242848 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:46542049 G>A maps to ENST00000242848 R1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr13:46619600 C>T maps to ENST00000242848 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr13:46549535 G>A maps to ENST00000242848 R784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:46541938 G>A maps to ENST00000242848 R1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr13:46542055 G>A maps to ENST00000242848 R1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr13:46539474 C>A maps to ENST00000242848 E1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr13:46554139 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:46543842 G>A maps to ENST00000242848 R946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr14:89039311 T>C maps to NM_024824.4 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:89039293 C>T maps to NM_024824.4 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr14:89061405 A>G maps to NM_207662.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:187373360 T>C maps to NM_018471.2 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:88675344 C>T maps to ENST00000452588 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr16:88643605 C>T maps to ENST00000452588 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr16:88643909 G>T maps to ENST00000452588 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr16:88691636 C>T maps to ENST00000452588 G714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:88664694 G>A maps to ENST00000452588 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:88691667 C>T maps to ENST00000452588 R725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr16:88691153 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:144589983 C>T maps to NM_015117.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:144550619 G>A maps to NM_015117.2 F679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:144620816 G>A maps to NM_015117.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:144523149 G>A maps to NM_015117.2 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:47588354 G>A maps to NM_015168.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:47597690 C>T maps to NM_015168.1 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:47572583 G>A maps to NM_015168.1 Y721Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:47597289 C>T maps to NM_015168.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:113088834 A>G maps to NM_198581.2 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:113069498 G>A maps to NM_198581.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:113088957 C>T maps to NM_198581.2 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr2:113089520 C>G maps to NM_198581.2 S1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:113089971 G>A maps to NM_198581.2 P1159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:113067713 C>T maps to NM_198581.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:11876153 C>T maps to NM_014153.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:11859518 A>G maps to NM_014153.3 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:11864747 C>T maps to NM_014153.3 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:11850095 A>G maps to NM_014153.3 V853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr22:41734150 C>T maps to ENST00000396532 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr22:41752791 C>T maps to ENST00000351589 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:41735848 C>T maps to ENST00000351589 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:41744075 C>A maps to ENST00000351589 C573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15Z-01A-11D-A122-09 chr22:41734255 T>G maps to ENST00000396532 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:113007845 G>A maps to NM_032494.2 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr7:138764687 G>A maps to ENST00000464606 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr7:138732366 A>G maps to ENST00000464606 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:129666065 G>A maps to NM_016478.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:129664191 G>T maps to NM_016478.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:64138962 G>A did not map to a codon.
Sequencing variant TCGA-AP-A1DQ-01A-11D-A135-09 chr23:64139014 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:64140106 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:64137683 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:64140095 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:64139979 C>A did not map to a codon.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr1:52954688 C>T maps to NM_001009881.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:52962761 C>A maps to NM_001009881.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:52911939 C>A maps to NM_001009881.2 E1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:52991747 C>A maps to NM_001009881.2 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:52933861 C>A maps to NM_001009881.2 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:52981591 C>A maps to NM_001009881.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:52941109 A>G maps to NM_001009881.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:117960105 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:117959856 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:117960244 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:117960400 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:117960323 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:117959720 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:117959891 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:117960400 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:117960111 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:73524409 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:73524564 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:73524328 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:73524121 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:73524328 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:87446127 G>A maps to NM_015144.2 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr16:87446541 C>G maps to NM_015144.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:111698205 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:111698453 C>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:111698343 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:111698249 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:111698157 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:111698677 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:111698686 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:111697979 A>G did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:111698754 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:31837018 C>T maps to NM_016505.2 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:103359611 T>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:103359806 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:103359336 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:103358884 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:103358877 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:103358884 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:103359497 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:103360142 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:103359336 C>A did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:103358979 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:60242409 C>T maps to NM_017742.4 Y1032Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:60242256 G>A maps to NM_017742.4 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr18:60241347 C>T maps to NM_017742.4 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:60207018 C>T maps to NM_017742.4 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr10:81154181 G>A maps to NM_153367.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:81154181 G>A maps to NM_153367.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr20:279028 G>T maps to NM_033089.6 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr4:25351205 A>G maps to NM_024936.2 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:77913050 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:77913481 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:77913641 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:77913244 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:77913163 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:77912824 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:77913544 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:77913637 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:77913178 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:77913567 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:77912807 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:77913659 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:77913021 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr23:77913700 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:88968087 G>A maps to NM_024617.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05H-01A-11W-A027-09 chr9:88958004 G>T maps to NM_024617.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:88916433 C>A maps to NM_024617.3 E1393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:88937267 G>T maps to NM_024617.3 I1000I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K4-01A-11W-A062-09 chr9:88938048 G>A maps to NM_024617.3 G872G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr9:88940282 C>T maps to NM_024617.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr9:88937964 G>A maps to NM_024617.3 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:37305608 C>T maps to NM_032226.2 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr9:37304270 C>T maps to NM_032226.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr9:37357263 A>G maps to NM_032226.2 *544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr9:37327830 G>A maps to NM_032226.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr12:122964735 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:42711179 G>A maps to NM_033114.3 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:100017498 T>C maps to NM_017984.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:100004909 C>A maps to NM_017984.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:28476732 C>T maps to NM_001040432.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:207170017 G>T maps to NM_020923.1 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:207176037 G>A maps to NM_020923.1 A2262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:207174948 T>C maps to NM_020923.1 I1899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:207161968 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:207169516 G>T maps to NM_020923.1 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr2:207174279 G>A maps to NM_020923.1 T1676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:207170244 G>A maps to NM_020923.1 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:207174222 C>T maps to NM_020923.1 S1657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:207174441 G>A maps to NM_020923.1 S1730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:207174544 G>T maps to NM_020923.1 E1765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:207171913 G>T maps to NM_020923.1 E888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:207169845 A>G maps to NM_020923.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:207173410 G>T maps to NM_020923.1 E1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:207169692 G>A maps to NM_020923.1 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:207173410 G>T maps to NM_020923.1 E1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:207174861 G>A maps to NM_020923.1 S1870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:207172813 G>T maps to NM_020923.1 E1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:207172828 C>T maps to NM_020923.1 Q1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:207172897 G>T maps to NM_020923.1 E1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:207172933 G>T maps to NM_020923.1 E1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:207170662 G>T maps to NM_020923.1 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:207175413 G>A maps to NM_020923.1 E2054E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:207172909 G>T maps to NM_020923.1 E1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:207175935 G>A maps to NM_020923.1 S2228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:67428934 G>A maps to NM_013304.2 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:825327 A>C maps to NM_024786.2 L325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:848658 G>A maps to NM_024786.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr9:131484863 C>T maps to ENST00000406904 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:19164614 G>T maps to NM_019028.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:19172281 T>C maps to NM_019028.2 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:158049495 C>T maps to NM_024630.2 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:74636952 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:74641703 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05T-01A-11W-A027-09 chr23:74698739 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:74670691 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:74698782 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:74670650 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:74698794 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:74742851 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:74641763 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:74644551 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:74641709 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:74641727 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:74641727 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:99212680 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:77244671 C>T maps to NM_015336.2 C602C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr12:77244666 C>T maps to NM_015336.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr12:77216187 C>T maps to NM_015336.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:27177694 C>T maps to NM_032283.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:27177047 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:195925261 C>T maps to NM_001039617.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:17072817 T>C maps to NM_016353.4 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr9:14674266 C>T maps to NM_178566.4 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:77600058 G>A maps to NM_174976.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:113677365 C>T maps to NM_173570.3 C399C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:113673125 G>A maps to NM_173570.3 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr3:113675204 G>T maps to NM_173570.3 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr3:45000805 G>A maps to NM_016598.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:44975391 G>A maps to NM_016598.2 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr11:57455980 T>C maps to NM_015457.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:57466161 C>T maps to NM_015457.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:57440571 G>T maps to NM_015457.2 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr11:57440645 G>A maps to NM_015457.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:114192134 G>A maps to NM_022494.1 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:85015573 C>T maps to NM_001145548.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:85012848 C>T maps to NM_001145548.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr22:20130755 G>T maps to NM_013373.3 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:128948661 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:128948664 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:128975762 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:128946704 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:128946756 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:128975839 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:128947681 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:31809684 C>A maps to NM_001174096.1 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:31815925 G>T maps to NM_001174096.1 E1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:31809756 C>T maps to NM_001174096.1 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:31809204 G>A maps to NM_001174096.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:31816158 G>A maps to NM_001174096.1 E1115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:31809280 C>T maps to NM_001174096.1 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:31810425 C>A maps to NM_001174096.1 Y722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr10:31784757 G>T maps to NM_001174096.1 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:145147449 C>T maps to NM_014795.3 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:145155992 G>A maps to NM_014795.3 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:145147128 C>T maps to NM_014795.3 T1178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:145147455 C>T maps to NM_014795.3 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:145274905 C>A maps to NM_014795.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:145147194 G>A maps to NM_014795.3 G1156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:145147311 G>A maps to NM_014795.3 T1117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:145157703 C>T maps to NM_014795.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:145154155 C>A maps to NM_014795.3 E964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:145156386 G>T maps to NM_014795.3 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:145157078 G>A maps to NM_014795.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:145158814 C>T maps to NM_014795.3 K289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:131497694 A>G maps to NM_006336.2 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:131515711 G>A maps to NM_006336.2 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr9:131517724 G>A maps to NM_006336.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:220072754 G>A maps to NM_138802.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr2:220072127 A>T maps to NM_138802.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:38029537 G>A maps to NM_021943.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K0-01A-11W-A062-09 chr6:38084516 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:74974437 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0IU-01A-11D-A10B-09 chr15:80429840 A>C maps to NM_019006.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:80429945 T>C maps to NM_019006.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:135614245 C>T maps to NM_020863.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr8:135614922 G>A maps to NM_020863.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:135490793 G>A maps to NM_020863.3 I1221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:135614560 G>A maps to NM_020863.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:135614560 G>A maps to NM_020863.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:135649718 C>A maps to NM_020863.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr8:135621015 G>A maps to NM_020863.3 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:135490745 C>T maps to NM_020863.3 E1237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:135614433 C>A maps to NM_020863.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:135614977 G>A maps to NM_020863.3 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr8:135614146 G>A maps to NM_020863.3 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:72026692 T>C maps to NM_144982.4 K930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:72025966 C>A maps to NM_144982.4 E1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:72037951 G>A maps to NM_144982.4 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:72057222 C>T maps to NM_144982.4 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr12:72050881 G>A maps to NM_144982.4 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A139-01A-11D-A122-09 chr12:72030802 A>G maps to NM_144982.4 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:72037951 G>A maps to NM_144982.4 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr12:72029252 G>A maps to NM_144982.4 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr16:72832236 A>G maps to NM_006885.3 L1448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr16:72822232 G>A maps to NM_006885.3 G3314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:72830346 C>T maps to NM_006885.3 P2078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:72831024 C>T maps to NM_006885.3 Q1852Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr16:72821682 G>A maps to NM_006885.3 Q3498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:72822283 C>T maps to NM_006885.3 S3297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:72827387 C>A maps to NM_006885.3 E3065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr16:72923722 G>A maps to NM_006885.3 R1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:72822727 C>T maps to NM_006885.3 P3149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:72829143 C>T maps to NM_006885.3 S2479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr16:72821590 C>T maps to NM_006885.3 S3528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr16:72831068 G>A maps to NM_006885.3 Q1838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr16:72827579 C>A maps to NM_006885.3 E3001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:72821191 C>T maps to NM_006885.3 S3661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:72828222 T>C maps to NM_006885.3 S2786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:72829281 C>T maps to NM_006885.3 A2433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:72832265 G>A maps to NM_006885.3 R1439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr16:72827657 C>A maps to NM_006885.3 E2975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr16:72992930 G>A maps to NM_006885.3 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:72830283 C>T maps to NM_006885.3 P2099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr16:72829700 G>A maps to NM_006885.3 R2294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:72822727 C>T maps to NM_006885.3 P3149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:72863755 C>A maps to NM_006885.3 E1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr8:77765709 C>T maps to NM_024721.4 R2185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr8:77768156 C>T maps to NM_024721.4 G3000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr8:77776581 T>C maps to NM_024721.4 S3544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R7-01A-31D-A10B-09 chr8:77618596 G>A maps to NM_024721.4 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:77768270 C>T maps to NM_024721.4 T3038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:77775511 G>T maps to NM_024721.4 E3188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:77620288 C>T maps to ENST00000458716 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:77768343 G>T maps to NM_024721.4 E3063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:77776173 C>A maps to NM_024721.4 C3408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:77617273 C>T maps to NM_024721.4 C317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:77764104 T>C maps to NM_024721.4 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:77767958 G>A maps to NM_024721.4 T2934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:77761246 G>A maps to NM_024721.4 E1176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr8:77764112 C>T maps to NM_024721.4 S1652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:77767472 T>G maps to NM_024721.4 S2772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr8:77767646 C>T maps to NM_024721.4 S2830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:77767082 C>T maps to NM_024721.4 V2642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr8:77766548 G>T maps to NM_024721.4 S2464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:77617507 G>A maps to NM_024721.4 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:77763410 T>G maps to NM_024721.4 Y1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:77764226 A>G maps to NM_024721.4 S1690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:77616535 C>A maps to NM_024721.4 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:77618176 C>T maps to NM_024721.4 C618C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:77761899 G>T maps to NM_024721.4 T1266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M0-01A-11W-A10C-09 chr8:77763297 C>T maps to NM_024721.4 Q1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr8:77768192 C>T maps to NM_024721.4 C3012C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:77763269 C>T maps to NM_024721.4 P1371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:77767448 G>A maps to NM_024721.4 P2764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:77775555 C>T maps to NM_024721.4 I3202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:77767661 G>A maps to NM_024721.4 P2835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:77765709 C>T maps to NM_024721.4 R2185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:77617402 C>T maps to NM_024721.4 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr8:77767953 C>T maps to NM_024721.4 R2933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr8:77767646 C>T maps to NM_024721.4 S2830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:77616913 C>T maps to NM_024721.4 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:77761301 G>T maps to NM_024721.4 E1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:77766677 C>A maps to NM_024721.4 L2507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:77775615 C>T maps to NM_024721.4 I3222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A212-01A-11D-A14K-09 chr8:77616658 C>T maps to NM_024721.4 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2D2-01A-11D-A17D-09 chr8:77768162 G>A maps to NM_024721.4 T3002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr16:75203727 C>T maps to NM_153688.2 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:42729504 T>C maps to NM_022473.1 V1534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:42742930 C>T maps to NM_022473.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr15:42720287 G>A maps to NM_022473.1 L1619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:44833373 C>A maps to ENST00000412927 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:44833244 G>A maps to ENST00000412927 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:36831767 G>T maps to NM_020917.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36831920 C>T maps to NM_020917.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr18:5292106 C>A maps to NM_003409.3 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:5291336 G>A maps to NM_003409.3 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZZ-01A-11D-A10M-09 chr18:5292191 G>A maps to NM_003409.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr18:5291240 T>C maps to NM_003409.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:178359133 C>T maps to NM_030613.2 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:178359222 C>T maps to NM_030613.2 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr5:178358394 T>C maps to NM_030613.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:178358466 T>C maps to NM_030613.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:57051086 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:57065162 G>T maps to NM_020828.1 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:57060414 A>G maps to NM_020828.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr17:4995134 T>C maps to NM_153018.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:4994874 G>T maps to NM_153018.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr17:4995170 G>A maps to NM_153018.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:4994835 G>T maps to NM_153018.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr17:4994939 G>A maps to NM_153018.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:38126621 C>A maps to NM_014898.2 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:38127119 T>G maps to NM_014898.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:39898384 C>T maps to NM_003407.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:43453430 G>T maps to NM_006887.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:115805994 A>C maps to NM_003408.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr9:115805504 C>A maps to NM_003408.1 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr8:144332507 C>T maps to NM_173832.3 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:144332456 C>T maps to NM_173832.3 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:188924180 G>T maps to NM_174900.3 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:188924752 G>A maps to NM_174900.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr4:188924185 C>T maps to NM_174900.3 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr4:188924890 G>A maps to NM_174900.3 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:188924293 C>T maps to NM_174900.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr4:188924785 C>T maps to NM_174900.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:29640335 C>A maps to NM_001109809.2 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LJ-01A-11W-A062-09 chr6:29640603 G>T maps to NM_001109809.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr6:29641020 T>C maps to NM_001109809.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:50701140 G>A maps to NM_199427.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:50701773 G>A maps to NM_199427.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:50701128 G>A maps to NM_199427.2 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:50769029 C>T maps to NM_018197.2 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr19:36883960 G>A maps to NM_133466.2 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36884305 G>A maps to NM_133466.2 C312C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:36884359 G>A maps to NM_133466.2 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:36900680 A>G did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:68598283 G>T maps to NM_133458.2 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:68597460 C>T maps to NM_133458.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr11:58385169 C>T maps to NM_053023.4 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:58381794 C>T maps to NM_053023.4 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:58377456 C>T maps to NM_053023.4 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:58385067 C>A maps to NM_053023.4 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:58384743 C>A maps to NM_053023.4 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M2-01A-11D-A10O-09 chr11:58384225 C>G maps to NM_053023.4 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr11:58377330 C>T maps to NM_053023.4 D133D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:64854490 C>T maps to NM_006782.3 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:64852273 T>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr11:64855519 C>T maps to NM_006782.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:106813605 G>A maps to NM_012082.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:106814622 C>A maps to NM_012082.3 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr5:32415107 A>G maps to NM_016107.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:32404115 A>G maps to NM_016107.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:32380222 G>A maps to NM_016107.3 C899C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:32403400 C>T maps to NM_016107.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr5:32420192 C>G maps to NM_016107.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:3827584 G>A maps to NM_015174.1 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:3834830 G>A maps to NM_015174.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:3852362 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:3831312 G>A maps to NM_015174.1 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr23:24228852 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:24197478 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:24229003 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:24228702 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:24228433 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0K1-01A-11W-A062-09 chr23:24229431 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:24228577 G>T did not map to a codon.
Sequencing variant TCGA-BG-A0MI-01A-11W-A062-09 chr23:24197519 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:24228865 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr23:24228841 T>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:24228534 C>T did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:24229431 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:24229220 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:73444741 C>A maps to NM_021260.2 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16E-01A-22D-A12J-09 chr14:73441496 G>A maps to NM_021260.2 N659N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:79734180 G>A maps to NM_014733.3 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:79733160 T>G maps to NM_014733.3 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:79773160 G>T maps to NM_014733.3 E1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr5:79768692 G>T maps to NM_014733.3 E1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:15115414 G>A maps to NM_022340.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:15131960 A>G maps to NM_022340.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:104198996 A>G maps to ENST00000216602 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr14:68249962 G>T maps to NM_015346.3 S1302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:68228121 G>A maps to NM_015346.3 H2183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr14:68252598 G>A maps to NM_015346.3 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr14:68252855 A>C maps to NM_015346.3 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr14:68238928 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr14:68250088 G>A maps to NM_015346.3 H1260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr14:68256193 G>T maps to NM_015346.3 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr14:68251148 A>G maps to NM_015346.3 H1176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:99509311 G>A maps to NM_001002261.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:99510205 G>A maps to NM_001002261.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:99512796 G>A maps to NM_001002261.3 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:99517040 G>A maps to NM_001002261.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:2274993 C>T maps to NM_020972.2 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:2307219 C>A maps to NM_020972.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:2341208 G>A maps to NM_020972.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr4:2307145 C>T maps to NM_020972.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:52704628 G>T maps to NM_004799.2 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:52704199 G>T maps to NM_004799.2 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr1:52704102 T>C maps to NM_004799.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:52811829 C>T maps to NM_004799.2 C1405C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:52704351 G>A maps to NM_004799.2 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:52704036 G>A maps to NM_004799.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:52704340 G>T maps to NM_004799.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17C-01A-11D-A12J-09 chr1:52704333 A>T maps to NM_004799.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr16:2882072 C>T maps to NM_145252.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:2881904 C>T maps to NM_145252.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:62366716 G>T maps to NM_032527.4 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:124265725 T>G maps to NM_007222.3 R821R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr8:124267678 C>A maps to NM_007222.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:124266350 G>A maps to NM_007222.3 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:123964115 C>T maps to NM_014943.3 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:123964115 C>T maps to NM_014943.3 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr8:123963863 A>G maps to NM_014943.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:123964286 C>T maps to NM_014943.3 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:123965669 T>G maps to NM_014943.3 V640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:39831624 G>A maps to NM_015035.3 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:39832347 C>T maps to NM_015035.3 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:39832899 C>T maps to NM_015035.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr20:39813831 C>A maps to NM_015035.3 *957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr20:39832107 G>A maps to NM_015035.3 C483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr3:147128501 C>T maps to NM_003412.3 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:147128474 G>A maps to NM_003412.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:147131142 C>A maps to NM_003412.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr3:147130392 G>A maps to NM_003412.3 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:136649448 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:136649579 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:136649635 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:136649638 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:136652124 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:136651133 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:136649653 C>T did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:136651208 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:136652112 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:136648925 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:136649755 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:136651210 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:136649782 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:136649508 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:136651224 G>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:136649224 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:136649604 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:136649871 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr3:147113929 G>A maps to NM_001168379.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:147109007 G>A maps to NM_001168379.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:147113999 C>T maps to NM_001168379.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:147114005 G>A maps to NM_001168379.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16R-01A-11D-A12J-09 chr3:147113699 C>A maps to NM_001168379.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:100617912 C>T maps to NM_033132.3 K570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr13:100617630 C>A maps to NM_033132.3 *664Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr19:58101760 C>A maps to NM_001010879.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:58101971 A>C maps to NM_001010879.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:58102327 G>A maps to NM_001010879.2 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:58102388 G>T maps to NM_001010879.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58102052 G>T maps to NM_001010879.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:58102388 G>T maps to NM_001010879.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:57286430 T>C maps to NM_001146326.1 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17S-01A-11D-A12J-09 chr19:57286802 C>T maps to NM_001146326.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:57647397 C>A maps to NM_052882.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:57647092 G>A maps to NM_052882.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:99631759 C>A maps to NM_003439.1 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:99631288 G>A maps to NM_003439.1 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:99621799 T>A maps to NM_003439.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:25252048 G>A maps to NM_001012981.4 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:25251334 A>G maps to NM_001012981.4 F902F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr16:25251796 G>A maps to NM_001012981.4 Y748Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:28327701 C>T maps to NM_024493.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:28333564 G>T maps to NM_024493.2 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:28327761 G>A maps to NM_024493.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:28333470 C>T maps to NM_024493.2 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:28217471 G>A maps to NM_019110.3 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:28214771 C>T maps to NM_019110.3 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:28219359 C>T maps to NM_019110.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr7:99103801 G>A maps to NM_014569.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:99129308 C>T maps to NM_014569.3 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:99103927 G>A maps to NM_014569.3 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:99128788 T>C maps to NM_014569.3 Y479Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:101139681 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:101138557 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:101139686 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:101141682 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:101153185 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:101139430 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:101139621 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101138492 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101138739 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101139557 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:101152903 T>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101138567 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101139629 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:101152902 T>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:101139731 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101138932 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101139113 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:101139128 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:101138792 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:101138556 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:101139405 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:101138956 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:101139666 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:101138877 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:101159273 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:140085313 C>T maps to NM_144723.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:178785386 C>A maps to NM_022470.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr3:178785417 C>T maps to NM_022470.3 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr8:40554818 G>T maps to NM_024645.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:81053451 A>G maps to ENST00000372347 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr10:80968134 C>T maps to NM_020338.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:81036950 C>T maps to NM_020338.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:81061874 C>T maps to NM_020338.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:44798890 G>A maps to NM_031449.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr7:44802912 C>T maps to NM_031449.3 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:44802586 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:44802855 A>C maps to NM_031449.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:44805113 C>T maps to NM_031449.3 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:44805065 C>T maps to NM_031449.3 H710H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:40756570 C>T maps to NM_005857.3 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:40724017 C>A maps to NM_005857.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr1:40751679 C>G maps to NM_005857.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:35578700 C>T maps to NM_024772.3 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:35580110 G>T maps to NM_024772.3 E894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:35580496 C>T maps to NM_024772.3 D1022D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:35578871 C>T maps to NM_024772.3 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:35579723 C>T maps to NM_024772.3 R765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:35579879 C>T maps to NM_024772.3 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr1:35580506 G>T maps to NM_024772.3 E1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr13:20577067 C>A maps to NM_001190965.1 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr13:20610977 G>T maps to NM_001190965.1 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:20567439 A>G maps to NM_001190965.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr13:20601371 C>T maps to NM_001190965.1 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr13:20656934 C>T maps to NM_001190965.1 R1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr13:20601371 C>T maps to NM_001190965.1 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr13:20625617 C>T maps to NM_001190965.1 R780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr13:20605499 G>A maps to NM_001190965.1 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:20605541 C>A maps to NM_001190965.1 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr13:20656173 C>T maps to NM_001190965.1 R1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:70460860 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:70469002 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70465882 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:70469430 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70464150 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70464739 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:70471419 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr23:70461175 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr23:70468137 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70467259 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:70468047 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:70464251 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70464181 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:70464277 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70471435 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:70472547 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:70473081 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:70468325 T>C did not map to a codon.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr23:70464192 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70461169 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:70467745 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr23:70460829 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70470034 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:70472662 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:70464301 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:70467266 G>T did not map to a codon.
Sequencing variant TCGA-D1-A15W-01A-11D-A122-09 chr23:70468155 C>G did not map to a codon.
Sequencing variant TCGA-FI-A2D2-01A-11D-A17D-09 chr23:70465835 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0G5-01A-11W-A062-09 chr1:35836100 C>T maps to NM_005095.2 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr1:35873675 C>T maps to NM_005095.2 C1288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:35852602 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:35859335 G>A maps to NM_005095.2 Q969Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:35885274 T>C maps to NM_005095.2 D1548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:35863015 T>C maps to NM_005095.2 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr1:35827383 T>C maps to NM_005095.2 N278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr1:35790986 T>C maps to NM_005095.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:20398718 T>G maps to NM_001142684.1 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr13:20412927 C>A maps to NM_001142684.1 G262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:35474489 G>A maps to NM_007167.3 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:35453697 T>C maps to NM_007167.3 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr1:35453861 C>A maps to NM_007167.3 E941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:35496145 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:35452886 C>A maps to NM_007167.3 E1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:35477598 C>T maps to NM_007167.3 Q318Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:35474439 T>A maps to NM_007167.3 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr1:35476598 C>T maps to NM_007167.3 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A168-01A-31D-A12J-09 chr1:35476598 C>G maps to NM_007167.3 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:35453319 T>C maps to NM_007167.3 S1121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:35484955 C>T maps to NM_007167.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:50379983 G>A maps to NM_015896.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr10:298376 G>A maps to NM_006624.4 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:267235 T>C maps to NM_006624.4 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr10:293391 G>T maps to NM_006624.4 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr10:288046 C>T maps to NM_006624.4 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:42896447 A>G maps to NM_032257.4 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:42915612 G>T maps to NM_032257.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:42915662 G>A maps to NM_032257.4 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr17:4648583 G>T maps to NM_001136046.1 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:4645752 G>T maps to NM_001136046.1 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:4644130 C>T maps to NM_001136046.1 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr17:4644178 G>A maps to NM_001136046.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr17:4648550 C>T maps to NM_001136046.1 Y646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:45839531 C>T maps to ENST00000471951 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:45850048 C>T maps to ENST00000471951 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:45927475 A>G maps to ENST00000471951 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:45938874 C>T maps to ENST00000471951 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:45910865 T>C maps to ENST00000471951 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr20:45878028 A>G did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr20:45865067 A>G did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr12:133732386 C>T maps to NM_015394.4 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:133732720 G>T maps to NM_015394.4 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:133727693 G>A maps to NM_015394.4 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:133733526 A>C maps to NM_015394.4 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr12:133733539 G>T maps to NM_015394.4 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:21910390 G>T maps to NM_173531.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:21910468 G>T maps to NM_173531.3 C215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:21910042 G>T maps to NM_173531.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:19788767 G>A maps to NM_033204.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:19790857 C>T maps to NM_033204.2 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:19790112 C>T maps to NM_033204.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:64167620 A>G maps to NM_016220.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:64167323 A>G maps to NM_016220.3 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:64168223 T>C maps to NM_016220.3 H514H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:64168431 G>T maps to NM_016220.3 E584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:64167167 T>C maps to NM_016220.3 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:64167644 T>A maps to NM_016220.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:64167948 C>T maps to NM_016220.3 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:48789375 C>T maps to NM_153608.1 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:48790095 A>G maps to NM_153608.1 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:48785665 C>T maps to NM_153608.1 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:64438523 A>G maps to NM_015852.3 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:64438562 T>C maps to NM_015852.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:64439792 G>A maps to NM_015852.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr7:64437572 C>G maps to ENST00000398695 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:6732197 C>T maps to ENST00000330442 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:6731681 G>A maps to ENST00000330442 Y354Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:6730646 G>A maps to ENST00000330442 F699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:6731512 C>A maps to ENST00000330442 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr7:6730964 A>C maps to ENST00000330442 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9677523 C>A maps to NM_001008727.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:9676972 C>T maps to NM_001008727.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:247323025 G>A maps to NM_003431.2 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:43161836 G>A maps to ENST00000509156 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:43173451 G>T maps to ENST00000509156 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:58945108 C>A maps to NM_003433.3 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:58131639 T>C maps to NM_003435.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:58131630 G>A maps to NM_003435.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58132284 G>A maps to NM_003435.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr19:58132651 C>T maps to NM_003435.3 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:58131630 G>A maps to NM_003435.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:58578880 G>A maps to NM_007134.1 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58578887 C>T maps to NM_007134.1 R370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:58578244 C>T maps to NM_007134.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:58572973 A>T maps to NM_007134.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr19:58578793 C>T maps to NM_007134.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:12298666 C>T maps to NM_003437.3 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:12297658 C>T maps to NM_003437.3 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:12297517 G>T maps to NM_003437.3 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:12298479 C>T maps to NM_003437.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:12297658 C>T maps to NM_003437.3 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:64275369 G>A maps to ENST00000307355 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr7:64292576 T>C maps to ENST00000307355 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:64291976 A>G maps to ENST00000307355 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:19822450 G>A maps to NM_021030.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:19824903 G>A maps to NM_021030.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:19822450 G>T maps to NM_021030.2 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19822366 G>A maps to NM_021030.2 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:19822450 G>A maps to NM_021030.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:19822366 G>A maps to NM_021030.2 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:19822667 G>T maps to NM_021030.2 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:19822366 G>A maps to NM_021030.2 R575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:19822954 G>A maps to NM_021030.2 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr4:366628 G>T maps to NM_003441.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:219508063 G>A maps to NM_001105537.1 R1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:219505489 G>A maps to NM_001105537.1 Y1497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:9492959 C>T maps to NM_003442.5 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:9530355 C>T maps to NM_003442.5 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:9516258 C>T maps to NM_003442.5 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:36727608 G>A maps to NM_007145.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LL-01A-12D-A127-09 chr3:124998004 C>T maps to NM_021964.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:124953162 T>C maps to NM_021964.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr3:124951268 T>C maps to NM_021964.2 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:58216269 G>T maps to NM_001085384.1 C37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:58213614 T>C maps to NM_001085384.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58213956 G>A maps to NM_001085384.1 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:58213007 G>A maps to NM_001085384.1 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44500312 C>T maps to NM_003445.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:44501160 C>T maps to NM_003445.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:44500666 C>T maps to NM_003445.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47270079 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47271932 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47271950 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:47272352 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47272756 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47272940 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47270118 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47271793 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:47272604 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47271932 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47272248 A>G did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr23:47272694 A>G did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:47272964 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:47272520 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:47270090 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:146156297 G>A maps to NM_006958.2 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:146157403 G>A maps to NM_006958.2 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:146157128 C>T maps to NM_006958.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr8:146156996 C>T maps to NM_006958.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:53571908 G>A maps to NM_001102603.1 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:28056965 A>C maps to NM_003447.3 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:44612096 G>T maps to NM_018651.2 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:57932467 G>A maps to NM_006959.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:57931063 G>A maps to NM_006959.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:57931129 C>T maps to NM_006959.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:57931984 T>C maps to NM_006959.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:57932035 G>A maps to NM_006959.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:57932224 C>T maps to NM_006959.2 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:3458702 G>A maps to NM_003450.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:3458427 C>T maps to NM_003450.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr16:3458396 G>A maps to NM_003450.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:52091485 A>G maps to NM_007147.2 Q634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:52091066 C>T maps to NM_007147.2 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:52090639 G>A maps to NM_007147.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:52076600 T>C maps to NM_007147.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:9491876 G>A maps to NM_001172651.1 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:9492420 C>T maps to NM_001172651.1 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:11881273 C>T maps to NM_144680.2 *550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:11895984 C>T maps to NM_144680.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:44981059 C>T maps to NM_013256.3 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:44981392 C>T maps to NM_013256.3 K435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:44981970 C>A maps to NM_013256.3 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:44980797 C>A maps to NM_013256.3 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:35231855 G>A maps to ENST00000392232 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr19:35232053 G>A maps to ENST00000392232 W300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:35232264 G>T maps to ENST00000392232 G371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47835605 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47837081 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47836136 C>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47837005 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47835859 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr23:47837014 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:47836168 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47835762 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47835968 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47837173 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr23:47836768 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:47861998 G>A did not map to a codon.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr23:47835840 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47836136 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47836220 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47836304 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47847975 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47836835 C>T did not map to a codon.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr23:47835700 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:27419213 G>A maps to NM_007149.2 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:27420059 G>T maps to NM_007149.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:27420425 T>C maps to NM_007149.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:27420178 C>A maps to NM_007149.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr6:27420590 G>T maps to NM_007149.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:27419786 A>C maps to NM_007149.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:152139047 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:152083369 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:152089257 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152083291 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152085893 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:152113954 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr23:152083324 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152083351 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr6:28244309 C>T maps to NM_001023560.2 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:104171852 T>C maps to NM_003452.2 C601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:104171624 T>C maps to NM_003452.2 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:71509098 C>A maps to NM_006961.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:28116538 C>T maps to NM_006298.2 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:28117262 C>A maps to NM_006298.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:28195027 C>T maps to ENST00000425468 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:3380860 A>G maps to NM_001130520.1 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr11:3381418 T>C maps to NM_001130520.1 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:3381467 G>T maps to NM_001130520.1 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:3380914 G>A maps to NM_001130520.1 D441D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:44685099 C>A maps to NM_006991.3 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr3:44672663 G>A maps to NM_006991.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:44672648 A>C maps to NM_006991.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M3-01A-11W-A10C-09 chr2:95845937 A>G maps to ENST00000453539 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:12244076 C>T maps to NM_021143.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:12244736 C>T maps to NM_021143.2 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:12243520 G>A maps to NM_021143.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:12244493 T>C maps to NM_021143.2 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:12244685 A>G maps to NM_021143.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr16:3273954 C>T maps to NM_198088.2 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:3283658 G>A maps to NM_198088.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:3283658 G>A maps to NM_198088.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:123601308 G>A maps to NM_003455.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr11:123601476 C>T maps to NM_003455.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:123598931 G>A maps to NM_003455.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:123600392 G>A maps to NM_003455.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr11:123598184 T>C maps to NM_003455.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:3169794 G>A maps to NM_001042428.1 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr16:3169602 C>T maps to NM_001042428.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:30692412 G>A maps to ENST00000394679 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:22154712 G>T maps to NM_007153.3 P1041P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:22156776 G>A maps to NM_007153.3 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:22157523 T>C maps to NM_007153.3 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:22154670 T>C maps to NM_007153.3 K1055K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:22157103 A>C maps to NM_007153.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:22155384 G>T maps to NM_007153.3 V817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:22154751 G>A maps to NM_007153.3 P1028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:58153236 C>A maps to NM_006385.3 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:58146082 C>T maps to NM_006385.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A2H5-01A-11D-A17D-09 chr7:148947809 C>T maps to NM_012256.3 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr7:148947473 C>T maps to NM_012256.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:3190915 G>A maps to NM_001134655.1 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:6964315 A>G maps to NM_013250.2 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr11:6977414 G>T maps to NM_013250.2 G403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:6977642 C>T maps to NM_013250.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr11:6964837 A>C maps to NM_013250.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:52193250 T>C maps to NM_006526.2 E684E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr10:45498899 G>A maps to NM_006963.4 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr10:45498917 C>T maps to NM_006963.4 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:45499133 G>A maps to NM_006963.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44469477 G>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:44469197 C>T maps to NM_013359.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:44470845 G>T maps to NM_013359.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44571022 G>T maps to NM_013361.4 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44571085 G>T maps to NM_013361.4 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:44564950 G>A maps to NM_013361.4 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:44570412 A>G maps to NM_013361.4 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr19:44610951 C>T maps to NM_013398.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:44605024 G>A maps to NM_013398.2 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:44612124 C>T maps to NM_013398.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44635399 G>A maps to NM_013362.2 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:44636173 G>A maps to NM_013362.2 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:44622656 T>C maps to NM_013362.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr19:44669960 G>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44681245 G>T maps to NM_001032372.1 G611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44681045 C>A maps to NM_001032372.1 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:44680206 C>T maps to NM_001032372.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:44681794 G>T maps to NM_001032372.1 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:44677076 G>A maps to NM_001032372.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:44681370 C>T maps to NM_001032372.1 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:44681500 G>T maps to NM_001032372.1 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44739728 C>T maps to NM_182490.1 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44739560 C>T maps to NM_182490.1 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:44721986 G>A maps to NM_182490.1 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:44738975 T>A maps to NM_182490.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:44934493 C>T maps to NM_014518.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44934345 T>A maps to NM_014518.2 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11O-01A-11D-A122-09 chr19:44933146 G>A maps to NM_014518.2 D603D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:44933583 C>A maps to NM_014518.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:44932999 G>A maps to NM_014518.2 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:71482991 G>A maps to NM_145911.1 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:71482922 A>C maps to NM_145911.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr16:71482553 G>A maps to NM_145911.1 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr16:71482574 A>G maps to NM_145911.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:44515208 G>T maps to NM_006300.3 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:5012844 C>T maps to NM_014519.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44777589 C>A maps to NM_181756.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:44777751 C>T maps to NM_181756.1 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr19:44661231 C>T maps to NM_006630.2 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:44791874 G>A maps to NM_004234.4 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:44791370 C>A maps to NM_004234.4 *739Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:74622022 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr18:74563831 T>C maps to NM_007345.3 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr18:74624252 A>G maps to NM_007345.3 Q951Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:74561576 G>T maps to NM_007345.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr18:74620344 G>A maps to NM_007345.3 Q787Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr18:74622021 A>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:244217801 G>A maps to NM_205768.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:244218008 C>T maps to NM_205768.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:244217378 G>A maps to NM_205768.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr1:244217423 T>C maps to NM_205768.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:244217714 C>T maps to NM_205768.2 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr1:244217658 C>T maps to NM_205768.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:44052666 G>A maps to NM_001099284.1 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:44053304 G>A maps to NM_001099284.1 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:32917291 G>A maps to NM_006965.2 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:32917279 C>T maps to NM_006965.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr10:38242017 A>G maps to NM_145011.2 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:38241543 G>A maps to NM_145011.2 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr10:38241060 C>T maps to NM_145011.2 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr8:146108177 C>T maps to NM_021061.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:146108163 G>T maps to NM_021061.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr8:146106971 G>A maps to NM_021061.3 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr8:146107282 G>A maps to NM_021061.3 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:146107502 G>A maps to NM_021061.3 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr8:146107076 C>T maps to NM_021061.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:145948420 G>T maps to NM_138367.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:145948675 G>A maps to NM_138367.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr8:145947690 G>A maps to NM_138367.1 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:19989319 G>T maps to NM_021047.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:20003027 C>A maps to NM_021047.2 C324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:20002479 G>T maps to ENST00000427401 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:20003484 C>T maps to NM_021047.2 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:20002479 G>T maps to ENST00000427401 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:58452701 C>A maps to NM_005773.2 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:58453269 T>C maps to NM_005773.2 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:22271724 G>A maps to NM_033468.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr11:116658316 C>A maps to NM_003904.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:116654313 C>A maps to NM_003904.3 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:37005187 G>T maps to NM_001166038.1 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:37005714 G>A maps to NM_001166038.1 G142G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:57724078 C>A maps to NM_003417.4 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:57723024 C>A maps to NM_003417.4 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:57724220 C>T maps to NM_003417.4 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:57724046 C>T maps to NM_003417.4 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:57724223 G>T maps to NM_003417.4 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:9524262 C>T maps to NM_006631.2 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:9524025 G>A maps to NM_006631.2 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:9524139 A>G maps to NM_006631.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:9528582 T>A maps to NM_006631.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9524829 C>T maps to NM_006631.2 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr16:31925806 G>A maps to NM_003414.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:31895848 G>T maps to NM_003414.4 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:31925795 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:133780299 C>A maps to NM_001165881.2 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr12:133779657 T>C maps to NM_001165881.2 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr12:133780020 T>G maps to NM_001165881.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr12:133779177 A>G maps to NM_001165881.2 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:133764633 G>A maps to NM_001165881.2 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:133780452 G>A maps to NM_001165881.2 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr12:133779657 T>C maps to NM_001165881.2 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:64389019 C>A maps to NM_021148.2 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:64377988 G>T maps to NM_021148.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:64388283 C>A maps to NM_021148.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NX-01A-11D-A16D-09 chr7:64363688 C>G did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:58718306 C>T maps to NM_133502.1 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:58723851 C>T maps to NM_133502.1 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr19:58718312 C>T maps to NM_133502.1 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr23:152612473 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:152612789 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:152612686 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:152608916 A>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:152612784 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:152612965 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:152612643 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:152613159 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:152612812 C>A did not map to a codon.
Sequencing variant TCGA-D1-A101-01A-12D-A10M-09 chr23:152613071 A>C did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:152612467 A>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:111979905 C>T maps to NM_021994.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:53303813 T>C maps to NM_006969.3 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:53302946 T>C maps to NM_006969.3 K717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:53303645 T>C maps to NM_006969.3 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:53311355 C>A maps to NM_006969.3 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr22:22869855 G>T maps to NM_080740.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr22:22869804 C>A maps to NM_080740.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr22:22868406 C>T maps to NM_080740.3 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:22868784 G>A maps to NM_080740.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr22:22869780 G>A maps to NM_080740.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:22842259 C>T maps to NM_080764.2 K488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr22:22842526 G>A maps to NM_080764.2 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr22:22842982 C>T maps to NM_080764.2 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:129360829 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129361711 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:129370483 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:129370576 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:129349176 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr23:129377603 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:129362961 T>C did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr23:129349772 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr23:129364606 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:129349998 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:129361731 G>T did not map to a codon.
Sequencing variant TCGA-FI-A2F8-01A-12D-A17D-09 chr23:129370208 A>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:56923982 G>A maps to NM_017661.2 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr15:56959142 A>C maps to NM_017661.2 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:56923706 C>A maps to NM_017661.2 E977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:56935195 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:56946658 A>G maps to NM_017661.2 D700D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A2AE-01A-11D-A16D-09 chr15:56993091 G>A maps to NM_001002844.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:56996376 G>A maps to NM_017661.2 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:56924163 G>A maps to NM_017661.2 I824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:56981335 G>T maps to NM_017661.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:200378491 C>T maps to NM_012482.3 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:200377297 C>T maps to NM_012482.3 E512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr7:148921516 C>A maps to NM_003575.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:148895723 G>A maps to NM_003575.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:148921543 C>T maps to NM_003575.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44351967 C>T maps to NM_181845.1 C405C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr19:44351862 T>C maps to NM_181845.1 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44591157 G>A maps to NM_001037813.2 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:44586166 G>A maps to NM_001037813.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:44591152 G>T maps to NM_001037813.2 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:44891008 C>T maps to NM_152354.3 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:44892201 C>A maps to NM_152354.3 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:44891808 C>A maps to NM_152354.3 G200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17B-01A-22D-A12J-09 chr19:44892259 G>A maps to NM_152354.3 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:15620186 A>G maps to NM_020652.2 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:15620109 G>T maps to NM_020652.2 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr17:15620339 A>G maps to NM_020652.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:18565495 A>G maps to NM_001145045.1 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:18566095 T>C maps to NM_001145045.1 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:18566461 C>T maps to NM_001145045.1 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:18584119 G>T maps to NM_001145045.1 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:16455333 C>A maps to NM_020653.2 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr17:16467082 T>C maps to NM_020653.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr17:16456450 T>C maps to NM_020653.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:16456558 G>A maps to NM_020653.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:87964706 C>T maps to NM_015021.1 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:87971290 C>T maps to NM_015021.1 S2648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:87970573 C>T maps to NM_015021.1 C2409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr6:87969152 G>T maps to NM_015021.1 E1936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:87967171 C>T maps to NM_015021.1 F1275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr6:87943238 C>T maps to NM_015021.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:87969796 C>T maps to NM_015021.1 V2150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr6:87965638 C>T maps to NM_015021.1 Y764Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr6:87968074 A>G maps to NM_015021.1 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr6:87971362 G>A maps to NM_015021.1 K2672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:87966269 G>T maps to NM_015021.1 E975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:87969796 C>T maps to NM_015021.1 V2150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:87970559 A>C maps to NM_015021.1 R2405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16N-01A-11D-A12J-09 chr6:87966982 T>C maps to NM_015021.1 N1212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:87971191 G>A maps to NM_015021.1 P2615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:87964843 T>G maps to NM_015021.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr21:43413649 A>G maps to NM_020727.4 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr21:43413337 G>T maps to NM_020727.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr21:43411491 C>A maps to NM_020727.4 E905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr21:43413483 A>G maps to NM_020727.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:45574966 A>G maps to NM_145288.1 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:45575140 G>A maps to NM_145288.1 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:35435318 C>A maps to NM_001099438.1 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:35435352 C>T maps to NM_001099438.1 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:35434571 C>T maps to NM_001099438.1 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr19:35435528 A>G maps to NM_001099438.1 G554G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AP-A059-01A-21D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:150275117 C>T maps to NM_001172831.1 K577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:150276441 G>T maps to NM_001172831.1 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:150276274 C>A maps to NM_001172831.1 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:150276460 C>A maps to NM_001172831.1 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:35175241 A>G maps to ENST00000221282 E179E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:35175701 G>T maps to ENST00000221282 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:57867668 C>T maps to ENST00000391705 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:57868022 G>A maps to ENST00000391705 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:9271022 C>T maps to NM_020933.4 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9271727 G>A maps to NM_020933.4 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:9268074 G>A maps to ENST00000419608 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:9271676 G>A maps to NM_020933.4 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr19:9270941 G>A maps to NM_020933.4 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:9269580 G>A maps to NM_020933.4 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr6:43325105 G>A maps to NM_014345.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:43305993 T>G maps to NM_014345.2 S1914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:43323118 G>A maps to NM_014345.2 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr6:43325208 C>T maps to NM_014345.2 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:43306271 C>A maps to NM_014345.2 E1822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr6:43305341 C>A maps to NM_014345.2 G2132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:43305314 C>A maps to NM_014345.2 E2141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:58031050 G>A maps to NM_020807.1 C373C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:58031335 G>A maps to NM_020807.1 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:58031932 G>A maps to NM_020807.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:44139578 G>A maps to NM_006973.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:44139578 G>A maps to NM_006973.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:53384796 G>A maps to NM_207333.2 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:53384933 G>A maps to NM_207333.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:53384139 G>A maps to NM_207333.2 Y413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr6:28295208 C>G maps to NM_030899.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:28297400 G>T maps to NM_030899.4 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:28297373 C>T maps to NM_030899.4 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:28293768 A>G did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:28297226 G>T maps to NM_030899.4 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr6:28295165 C>A maps to NM_030899.4 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:28297172 C>T maps to NM_030899.4 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:28297349 G>T maps to NM_030899.4 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr6:28294229 G>A maps to NM_030899.4 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:58983055 C>T maps to NM_014347.2 C399C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:58982761 G>A maps to NM_014347.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:58982225 C>T maps to NM_014347.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:58967675 C>T maps to NM_207395.2 C455C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58967489 C>T maps to NM_207395.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:58966460 C>A maps to ENST00000391696 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:58967501 C>T maps to NM_207395.2 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:58967753 C>T maps to NM_207395.2 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr19:58967573 C>T maps to NM_207395.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:90484284 G>A maps to NM_182976.2 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:90473242 T>C maps to NM_182976.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:90478722 C>T maps to NM_182976.2 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:58640156 C>T maps to NM_024620.3 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:142145763 G>A maps to NM_014487.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:142153677 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:142155040 C>G maps to NM_014487.4 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:54080884 C>T maps to NM_001079907.1 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:54081145 C>T maps to NM_001079907.1 C444C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr19:54080863 G>A maps to NM_001079907.1 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr19:14829707 G>A maps to NM_032433.2 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:14829269 C>T maps to NM_032433.2 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:14829566 G>A maps to NM_032433.2 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:14829698 T>C maps to NM_032433.2 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:45129934 T>G maps to NM_018102.3 *681Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr20:45131653 C>A maps to NM_018102.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:44589332 G>T maps to NM_022095.3 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:44577618 G>A maps to NM_022095.3 Y1334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:44588945 A>G maps to NM_022095.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr20:44580950 C>T maps to NM_022095.3 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:44581338 G>A maps to NM_022095.3 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:44587980 G>A maps to NM_022095.3 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr20:44588937 G>A maps to NM_022095.3 H643H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:44578025 G>A maps to NM_022095.3 G1255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:44587994 G>A maps to NM_022095.3 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:25657545 G>A maps to NM_015655.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr20:25657017 G>A maps to NM_015655.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr20:25657521 G>A maps to NM_015655.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr10:38344992 C>T maps to NM_006954.1 C647C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:38344398 C>A maps to NM_006954.1 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr10:38345154 C>T maps to NM_006954.1 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr10:38345238 C>A maps to NM_006954.1 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:38305826 C>A maps to NM_006954.1 S13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr10:38345035 G>T maps to NM_006954.1 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr10:38344671 C>A maps to NM_006954.1 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:43089047 G>A maps to NM_006955.1 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:43090130 A>G maps to NM_006955.1 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:43088308 C>A maps to NM_006955.1 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:43089422 T>C maps to NM_006955.1 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr10:43088759 C>T maps to NM_006955.1 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:43088102 A>G maps to NM_006955.1 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr10:43089310 C>A maps to NM_006955.1 G363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:146003435 G>A maps to NM_030580.3 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:146003534 G>A maps to NM_030580.3 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:32336829 C>A maps to ENST00000375200 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr20:32341132 C>T maps to ENST00000375200 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:32357900 T>C maps to ENST00000375200 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr20:32376705 G>A maps to ENST00000375200 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr20:32349787 C>T maps to ENST00000375200 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:2473383 C>A maps to NM_024325.4 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:37367975 C>T maps to NM_003419.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:176468187 C>T maps to ENST00000503039 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr5:176468872 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:53645384 G>A maps to NM_001172674.1 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:53652584 G>A maps to NM_001172674.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:53652057 G>T maps to NM_001172674.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:44700823 G>A maps to NM_003420.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:178139075 G>A maps to NM_005649.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:178139969 A>G maps to NM_005649.2 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:178139257 G>A maps to NM_005649.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:178139075 G>A maps to NM_005649.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:178139540 G>T maps to NM_005649.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:178309719 C>T maps to NM_058230.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:178506329 G>A maps to NM_014594.1 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:178506944 C>A maps to NM_014594.1 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:178506422 C>T maps to NM_014594.1 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:7584361 G>A maps to NM_018083.4 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:33742028 G>A maps to NM_152493.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr10:64136197 G>A maps to NM_199451.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:64239642 G>A maps to NM_199450.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr10:64136663 G>T maps to NM_199451.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr10:64136239 G>A maps to NM_199451.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K9-01A-21D-A10O-09 chr5:71743088 C>T maps to NM_152625.1 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr5:71756234 G>A maps to NM_152625.1 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:71756024 C>T maps to NM_152625.1 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr5:71757278 G>A maps to NM_152625.1 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr9:99154744 C>T maps to NM_153695.3 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:99160586 G>A maps to NM_153695.3 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr9:99160474 G>T maps to NM_153695.3 S181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr10:38407629 C>T maps to NM_003421.2 H517H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:38406316 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:38407069 G>T maps to NM_003421.2 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr10:38407731 A>C maps to NM_003421.2 I551I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:37117072 G>T maps to NM_032825.3 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:37117840 G>T maps to NM_032825.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:37101603 G>A maps to NM_032825.3 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:37100577 G>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:37117863 C>T maps to NM_032825.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:37733755 C>T maps to NM_152604.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:37733620 A>G maps to NM_152604.1 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:37733429 G>T maps to NM_152604.1 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:37734187 C>T maps to NM_152604.1 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:37733692 T>C maps to NM_152604.1 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr12:6788169 C>T maps to NM_001135734.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr12:54778301 C>T maps to NM_001130967.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr12:54764493 G>A maps to NM_001130967.1 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr2:180383278 G>T maps to NM_152520.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:180634448 C>A maps to NM_152520.4 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:21706452 C>T maps to NM_024697.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr6:27368800 G>T maps to NM_001076781.1 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr6:27369057 G>A maps to NM_001076781.1 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr6:27368871 A>C maps to NM_001076781.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:27369094 C>T maps to NM_001076781.1 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Y-01A-11W-A027-09 chr7:99097347 C>T maps to NM_032164.2 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:99091607 G>T maps to NM_032164.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr7:99096378 T>C maps to NM_032164.2 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:99091337 G>A maps to NM_032164.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr8:28217122 G>A maps to NM_018660.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:28209104 T>C maps to NM_018660.2 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr8:28214226 A>G maps to NM_018660.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:28206718 G>A maps to NM_018660.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:32949589 A>G maps to NM_145756.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:32949624 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:32948409 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:32954061 C>T maps to NM_145756.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr18:32949561 C>A maps to NM_145756.2 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:32825919 A>G maps to NM_001135178.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:32825333 T>G maps to NM_001135178.2 L222*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AP-A0LM-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:32834265 C>T maps to NM_032347.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr18:32825964 A>G maps to NM_001135178.2 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:32825305 C>T maps to NM_001135178.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:148873566 T>C maps to NM_170686.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:148875740 T>C maps to NM_170686.2 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44376931 A>C maps to ENST00000324394 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr18:72589189 G>T maps to NM_017757.2 E1639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:72345333 G>T maps to NM_017757.2 E787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:72632631 C>T maps to NM_017757.2 L1804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:72344951 G>A maps to NM_017757.2 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:72347066 G>A maps to NM_017757.2 K1364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:72632631 C>T maps to NM_017757.2 L1804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr18:72775292 C>T maps to NM_017757.2 Y1872Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr18:72343397 T>C maps to NM_017757.2 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr18:72343484 G>A maps to NM_017757.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:72343145 G>A maps to NM_017757.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:72346575 G>T maps to NM_017757.2 E1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:72775976 C>T maps to NM_017757.2 D2100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr18:72775832 C>T maps to NM_017757.2 A2052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr18:72347654 T>G maps to NM_017757.2 T1560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr18:72346634 G>A maps to NM_017757.2 S1220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:46726890 C>T maps to NM_024741.2 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr11:46726734 T>G maps to NM_024741.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr11:46727370 C>T maps to NM_024741.2 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:46727370 C>T maps to NM_024741.2 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr11:46724539 A>G maps to NM_024741.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47308389 T>C did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47308818 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47308220 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47308466 C>A did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:47308572 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:47315386 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47307438 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47307515 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr23:47307645 G>C did not map to a codon.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr23:47315701 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:47308858 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47308501 T>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47307602 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:47307708 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:47307834 C>A did not map to a codon.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr23:47307374 C>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr14:74360553 G>T maps to NM_021188.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr14:74363230 A>C maps to NM_021188.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:53613050 C>A maps to NM_001164309.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:53612904 T>C maps to NM_001164309.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:58089427 T>G maps to NM_017879.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58084956 G>T maps to NM_017879.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:58084965 C>T maps to NM_017879.1 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:58084980 A>G maps to NM_017879.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58420319 C>A maps to NM_152475.2 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58421126 G>A maps to NM_152475.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:58421036 T>C maps to NM_152475.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:58423431 C>T maps to NM_152475.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:58437518 C>A maps to NM_133460.1 *677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:58437518 C>A maps to NM_133460.1 *677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:58439278 G>T maps to NM_133460.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0RA-01A-21D-A10B-09 chr19:58005428 C>T maps to NM_001098491.1 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:37581952 C>T maps to NM_144689.3 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:37618408 C>T maps to NM_144689.3 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:37618096 C>T maps to NM_144689.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:37618193 G>T maps to NM_144689.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:37619945 C>T maps to NM_144689.3 Q685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:37619047 C>T maps to NM_144689.3 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:37619512 T>C maps to NM_144689.3 F540F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:49671829 G>T maps to NM_015069.2 C411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr16:49672267 G>A maps to NM_015069.2 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:49670422 G>A maps to NM_015069.2 D880D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr16:49672594 G>A maps to NM_015069.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr16:49672150 G>A maps to NM_015069.2 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:49671790 C>T maps to NM_015069.2 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E6-A1LZ-01A-11D-A142-09 chr16:49670875 G>A maps to NM_015069.2 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr7:148801975 G>A maps to NM_001001661.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:148802506 C>T maps to NM_001001661.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:148801708 C>T maps to NM_001001661.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:148801174 C>T maps to NM_001001661.2 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:148801429 C>T maps to NM_001001661.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17N-01A-11D-A12J-09 chr7:148801597 G>A maps to NM_001001661.2 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9640060 T>C maps to NM_024106.1 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9640300 G>A maps to NM_024106.1 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:9639078 G>A maps to NM_024106.1 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:9639397 C>T maps to NM_024106.1 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:9639318 G>A maps to NM_024106.1 R468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:44112164 G>A maps to NM_182498.3 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:21719787 A>G maps to NM_001001415.2 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:21719751 C>A maps to NM_001001415.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:21720862 C>T maps to NM_001001415.2 R670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr19:21688577 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:21992054 C>A maps to NM_003423.2 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:22001992 C>A maps to NM_003423.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:21991005 T>C maps to NM_003423.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:21992124 G>T maps to NM_003423.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:21990426 A>C maps to NM_003423.2 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:21991860 G>T maps to NM_003423.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:21240655 A>G maps to NM_025189.3 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:21216291 G>T maps to NM_025189.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:21205620 T>G maps to NM_025189.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:21349167 G>T maps to NM_133473.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:21365837 C>T maps to NM_133473.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:21366173 C>T maps to NM_133473.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A05A-01A-11W-A027-09 chr19:21365600 C>T maps to NM_133473.2 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:21349216 T>G maps to NM_133473.2 L59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:52538445 C>T maps to NM_014650.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:52538417 C>A maps to NM_014650.2 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:52538417 C>A maps to NM_014650.2 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:12125781 G>A maps to NM_001080411.1 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:12126117 G>A maps to NM_001080411.1 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:12126466 A>G maps to NM_001080411.1 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:12126955 T>G maps to NM_001080411.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:12125803 A>G maps to NM_001080411.1 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:3434672 G>T maps to ENST00000396852 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:23689411 G>A maps to NM_001077195.1 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr10:31138706 G>A maps to NM_182755.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:31133934 G>T maps to NM_182755.2 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr10:31134276 G>A maps to NM_182755.2 D700D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:11979026 G>A maps to NM_152262.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:11977030 T>G maps to NM_152262.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:11978655 C>T maps to NM_152262.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:12383896 G>A maps to NM_001164276.1 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:12384825 C>A maps to NM_001164276.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:12384094 T>C maps to NM_001164276.1 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:11943544 C>T maps to NM_152357.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:11891151 T>C maps to NM_152355.2 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:11891133 A>G maps to NM_152355.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr19:11890917 G>A maps to NM_152355.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:11891857 C>T maps to NM_152355.2 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:12474373 T>C maps to NM_030824.2 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr3:44489026 G>A maps to NM_181489.5 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr3:44489341 G>A maps to NM_181489.5 H607H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:44489236 A>G maps to NM_181489.5 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:44488158 G>A maps to NM_181489.5 R1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:44489290 G>A maps to NM_181489.5 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:58988773 G>A maps to NM_017908.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:58991008 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:58989176 C>T maps to NM_017908.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GV-01A-31W-A062-09 chr23:134481131 G>A did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:134494443 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:134494560 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:134494752 T>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134481425 T>G did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134494419 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134494614 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:134481499 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:134494639 G>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:134494956 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:134494858 T>G did not map to a codon.
Sequencing variant TCGA-BK-A0CC-01A-21W-A027-09 chr23:134483145 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:134481295 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:134494414 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:134494807 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:134494891 G>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZN-01A-11D-A122-09 chr23:134494127 C>T did not map to a codon.
Sequencing variant TCGA-D1-A0ZQ-01A-11D-A122-09 chr23:134494251 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:134494165 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:44418696 A>C maps to NM_003425.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:44423063 G>A maps to NM_003425.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr6:57015532 G>A maps to NM_001031623.2 E875E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr6:57011897 C>T maps to NM_001031623.2 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:57013192 T>A maps to NM_001031623.2 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:57018780 C>T maps to NM_001031623.2 N1002N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr6:57012047 C>T maps to NM_001031623.2 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:57012839 C>T maps to NM_001031623.2 R653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:57017085 C>T maps to NM_001031623.2 C940C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr6:57012052 C>A maps to NM_001031623.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr5:178391815 G>A maps to NM_182594.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr5:178392053 G>T maps to NM_182594.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:178391989 A>G maps to NM_182594.2 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:178391890 T>C maps to NM_182594.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:178392904 A>G maps to NM_182594.2 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:57802703 G>A maps to NM_006635.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:57802832 C>T maps to NM_006635.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K3-01A-11W-A062-09 chr19:57802715 G>A maps to NM_006635.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr19:57802658 G>A maps to NM_006635.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr19:37129665 G>A maps to NM_153257.2 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:37130172 T>C maps to NM_153257.2 E358E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:109687140 C>T maps to NM_021224.4 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:109690917 C>T maps to NM_021224.4 G1575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:109691076 C>T maps to NM_021224.4 S1628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:109686672 G>A maps to NM_021224.4 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:109686910 C>T maps to NM_021224.4 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:109689057 C>T maps to NM_021224.4 N955N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:109690167 C>T maps to NM_021224.4 N1325N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:109687543 C>T maps to NM_021224.4 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:109773205 C>T maps to NM_021224.4 D2472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr9:109689702 C>T maps to NM_021224.4 P1170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:109688664 C>A maps to NM_021224.4 I824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:109689081 C>T maps to NM_021224.4 V963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:109734436 C>T maps to NM_021224.4 C2193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr9:109685829 G>T maps to NM_021224.4 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:109688820 C>A maps to NM_021224.4 I876I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:149467624 C>A maps to NM_207336.1 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:53352445 G>A maps to NM_001008801.1 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:53352435 C>A maps to NM_001008801.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:53344538 G>A maps to NM_001008801.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:57089806 T>A maps to NM_001001668.3 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:57085971 G>A maps to ENST00000446235 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:57088192 T>C maps to NM_001001668.3 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:57086063 G>A maps to NM_001001668.3 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr19:57085905 C>A maps to ENST00000446235 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:57036399 G>T maps to NM_020813.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:57036137 T>C maps to NM_020813.2 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:57035886 G>T maps to NM_020813.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:57035886 G>T maps to NM_020813.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr19:57029947 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:57035868 G>T maps to NM_020813.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:50548080 C>T maps to NM_015428.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:50548035 C>T maps to NM_015428.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:50542497 G>A maps to NM_015428.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:50548146 T>C maps to NM_015428.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:50549874 A>G maps to NM_015428.1 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr19:50548164 A>G maps to NM_015428.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:50549145 C>A maps to NM_015428.1 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr5:121488146 C>T maps to NM_207317.1 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:121488578 C>T maps to NM_207317.1 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:57187858 G>A maps to NM_033273.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:57188023 C>T maps to NM_033273.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:57188749 T>C maps to NM_033273.1 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:57188059 G>T maps to NM_033273.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:57187651 C>T maps to NM_033273.1 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:57188023 C>T maps to NM_033273.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:57188566 G>A maps to NM_033273.1 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:57187987 C>T maps to NM_033273.1 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:57188626 G>T maps to NM_033273.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:57187690 G>T maps to NM_033273.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:30409635 C>T maps to ENST00000495929 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:30409932 T>C maps to ENST00000495929 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:52825570 G>A maps to NM_144684.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:52825754 C>T maps to NM_144684.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:52825903 G>A maps to NM_144684.2 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:52803645 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:114304186 C>A maps to NM_133464.2 Y324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:114296128 G>A maps to NM_133464.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0T9-01A-11D-A12J-09 chr9:114304148 A>T maps to NM_133464.2 K312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:95609568 C>T maps to NM_031486.1 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:95609487 G>A maps to NM_031486.1 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr10:44111817 G>A maps to NM_145312.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:20308334 C>T maps to ENST00000428290 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:20308277 T>C maps to ENST00000428290 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11S-01A-11D-A122-09 chr19:20307779 T>A maps to NM_052852.2 C87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:12691832 G>A maps to NM_020714.2 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:12691588 G>A maps to NM_020714.2 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr19:12691817 G>A maps to NM_020714.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A165-01A-11D-A12J-09 chr19:12691748 G>A maps to NM_020714.2 H380H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr19:11917794 C>T maps to NM_152356.3 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:11917794 C>T maps to NM_152356.3 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:11917166 T>C maps to NM_152356.3 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:11917103 C>T maps to NM_152356.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:11917290 C>T maps to NM_152356.3 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:22846756 G>T maps to NM_020855.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:22847239 G>T maps to NM_020855.2 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:21605910 G>A maps to NM_001076678.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:21607197 C>T maps to NM_001076678.2 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:21607357 G>T maps to NM_001076678.2 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:21606937 G>T maps to NM_001076678.2 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:21607716 G>A maps to NM_001076678.2 R752R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:21606918 G>A maps to NM_001076678.2 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr1:247463859 G>A maps to NM_032752.1 H575H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr1:247464264 G>A maps to NM_032752.1 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:247464243 G>A maps to NM_032752.1 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:247492553 G>A maps to NM_032752.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr1:247492721 C>T maps to NM_032752.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:247464519 G>A maps to NM_032752.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:247464563 G>A maps to NM_032752.1 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:247473644 G>A maps to NM_032752.1 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr1:247473644 G>A maps to NM_032752.1 Y255Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:99217255 G>A maps to NM_145115.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr7:99227336 G>A maps to NM_145115.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr7:99227618 C>T maps to NM_145115.2 H537H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr7:99227117 C>T maps to NM_145115.2 H370H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:4802847 C>T maps to NM_021646.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr16:4810553 A>C maps to NM_021646.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0L8-01A-11W-A062-09 chr3:44776146 T>C maps to NM_145044.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:44763221 C>T maps to NM_033210.4 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:44763241 G>A maps to NM_033210.4 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:44763274 C>T maps to NM_033210.4 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr3:44762830 G>A maps to NM_033210.4 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:77159046 C>T maps to NM_032772.4 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:32845598 C>T maps to NM_014910.4 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:32845206 C>T maps to NM_014910.4 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:32844470 C>T maps to NM_014910.4 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:32873796 A>G maps to NM_014910.4 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:32845538 C>T maps to NM_014910.4 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:32844314 C>T maps to NM_014910.4 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:32845206 C>T maps to NM_014910.4 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:32845640 G>A maps to NM_014910.4 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:32873799 T>C maps to NM_014910.4 Y891Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:99521734 G>A maps to NM_014930.1 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:99522523 A>C maps to NM_014930.1 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr9:99538315 C>T maps to NM_014930.1 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:99522514 C>T maps to NM_014930.1 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr10:135126328 C>T maps to NM_145806.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr2:27826143 T>C maps to NM_032434.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:27844108 G>A maps to NM_032434.2 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:27839130 C>T maps to NM_032434.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr2:27844102 G>A maps to NM_032434.2 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr2:27826131 G>A maps to NM_032434.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr20:62596056 G>A maps to NM_020713.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:27601106 G>A maps to NM_144631.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr2:27601361 C>T maps to NM_144631.4 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:95818953 C>T maps to NM_032788.1 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr18:74092149 G>A maps to ENST00000443185 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:146032852 G>A maps to NM_213605.2 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr10:97916762 A>G maps to NM_014803.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr10:97918205 T>A maps to NM_014803.3 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr10:97919537 T>C maps to NM_014803.3 N1153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr10:97916798 T>C maps to NM_014803.3 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr4:10446119 A>G maps to NM_053042.2 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr4:10446850 C>A maps to NM_053042.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr4:10445093 C>T maps to NM_053042.2 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr4:10445927 G>T maps to NM_053042.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:10447439 C>T maps to NM_053042.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr18:14105064 C>A maps to NM_145287.3 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr18:14105778 C>A maps to NM_145287.3 G254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr18:14106148 A>G maps to NM_145287.3 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr18:14106079 G>A maps to NM_145287.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GJ-01A-11W-A062-09 chr18:22662577 T>C maps to ENST00000399425 Q1310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr18:22806756 C>T maps to NM_015461.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr18:22805886 G>T maps to NM_015461.2 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:22807335 C>T maps to NM_015461.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr18:22775133 A>G maps to NM_015461.2 N1216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr18:22804664 C>A maps to NM_015461.2 E1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr18:22805106 G>T maps to NM_015461.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr18:22804503 G>A maps to NM_015461.2 A1126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr18:22804578 C>T maps to NM_015461.2 K1101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:22804548 G>A maps to NM_015461.2 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:56113510 G>A maps to NM_153219.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr19:42729211 C>T maps to NM_133444.1 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:42729172 C>T maps to NM_133444.1 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:42728731 C>A maps to NM_133444.1 C59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:42730319 C>T maps to NM_133444.1 R589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:37879673 T>C maps to NM_032453.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:37879440 G>T maps to NM_032453.1 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:37880729 T>C maps to NM_032453.1 C593C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:52918686 C>A maps to NM_032423.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:52909771 C>A maps to NM_032423.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:52919439 G>A maps to NM_032423.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:37037833 G>T maps to NM_001145649.1 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:37038766 T>C maps to NM_001145649.1 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:37038922 G>T maps to NM_001145649.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:37037899 G>T maps to NM_001145649.1 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:37037881 G>A maps to NM_001145649.1 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58118186 G>T maps to NM_020880.3 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:58118485 C>T maps to NM_020880.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:56586448 C>A maps to NM_018181.4 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr18:56587789 G>A maps to NM_018181.4 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr18:56615352 G>A maps to NM_018181.4 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr18:56586562 G>A maps to NM_018181.4 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:56585911 G>A maps to NM_018181.4 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr18:56585984 C>T maps to NM_018181.4 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JV-01A-11D-A10B-09 chr18:56651406 C>T maps to NM_018181.4 C1205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr18:56587676 C>T maps to NM_018181.4 Q720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:56585746 C>T maps to NM_018181.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr18:56646390 C>T maps to NM_018181.4 Y1085Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:52937237 G>T maps to NM_001143939.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:52941177 C>T maps to NM_001143939.1 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:52942302 C>A maps to NM_001143939.1 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:52941729 T>C maps to NM_001143939.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:52942327 C>T maps to NM_001143939.1 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:52937237 G>T maps to NM_001143939.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:52942000 C>T maps to NM_001143939.1 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:52941516 A>G maps to NM_001143939.1 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:52937237 G>T maps to NM_001143939.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr19:31039267 C>T maps to NM_014717.1 F914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:30934885 C>T maps to NM_014717.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:30935863 G>A maps to NM_014717.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:31038892 G>A maps to NM_014717.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:31039804 C>T maps to NM_014717.1 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:31038886 C>T maps to NM_014717.1 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:31039312 C>A maps to NM_014717.1 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr19:30935554 T>C maps to NM_014717.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:30934553 C>T maps to NM_014717.1 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MT-01A-11D-A10B-09 chr19:31040281 G>A maps to NM_014717.1 E1252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VT-01A-11D-A10M-09 chr19:31040278 G>A maps to NM_014717.1 P1251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:30934834 C>T maps to NM_014717.1 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:30935959 G>A maps to NM_014717.1 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:31039864 G>A maps to NM_014717.1 K1113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr19:30934972 G>A maps to NM_014717.1 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:31040308 G>A maps to NM_014717.1 P1261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:31040008 C>A maps to NM_014717.1 L1161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:38103830 C>A maps to NM_152606.3 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:38102612 C>T maps to NM_152606.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:38103614 T>G maps to NM_152606.3 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr19:38103609 C>T maps to NM_152606.3 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:40514452 G>A maps to NM_178544.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:40520173 G>T maps to NM_178544.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:40520173 G>T maps to NM_178544.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:40520929 G>T maps to NM_178544.3 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:40513236 C>T maps to NM_178544.3 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:40520391 A>G maps to NM_178544.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:40521727 G>T maps to ENST00000392042 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:40520655 T>C maps to NM_178544.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:57889366 A>G maps to NM_173631.2 Q341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:57889378 T>C maps to NM_173631.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:57879946 G>A maps to NM_173631.2 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:57888526 A>G maps to NM_173631.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:57910872 C>T maps to NM_001172773.1 C418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:57910856 C>A maps to NM_001172773.1 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:58046522 C>A maps to ENST00000376233 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58049808 G>A maps to ENST00000376233 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:58049503 C>T maps to ENST00000376233 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:58049982 C>T maps to ENST00000376233 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:58049211 T>C maps to ENST00000376233 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58059317 C>T maps to NM_001039654.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:58198746 C>T maps to ENST00000356715 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr19:58199628 G>A maps to ENST00000356715 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:58324692 C>T maps to NM_024762.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:58320160 C>T maps to NM_024762.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:2834540 C>T maps to NM_001102651.1 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:2834798 C>A maps to NM_001102651.1 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MS-01A-11D-A10B-09 chr19:2827634 C>T maps to NM_001102651.1 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr19:2823050 G>T maps to NM_001102651.1 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:2853460 C>T maps to NM_152791.4 C466C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:2853265 C>T maps to NM_152791.4 C401C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:2852876 C>T maps to NM_152791.4 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:2878077 G>A maps to NM_024967.1 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17M-01A-21D-A12J-09 chr19:2878236 C>T maps to NM_024967.1 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:7083364 C>T maps to NM_024341.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:7083375 C>A maps to NM_024341.2 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:7083586 C>A maps to NM_024341.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:8922676 C>T maps to NM_144693.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A102-01A-11D-A10M-09 chr19:8922211 T>C maps to NM_144693.1 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:8931925 C>T maps to NM_144693.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:8932717 G>A maps to NM_144693.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:9452762 A>G maps to NM_032497.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:9452882 G>A maps to NM_032497.1 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:9453632 T>C maps to NM_032497.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:9578581 G>T maps to NM_152476.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A052-01A-11W-A027-09 chr19:9578899 C>T maps to NM_152476.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9577833 C>A maps to NM_152476.2 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9577905 C>A maps to NM_152476.2 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9579863 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:9578673 C>A maps to NM_152476.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:9578809 T>C maps to NM_152476.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:9583906 G>T maps to NM_152476.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:9720989 G>A maps to NM_152289.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:9727720 C>A maps to NM_152289.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:9764476 G>A maps to NM_001130032.1 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:9764074 T>C maps to NM_001130032.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr19:12433414 C>T maps to NM_145276.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:12429418 C>A maps to NM_145276.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TI-01A-11D-A10B-09 chr19:12430166 C>G maps to NM_145276.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:12638344 C>A maps to NM_144976.3 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:12638452 G>A maps to NM_144976.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:36674273 C>T maps to ENST00000355114 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:36674585 G>A maps to ENST00000355114 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:36685204 G>A maps to ENST00000355114 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:36686037 G>A maps to ENST00000355114 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:36673742 G>A maps to ENST00000355114 H396H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:36674372 T>C maps to ENST00000355114 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:36940724 T>A maps to NM_001145343.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:36940276 C>A maps to NM_001145343.1 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17F-01A-11D-A12J-09 chr19:36964303 G>A maps to NM_001145343.1 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:37210093 A>G maps to ENST00000423498 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:37441155 T>C maps to NM_198539.2 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:37440778 C>T maps to NM_198539.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:37488162 C>T maps to ENST00000444991 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:37441525 C>T maps to NM_198539.2 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:37441779 T>G maps to NM_198539.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:37441227 A>G maps to NM_198539.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr19:37428067 G>C maps to NM_198539.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U7-01A-21D-A10B-09 chr19:37904092 A>G maps to NM_152484.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:37903657 G>A maps to NM_152484.2 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:2918070 C>A maps to NM_173480.2 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:2917689 G>A maps to NM_173480.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:2917326 C>T maps to NM_173480.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:2918140 C>T maps to NM_173480.2 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:2917437 A>G maps to NM_173480.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:2916920 G>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:2916105 C>A maps to NM_173480.2 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:37967298 G>A maps to NM_144694.1 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:37975129 T>C maps to NM_144694.1 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:37975522 C>T maps to NM_144694.1 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:125989059 G>T maps to NM_152412.2 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr8:125989526 T>C maps to NM_152412.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr8:125989970 G>T maps to NM_152412.2 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:38230868 G>T maps to NM_001172690.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:38229626 T>C maps to NM_001172690.1 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:44103343 T>C maps to NM_024327.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:53014447 C>T maps to NM_001099694.1 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr19:53014344 C>T maps to NM_001099694.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:53014447 C>T maps to NM_001099694.1 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:53014536 C>A maps to NM_001099694.1 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:56895243 G>A maps to NM_144690.1 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:56895387 G>A maps to NM_144690.1 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:56895678 G>T maps to NM_144690.1 C369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:56895855 G>T maps to NM_144690.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr19:56895621 A>G maps to NM_144690.1 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:56895948 G>A maps to NM_144690.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:56934276 A>T maps to NM_001159861.1 K84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:56935166 C>T maps to NM_001159861.1 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56935010 A>G maps to NM_001159861.1 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56935325 G>A maps to NM_001159861.1 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:56935070 A>T maps to NM_001159861.1 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:56935335 G>T maps to NM_001159861.1 E437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:58927205 T>C maps to ENST00000322834 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GE-01A-11W-A062-09 chr19:37647248 C>A maps to ENST00000356958 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:37660752 G>A maps to ENST00000356958 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:37680938 G>A maps to NM_152279.3 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:37677409 T>C maps to NM_152279.3 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:37677637 C>T maps to NM_152279.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:37676977 A>C maps to NM_152279.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:37676707 G>T maps to NM_152279.3 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:58290741 G>T maps to NM_017652.2 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:58290763 C>A maps to NM_017652.2 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr19:58290291 A>C maps to NM_017652.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:58352203 A>G did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr19:58370031 A>G maps to NM_032828.2 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:58353905 C>T did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:58370388 A>G maps to NM_032828.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:58370247 G>A maps to NM_032828.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:58353514 G>T did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:58353906 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:58371231 G>A maps to NM_032828.2 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:58353599 A>C did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:48309759 G>A maps to NM_016089.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr15:85341671 C>T maps to NM_014630.2 F901F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:85327369 G>A maps to NM_014630.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:85341575 C>A maps to NM_014630.2 V869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr15:85341258 G>A maps to NM_014630.2 Q853Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:5086639 G>A maps to NM_032530.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:5086690 T>C maps to NM_032530.1 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr17:5085451 T>C maps to NM_032530.1 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16I-01A-11D-A12J-09 chr17:5085166 C>T maps to NM_032530.1 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr8:196238 T>C maps to NM_001042416.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:193761 G>A maps to NM_001042416.1 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr16:3490833 C>A maps to NM_152457.1 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr16:3487221 A>G maps to NM_152457.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:2050465 C>T maps to ENST00000431526 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr16:2053672 C>T maps to ENST00000431526 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr16:2049845 G>A maps to ENST00000431526 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:35250400 G>A maps to NM_001007248.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:35251126 A>G maps to NM_001007248.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:35260355 G>T maps to NM_001007248.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:35250451 G>A maps to NM_001007248.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:53270003 A>G maps to NM_198457.2 C335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:53270576 C>T maps to NM_198457.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GQ-01A-11D-A122-09 chr19:58490829 C>A maps to NM_025027.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:58489785 A>G maps to NM_025027.3 H754H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:58490337 A>G maps to NM_025027.3 C570C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:38189263 C>A maps to NM_032689.4 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:38190649 C>A maps to NM_032689.4 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:38189105 T>C maps to NM_032689.4 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr19:38190422 C>T maps to NM_032689.4 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:38190386 A>G maps to NM_032689.4 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr5:123980159 A>G maps to NM_020747.2 H1300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr5:124080384 C>A maps to NM_020747.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr5:123984141 G>A maps to NM_020747.2 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr5:123980343 G>T maps to NM_020747.2 S1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:64970577 G>A maps to NM_015042.1 Q1222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:64966760 C>T maps to NM_015042.1 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:64967578 C>T maps to NM_015042.1 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr15:64791993 G>T maps to NM_015042.1 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:64972874 C>T maps to NM_015042.1 R1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr15:64967596 C>A maps to NM_015042.1 I848I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0RY-01A-11D-A10B-09 chr15:64792055 G>A maps to NM_015042.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr15:64968077 C>T maps to NM_015042.1 Q1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr15:64972874 C>T maps to NM_015042.1 R1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:64792407 G>T maps to ENST00000416172 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:52869671 T>C maps to NM_001161425.1 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:52869026 T>C maps to NM_001161425.1 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:53219082 A>G did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:53209625 C>A maps to NM_001161500.1 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:53209625 C>A maps to NM_001161500.1 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:53209982 C>A maps to NM_001161500.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K6-01A-11W-A062-09 chr19:53208438 C>T maps to NM_001161500.1 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:53209268 C>A maps to NM_001161500.1 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:52443550 C>T maps to NM_001031721.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:52448390 C>T maps to NM_001031721.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:52448489 G>T maps to NM_001031721.3 G452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:52443577 C>T maps to NM_001031721.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:52519094 A>G maps to NM_025040.3 *586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:52519160 C>A maps to NM_025040.3 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr19:52519707 G>A maps to NM_025040.3 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:52519415 C>A maps to NM_025040.3 G479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:52505449 G>T maps to ENST00000354939 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:52496174 C>T maps to ENST00000354939 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:52496174 C>T maps to ENST00000354939 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:52496273 G>A maps to ENST00000354939 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:52496201 T>A maps to ENST00000354939 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr19:52618313 A>G maps to NM_178523.3 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:52627271 C>A maps to NM_178523.3 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:116812206 C>T maps to ENST00000374126 Y875Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr9:116812119 C>T maps to ENST00000374126 F846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:116812266 C>T maps to ENST00000374126 C895C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr9:116812341 C>T maps to ENST00000374126 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr9:116811399 C>T maps to ENST00000374126 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:40529864 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr3:40524128 G>T maps to NM_001145082.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:40529914 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:40529863 T>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr3:40529117 G>T maps to NM_001145082.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:40558356 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:40558066 C>T maps to NM_175888.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:40574031 C>T maps to NM_001098414.1 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr3:40573647 G>A maps to NM_001098414.1 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr3:40573693 C>T maps to NM_001098414.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr5:16451821 C>A maps to NM_033414.2 G460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr5:16463720 C>T maps to NM_033414.2 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr5:16453218 T>C maps to NM_033414.2 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr5:16465443 C>A maps to NM_033414.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr5:16453119 A>G did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr5:16465180 G>A maps to NM_033414.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr8:144732947 T>C maps to NM_014789.3 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr8:144732672 C>T maps to NM_014789.3 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A1MY-01A-11D-A142-09 chr8:144733544 C>T maps to NM_014789.3 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr8:144732158 G>A maps to NM_014789.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr8:144733082 C>T maps to NM_014789.3 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr17:16525618 C>A maps to NM_020787.3 E861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:16525702 C>A maps to NM_020787.3 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:16526069 G>A maps to NM_020787.3 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:16526498 A>G maps to NM_020787.3 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:16537199 C>A maps to NM_020787.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:16526015 G>A maps to NM_020787.3 D728D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr17:16526137 G>A maps to NM_020787.3 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A177-01A-21D-A12J-09 chr17:16526900 T>C maps to NM_020787.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:16525618 C>A maps to NM_020787.3 E861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:12258605 G>T maps to ENST00000439556 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:12256527 G>A maps to ENST00000439556 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:20808274 A>G maps to NM_001076675.2 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:20807842 C>T maps to NM_001076675.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:11728116 C>T maps to NM_145295.3 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr19:11728496 T>C maps to NM_145295.3 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:11727864 C>T maps to NM_145295.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:11728368 C>T maps to NM_145295.3 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:11725642 A>T maps to NM_145295.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R9-01A-11D-A10B-09 chr19:55994491 C>T maps to NM_033113.2 H640H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:55994966 C>T maps to NM_033113.2 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:55993063 C>T maps to NM_033113.2 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:55992658 G>A maps to NM_033113.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr23:47918478 C>T did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47918711 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47919272 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:47919231 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47918205 G>T did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr23:47917907 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47918310 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:47919547 C>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:47918094 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:47918467 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47918294 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47919429 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:47918821 G>A did not map to a codon.
Sequencing variant TCGA-BG-A0VW-01A-11D-A122-09 chr23:47918042 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47918631 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47919189 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:47920306 C>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47918558 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:47918966 C>A did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:47918336 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LD-01A-11W-A062-09 chr2:71650294 T>C maps to NM_014497.3 I1217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:71654179 C>T maps to NM_014497.3 P1727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:71631008 G>T maps to NM_014497.3 E947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:71658541 G>A maps to NM_014497.3 A1912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:71633281 C>T maps to NM_014497.3 R1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:71653994 C>T maps to NM_014497.3 L1666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:71655768 C>T maps to NM_014497.3 Q1880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr2:71576704 T>C maps to NM_014497.3 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr2:71576788 T>C maps to NM_014497.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:71591333 C>T maps to NM_014497.3 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr2:71577100 G>A maps to NM_014497.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:179051879 T>C maps to NM_016331.1 C376C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:179051766 G>T maps to NM_016331.1 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr3:179052170 G>A maps to NM_016331.1 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr3:179051330 G>A maps to NM_016331.1 W193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:179052047 A>G maps to NM_016331.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr3:179051975 T>C maps to NM_016331.1 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr12:48737361 G>T maps to NM_152320.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr12:48736908 C>T maps to NM_152320.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr1:40945116 G>C maps to NM_198494.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:40961388 C>T maps to NM_198494.2 C413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:40960986 C>A maps to NM_198494.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:40961574 C>A maps to NM_198494.2 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:40961716 C>T maps to NM_198494.2 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:40928222 C>T maps to NM_023070.2 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:40928927 T>C maps to NM_023070.2 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:40919908 C>T maps to NM_023070.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:91404728 C>A maps to NM_201269.1 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:91405065 A>G maps to NM_201269.1 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr1:91383649 T>C maps to NM_201269.1 T1250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:91406448 A>T maps to NM_201269.1 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr1:91406184 C>T maps to NM_201269.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:22291567 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:22291472 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:22291567 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:22291372 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:22291583 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:22291956 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr23:22292159 C>T did not map to a codon.
Sequencing variant TCGA-BG-A18A-01A-21D-A12J-09 chr23:22291375 T>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:22291513 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:22291135 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:22291301 A>C did not map to a codon.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr23:22291567 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr23:22291387 C>A did not map to a codon.
Sequencing variant TCGA-D1-A176-01A-11D-A12J-09 chr23:22291874 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:31089639 G>T maps to NM_014699.3 R665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr16:31089027 C>T maps to NM_014699.3 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:31089879 G>A maps to NM_014699.3 E745E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:31087726 G>T maps to NM_014699.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:31091073 G>A maps to NM_014699.3 G1143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr16:31087689 C>T maps to NM_014699.3 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr16:31090566 G>A maps to NM_014699.3 E974E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr16:31092801 T>G maps to NM_014699.3 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr1:182025534 G>A maps to NM_001009992.1 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:182026461 C>T maps to NM_001009992.1 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:52394853 C>A maps to NM_023074.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:52394853 C>A maps to NM_023074.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:47394292 G>A maps to NM_014897.2 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:11606858 C>T maps to NM_138783.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:11609114 C>T maps to NM_138783.3 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:11598296 G>A maps to NM_138783.3 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:88189842 C>A maps to NM_018293.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0WQ-01A-21D-A10G-09 chr3:88189042 C>T maps to NM_018293.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:99160004 C>T maps to NM_024061.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:99169893 C>T maps to NM_001083956.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:40774335 A>G maps to NM_033160.5 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr9:40772207 C>A maps to NM_033160.5 E1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr9:40773861 A>G maps to NM_033160.5 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:40773215 C>A maps to NM_033160.5 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr9:40774535 C>A maps to NM_033160.5 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr9:40773290 C>A maps to NM_033160.5 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17D-01A-12D-A12J-09 chr9:40774962 G>T maps to NM_033160.5 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr9:40773321 A>G maps to NM_033160.5 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr3:44636228 C>T maps to NM_173658.1 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:44635903 G>A maps to NM_173658.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:42950328 C>T maps to NM_001134656.1 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr3:42956791 C>T maps to NM_001134656.1 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:42950306 G>A maps to NM_001134656.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:42956155 C>T maps to NM_001134656.1 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:42949562 G>A maps to NM_001134656.1 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:42956030 G>T maps to NM_001134656.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr3:42956402 G>T maps to NM_001134656.1 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UA-01A-11D-A122-09 chr3:42956104 T>C maps to NM_001134656.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:42956030 G>T maps to NM_001134656.1 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16D-01A-11D-A12J-09 chr3:42949566 C>A maps to NM_001134656.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:53668551 G>A maps to NM_024733.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:53668901 G>A maps to NM_024733.3 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:56973781 G>T maps to ENST00000342634 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:56953900 G>A maps to ENST00000342634 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:56953007 G>A maps to ENST00000342634 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:56953298 C>T maps to ENST00000342634 E483E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:56953841 G>A maps to ENST00000342634 C302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:56953007 G>A maps to ENST00000342634 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DI-A0WH-01A-12D-A12J-09 chr19:56952551 T>C maps to ENST00000342634 T732T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B5-A0JR-01A-13W-A062-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-B5-A11Q-01A-11D-A122-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:247264206 A>G maps to NM_024804.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:247264257 A>C maps to NM_024804.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:247201248 G>T maps to NM_033213.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:247201239 A>G maps to NM_033213.3 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:58232361 C>T maps to ENST00000335820 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:58232505 G>A maps to ENST00000335820 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:249142663 C>T maps to NM_024836.1 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:249142606 C>T maps to NM_024836.1 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05S-01A-11W-A027-09 chr1:249142830 A>C maps to NM_024836.1 *453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:46332263 C>G did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:46332343 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:46359305 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:46388265 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:46359893 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:46388269 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr23:46359380 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LI-01A-11W-A062-09 chr23:46359559 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:46360490 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:46360674 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:46360736 T>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:46359974 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:46360258 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:46388269 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:46359625 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:46359725 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:46359809 C>T did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:46359809 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:46359809 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr23:46360497 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:46359641 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:46359809 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:46360376 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:46359459 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:46359641 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:46360318 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:46359893 C>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:23836426 G>T maps to NM_138330.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:23836888 T>C maps to NM_138330.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:23845929 C>A maps to NM_138330.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:23836291 C>T maps to NM_138330.2 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:23837076 T>G maps to NM_138330.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:22363726 G>A maps to NM_001001411.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:22375862 C>A maps to NM_001001411.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:53740593 A>G maps to NM_182609.2 N462N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A1C7-01A-11D-A135-09 chr19:53747108 T>C maps to NM_182609.2 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16Y-01A-31D-A12J-09 chr19:53741031 C>T maps to NM_182609.2 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr1:227842046 T>G maps to NM_178549.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:227842671 G>T maps to NM_178549.3 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZS-01A-11D-A122-09 chr1:227842418 C>T maps to NM_178549.3 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:63721221 C>A maps to NM_153363.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr7:63726331 C>T maps to NM_153363.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:63726373 C>T maps to NM_153363.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:63982234 A>G maps to NM_178558.4 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:63981868 A>G maps to NM_178558.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr7:63981623 G>T maps to NM_178558.4 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:23927271 A>G maps to NM_138286.2 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:23926863 A>G maps to NM_138286.2 H496H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:20117928 C>A maps to NM_033196.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:20117851 G>T maps to NM_033196.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:26691715 C>T maps to ENST00000436292 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:41007368 C>T maps to NM_152373.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:41006373 C>A maps to NM_152373.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:41012465 C>T maps to NM_152373.3 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr1:41012684 C>T maps to NM_152373.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0R8-01A-11D-A10B-09 chr1:151259081 C>T maps to NM_020832.1 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:151258973 C>A maps to NM_020832.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:151259342 G>A maps to NM_020832.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:151259492 C>T maps to NM_020832.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:151261868 C>T maps to NM_020832.1 C829C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:151263366 T>C maps to NM_020832.1 D1132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:151262467 G>A maps to NM_020832.1 K983K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr1:151259294 G>A maps to NM_020832.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:30581395 G>A maps to NM_145271.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr16:30616382 G>A maps to NM_138447.1 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr16:30615593 G>A maps to NM_138447.1 N498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr19:12016513 T>C maps to ENST00000429654 H434H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr1:43317576 C>T maps to ENST00000372503 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:43317423 G>A maps to ENST00000442768 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:249151511 C>T maps to NM_001136036.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:249151676 T>C maps to NM_001136036.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:247150604 C>T maps to NM_020394.3 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr1:247151060 G>A maps to NM_020394.3 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:247150322 G>T maps to NM_020394.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr1:247151183 C>T maps to NM_020394.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr8:144378624 C>T maps to NM_030895.2 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:120168575 C>A maps to NM_001080470.1 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr19:9413060 G>T maps to NM_198535.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:9406272 G>A maps to NM_198535.1 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:9406960 G>A maps to NM_198535.1 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:9407497 G>T maps to NM_198535.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:9406752 G>A maps to NM_198535.1 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr8:146067085 C>T maps to ENST00000446747 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:146067238 G>A maps to ENST00000446747 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:24086397 G>A maps to NM_021916.2 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr22:24086397 G>A maps to NM_021916.2 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr22:24087147 A>G maps to NM_021916.2 N60N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:12059357 A>G maps to NM_144566.1 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:12059124 G>T maps to NM_144566.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:12060677 T>C maps to NM_144566.1 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:12059391 G>T maps to NM_144566.1 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:12060492 C>T maps to NM_144566.1 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:12060660 C>T maps to NM_144566.1 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:53077411 T>C maps to NM_001172655.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:53085968 G>A maps to NM_001172655.1 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr19:53086579 C>G maps to NM_001172655.1 S489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr8:81553672 G>A maps to NM_001033723.2 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr8:81577109 C>T maps to NM_001033723.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr12:8327894 G>T maps to NM_001004328.2 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr12:8330010 A>G maps to NM_001004328.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr8:102213963 A>G maps to NM_016096.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0MQ-01A-11D-A10B-09 chr8:144776687 C>T maps to NM_173831.3 H368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:21476329 C>A maps to NM_021269.2 E480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:21477461 T>C maps to NM_021269.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11V-01A-11D-A10M-09 chr19:21477020 C>T maps to NM_021269.2 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:21477131 C>T maps to NM_021269.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:21476837 A>G maps to NM_021269.2 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:12575673 A>G maps to ENST00000428311 H354H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr19:12576176 C>A maps to ENST00000428311 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:12576017 G>A maps to ENST00000428311 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:12577664 C>A did not map to a codon.
Sequencing variant TCGA-D1-A174-01A-11D-A12J-09 chr19:12576281 G>A maps to ENST00000428311 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:57133899 C>T maps to NM_021216.4 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:57133098 C>T maps to NM_021216.4 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:57133821 G>A maps to NM_021216.4 K389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:57134040 C>T maps to NM_021216.4 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:57134053 C>T maps to NM_021216.4 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:90611250 C>T maps to NM_198526.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr15:90611130 C>T maps to NM_198526.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr15:90611604 C>T maps to NM_198526.2 C412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:90610809 C>T maps to NM_198526.2 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr15:90611130 C>T maps to NM_198526.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr15:90611565 G>T maps to NM_198526.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr23:84526799 A>C did not map to a codon.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr23:84526278 T>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:84525717 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:84526416 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:84510353 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:84519342 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:84526682 G>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:84525066 A>C did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:84525756 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:84510588 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:84510293 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:84526416 C>G did not map to a codon.
Sequencing variant TCGA-B5-A11G-01A-13D-A122-09 chr23:84525986 A>G did not map to a codon.
Sequencing variant TCGA-BG-A0VX-01A-11D-A122-09 chr23:84525090 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:84510493 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:84510623 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:84525738 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr23:84526236 A>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:84525769 C>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:84525895 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:84526090 C>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:84526519 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:84526668 G>T did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:84526780 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:84526107 C>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:55991327 C>T maps to NM_182633.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:21300876 A>G maps to NM_182515.3 K469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:57529246 C>A maps to NM_001159279.1 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr7:57522779 T>C maps to NM_001159279.1 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:57529615 G>A maps to NM_001159279.1 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:57529183 T>C maps to NM_001159279.1 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:57529064 G>T maps to NM_001159279.1 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr16:31733951 G>T maps to NM_001130913.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr4:436023 C>T maps to NM_133474.2 K744K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr4:435491 G>A maps to NM_133474.2 Q922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:437750 C>A maps to NM_133474.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr4:435780 A>G maps to NM_133474.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:436635 C>T maps to NM_133474.2 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:435882 C>T maps to NM_133474.2 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17R-01A-11D-A12J-09 chr4:435960 G>T maps to NM_133474.2 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr4:266263 C>A maps to ENST00000419098 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr4:289322 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr4:265205 G>T maps to ENST00000419098 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr4:266311 C>A maps to ENST00000419098 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:266363 C>T maps to ENST00000419098 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr4:289913 C>A maps to ENST00000419098 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr4:266086 C>A maps to ENST00000419098 G187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr4:265322 A>G maps to ENST00000419098 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:63809155 A>C maps to NM_001170905.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:63808726 A>G maps to NM_001170905.1 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:20736527 G>A maps to NM_001159293.1 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:20728762 G>A maps to NM_001159293.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:20727799 G>A maps to NM_001159293.1 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:20736610 C>A maps to NM_001159293.1 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:20727495 C>A maps to NM_001159293.1 G505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr22:20760528 C>T maps to NM_003426.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LP-01A-12D-A10B-09 chr22:20748843 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr12:53580193 C>T maps to NM_001004304.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr7:149174748 C>T maps to NM_001163474.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr7:149172575 T>C did not map to a codon.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr7:149191450 G>A maps to NM_001163474.1 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:149171867 C>T maps to NM_001163474.1 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:57956277 G>T maps to NM_001023561.2 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:57955494 G>T maps to NM_001023561.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:57955046 G>A maps to NM_001023561.2 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VQ-01A-11D-A10B-09 chr17:80789037 G>A maps to NM_024702.2 Y431Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr17:80789802 G>A maps to NM_024702.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr17:80789955 G>A maps to NM_024702.2 C125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr17:80788674 C>T maps to NM_024702.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr17:80789049 G>A maps to NM_024702.2 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A18B-01A-11D-A12J-09 chr17:80789424 G>A maps to NM_024702.2 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:134421136 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:134427910 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:134421610 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:134426230 C>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:134427984 C>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:134421701 G>A did not map to a codon.
Sequencing variant TCGA-AX-A05U-01A-11W-A027-09 chr23:134424988 T>G did not map to a codon.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr23:134427805 C>A did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:134421447 C>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:134421701 G>A did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:134426247 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:35258083 G>A maps to NM_003427.3 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:53959098 C>A maps to NM_001008401.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr19:53959461 C>A maps to NM_001008401.3 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:53952847 C>T maps to NM_001008401.3 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:53958639 T>C maps to NM_001008401.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:53959104 C>T maps to NM_001008401.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:53959647 C>T maps to NM_001008401.3 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:12089300 C>T maps to NM_001012753.1 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LG-01A-11W-A062-09 chr19:12089468 C>T maps to NM_001012753.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:12089264 G>T maps to NM_001012753.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:12089300 C>T maps to NM_001012753.1 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:53911542 C>T maps to NM_001040185.1 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:53911578 C>T maps to NM_001040185.1 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr19:53911668 A>T maps to NM_001040185.1 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:52793401 G>T maps to NM_001010851.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:52794309 G>A maps to NM_001010851.2 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr19:52793484 G>A maps to NM_001010851.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:52793572 G>T maps to NM_001010851.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr16:30536962 T>C maps to NM_024671.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr16:30536628 G>A maps to NM_024671.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:2934575 C>T maps to NM_021217.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:2933630 C>T maps to NM_021217.2 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr15:35275289 T>G maps to NM_014106.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr15:35274941 G>A maps to NM_014106.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr15:35273759 G>A maps to NM_014106.3 R626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr19:57985397 G>A maps to NM_001024596.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:57984968 G>A maps to NM_001024596.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:58018350 C>A maps to NM_198542.1 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:58018434 T>C maps to NM_198542.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr15:90904217 C>T maps to NM_001004309.2 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr15:90904268 C>T maps to NM_001004309.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0K8-01A-11D-A14K-09 chr7:150094993 G>A maps to NM_173680.3 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr7:150094999 C>T maps to NM_173680.3 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:150093892 A>G maps to NM_173680.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr19:58265197 G>T maps to NM_173632.3 G234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:58265271 C>T maps to NM_173632.3 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58265719 G>T maps to NM_173632.3 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:58264938 G>A maps to NM_173632.3 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:149129022 G>A maps to ENST00000440594 C781C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr16:89294507 A>G maps to NM_182531.2 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr16:89293466 G>A maps to NM_182531.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr16:89294057 C>T maps to NM_182531.2 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:89289663 G>T maps to NM_182531.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:89294207 C>A maps to NM_182531.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr16:89293932 C>T maps to NM_182531.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:89293932 C>T maps to NM_182531.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:89294387 G>A maps to NM_182531.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:40581405 G>A maps to NM_001142577.1 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:40581376 G>A maps to NM_001142577.1 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:40580706 G>A maps to NM_001142577.1 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:40541799 T>C maps to NM_001005851.2 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:40541835 A>G maps to NM_001005851.2 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:40541778 G>A maps to NM_001005851.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:40541304 C>T maps to NM_001005851.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:40541574 G>T maps to NM_001005851.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:40540575 G>A maps to NM_001005851.2 C730C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr19:40540722 A>G maps to NM_001005851.2 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:40554702 C>A maps to NM_001005851.2 G4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:38160134 T>C maps to NM_152605.3 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:38160220 C>A maps to NM_152605.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:38160220 C>A maps to NM_152605.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:38160220 C>A maps to NM_152605.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:38160220 C>A maps to NM_152605.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr9:99589419 T>C maps to NM_001001662.1 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:99580534 A>C maps to NM_001001662.1 Y590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr9:99580912 G>A maps to NM_001001662.1 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr16:30594426 G>A maps to NM_152458.6 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A06H-01A-11D-A122-09 chr16:30594327 C>T maps to NM_152458.6 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:148771558 C>A maps to NM_152411.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:148771550 C>T maps to NM_152411.3 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:148769329 G>A maps to NM_152411.3 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr7:148768375 C>T maps to NM_152411.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr9:130207085 C>A maps to NM_007135.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr9:130207397 C>T maps to NM_007135.2 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:37309643 G>A maps to NM_206894.2 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:37314274 G>A maps to NM_206894.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:37309640 T>C maps to NM_206894.2 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:37309594 G>A maps to NM_206894.2 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:12735513 C>T maps to NM_153358.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:35451775 C>T maps to NM_175872.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr19:35449333 C>T maps to NM_175872.4 E475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:38028711 A>G maps to NM_001013659.2 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:38028285 C>T maps to NM_001013659.2 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:38028240 C>T maps to NM_001013659.2 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:12501902 G>A maps to NM_001080821.2 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:12501618 C>T maps to NM_001080821.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:12502451 C>A maps to NM_001080821.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr19:58805557 G>A maps to NM_021089.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:58805719 C>T maps to NM_021089.2 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr19:58806130 G>A maps to NM_021089.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:58806562 C>T maps to NM_021089.2 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:113955339 G>A maps to NM_007136.3 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr3:113955645 G>A maps to NM_007136.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr3:113955600 G>A maps to NM_007136.3 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr3:113955492 G>A maps to NM_007136.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr3:113955906 G>A maps to NM_007136.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr7:127014843 C>T maps to NM_176814.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:127014945 C>T maps to NM_176814.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr7:127014677 C>A maps to NM_176814.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:127014677 C>A maps to NM_176814.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr7:127014945 C>T maps to NM_176814.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:127013393 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:127014332 C>A maps to NM_176814.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr7:127014980 C>A maps to NM_176814.3 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:185801718 C>T maps to NM_194250.1 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:185803686 C>T maps to NM_194250.1 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:185802233 C>A maps to NM_194250.1 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:185802717 C>T maps to NM_194250.1 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr2:185803011 G>A maps to NM_194250.1 Q963Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr2:185800794 G>T maps to NM_194250.1 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11F-01A-11D-A10M-09 chr2:185802430 C>T maps to NM_194250.1 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr2:185802717 C>T maps to NM_194250.1 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:185802000 C>T maps to NM_194250.1 Y626Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:185802502 G>T maps to NM_194250.1 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:185801019 C>A maps to NM_194250.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr2:185802288 C>T maps to NM_194250.1 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr7:88964770 C>T maps to NM_181646.2 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:88963245 C>A maps to NM_181646.2 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr7:88847527 C>T maps to NM_181646.2 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr7:88964092 G>A maps to NM_181646.2 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:88963216 C>T maps to NM_181646.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:88964395 T>C maps to NM_181646.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:88956755 T>C maps to NM_181646.2 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LW-01A-11W-A062-09 chr7:88963753 G>A maps to NM_181646.2 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:88965184 C>T maps to NM_181646.2 C963C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr7:88963160 G>T maps to NM_181646.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:57765335 C>T maps to NM_001023563.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr19:57765113 C>T maps to NM_001023563.3 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FI-A2EW-01A-11D-A17D-09 chr19:57764654 C>A maps to NM_001023563.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr19:53058550 G>A maps to NM_001039886.3 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr19:53057923 T>C maps to NM_001039886.3 H585H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr19:53056765 G>A maps to NM_001039886.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:47747451 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47774499 G>A did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47774689 G>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47774968 A>C did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:47775305 A>C did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:47774572 T>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:47774360 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:47775055 G>T did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:47775884 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47774499 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr23:47775513 G>T did not map to a codon.
Sequencing variant TCGA-D1-A161-01A-11D-A122-09 chr23:47774614 T>G did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:47775780 A>G did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:47775350 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:47705706 G>A did not map to a codon.
Sequencing variant TCGA-DI-A1NN-01A-11D-A16D-09 chr23:47775607 T>C did not map to a codon.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:53995085 C>T maps to NM_001004301.3 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:53994334 G>A maps to NM_001004301.3 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr19:53993755 T>C maps to NM_001004301.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:58388364 C>A maps to NM_001144989.1 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:58386367 A>G maps to NM_001144989.1 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr16:71898858 C>A maps to ENST00000425432 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:11833580 G>T maps to NM_001080493.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:11836079 A>G maps to NM_001080493.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:11833412 C>T maps to NM_001080493.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:11832637 G>A maps to NM_001080493.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr19:11833229 C>T maps to NM_001080493.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:11833306 G>A maps to NM_001080493.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GI-01A-11W-A062-09 chr4:146686735 G>A maps to ENST00000508784 S1005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GW-01A-11W-A062-09 chr4:146824170 C>T maps to ENST00000508784 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr4:146823495 C>T maps to ENST00000508784 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:37398888 C>T maps to NM_001171979.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:53116457 C>A maps to NM_018300.3 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:53117118 G>A maps to NM_018300.3 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:53117465 C>A maps to NM_018300.3 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:53164096 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17A-01A-11D-A12J-09 chr17:33288788 T>G maps to NM_052857.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr20:57766295 C>T maps to NM_178457.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:57766658 G>A maps to NM_178457.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr20:57829789 G>T maps to NM_178457.1 E1676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:57769616 G>A maps to NM_178457.1 P1181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:57768533 A>G maps to NM_178457.1 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:57175945 C>T maps to NM_001005850.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:57174988 G>A maps to NM_001005850.1 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:57176230 G>A maps to NM_001005850.1 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:57175249 C>T maps to NM_001005850.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11H-01A-11D-A122-09 chr19:57175129 G>A maps to NM_001005850.1 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:57175726 G>A maps to NM_001005850.1 C302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:52659623 C>A maps to NM_001102657.1 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:52659959 C>A maps to NM_001102657.1 G326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:52663813 C>A maps to NM_001102657.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr14:102807771 A>G maps to NM_018335.3 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr14:102808332 C>T maps to NM_018335.3 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr14:102798158 G>A maps to NM_018335.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr14:102792357 G>T maps to NM_018335.3 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:52570423 T>C maps to NM_001136499.1 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:52570089 C>A maps to NM_001136499.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:52568527 T>G maps to NM_001136499.1 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr19:52569475 A>G maps to NM_001136499.1 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:52569285 G>A maps to NM_001136499.1 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:12186585 A>G maps to NM_001136501.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr19:12186451 G>T maps to NM_001136501.1 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:12187551 A>G maps to NM_001136501.1 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:53854365 G>A maps to NM_138374.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:53855457 T>C maps to NM_138374.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:53855870 C>A maps to NM_138374.1 S648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr19:21116859 G>T maps to NM_003429.4 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:21132894 T>G maps to NM_003429.4 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr19:21132216 A>G maps to NM_003429.4 S299S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-D1-A17Q-01A-11D-A12J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr3:32031755 G>A maps to NM_001137674.1 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr3:32031356 A>G maps to NM_001137674.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr7:149558039 G>A maps to NM_001099220.1 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr7:149557916 G>A maps to NM_001099220.1 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr7:149559176 C>T maps to NM_001099220.1 F976F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr7:149558306 G>T maps to NM_001099220.1 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr7:149559176 C>T maps to NM_001099220.1 F976F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:12154643 C>T maps to NM_001080404.1 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:12155459 C>T maps to NM_001080404.1 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:52887738 C>T maps to NM_001145434.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr19:52887562 G>T maps to NM_001145434.1 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr9:115759443 G>A maps to NM_001101338.1 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr9:115760053 G>A maps to NM_001101338.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:20229796 G>A maps to NM_007138.1 E478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:23556598 C>T maps to NM_003430.2 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:23543170 C>T maps to NM_003430.2 T870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:23544790 A>C maps to NM_003430.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:23545371 C>A maps to NM_003430.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:23557530 G>A maps to NM_003430.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:23557535 C>A maps to NM_003430.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr7:64863891 G>T maps to NM_152626.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr7:64864589 C>A maps to NM_152626.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:20044039 A>G maps to NM_031218.3 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:20026118 G>T maps to NM_031218.3 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr19:20044255 T>C maps to NM_031218.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:20045074 C>T maps to NM_031218.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:20045515 G>A maps to NM_031218.3 K584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:22574905 G>T maps to NM_001098626.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:22575370 G>T maps to NM_001098626.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:22574640 C>A maps to NM_001098626.1 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr19:22585635 C>A maps to NM_001098626.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:22940307 G>T maps to ENST00000397104 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:22939404 G>A maps to ENST00000397104 G922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:22941761 C>A maps to ENST00000397104 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr19:22940427 G>A maps to ENST00000397104 C670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:22940095 G>T maps to ENST00000397104 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr19:22942299 C>T maps to ENST00000397104 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr19:22939830 C>A maps to ENST00000397104 E834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VP-01A-21D-A10B-09 chr20:47869319 A>T maps to NM_021035.2 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr20:47864310 G>A maps to NM_021035.2 S1750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:47864724 G>A maps to NM_021035.2 V1612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:47864729 C>A maps to NM_021035.2 E1611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr20:47865696 G>A maps to NM_021035.2 C1288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr20:47887420 G>A maps to NM_021035.2 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr20:47865237 G>A maps to NM_021035.2 C1441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr20:47887208 G>A maps to NM_021035.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr11:64884275 G>A maps to NM_014205.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:86173388 G>A maps to NM_017953.3 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:86171988 G>A maps to NM_017953.3 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr1:86167898 T>C maps to NM_017953.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr1:86171988 G>A maps to NM_017953.3 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:75127536 T>C maps to ENST00000320619 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:29440866 C>T maps to NM_032173.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr22:29445386 C>T maps to NM_032173.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr22:29445206 G>A maps to NM_032173.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr11:60638697 C>T maps to NM_207341.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr11:60638479 G>T maps to NM_207341.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr11:60638457 C>A maps to NM_207341.2 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr11:60640950 C>T maps to NM_207341.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr11:60638457 C>T maps to NM_207341.2 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr11:60636619 G>T maps to NM_207341.2 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr16:21222862 C>T maps to NM_003460.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:21210893 G>A maps to NM_003460.1 R642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr16:21215509 T>C maps to NM_003460.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr16:21214545 C>T maps to NM_003460.1 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr16:21218197 C>T maps to NM_003460.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr16:21211171 C>T maps to NM_003460.1 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:76069797 C>T maps to NM_001110354.1 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UM-01A-11W-A10C-09 chr7:76071157 G>A did not map to a codon.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:238053191 C>T maps to NM_021186.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:238053193 G>A maps to NM_021186.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JR-01A-13W-A062-09 chr1:238051655 A>G did not map to a codon.
Sequencing variant TCGA-BS-A0U8-01A-11D-A10B-09 chr1:238053461 G>A maps to NM_021186.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GA-01A-11W-A062-09 chr7:49977132 C>T maps to NM_007009.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr7:50129252 C>T maps to NM_007009.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr7:50121487 C>T maps to NM_007009.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A05Z-01A-11W-A027-09 chr17:38027873 C>A maps to NM_199321.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr3:102175035 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:126631520 G>A maps to NM_017580.2 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr10:126660592 A>G maps to NM_017580.2 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:71534966 C>T maps to NM_203350.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:71544138 C>T did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr1:71544350 G>A maps to NM_203350.2 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11R-01A-11D-A122-09 chr1:71546639 C>T maps to NM_203350.2 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UJ-01A-12D-A10B-09 chr1:71544237 A>C maps to NM_203350.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr2:136261909 T>C maps to NM_032143.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:135965228 C>T maps to NM_032143.2 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr2:135988494 G>A maps to NM_032143.2 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:135985427 T>C maps to NM_032143.2 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr2:136107736 G>A maps to NM_032143.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr2:135965173 G>A maps to NM_032143.2 R947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16F-01A-11D-A12J-09 chr2:135988146 G>A maps to NM_032143.2 C630C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr23:15841112 T>C did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:15836764 C>T did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:15840882 G>T did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:15809113 A>G did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:15822289 G>T did not map to a codon.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr23:15838411 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17U-01A-21D-A12J-09 chr23:15841225 G>A did not map to a codon.
Sequencing variant TCGA-B5-A0JZ-01A-11W-A062-09 chr19:58564854 C>T maps to NM_182572.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr19:58565097 C>A maps to NM_182572.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr16:3140387 G>A maps to NM_032805.1 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr16:3142761 C>A maps to NM_032805.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A1NU-01A-11D-A14G-09 chr16:3141574 C>A maps to NM_032805.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr6:28366170 A>C maps to ENST00000396827 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:28359366 C>A maps to ENST00000396827 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr6:28360756 C>A maps to ENST00000396827 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr6:28358884 A>G maps to ENST00000396827 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:28097709 C>T maps to NM_025231.1 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr19:58619250 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr19:58619924 C>A did not map to a codon.
Sequencing variant TCGA-D1-A17H-01A-11D-A12J-09 chr19:58619357 A>G did not map to a codon.
Sequencing variant TCGA-A5-A0GH-01A-21W-A062-09 chr1:33959108 G>A maps to NM_145238.3 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr1:33956668 G>T maps to NM_145238.3 G271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:33959906 G>T maps to NM_145238.3 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EY-A1GS-01A-11D-A13L-09 chr1:33954721 C>T maps to NM_145238.3 L204L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A5-A0GA-01A-11W-A062-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr19:58850364 C>T maps to NM_181846.2 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:28402286 G>A maps to NM_001012455.1 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:28402616 G>A maps to NM_001012455.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr6:28403737 C>T maps to NM_001012455.1 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A051-01A-21W-A027-09 chr15:43653546 G>T maps to NM_152455.3 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr15:43656578 A>G maps to NM_152455.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr15:43658788 G>A maps to NM_152455.3 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TJ-01A-11D-A10B-09 chr19:58189813 C>A maps to NM_152677.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr19:58187870 G>T maps to NM_152677.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:56736247 C>T maps to NM_024303.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr19:56736304 G>A maps to NM_024303.1 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr19:56733195 C>T maps to NM_024303.1 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0LX-01A-11W-A062-09 chr19:56701372 C>T maps to NM_001080456.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A060-01A-11W-A027-09 chr20:44511875 A>G maps to NM_080603.4 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr20:44511372 C>T maps to NM_080603.4 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr20:44512484 G>A maps to NM_080603.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GP-01A-11W-A062-09 chr2:187702136 G>A maps to NM_182521.2 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr2:187709484 C>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr2:187702088 G>A maps to NM_182521.2 H229H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr2:187713815 G>A maps to NM_182521.2 H14H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr2:187692718 G>A maps to NM_182521.2 Q632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0VO-01A-21D-A10G-09 chr19:13941179 C>T maps to NM_023072.2 C762C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr19:13928534 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr1:45553825 G>A maps to NM_020883.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:45504674 G>A maps to NM_020883.1 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BK-A0C9-01A-11W-A027-09 chr1:45524298 G>A maps to NM_020883.1 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:45553825 G>A maps to NM_020883.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr6:116977970 T>C maps to NM_145062.2 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0M4-01A-11W-A10C-09 chr6:116987839 A>G maps to NM_145062.2 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11Y-01A-21D-A10M-09 chr11:113614597 G>T maps to NM_004724.2 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11U-01A-11D-A122-09 chr15:66801171 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:66801171 G>A did not map to a codon.
Sequencing variant TCGA-D1-A15X-01A-11D-A122-09 chr15:66840998 T>A did not map to a codon.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr10:58119845 C>T maps to NM_032997.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A5-A0GB-01A-11W-A062-09 chr23:57935716 G>A did not map to a codon.
Sequencing variant TCGA-AP-A054-01A-11W-A062-09 chr23:57935546 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:57935216 C>T did not map to a codon.
Sequencing variant TCGA-AP-A056-01A-11W-A027-09 chr23:57935840 G>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:57935705 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:57935804 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:57934545 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LM-01A-11D-A122-09 chr23:57936184 G>A did not map to a codon.
Sequencing variant TCGA-AP-A0LT-01A-11W-A062-09 chr23:57935315 A>G did not map to a codon.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr23:57935741 C>T did not map to a codon.
Sequencing variant TCGA-B5-A0K2-01A-12W-A10C-09 chr23:57935853 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0TA-01A-11D-A10B-09 chr23:57935817 T>G did not map to a codon.
Sequencing variant TCGA-BS-A0TE-01A-11D-A10B-09 chr23:57935262 G>A did not map to a codon.
Sequencing variant TCGA-BS-A0UL-01A-11D-A10G-09 chr23:57935668 A>G did not map to a codon.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr23:57934963 T>C did not map to a codon.
Sequencing variant TCGA-D1-A16X-01A-11D-A12J-09 chr23:57935852 C>T did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:57935324 G>A did not map to a codon.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr23:57935421 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:57620064 C>T did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:57620130 G>A did not map to a codon.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr23:57620267 G>T did not map to a codon.
Sequencing variant TCGA-AP-A0LF-01A-11D-A122-09 chr23:57620424 C>A did not map to a codon.
Sequencing variant TCGA-AX-A063-01A-11W-A027-09 chr23:57619723 C>T did not map to a codon.
Sequencing variant TCGA-AX-A064-01A-11W-A027-09 chr23:57620267 G>A did not map to a codon.
Sequencing variant TCGA-AX-A0J0-01A-11D-A117-09 chr23:57620488 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr23:57619642 G>A did not map to a codon.
Sequencing variant TCGA-B5-A11N-01A-11D-A122-09 chr23:57619914 C>T did not map to a codon.
Sequencing variant TCGA-D1-A160-01A-11D-A122-09 chr23:57620825 C>T did not map to a codon.
Sequencing variant TCGA-D1-A16J-01A-11D-A12J-09 chr23:57619770 C>T did not map to a codon.
Sequencing variant TCGA-A5-A0G9-01A-11W-A062-09 chr3:126191100 G>A maps to NM_025112.4 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A167-01A-11D-A12J-09 chr3:126160634 C>T maps to NM_025112.4 A789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:53279585 T>C did not map to a codon.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr1:53237430 C>T maps to NM_024646.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr1:53282301 G>A did not map to a codon.
Sequencing variant TCGA-D1-A0ZO-01A-11D-A122-09 chr7:143079446 C>A maps to NM_001010972.1 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A163-01A-11D-A12J-09 chr7:143085431 G>T maps to NM_001010972.1 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A0LE-01A-11D-A127-09 chr17:3968073 C>A maps to NM_015113.3 T1433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:3920904 G>A maps to NM_015113.3 S2587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr17:3984768 G>A maps to NM_015113.3 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:3921171 G>A maps to NM_015113.3 S2533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr17:3968117 C>A maps to NM_015113.3 E1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11E-01A-11D-A10M-09 chr17:3937465 A>G maps to NM_015113.3 L2143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A11J-01A-11D-A122-09 chr17:3955431 T>C did not map to a codon.
Sequencing variant TCGA-BG-A0VZ-01A-11D-A10G-09 chr17:3981219 C>T maps to NM_015113.3 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UF-01A-11D-A10B-09 chr17:3989046 C>A maps to NM_015113.3 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:3920916 G>A maps to NM_015113.3 R2583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:3935506 C>A maps to NM_015113.3 E2269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BS-A0UV-01A-11D-A10B-09 chr17:3984716 C>A maps to NM_015113.3 E928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr17:3916780 G>A maps to NM_015113.3 I2847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A17Q-01A-11D-A12J-09 chr17:3970467 G>A maps to NM_015113.3 R1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:78031829 G>T maps to NM_015534.4 R835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AP-A059-01A-21D-A122-09 chr1:78044473 A>G maps to NM_015534.4 Y721Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AX-A0J1-01A-11W-A062-09 chr1:78046739 G>A maps to NM_015534.4 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B5-A0JY-01A-11D-A10B-09 chr1:78098927 C>A maps to NM_015534.4 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BG-A0W1-01A-12D-A10G-09 chr1:78045209 A>C did not map to a codon.
Sequencing variant TCGA-BS-A0TC-01A-11D-A10B-09 chr1:78098978 C>A maps to NM_015534.4 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:78031417 A>G maps to NM_015534.4 Y873Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D1-A103-01A-11D-A10M-09 chr1:78044497 T>C maps to NM_015534.4 V713V. Only missense variants will be evaluated by CHASM.
